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Discover why a humidity checker is essential for comfort, health, and home protection—get accurate moisture control insights today! < Back Why You Need a Humidity Checker Today Humidity is invisible, yet it has a powerful effect on your comfort, health, and even the condition of your home. Too much moisture in the air encourages mould growth, triggers allergies, and damages furniture. Too little humidity leads to dry skin, irritated sinuses, and uncomfortable living conditions. The easiest way to stay in control? A humidity checker. Whether you call it a hygrometer, humidity sensor, or indoor comfort monitor, it gives you accurate readings so you can make quick adjustments and protect your home. What is a humidity checker? A humidity checker is a simple device that measures the relative humidity (RH) inside your home. It’s also known as a hygrometer or humidity sensor. Two main types are available: Analog hygrometers – traditional dial-style tools that give a rough estimate. Digital hygrometers – modern versions with LCD displays, often offering more accuracy, memory, or smartphone connectivity. By reading RH as a percentage, they help you see when your indoor environment is too dry, too damp, or just right. Why monitoring humidity matters Monitoring indoor humidity isn’t just about comfort, it's about wellbeing and protecting your home. Health: High humidity above 55 to 60% RH encourages mould, dust mites, and allergens. Low humidity below 30% RH dries out skin, eyes, and sinuses, and may worsen respiratory issues. Comfort: Humidity affects how warm or cool a room feels. Dry air can make winter feel colder, while damp air makes summer heat harder to tolerate. Home Protection: Excess humidity can warp wooden floors, damage furniture, and cause paint to peel. Dry air can crack wood and shrink caulking. The EPA recommends keeping indoor humidity between 30–50% RH for best comfort and safety. How a humidity checker works Modern humidity checkers use different types of sensors to convert moisture levels into readings: Capacitive sensors – measure changes in electrical capacity as air moisture changes. Resistive sensors – detect changes in electrical resistance caused by humidity. Thermal sensors – calculate absolute humidity by comparing temperature differences. Most digital hygrometers combine these technologies for fast, accurate readings, often within ±2 to 3% RH accuracy. Choosing the right humidity checker When buying a humidity checker, keep these factors in mind: Accuracy: High quality models offer accuracy of ±2 to 3% RH. Cheaper devices may only give ±5% RH, which can make a big difference. Placement: For best results, place your checker at mid-room height, away from direct sunlight, heaters, vents, or corners that may skew readings. Features: Look for clear digital displays, comfort icons (showing dry/normal/humid ranges), memory or logging functions, smartphone connectivity, and calibration options. Simple ways to check indoor humidity The best way is to use a hygrometer. But if you don’t have one yet, here are a few quick (though less accurate) methods: Ice cube test: Place a glass of water with ice cubes in a room for a few minutes. If condensation forms on the outside, humidity may be high. If there’s no condensation, the air may be too dry. Wet and dry bulb test: A more old-fashioned but useful way to measure relative humidity using two thermometers, one wrapped in a wet cloth. Phone apps: While convenient, most only pull data from outdoor weather services, not your actual indoor conditions. What to do with the results Once you know your home’s humidity levels, here’s how to respond: If humidity is too high: Run exhaust fans or improve ventilation. Use a dehumidifier. Fix leaks and reduce moisture sources like drying clothes indoors. If humidity is too low: Run a humidifier. Add houseplants, which naturally release moisture. Place bowls of water near heating sources for gentle evaporation. The sweet spot is 30 to 50% RH, balancing comfort, health, and home protection. Benefits at a glance A humidity checker can improve life at home in many ways: Better health: fewer respiratory issues, reduced risk of mould. Increased comfort: stable indoor air that feels warmer in winter and cooler in summer. Stronger home integrity: protection for wood, furniture, and paintwork. Greater energy efficiency: optimised HVAC use by avoiding unnecessary heating or cooling. Why you need one today Humidity is silent and invisible, but its effects are real. A simple, affordable humidity checker gives you the power to take control. By keeping your home within the recommended 30 to 50% RH range, you can improve your health, feel more comfortable, and protect your home. Ready to take control of your home’s comfort and health? Contact us and start monitoring your air today! FAQs Previous Next

Learn why autoclave calibration matters in labs—assuring sterility, accuracy, and compliance with limited downtime and maximum safety. < Back Why Autoclave Calibration Is Critical for Laboratory Safety and Accuracy Autoclaves are essential in laboratories, hospitals, and research facilities. They sterilize instruments, glassware, and materials by applying high-pressure steam at elevated temperatures. For sterilization to be effective, temperature and pressure inside the chamber must be accurate and consistent. Even minor deviations can compromise sterility, posing risks to lab safety, patient health, and experimental outcomes. Autoclave calibration is the process of ensuring that the device’s sensors such as temperature probes, pressure gauges, and timers are working within specified tolerances. Without regular calibration, results can be unreliable, and compliance with laboratory standards can be compromised. A well-calibrated autoclave not only ensures accurate sterilization but also extends the lifespan of equipment by reducing unnecessary stress from improper operating conditions. What Is Autoclave Calibration? Calibration is the verification and adjustment of an autoclave’s measurement systems. It involves comparing the readings of sensors like temperature, pressure, and timer against traceable reference standards and adjusting them as needed to maintain accuracy. It is important to distinguish calibration from validation. Calibration ensures that measurement devices inside the autoclave are reading accurately. Validation, on the other hand, goes further to confirm that the entire sterilization process including temperature, pressure, steam penetration, and cycle duration consistently meets operational requirements and produces sterile outcomes. Both processes are complementary, and in most regulated industries, laboratories are required to perform both to ensure full compliance. Why Is Autoclave Calibration Critical? Accurate calibration ensures sterilization cycles reach the required conditions for destroying microorganisms. A drop of even 2 °C can drastically reduce sterilization effectiveness. For example, a cycle at 120 °C instead of 122 °C may fail to kill certain heat-resistant spores, which could lead to contaminated instruments being reintroduced into a sterile environment. Calibration also supports: Laboratory safety : Prevents incomplete sterilization that could expose staff and researchers to infectious agents. Patient and research integrity : Ensures sterile equipment for reliable medical and scientific outcomes. Inaccurate sterilization can compromise experimental results or, worse, patient safety in clinical applications. Operational efficiency : Prevents equipment failures, costly downtime, and repeat sterilization cycles that waste energy, increase maintenance costs, and reduce productivity. Regular calibration also minimizes unexpected breakdowns by catching performance issues early. Compliance, Standards, and Frequency Accredited calibration is required for labs working under regulated frameworks, particularly in pharmaceuticals, biotechnology, and healthcare. These industries must comply with rigorous standards to pass audits and maintain certifications. ISO/IEC 17025 accreditation ensures competence and traceability in calibration services, offering assurance that processes meet international best practices. NIST-traceable instruments guarantee that calibration results are accurate and defensible in audits. Frequency : Most guidelines recommend calibrating autoclaves every 6 to 12 months, depending on usage, regulatory requirements, and the risk profile of the work being conducted. Safety checks : Annual inspection of safety valves, pressure switches, gaskets, and control sensors is considered best practice to maintain reliable performance and avoid hazardous failures. By adhering to these standards, laboratories protect not only their compliance standing but also the integrity of their operations and the safety of their personnel. The Calibration Process: Step-by-Step A typical autoclave calibration process includes multiple checks to ensure reliability and accuracy of sterilization cycles: Prepare NIST-traceable reference instruments, such as precision temperature probes and pressure gauges. Record baseline “as-found” data before making any adjustments. Check and adjust zero and gain settings of the sensors. Conduct multipoint measurements across relevant temperature and pressure ranges to confirm accuracy at various operating points. Compare results with reference standards to identify discrepancies. Apply regression analysis where required to establish correction factors. Adjust calibration values accordingly using the autoclave’s control system. Verify readings with repeat measurements to confirm adjustments were successful. Document all results for traceability and compliance records. Label equipment with calibration status and due date for next calibration. Issue a traceable calibration certificate for regulatory and audit purposes. Standard operating procedures often include additional steps such as temperature mapping of the chamber to ensure even distribution, pressure gauge testing, and verification of cycle timer accuracy. Together, these steps ensure both accuracy and reproducibility of sterilization cycles. Professional Calibration Best Practices Professional autoclave calibration ensures compliance, accuracy, and reliability beyond what in-house checks can provide. Accredited service providers follow strict methodologies to maintain consistency and meet regulatory requirements. Key Best Practices Traceability : Use of NIST-traceable equipment ensures every calibration point is linked back to international standards. Controlled environment : Professional calibration is performed under stable conditions to reduce environmental influence on results. Documentation : Detailed calibration certificates are issued, including uncertainty measurements, procedures followed, and results obtained. Preventive maintenance : Professionals often combine calibration with preventive inspections, checking gaskets, safety valves, and heating elements. Audit support : Accredited calibration records provide defensible evidence during regulatory inspections and audits. Professional calibration services are indispensable in industries where sterility, compliance, and accuracy are critical, such as pharmaceuticals, food production, and clinical research. Validation vs Calibration: What Labs Should Know While calibration ensures instruments read accurately, validation verifies that the sterilization process consistently delivers sterile outcomes. Both are required for complete quality assurance. Validation typically includes: Installation Qualification (IQ) : Ensuring autoclave installation meets design and manufacturer specifications. Operational Qualification (OQ) : Confirming the autoclave operates correctly across intended parameters. Performance Qualification (PQ) : Testing actual sterilization performance using biological and chemical indicators in both empty and fully loaded conditions. Together, calibration and validation create a complete framework that ensures not only the accuracy of measurements but also the effectiveness and reproducibility of the sterilization process. Ensure Sterility and Lab Compliance Autoclave calibration is essential for ensuring sterilization efficacy, maintaining laboratory safety, meeting regulatory requirements, and extending equipment lifespan. Neglecting calibration exposes laboratories to risks such as contamination, failed audits, and potential health hazards. Both calibration and validation are critical for reliable laboratory operations, and together they form the foundation of effective quality management. Ensure sterility and lab compliance with expert autoclave calibration with CISCAL Frequently Asked Questions (FAQs) Previous Next

Discover the leading causes of calibration error in devices, from environmental factors to human mistakes, and learn how to avoid them. < Back Top Causes of Calibration Error in Devices (and How to Prevent Them) Top Causes of Calibration Error in Devices Calibration error is a deviation between a device’s measured value and the true reference standard. In simple terms, it means the instrument does not provide the exact reading it should. Even small errors can create significant consequences, particularly in industries where precision is essential such as healthcare, energy, manufacturing, and scientific research. A scale off by just a fraction of a gram can ruin a pharmaceutical batch. A miscalibrated pressure sensor could compromise plant safety. For laboratories and production facilities, calibration error is not just about faulty numbers it directly affects compliance, safety, and reputation. The importance of identifying the sources of calibration error and preventing them cannot be overstated. By understanding what drives these deviations, organizations can reduce risk, minimize downtime, and maintain accuracy across their operations. What Is Calibration Error? Calibration error occurs when an instrument provides readings that deviate from the known true value or standard. Errors are often categorized into two primary types: Systematic error : Consistent bias in one direction, such as a thermometer that always reads 0.5 °C high. These errors are predictable and often stem from instrument drift, poor reference standards, or misalignment. Random error : Unpredictable fluctuations caused by environmental noise, operator mistakes, or unstable power sources. These errors reduce repeatability and can only be quantified statistically. Examples of calibration error include a laboratory balance that consistently weighs 1 g too high, an oscilloscope that distorts signal amplitude, or a flow meter that underreports fluid volume. In accredited calibration laboratories, these errors are accounted for in the measurement uncertainty budget. Uncertainty combines all potential sources of deviation into a documented value, giving a quantified confidence range for the calibration. Without proper management of calibration error, uncertainty expands, certificates lose validity, and compliance with ISO/IEC 17025 and regulatory bodies may be jeopardized. Examples of calibration error include a laboratory balance that consistently weighs 1 g too high, an oscilloscope that distorts signal amplitude, or a flow meter that underreports fluid volume. In accredited calibration laboratories, these errors are accounted for in the measurement uncertainty budget. Uncertainty combines all potential sources of deviation into a documented value, giving a quantified confidence range for the calibration. Without proper management of calibration error, uncertainty expands, certificates lose validity, and compliance with ISO/IEC 17025 and regulatory bodies may be jeopardized. Top Causes of Calibration Error Several factors contribute to calibration error. Understanding them helps in preventing costly mistakes. 1. Environmental Factors Temperature fluctuations, humidity, vibrations, and electromagnetic interference can skew readings. Sensitive instruments like balances or oscilloscopes are particularly vulnerable. Even minor air drafts or floor vibrations in a laboratory can cause inaccurate measurements. For example, in pharmaceutical labs, balances may require isolation chambers to protect from drafts. Similarly, electromagnetic interference from nearby machinery can cause signal drift in electronic sensors. 2. Instrument Drift and Wear All devices degrade over time. Electronic sensors drift, mechanical parts wear, and optical systems lose alignment. Without recalibration at recommended intervals, these changes accumulate into significant error. Drift is particularly problematic in continuous monitoring systems, such as those used in energy plants, where even small deviations over time can mislead performance data. 3. Poor Reference Standards Calibration depends on comparing instruments to reference standards. If the standards themselves are uncalibrated, non-traceable, or physically degraded, every calibration performed against them will inherit their inaccuracy. For example, using a reference weight that has not been re-certified in years could result in entire batches of incorrectly measured products. 4. Human Error. Operators may incorrectly set up equipment, misread scales, or record data inaccurately. Simple oversights such as skipping warm-up times or applying the wrong test load are common contributors to calibration error. In busy facilities, documentation mistakes are also frequent, leading to data inconsistency and invalid results. 5. Improper Procedures Deviation from standard operating procedures (SOPs) leads to unreliable results. Examples include skipping stabilization steps, failing to account for load conditions, or calibrating outside the recommended environment. Many errors occur because staff rush through calibration without following the documented sequence. 6. Unstable Power Supply Electronic instruments are highly sensitive to voltage fluctuations. Power surges or unstable supply can cause inconsistent readings during calibration, introducing error into results. Laboratories often mitigate this with uninterruptible power supplies (UPS) or stabilized power sources. 7. Inadequate Calibration Frequency When calibration intervals are extended too long, drift and wear accumulate unnoticed. Instruments may operate out of tolerance for months before being checked, resulting in poor data and costly recalls. Extending calibration cycles beyond recommended schedules may appear cost-saving in the short term, but it leads to greater risks of product recalls and compliance failures. Case Examples of Calibration Error Impact Calibration error has caused real-world failures across industries: Manufacturing : A miscalibrated scale in a chemical plant produced defective product batches. The issue led to wasted raw materials, customer complaints, and a costly investigation. In the food industry, packaging scales that drift caused underfilled products, leading to fines and recalls. Healthcare : Infusion pumps or blood pressure monitors that drift out of calibration put patients at serious risk. Even slight deviations in medication delivery volumes can have life-threatening consequences. Hospitals often face legal and regulatory action when such errors occur. Energy Sector : Incorrectly calibrated flow meters in pipelines have led to billing disputes, safety concerns, and regulatory penalties. In one case, turbine efficiency analysis was compromised by anemometer error, costing operators significant lost revenue. Aviation incidents have also been linked to faulty pitot tubes and anemometers with calibration errors. These cases highlight why calibration error is not a minor technical issue, it directly influences safety, efficiency, and financial stability. How to Minimize Calibration Errors Organizations can take proactive steps to reduce calibration errors and their consequences: Follow ISO/IEC 17025 guidelines : This international standard ensures laboratories meet strict requirements for competence, traceability, and reporting of uncertainty. Use accredited calibration labs : Partnering with NATA or ILAC -accredited providers ensures compliance and internationally recognized results. Certificates from accredited labs are trusted in audits and inspections. Maintain a controlled environment : Keep temperature, humidity, and vibration within recommended limits. Isolation chambers or stabilized benches may be required for sensitive equipment. For portable instruments, field calibration kits with protective shielding can reduce environmental effects. Train personnel : Well-trained staff reduce the chance of operator error. Consistent training ensures procedures are followed accurately. Regular refresher courses reinforce best practices. Use reliable standards : All reference standards should be traceable to national measurement institutes ( NIST , PTB, NPL) and recalibrated at appropriate intervals. Using degraded or expired reference standards introduces errors across an entire lab. Set optimal calibration intervals : Base calibration schedules on manufacturer recommendations, historical performance, and environmental conditions. High-use devices or those exposed to harsh environments may need shorter intervals. Calibration management software can automate scheduling and reminders, minimizing the chance of overdue calibrations. By applying these practices, companies reduce error risks, improve audit readiness, and maintain consistent product quality. Role of Measurement Uncertainty in Calibration Errors Measurement uncertainty is not the same as error, but it quantifies the potential range of error sources. When a calibration certificate lists uncertainty, it accounts for environmental influences, equipment repeatability, operator handling, and reference standard accuracy. Why it matters : Without reporting uncertainty, a calibration result cannot be compared or trusted. For example, if a flow meter shows an error of 0.2% but the uncertainty is ±0.5%, then the measurement cannot be relied upon for high-stakes billing. How it is calculated : Labs combine Type A uncertainties (statistical, from repeated measurements) and Type B uncertainties (systematic, from standards and procedures). The final reported value gives clients confidence in the reliability of the instrument. Examples : Type A might involve repeated weighing tests on a balance to establish repeatability. Type B may come from uncertainty in the calibration of the reference weights themselves. Advanced labs may use Monte Carlo simulations to propagate uncertainties across multiple sources. Regulators and auditors require uncertainty budgets to be documented. They serve as evidence that calibration results are valid and within tolerance. Ignoring uncertainty not only undermines data quality but can also invalidate certifications. Manage Calibration Error Calibration error results from a combination of environmental influences, equipment drift, poor reference standards, human mistakes, and inadequate procedures. Left unchecked, it can compromise safety, compliance, and efficiency. The solution lies in rigorous processes: working with accredited labs, adhering to ISO/IEC 17025, using traceable standards, and ensuring personnel training. By managing calibration error, companies not only protect compliance but also safeguard safety, quality, and reputation. Avoid costly calibration errors partner with accredited labs that guarantee accuracy, compliance, and traceable results. Contact us today for expert support. Frequently Asked Questions Previous Next

Learn why NATA pressure calibration sets the industry benchmark for accuracy and compliance. Essential for manufacturing, pharma, and industrial safety. < Back Why NATA Pressure Calibration Is the Industry Standard Pressure measurement underpins some of the most safety-critical processes in modern industry. From monitoring gas pipelines in oil & gas, to ensuring autoclaves maintain sterile conditions in pharmaceuticals, to verifying packaging vacuum levels in food production, reliable pressure data directly influences quality, compliance, and human safety. The consequences of inaccurate readings range from minor inefficiencies to catastrophic failures, leaks, contamination, equipment breakdowns, or even loss of life. This is why NATA-accredited pressure calibration is considered the benchmark in Australia. It assures not only technical accuracy but also compliance with international standards such as ISO/IEC 17025 . This guide explores what pressure calibration involves, the instruments covered, how the NATA process works, and why accredited calibration is indispensable across industries. What Is Pressure Calibration? At its core, pressure calibration is the process of comparing the output of a pressure-measuring instrument against a reference standard that is itself traceable to SI units. This ensures that the instrument’s readings remain consistent and accurate over time. Instruments commonly calibrated include: Manometers & Pressure Gauges – used to measure positive and negative pressures in industrial processes. Vacuum Gauges – critical for food packaging, semiconductor production, and research labs. Differential Pressure Gauges – essential in cleanrooms, filter monitoring, and HVAC validation . Pressure Transducers & Indicators – convert pressure into electrical signals for automated systems. Pressure Loggers – used in pharmaceutical QA to record and validate environmental conditions. Leak Test Apparatus – verify pressure integrity in tanks, pipelines, and packaging. Medical Devices – such as sphygmomanometers, where human safety depends on reliable readings. The value of calibration lies not only in aligning instruments with standards but in ensuring decisions made based on pressure data, whether regulatory, operational, or safety-related, are sound and defensible. Why NATA Pressure Calibration Matters Accuracy & Repeatability Pressure sensors and gauges naturally drift over time due to wear, environmental stress, or electrical degradation. In high-risk settings such as pharmaceutical sterilisation cycles, a minor deviation can compromise entire product batches. In oil & gas pipelines, inaccurate readings may cause premature shutdowns or undetected leaks. Regular calibration restores accuracy and ensures measurements remain repeatable across multiple uses and conditions. Compliance & Accreditation NATA accreditation proves that a calibration has been performed by a lab meeting ISO/IEC 17025 standards for technical competence and traceability. For companies operating under ISO 9001, GMP, or TGA regulations, this is not optional it is a core requirement. Without NATA certification, audit trails weaken, product certifications may be questioned, and regulatory non-compliance becomes a tangible risk. Safety Incorrect pressure readings directly threaten safety. Over-pressurisation of pipelines can cause ruptures; under-vacuum in sterile environments can lead to microbial contamination. In mining, inaccurate pressure monitoring of hydraulic systems can endanger workers and machinery alike. NATA calibration minimises such risks by ensuring instruments remain trustworthy. Operational Efficiency Calibrated instruments reduce false alarms, avoid unnecessary downtime, and optimise production output. For example, food packaging facilities avoid wasted packaging film and product recalls by maintaining accurate vacuum pressure. Efficiency gains are compounded when calibration is built into preventive maintenance schedules. Instruments That Require NATA Pressure Calibration Pressure instruments exist in nearly every sector of industry. Each has specific calibration needs: Manometers & Pressure Gauges – used across manufacturing and utilities for line pressure monitoring. Even small deviations can cause under- or over-pressurisation. Vacuum Gauges – vital in food & beverage packaging (modified atmosphere packaging), pharmaceuticals, and R&D. Calibration ensures vacuum levels prevent spoilage or contamination. Differential Pressure Gauges – used in hospitals, cleanrooms, and pharma labs to ensure airflow prevents contamination. Pressure Transducers & Indicators – critical in automated systems where pressure is converted to electronic signals for PLCs. Incorrect calibration here can disrupt entire production lines. Pressure Loggers – used in long-term monitoring of storage tanks or autoclaves. If uncalibrated, they may provide misleading trends. Leak Test Apparatus – ensure that containers, pipelines, or tanks remain sealed. A wrongly calibrated leak tester can allow hazardous leaks to go unnoticed. Medical Devices – inaccurate blood pressure monitors can lead to incorrect diagnoses and treatments, demonstrating the direct link between calibration and human health. Each instrument type has its own operating range, uncertainty level, and calibration interval requirements. NATA Pressure Calibration Process (Step-by-Step) A NATA-accredited pressure calibration follows rigorous methodology: Visual Inspection & Baseline Check – identifying mechanical damage, contamination, or sensor wear before testing. Application of Controlled Pressure – reference standards (deadweight testers, pressure controllers) apply stable pressures across the operating range. Comparison of Readings – the device under test is measured against the standard at multiple calibration points. Adjustment & Retesting – instruments are corrected where possible, then retested for verification. Recording Results – deviations, corrections, and measurement uncertainty are documented. Issuing Calibration Certificate – includes SI traceability, uncertainty, environmental conditions, and NATA accreditation details. The emphasis on traceability and uncertainty ensures that calibration results hold weight in audits, certifications, and global trade. Calibration Standards & Compliance Pressure calibration is rooted in recognised international frameworks: ISO/IEC 17025 defines competence for calibration labs, ensuring processes, staff, and equipment meet stringent requirements. NATA Accreditation validates that Australian labs comply with ISO/IEC 17025 and that results are accepted internationally. Industry-Specific Regulations: Pharmaceuticals – TGA and GMP guidelines require calibrated pressure for sterilisation, cleanrooms, and process validation. Food & Beverage – HACCP and export certification depend on validated pressure control in packaging and processing. Oil & Gas / Mining – regulated by safety codes that mandate traceable pressure calibration for high-risk systems. NATA accreditation therefore provides both technical assurance and regulatory compliance, making it the industry standard across Australia. Frequency & Best Practices Typical Calibration Intervals General Industry – annual calibration is standard practice. High-Use Applications – 3–6 months, especially in pharma, cleanrooms, and high-pressure manufacturing. Event-Driven – recalibration after overload, exposure to extreme environments, or repairs. Best Practices for Reliability Avoid overpressure that strains sensors. Store gauges away from vibration, moisture, and temperature extremes. Keep detailed calibration logs for traceability and trend analysis. Rotate instruments to manage workload and avoid overuse of single devices. Embedding these practices into preventive maintenance strategies enhances reliability and reduces operational risks. Choosing a NATA-Accredited Calibration Partner Calibration quality depends on the competence of the provider. Choosing a NATA-accredited partner ensures your certificates are audit-ready and globally recognised. Benefits of working with CISCAL: Over 60 years of calibration expertise across industries. NATA-accredited scope for pressure and multi-parameter instruments. Nationwide coverage & Pacific Islands reach. The CISCAL SMART portal for certificate access, compliance tracking, and calibration scheduling. With CISCAL, clients gain more than calibration, they gain compliance assurance, operational reliability, and confidence for audits. Trusted Partner for Pressure Calibration From safety in mining operations to sterility in pharmaceuticals, accurate pressure measurement protects lives, ensures compliance, and drives operational efficiency. NATA pressure calibration is the benchmark because it delivers not just accuracy, but traceability, audit readiness, and international recognition. With over 60 years of expertise and NATA-accredited services, CISCAL is the trusted partner for pressure calibration across Australia. CISCAL NATA Pressure Calibration Frequently Asked Questions (FAQs) Previous Next

Discover what calibration is, why it matters, and its applications in pharma, food, biotech, and manufacturing. Learn from NATA-accredited experts. < Back What Is Calibration? Definition, Importance, and Real-World Applications How can industries ensure every measurement they rely on is accurate, compliant, and reliable? The answer lies in calibration. From pharmaceutical labs safeguarding patient safety to food producers maintaining product consistency, calibration underpins compliance, quality, and safety. At its core, calibration is the process of comparing a measurement instrument against a recognised standard to verify accuracy. In Australia, this process is tightly linked to NATA-accredited laboratories, ISO/IEC 17025 standards, and industry-specific compliance requirements. For organisations in pharmaceuticals, biotechnology, food and beverage, manufacturing, and scientific research, calibration isn’t just technical, it’s operational survival. Without it, compliance, efficiency, and credibility are all at risk. What Is Calibration? Calibration is the process of checking and adjusting measurement instruments by comparing them against standards that are traceable to recognised references, such as those defined by the National Measurement Institute (NMI). In Australia, accredited calibration providers follow the ISO/IEC 17025 standard, ensuring that results are accurate, consistent, and legally defensible. When an instrument is calibrated, its readings are tested against a known standard. Any deviations are recorded and, if necessary, the instrument is adjusted. This ensures traceability and compliance, giving organisations confidence in the reliability of their data. Traceability is critical, as it creates a documented link between the measurement equipment and international standards, providing legal and regulatory assurance. Calibration matters because even small inaccuracies can lead to regulatory non-compliance, product recalls, financial loss, or, in critical sectors like pharma and healthcare, risks to human safety. For example, a miscalibrated medical thermometer could impact patient diagnosis, while an uncalibrated pressure gauge in a factory could cause unsafe operating conditions. Why Calibration Is Important Accurate measurement is central to quality control, compliance, and safety. Without it, industries risk: Loss of accuracy and precision: Instruments drift over time. Regular calibration ensures consistent, reliable data and prevents small errors from accumulating into major failures. Regulatory non-compliance: Agencies like the Therapeutic Goods Administration (TGA) enforce strict calibration and Good Manufacturing Practice (GMP) standards . Non-compliance can lead to penalties, product seizures, or reputational damage. Audit failures: Uncalibrated equipment can cause businesses to fail compliance audits, leading to costly corrective actions or halted operations. Downtime and costs: Faulty readings may cause entire production lines to shut down or products to be scrapped, resulting in financial losses and wasted resources. For example, in pharmaceutical manufacturing, an improperly calibrated autoclave risks producing non-sterile batches, directly endangering patient safety. In the food sector, incorrect weighing systems could result in product inconsistency, mislabelling, and legal action. In biotechnology research, even minor deviations in pipette calibration can distort experimental results, undermining years of work. Proper calibration not only protects consumers but also saves organisations from costly downtime and reputational damage. Types of Calibration CISCAL provides NATA-accredited calibration services across multiple parameters, ensuring full industry coverage. Key types include: Dimensional Calibration Tools such as micrometers, calipers, and gauges must be precise to ensure accurate manufacturing tolerances. Even slight measurement errors can compromise product fit and performance, leading to costly recalls or safety issues. Dimensional calibration ensures equipment used in machining, engineering, and research delivers precise results. Learn More With Dimentional Calibration Mass & Weighing Calibration Balances, scales, and tanks are used daily in laboratories and industrial production. CISCAL calibrates equipment from microbalances to large weighing systems, ensuring compliance with trade measurement regulations (Reg 13). In food and pharmaceutical industries, weighing errors can alter formulations and compromise safety. Weight Classes We Handle Temperature & Humidity Calibration Temperature-controlled environments—autoclaves, freezers, incubators—are critical in biotech, food production, and pharma. Calibration ensures accuracy within strict ranges, guaranteeing sterile environments and product stability. For example, vaccine storage relies on calibrated refrigeration units to maintain efficacy. Plan Your Schedule Pressure Calibration Pressure gauges and transducers used in manufacturing and processing industries must be calibrated to avoid errors in system control. Inaccuracies can compromise safety in industries like oil and gas, where correct pressure readings are critical to preventing accidents. Who Needs It Electrical Calibration Instruments like multimeters, oscilloscopes, and calibrators require precise adjustment for safe and efficient electrical testing. Miscalibrated electrical devices can lead to faulty readings, causing production downtime or safety hazards. See What We Calibrate Chemical Properties Calibration Laboratories rely on accurate pH meters, conductivity meters, and viscometers. Even minor deviations can compromise research outcomes or product formulations. For example, an incorrect pH measurement could ruin entire production batches in food manufacturing. Why It’s Critical Torque & Force Calibration From torque wrenches to hardness testers, force measurement devices are essential in engineering and manufacturing. Calibration ensures correct tolerances and safety compliance, preventing product failures and mechanical accidents. Where Torque Matters Most Calibration Process: Step by Step Calibration is not a one-step check; it’s a rigorous process designed to guarantee traceability: Instrument inspection: Check for damage, wear, or contamination that could affect performance. Comparison with a reference standard: Measure outputs against certified reference equipment traceable to international standards. Adjustment: Correct deviations when possible to restore accuracy. If adjustment isn’t possible, the instrument may be marked as “out of tolerance.” Documentation: Record results in compliance with ISO/IEC 17025, ensuring audit traceability. Certificates typically include measurement results, uncertainty, and traceability information. By following NATA-accredited procedures, calibration ensures that every measurement is traceable to national and international standards. This traceability is essential for compliance, quality assurance, and legal defensibility, providing businesses with a documented chain of accuracy. Real-World Applications of Calibration Pharmaceutical Sterile environments depend on accurate autoclaves, incubators, and balances. Calibration ensures compliance with TGA and GMP standards, directly affecting patient safety. Incorrect calibration could lead to the release of ineffective or unsafe drugs, which carries life-threatening consequences. Food & Beverage Weighing systems, moisture analysers, and temperature controls are vital for consistency and compliance. Trade measurement verification ensures fair and legal product labelling, protecting both producers and consumers. Inconsistent calibration can lead to consumer complaints, product recalls, and regulatory fines. Biotechnology Research validity relies on precise pipettes, microscopes, and chemical analysis tools. Calibration safeguards the integrity of experimental results, ensuring reproducibility. Poor calibration could invalidate research, jeopardising funding and delaying scientific progress. Manufacturing Torque measurement, flow meters, and pressure gauges are central to safe and efficient production lines. Inaccuracies can cause costly shutdowns or defective products. Calibrated instruments ensure product quality and reduce waste in lean manufacturing environments. Scientific Research Balances, spectrophotometers, and environmental chambers must be calibrated to guarantee reliable research data and reproducibility. Calibration builds trust in scientific results, enabling discoveries to be replicated across labs worldwide. Challenges Without Calibration Failing to calibrate equipment exposes organisations to major risks: Regulatory risk: Non-compliance with NATA or ISO/IEC 17025 standards, leading to audit failures. Quality failures: Inconsistent or unreliable product outputs, reducing consumer trust. Financial losses: Downtime, wasted batches, product recalls, or reputational damage. One Australian case study involved a food manufacturer halting production for three days due to inaccurate weighing systems. The unplanned downtime cost millions in lost revenue and damaged client trust. This example illustrates how calibration is not only about compliance but also about maintaining uninterrupted operations. Choosing the Right Calibration Partner Not all calibration services are equal. The gold standard in Australia is NATA accreditation , proving compliance with ISO/IEC 17025. Choosing a partner like CISCAL ensures: 60+ years of continuous accreditation and expertise across industries. Multi-parameter calibration covering dimensional, mass, temperature, pressure, electrical, and more. Nationwide reach with service centres in NSW, VIC, QLD, and coverage across WA, SA, TAS, NT, New Zealand, and Pacific Islands. Access to the CISCAL SMART portal, offering real-time asset management, job tracking, and digital certification, enabling organisations to streamline compliance management. Working with an accredited partner gives businesses assurance that their calibration certificates will be recognised during audits, regulatory inspections, and client quality checks. Getting the Most Value from CISCAL Services Calibration is more than ticking a compliance box—it’s about ensuring operational reliability, safety, and efficiency. Partnering with CISCAL gives enterprises access to Australia’s most experienced NATA-accredited calibration provider, a nationwide technical team, and advanced digital tools for compliance management. Stay compliant. Minimise downtime. Ensure absolute accuracy. Partner with CISCAL today to safeguard your operations and request a quote. Contact Ciscal for more information Frequently Asked Questions (FAQs) Previous Next

Learn how accurate instrument calibration supports autoclave repair and compliance. Trusted guidance for Australian pharma, biotech, and food industries. < Back Guide to Accurate Instrument Calibration: Autoclave Repair Insights In highly regulated industries such as pharmaceuticals, biotechnology, food production, and research, accuracy is everything. Instruments used for monitoring and validating processes must deliver precise readings, especially when it comes to sterilisation equipment like autoclaves. Incorrect measurements can lead to compliance failures, compromised product safety, and costly downtime. That’s where instrument calibration plays a vital role. By comparing an instrument’s readings against recognised reference standards, calibration ensures measurement accuracy, reliability, and compliance with industry regulations. For more than 60 years, CISCAL has been Australia’s trusted provider of NATA-accredited calibration services, helping organisations keep their autoclaves and supporting equipment in peak condition. What Is Instrument Calibration? Instrument calibration is the process of comparing the measurements from an instrument to a reference standard that is traceable to international or national measurement systems. If discrepancies are found, the instrument can be adjusted to bring it back into specification. Purpose of Calibration Ensures accuracy and reliability of measurements. Demonstrates compliance with regulatory requirements. Provides traceability through documentation and certificates. Examples of Instruments Requiring Calibration Temperature probes : essential for autoclave sterilisation cycles. Pressure gauges : used in autoclave chambers and pressure vessels. Sound meters : for workplace noise compliance and autoclave diagnostics. Torque wrenches : for ensuring correct fastening of autoclave seals and fittings. In Australia, traceability for calibration is supported by the National Measurement Institute (NMI), ensuring instruments are benchmarked against internationally recognised standards. Learn more about calibration Why Calibration Matters in Autoclave Repair Autoclaves rely on multiple instruments and sensors: including temperature, pressure, and humidity sensors to validate sterilisation. If these instruments are not properly calibrated: Sterilisation failures may occur, leaving equipment or materials contaminated. Compliance risks increase, with potential non-conformities during TGA audits for pharma or FSANZ HACCP inspections in food production. Downtime becomes more likely due to unexpected failures or repeat cycles. Industry-Specific Implications Pharma & Biotech : The TGA’s GMP guidelines require validated sterilisation processes. Inaccurate sensors can lead to failed sterility assurance and costly batch recalls. Food & Beverage : Under FSANZ HACCP programs, temperature data must be accurate and verifiable. Poor calibration can result in unsafe food release and reputational damage. Healthcare & Research : Patient safety and research outcomes rely on validated sterilisation. Non-compliance may lead to failed accreditations or compromised results. Case Example: In 2021, a Victorian pharmaceutical manufacturer faced a regulatory warning after a TGA inspection found calibration records for autoclave pressure sensors were outdated. Implementing a NATA-accredited calibration program prevented further penalties and restored compliance. How Instrument Calibration Is Done (Step-by-Step) Calibration is a controlled, traceable process that ensures instruments remain accurate and compliant. Typical Calibration Steps Inspection : The instrument is visually checked for physical damage, wear, or contamination. Reference Setup : The instrument is connected to a reference device or standard with higher accuracy, certified by NATA or the National Measurement Institute (NMI). Testing : Measurements are taken at multiple points across the instrument’s operating range. Deviation Recording : Differences between the instrument and the standard are documented. Adjustment : If possible, the instrument is adjusted back into tolerance. Certification : A NATA-accredited calibration certificate is issued, documenting results, uncertainty, and traceability. Example: Autoclave Temperature Probe Calibration A temperature probe is tested against a certified dry block calibrator. Readings are compared at validation temperatures such as 121°C and 134°C. If deviations are outside the ±0.5°C tolerance specified in ISO/IEC 17025 testing protocols, the probe is adjusted, and results are documented in a NATA-traceable certificate. Applications Across Australian Industries Accurate instrument calibration underpins quality and compliance in many sectors: Pharmaceuticals Validating sterilisation cycles in cleanrooms and production facilities. Supporting TGA GMP compliance and ensuring audit readiness. Food & Beverage Confirming sterilisation and cooking processes meet FSANZ safety standards. Supporting HACCP certification by maintaining calibration traceability. Biotechnology & Research Ensuring accurate operation of incubators, UV sterilisation chambers, and autoclaves. Supporting laboratory accreditation and compliance with biosafety regulations. Engineering & Manufacturing Calibrating torque tools, dimensional measurement devices, and sound meters. Supporting ISO-certified quality management systems where calibration records are mandatory. Calibration Standards & Compliance Calibration is not just a best practice. it’s a regulatory requirement. ISO/IEC 17025 : The international standard defining competence and quality for calibration and testing laboratories. NATA accreditation : Provides independent assurance that calibration services are reliable, traceable, and recognised globally. TGA GMP compliance : Requires pharmaceutical companies to demonstrate validated sterilisation processes with traceable calibration. FSANZ HACCP standards : Depend on calibrated equipment to ensure food safety compliance. Safe Work Australia : Recognises calibration as part of workplace safety requirements when instruments are used for monitoring. By adhering to these standards, organisations safeguard quality, demonstrate due diligence, and avoid costly non-compliance penalties. Best Practices & Calibration Intervals Typical Calibration Intervals Every 6–12 months for most instruments. More frequent calibration (every 3–6 months) for critical tools in pharma, aerospace, or food manufacturing. Usage-based intervals : Instruments with heavy daily use may require recalibration sooner. Best Practices Maintain a centralised asset register of all calibrated instruments. Store instruments in protective cases to prevent contamination or damage. Train staff in correct usage to reduce drift or premature wear. Integrate calibration into preventive maintenance schedules. Use digital systems, such as CISCAL’s SMART portal, to manage calibration records and audit readiness. Getting the Most Value from Instrument Calibration Instrument calibration is the foundation of reliable measurement and compliance. For autoclaves, it ensures sterilisation processes are validated and trusted. Across industries, it reduces risks, extends equipment life, and protects reputations. By choosing a NATA-accredited provider, organisations demonstrate compliance with ISO/IEC 17025, satisfy TGA and FSANZ audit requirements, and ensure traceability through internationally recognised certificates. CTA: Ensure precision and compliance across your operations with CISCAL’s NATA-accredited instrument calibration services. From autoclaves to torque wrenches, our experts deliver nationwide coverage, quick turnaround, and tailored compliance documentation. Contact us today. Stay Compliant with CISCAL FAQs Previous Next

Learn the essentials of electrical calibration, from methods and tools to industry standards. Stay compliant with NATA and ISO/IEC 17025 requirements. < Back Electrical Calibration: A Complete Guide for Professionals Electrical calibration underpins accuracy, safety, and compliance across critical industries. In pharmaceuticals, biotechnology, food and beverage, manufacturing, and utilities, every decision relies on precise electrical measurements. Instruments such as multimeters, oscilloscopes, and PAT testers are essential for quality assurance and maintenance, yet their readings can drift over time. Without calibration, even minor deviations can trigger costly downtime, safety hazards, or audit failures. This guide explores what electrical calibration is, why it matters, the instruments involved, calibration methods, compliance requirements, and best practices, equipping professionals with practical insights to keep operations running safely and efficiently. What Is Electrical Calibration? Electrical calibration is the process of comparing the output of an electrical measuring instrument against a known reference standard, which is traceable to national or international benchmarks. Key parameters include voltage, current, resistance, frequency, and capacitance. Instruments requiring calibration include: Multimeters and clamp meters : used daily for current, resistance, and voltage checks. Oscilloscopes and scopemeters : for waveform analysis in R&D and troubleshooting. Portable Appliance Testers (PAT testers) : mandated for workplace safety compliance. Insulation testers and Hi-Pot testers : critical in utilities and manufacturing. Resistance boxes and power supplies : for calibration and testing environments. Timers, stopwatches, and tachometers : time- and speed-based instruments requiring consistent repeatability. Accreditation frameworks such as ISO/IEC 17025 and NATA ensure calibration is not just accurate but traceable, meaning results can be verified during audits and accepted internationally. This level of rigour is vital in regulated industries like pharmaceuticals and aerospace, where errors can have wide-reaching consequences. Why Electrical Calibration Matters Accuracy & Repeatability Over time, electrical instruments degrade due to component ageing, wear, and environmental factors. Drift in readings can compromise accuracy and lead to repeated measurement errors. Calibration corrects these deviations, ensuring results remain accurate and reproducible, a non-negotiable requirement in fields like pharmaceutical testing or quality assurance in electronics. Compliance & Audit Readiness Industries regulated by ISO, GMP, and Australian Standards must prove that their measurements are accurate and traceable. In a pharmaceutical audit, for example, an uncalibrated oscilloscope used in equipment validation could invalidate the entire process, delaying product release. Regular calibration ensures audit readiness and maintains certifications. Safety & Risk Reduction Safety risks increase significantly when instruments are out of calibration. A miscalibrated insulation tester may fail to identify dangerous faults, leaving staff exposed to live electrical hazards. In utilities, poor calibration of protective relays could lead to power system instability or equipment failure. Accurate calibration protects both people and infrastructure. Operational Efficiency Calibration not only ensures compliance but also reduces costly downtime. For example, in food production, inaccurate PAT testers could incorrectly tag safe equipment as faulty, delaying production unnecessarily. Conversely, failure to detect faulty equipment could lead to contamination or recalls. Regular calibration keeps operations efficient by ensuring reliable decision-making. Common Instruments in Electrical Calibration Multimeters & Clamp Meters The most frequently used tools for electrical measurements. Drift can lead to significant miscalculations in system diagnostics, impacting everything from consumer electronics to heavy industry. Oscilloscopes & Scopemeters Used for observing waveforms in electronic circuits. An uncalibrated scope may distort signal shapes, leading to incorrect diagnoses in R&D or failure analysis. Portable Appliance Testers (PAT) Vital for workplace compliance with Australian electrical safety regulations. A miscalibrated PAT tester can either flag safe devices as unsafe or, worse, pass unsafe devices. Insulation Testers & Hi-Pot Testers These instruments check insulation integrity at high voltages. Inaccuracies could expose staff to shock hazards or allow defective products into service. Power Supplies & Resistance Boxes Often used as part of wider calibration setups. If their outputs are incorrect, they can compromise the calibration of other instruments. Timers, Stopwatches, Tachometers Critical in manufacturing and research environments where precise timing dictates performance outcomes. Drift in these tools can delay production cycles or skew experimental data. Methods of Electrical Calibration Direct Comparison with Reference Standards This method uses high-precision reference standards, traceable to NMI or international equivalents, to verify instrument accuracy. It provides the most reliable results but requires access to accredited labs. Simulation Methods Signal simulators generate known voltages, currents, or frequencies to test instruments in situ. This is faster and less disruptive but still requires traceability to reference standards. Automated Calibration Systems Automation improves repeatability and reduces human error. Large organisations with hundreds of instruments often rely on automated systems to maintain calibration efficiency and accuracy. In-Situ vs Laboratory Calibration In-Situ Calibration : Conducted onsite, minimising downtime. Useful in factories, power plants, or hospitals where removing instruments is impractical. Laboratory Calibration : Conducted in controlled environments with advanced standards. While more accurate, it requires downtime and logistics. Step-by-Step Calibration Process Preparation : Stabilise the environment, control temperature, humidity, and interference. Verify reference standards are in date. Zero Check : Confirm baseline readings with no input applied. Apply Known Inputs : Test across low, mid, and high ranges relevant to the instrument. Adjust for Deviations : Correct settings internally or apply compensation factors. Record Results : Document readings, tolerances, and traceability. Certification : Issue a calibration certificate, ensuring compliance with ISO/IEC 17025 and NATA. Calibration Frequency & Compliance Typical Intervals : Most instruments should be calibrated annually. However, high-use or safety-critical devices may need calibration quarterly or biannually. Factors Influencing Frequency : Environment (temperature, dust, humidity), intensity of use, and application criticality. Instruments used in harsh industrial settings degrade faster. Compliance : Calibration records must be retained for audits. ISO/IEC 17025 and NATA specify requirements for traceability and uncertainty calculations. Challenges & Best Practices Environmental Factors Electrical instruments are sensitive to their environment. High humidity, heat, or electrical noise can accelerate drift. Calibrating in stable, controlled environments minimises these effects. Avoiding Common Errors Using outdated or uncertified reference standards. Poor documentation of calibration results. Ignoring early warning signs of instrument drift. Best Practices Implement digital calibration management systems like the CISCAL SMART portal to track schedules and results. Train staff to recognise signs of calibration drift. Partner with accredited providers to ensure compliance and traceability. Partner With Accredited Providers Electrical calibration is not just a compliance requirement. It is a safeguard for accuracy, safety, and operational efficiency. Whether for multimeters in manufacturing, oscilloscopes in R&D, or PAT testers in food production, calibrated instruments keep businesses compliant and productive. Partnering with accredited providers ensures traceability and confidence. Ensure compliance and accuracy with CISCAL’s NATA-accredited electrical calibration services. With nationwide reach, multi-parameter expertise, and over 60 years of experience, we keep your instruments reliable and audit-ready. Frequently Asked Questions (FAQs) Previous Next

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Kaye ValProbe RT Product Tags KAYE Measurement and Calibration Equipment Validation System Kaye ValProbe RT is a wireless real-time validation and monitoring system that provides precise, reliable temperature and humidity data for thermal validation processes in GMP and FDA-regulated environments. Request A Quote * First name * Email * Phone * State How can we help? Submit Description Kaye ValProbe® RT (Real-Time) is a cutting-edge wireless thermal validation system tailored to meet the thermal validation and regulatory requirements of the Pharmaceutical and Biotech industries. As the reliability, repeatability, and accuracy of real-time wireless technology evolve, Kaye has harnessed the latest advances in RF and battery technology to design the most sophisticated wireless thermal validation system on the market, centered around the wireless data logger. The ValProbe RT wireless thermal validation system is comprised of: A wide range of wireless data loggers for accurate, in-situ measurements of critical process temperatures, pressures, and humidity (-80C to 140C). These wireless data loggers ensure precise monitoring in even the most demanding conditions. A Base Station that guarantees reliable real-time wireless communications, collecting process data efficiently from the wireless data loggers. The use of advanced technologies, like antenna diversity, ensures unmatched signal strength and communication reliability with each wireless data logger. A robust Validation Console running Windows 10 LTSC, preloaded with ValProbe RT® software dedicated to validation tasks. This setup enhances security and reduces software validation efforts. The software’s intuitive interface supports all validation tasks, including Setups, Qualifications, Logger Verifications, Reporting, and Data Storage/Backup, conforming to all current regulatory requirements for 21 CFR Part 11, Data Integrity, and Cyber Security. The ValProbe RT® family of wireless data loggers provides precise, convenient, and reliable process measurements for various pharmaceutical and medical device applications. These wireless data loggers are part of a system that integrates high-accuracy measurements and automated sensor verification, supported by an intuitive metro-style user interface and extensive reporting capabilities. Kaye ValProbe RT Datalogger Steam Sterilizers Dry Heat Sterilizers Steam in Place (SIP) Water Cascade/Fall Sterilizer Incubators Stability Chambers Freezers Freeze Dryer /Lyophilization Vessels Temperature Rigid Logger Yes Yes Yes Yes Yes Yes Yes Yes Temperature Flexible Logger Yes Yes Yes Yes Yes Yes Yes Yes Temperature Bendable Logger Yes Yes Yes Yes Yes Yes Yes Yes Yes Temperature Freeze Dryer Logger Yes Yes Yes Yes Pressure/Temp Logger Yes Yes Yes Yes The ValProbe RT system combines high accuracy measurements, automated sensor verification, an intuitive metro style user interface, and extensive reporting to simplify the complete validation process and the compliant reporting of all Real Time data Loggers used. Take the next step and see how the Kaye ValProbe® RT wireless thermal validation system greatly simplifies monitoring and validation of severe and hard-to-reach environments while also providing validation efficiency and time savings. Users of the current Kaye ValProbe System can easily upgrade their existing fleet to the Real Time Datalogger family entering the next stage of wireless thermal validation. Common Reporting Tool Software Sometimes the reporting and post analysis of your validation studies are better done in the convenience of your office on a separate PC. That is possible with the Kaye Common Reporting Tool that opens study files generated with Kaye ValProbe RT and Kaye Validator AVS systems. This provides added flexibility and efficiency with the use of your Validation Console. Key Features Life data under harsh conditions via RF during validation study RF-Range up to 150 meters Temperature Range -85 to 400°C Up to 100,000 samples per sensor Scan rate down to 1 second ValProbe system capacity 25 loggers / 50 sensors Customer interchangeable batteries Accuracy up to 0.1°C Unmatched battery life Applications Steam Sterilizer Dry Heat Sterilizers Steam in Place (SIP) Water Cascade/Fall Sterilizer Incubators Stability Chambers Freezers Freeze Dryer/Lyophilization Washer Disinfectors Vessels Specifications Kaye ValProbe RT Generic Specifications Base Station Dimensions 7.6 in x 5.2 in x 2.2 in 190mm x 130 mm x 55 mm Logger Dimensions Hight: 1,9'' / Diameter 1,4'' 48mm / 36mm Logger Material Stainless Steel 316L and Peek Battery Field replaceable - 3.6V Lithium Sampling Rate Starting at 1 sec Data Storage 100.000 Samples retained in non-volatile memory Real-Time Clock Accuracy < 15sec/day Kaye ValProbe RT Generic Specifications Calibration NVLAP (NVLAP LAB CODE 200913-0)/DAkkS Calibration Verification Automated User Verification capability Sensing Element Precision Platinum RTD Environmental Temperature -85°C to 140°C Environmental Pressure 0-5bar absolute Environmental Humidity 0-100% condensing Regulatory Compliance UL and CE Temperature Loggers Pressure & Temp. Logger Specifications Rigid Bendable Flexible Surface Pressure Sensor Type Single Sensor Single and Dual Sensor Single, Dual and 5-Channel Ultra Flat Surface Sensor Single P/T Sensor Sensor Length 1.5, 3, 6, 9" inches 38, 76, 152, 229 mm 12, 24, 36" inches 305, 610, 915 mm 40" inches 1000 mm - - Tip Diameter 0.118"; 3mm 0.095"; 2.4mm 0.095"; 2.4mm 32mm diameter 1/4 NPT Connection fitting Measurement Range -85°C to 140°C -85°C to 400°C -85°C to 140°C -85°C to 140°C 0°C to 140°C / 0-5bar abs. Accuracy -85°C to 140°C, ±0.1°C -85°C to 140°C, ±0.1°C 140°C to 400°C ±0.25°C -85°C to 140°C, ±0.1°C -85°C to 140°C, ±0.1°C 0°C to 120°C ±25mb 120°C to 135°C ±10mb 135°C to 140°C ±25mb 0°C to 140°C, ±0.1°C Enquire Now Fill out the form below and together we will find a perfect customised solution tailored for your business. * First name * Email * Phone * State How can we help? Submit

PRODUCTS CISCAL is Australia’s trusted partner for precision laboratory and industrial equipment, delivering cutting-edge solutions across food and beverage analysis, grain processing, weighing systems, plastic testing, and temperature calibration. We supply high-performance tools that drive accuracy, compliance, and efficiency in every environment. Backed by over 60 years of industry expertise, our catalog supports industries including winemaking, dairy, grain, pharma, and more. Browse below to find the equipment that powers smarter science and streamlined operations. Filter by Brand Select Brand Filter by Category Select Category Filter by Equipment type Select Equipment type ValProbe RT Humidity orTemperature Logger The Kaye ValProbe RT Humidity & Temperature Logger offers precise real-time monitoring of temperature and relative humidity for validation of controlled environments and stability chambers. Click Here ValProbe RT Temp Logger The Kaye ValProbe RT Surface Sensor Logger ensures precise real-time temperature validation for freeze-dryers and other critical surface monitoring applications. Click Here ValProbe RT Temperature Data Loggers - Bendable Sensors The ValProbe RT Temperature Data Loggers with bendable sensors provide a vast temperature range from -85°C to + 400°C and are available as single and dual and five channel bendable sensor. Click Here ValProbe RT Base Station The base station is used for qualification, calibration, and verification studies. Compatible with the entire line of high-accurate temperature and pressure loggers Click Here HYPERLAB PLUS wine analyzer Hyperlab wine analyzer represents the most advanced solution for analytical control automation in the oenological field. Click Here ValProbe RT Pressure or Temperature Logger The Kaye ValProbe RT Flexible Sensor Logger (Dual) provides accurate real-time temperature validation with dual flexible sensors for simultaneous multi-point monitoring in regulated thermal processes. Click Here ValProbe RT Temp Logger Rigid Sensors The Kaye ValProbe RT Rigid Sensor Logger provides accurate real-time temperature validation for fixed-point thermal applications in GMP-regulated environments. Click Here ValProbe RT Flexible Real-Time Temperature Data Logger The Kaye ValProbe RT Flexible Sensor Logger delivers precise real-time temperature validation for complex thermal processes in regulated environments. Click Here Kaye ValProbe RT Kaye ValProbe RT is a wireless real-time validation and monitoring system that provides precise, reliable temperature and humidity data for thermal validation processes in GMP and FDA-regulated environments. Click Here Automatic Titrator FLASH Flash Automatic Titrator has been designed to simply and precisely perform the widest range of potentiometric titrations. Click Here Weighing and Inspection Solutions Food and Beverage Analysis Grain Quality and Processing PRODUCT CATALOGUES Laboratory Equipment Download PDF Download PDF Download PDF Download PDF OUR PARTNERS

ValProbe RT Pressure or Temperature Logger Product Tags KAYE Measurement and Calibration Equipment Validation System The Kaye ValProbe RT Flexible Sensor Logger (Dual) provides accurate real-time temperature validation with dual flexible sensors for simultaneous multi-point monitoring in regulated thermal processes. Request A Quote * First name * Email * Phone * State How can we help? Submit Description The ValProbe RT Pressure/Temp Logger provides a wide temperature range from 0°C to 140°C and is a single solution for pressure and temperature measurement for pressure up to 5bar absolute. RTD Technology delivers measurement accuracy and the new logger electronic design guarantees long battery lifetime. The antenna diversity concept secures an unmatched RF communication reliability. Key Features Temperature range for complete logger: 0°C to 140°C Pressure range 0 to 5 bar absolute, 1mbar resolution ¼ NPT connection fitting Applications Steam Sterilizer Steam in Place (SIP) Water Cascade/Fall Sterilizer Vessels Specifications Specifications Pressure/Temp Sensor Type Single P/T Sensor Sensor Length - Tip Diameter 1/4 NPT Connection fitting Measurement Range 0°C to 140°C / 0-5bar abs. Accuracy 0°C to 120°C ±25mb 120°C to 135°C ±10mb 135°C to 140°C ±25mb 0°C to 140°C, ±0.1°C Kaye ValProbe RT Generic Specifications Logger Dimensions Hight: 1,9'' / Diameter 1,4'' 48mm / 36mm Logger Material Stainless Steel 316L and Peek Battery Field replaceable - 3.6V Lithium Sampling Rate Starting at 1 sec Data Storage 100.000 Samples retained in non-volatile memory Real-Time Clock Accuracy < 15sec/day Kaye ValProbe RT Generic Specifications Calibration NVLAP (NVLAP LAB CODE 200913-0)/DAkkS Calibration Verification Automated User Verification capability Environmental Pressure 0-5bar absolute Environmental Humidity 0-100% condensing Regulatory Compliance UL and CE Enquire Now Fill out the form below and together we will find a perfect customised solution tailored for your business. * First name * Email * Phone * State How can we help? Submit

Biological Safety Cabinet Class II A2 Product Tags Biosafety Cabinet Laboratory Equipment Scitek This Class II Biosafety Cabinet provides a compact, energy-efficient workspace that ensures operator, product, and environmental protection through advanced HEPA filtration and airflow control. Request A Quote * First name * Email * Phone * State How can we help? Submit Key Features UV sterilization function and timing function can be set by appointment. Motorized front window, control limit and travel limit double protection, ergonomic 10° tilt Angle, improve the operation comfort. With memory function in case of power-failure. Work area surrounded by negative pressure, prevent leakage,improve Biosafety. Audio and visual alarm (Abnormal airflow velocity, HEPA filter failure, UV lamp failure, Front window at unsafe height). Interlock function: UV lamp and front window; UV lamp and blower, LED lamp; blower and front window. Standard with foot switch: adjust front window to up and down, to avoid airflow turbulence caused by arm movement. Color Rendering Index up to Ra98, Truly restore the true color of the experimental object, the experimental results are more accurate. RG0 without blue light, protects the operator from blue light. Optional upgraded LED lamp. Specifications Model BSC-IIA2-2F Internal Size (W×D×H)(mm) 610×550×600 External Size (W×D×H)(mm) 710x760x1430 (Without base stand), 710x760x2050 (With base stand) Max.Opening 370mm Work Surface Height 750mm Control System Display 7”LCD touch screen Airflow System Alarm Abnormal airflow velocity, HEPA filter failure, UV lamp failure, Front window at unsafe height Airflow Mode 70% air recirculation, 30% air exhaust Downflow Velocity 0.35m/s±0.025m/s Inflow Velocity 0.52 m/s±0.025m/s Inflow Air Volume 240m³/h (141CFM) Downflow Air Volume 560m³/h (330CFM) Exhaust Air Volume 240m³/h (141CFM) Air filtration System HEPA Filter 2pcs H14 HEPA filter, ≥99.995% efficiency at 0.3μm Cleanliness Grade Class 100 (ISO14644.1 Class 5) Cabinet Construction Main Body Electro-galvanized steel with antimicrobial Powder Coating Work Surface 304 stainless steel Front Window Motorized, toughened glass Electrical System UV Lamp 15W×1 (Emission of 253.7 nanometers for most efficient decontamination, UV life indicator, UV timer) LED Lamp 10W×2 Max.Consumption 350W (Not include socket consumption) Power Supply AC220V±10%, 50/60Hz; 110V±10%, 60Hz Illumination ≥900Lux Sound Emission ≤65dB(A) Vibration of Work Surface ≤2μm Standard Accessory 1. Air Velocity Sensor; 2. LCD Touch Screen; 3. LED Lamp×2; 4. UV Lamp×1; 5. Explosion-Proof/Waterprof Socket×1; 6. Motorized Front Window; 7. Footmaster Caster; 8. Foot Switch; 9. Removable shallow-plate stainless steel work surface; Optional Accessory 1. Base Stand; 2. Gas tap; 3. Water tap; 4. Pressure Sensor; 5. IV Bar With Hooks; 6. ULPA filter; 7. Upgraded LED Lamp; Net Weight 130kg (Without base stand), 140kg (With base stand) Gross Weight 165kg (Without base stand), 175kg (With base stand) Shipping Size (W×D×H)(mm) 850×990×1640 Shipping Volume 1.4 m³ Environment conditions: Temperature range: 5∽40℃ Relative humidity: ≤90%(At +40℃) Atmospheric pressure: 86kPa-106kPa Maximum dust concentration: 3500 particles /L(particle size ≥0.5μm) Optional upgrade LED lamp can be choosed. Color Rendering Index up to Ra98, Truly restore the true color of the experimental object, the experimental results are more accurate. RG0 without blue light, protects the operator from blue light. Class II A2 Biosafety Cabinet Details Show 7'' LCD Touch Screen (Real-time monitoring and display Front window status/Airvelocity/Date/Time/Temperaturel-Filter and UV lamp life/System working status etc.) Air Velocity sensor (Real-time monitoring and display air velocity and precise control.) Removable work zone, 304 Stainless steel. (Easy to pull out, convenient for cleaning and disinfection.) Waterproof Socket (IP54) Water Tap (Optional) Optional upgrade LED lamp Details of Class II Cabinet This BSC Class II Type A2 has a front protective screen and transparent window design, and is equipped with multiple safety indicators and alarm devices to monitor the operating status of the equipment in real time to ensure the safety of use. The Class II type A2 biological safety cabinet's compact construction saves laboratory space and is suitable for placement in tight working environments. This class ii cabinet ensures efficient circulation and filtration of internal air, providing a clean working environment. The interior is equipped with a HEPA filter, which effectively filters microorganisms and particles in the air to ensure the cleanliness of the operating environment. Real-time monitoring and display front window status/Velocity/Pressure, Date/Time/Temperature/filter and UV lamp life/System working status etc. Accessories include power cord, Air velocity sensor, Foot switch, LED lamp, and instructions. Enquire Now Fill out the form below and together we will find a perfect customised solution tailored for your business. * First name * Email * Phone * State How can we help? Submit

GRANIFRIGOR™ Europe Product Tags Cooling Unit Frigortec Grain Quality and Processing Equipment The GRANIFRIGOR™ Europe range of grain cooling units are performance- and energy consumption-optimised for the temperature and humidity of European temperate conditions. Request A Quote * First name * Email * Phone * State How can we help? Submit Fields of Application Reliable grain cooling in temperate climates (rain, fog, heat and cold) - assured control of air humidity due to HYGROMAT™ automatic Complete suitability and reliable operation even at high ambient temperatures due to safe refrigerants Standard medium pressure version - ideal for tower silos too Product Overview GRANIFRIGOR™GC 40 Europe Storage size 1.300 t Cools 30-60 tons in 24 hours Up to 1,300 tons in 3 weeks GRANIFRIGOR™GC 80 Europe Storage size 2.500 t Cools 55-120 tons in 24 hours Up to 2,500 tons in 3 weeks GRANIFRIGOR™GC 140 Europe Storage size 4.600 t Cools 140-220 tons in 24 hours Up to 4,600 tons in 3 weeks GRANIFRIGOR™GC 180 Europe Storage size 5.800 t Cools 170-280 tons in 24 hours Up to 5,800 tons in 3 weeks GRANIFRIGOR™GC 240 Europe Storage size 8.200 t Cools 220-390 tons in 24 hours Up to 8,200 tons in 3 weeks GRANIFRIGOR™GC 320 Europe Storage size 10.000 t Cools 310-520 tons in 24 hours Up to 10,000 tons in 3 weeks GRANIFRIGOR™GC 500 Europe Storage size 16.000 t Cools 460-750 tons in 24 hours Up to 16,000 tons in 3 weeks GRANIFRIGOR™GC 700 Europe Storage size 25.000 t Cools 700-1200 tons in 24 hours Up to 25,000 tons in 3 weeks Handling and Operation Quiet normal running due to frequency-controlled fans and sound-optimised compressors Different operating modes through fully automatic Siemens S7 controller: very quiet (whisper operation - often needs to be run at night), rapid cooling (booster operation), ventilation operation (only air) and normal operation Efficient, large-area filter with integrated filter monitoring Increased safety through counter pressure display Optimal control through viewing window in air cooler Effective device protection through integrated phase and undervoltage monitoring Reliable start even at low outside temperatures due to speed-controlled condenser fans Easy and thorough cleaning due to easy accessibility e.g. by heat exchangers with wide fin spacing, housing doors, manholes and inspection openings in the air duct Energy and Environmental Balance Economical solution due to low power consumption Energy-efficient design due to frequency controls and state-of-the-art motors Environment friendly safety refrigerant - without CFCs and without HCFCs Further energy savings through winter and summer thermostats Permanent compliance and monitoring of setpoint cooling air humidity and temperature with HYGROTHERM™ Standard sound insulation for GC 180-GC 500 Workmanship and Quality Standard HYGROTHERM™ heating coil Electrical heating coil as standard Robust construction with stainless steel condensate tray Corrosion protection through coated heat exchangers Chassis fitted with robust pneumatic tyres for increased puncture protection with GC 40 - GC 180, optionally swivel castors Extra secure chassis equipment with puncture-proof solid rubber tyres for GC 240 - GC 500, optionally swivel castors Multi-stage quality control with factory test run Easy maintenance due to large, fully panelled doors Robust industrial design Depending on design, large TÜV-tested refrigerant collector and subcooler CE-compliant designs Options High pressure blower (HP) for slimline silo cells Protective grille against animals Parking supports Forklift pockets for easy device transport using a forklift Alarm modem (notification by SMS/email) for permanent monitoring Modem for remote diagnosis/remote display (app, LAN, WiFi/WLAN, GSM) Sound-proof cabin for -15 to -20 dB(A) Additional heating for seeds and/or brewer's malt Rotary field monitoring for effective device protection Signalling light for convenient remote device monitoring Fully automatic cool stop function FrigorTec app Key Features Fully automatic Siemens S7 controller Remote-controlled operation via FrigorTec app Low power consumption Large area filter Pressure-stable cooling air high pressure fans Rigid, welded frame construction Multi-coated steel parts Partially soundproofed housing UV-resistant external cable Eyelets for lashing on every housing corner Compressor from renowned manufacturer, e.g. Bitzer Many options available Factory test run before delivery Made in Germany Enquire Now Fill out the form below and together we will find a perfect customised solution tailored for your business. * First name * Email * Phone * State How can we help? Submit

ValProbe RT Humidity orTemperature Logger Product Tags KAYE Measurement and Calibration Equipment Validation System The Kaye ValProbe RT Humidity & Temperature Logger offers precise real-time monitoring of temperature and relative humidity for validation of controlled environments and stability chambers. Request A Quote * First name * Email * Phone * State How can we help? Submit Description The ValProbe RT logger with humidity and temperature sensors comes with RF technology to give users real-time data viewable on their Validation Console. With a humidity range of 15% to 95%, and a temperature range from 0°C to 70°C, this logger has a wide range of capabilities for temperature and humidity mappings. Digital sensor technology delivers unrivalled measurement accuracy and the new logger electronic design guarantees long battery life. Operator programmable sample rates starting at 1 second, allow collection of up to 100,000 data points per sensor. FIELD-REPLACEABLE DIGITAL SENSOR We designed this humidity logger with the end user in mind. At Kaye we understand that sending loggers back to the manufacturer for factory calibration, verifications, or repairs can slow down your production. That’s why this new ValProbe RT logger is built with a field-replaceable digital sensor. This allows users to quickly and cost-effectively replace the sensor without having to send the entire logger back to the calibration lab. The sensors are pre-calibrated before being sent to the user, guaranteeing precision and accuracy right from the start. EASY VERIFICATIONS IN YOUR LAB When verifying for temperature, simply attach the 1-meter extendable cable sensor for easy verification in a drywell, like the Kaye LTR-150. This dry block allows users to verify up to 18 humidity/temperature ValProbe RT loggers at once, saving a substantial amount of time. Once the probe is inserted into the dry block, the ValProbe RT software will perform an automatic verification and verify the temperature at multiple set points, determining the accuracy of the logger. Verifying relative humidity is also easy by using a portable humidity test chamber, which will evaluate the performance of multiple ValProbes at a time. The RT software will perform an automatic verification of the humidity sensors to show if the loggers have drifted. Additionally, reports can be generated automatically inside the ValProbe RT software, simplifying the process to review the report of the loggers. Key Features High accuracy measurement: 2% on humidity and 0.15°C for temperature 100,000 data samples per sensor Field-replaceable digital temp/humidity sensor 1 meter sensor extension cable Economical field-replaceable battery Operator programmable sample rate, start, delay and stop function Applications Stability chambers Incubators Warehouses Temperature chambers Specifications Specifications Humidity/Temperature Sensor Type Digital RH/T Sensor Sensor Length Up to 1 meter Tip Diameter Sensor tip: 0.295”, 7mm Outer filter: 0.472”, 12mm Measurement Range Temp: 0°C to 70°C Humidity: 15% to 95% Accuracy 0°C to 70°C, ±0.15°C 15% to 95% RH, 2% Kaye ValProbe RT Generic Specifications Logger Dimensions Hight: 1,9'' / Diameter 1,4''48mm / 36mm Logger Material Stainless Steel 316L and Peek Battery Field replaceable - 3.6V Lithium Sampling Rate Starting at 1 sec Data Storage 100.000 Samples retained in non-volatile memory Real-Time Clock Accuracy < 15sec/day Calibration NVLAP (NVLAP LAB CODE 200913-0) /DAkkS Calibration Verification Automated User Verification capability Sensing Element Digital Sensor Environmental Temperature 0°C to 70°C Environmental Humidity Non-condensing Regulatory Compliance UL and CE Enquire Now Fill out the form below and together we will find a perfect customised solution tailored for your business. * First name * Email * Phone * State How can we help? Submit

ValProbe RT Flexible Real-Time Temperature Data Logger Product Tags KAYE Measurement and Calibration Equipment Validation System The Kaye ValProbe RT Flexible Sensor Logger delivers precise real-time temperature validation for complex thermal processes in regulated environments. Request A Quote * First name * Email * Phone * State How can we help? Submit Description ValProbe RT Flexible Real-Time Temperature Data Logger - Single, Dual or 5-Sensor Logger The Kaye ValProbe RT Real-Time Data Loggers are available in various sensor configurations, including rigid, bendable, and flexible sensors. The flexible real-time data loggers offer configurations with one, two, or five temperature sensors. Each flexible real-time data logger has a storage capacity of 100,000 data points per sensor to ensure extensive data storage and backup. The flexible real-time data logger is equipped with a 1m/40-inch long, flexible, Teflon™-coated sensor cable and a stainless-steel tip to protect the RTD sensor. The operating temperature range of the logger extends from -85°C to +140°C. The 5-channel version is an ideal and cost-effective alternative when multiple measurement points are needed in a single application, such as qualifying an incubator or refrigerator. The flexibility and length of the sensors make them excellent for applications such as sterilizer drains, SIP processes (Steam-In-Place), and penetration studies in vials. The compact and flexible sensor of the logger allows for use in most pharmaceutical applications and is ideal for penetration studies even with very small vials. This versatility makes the Kaye ValProbe RT Real-Time Data Loggers an excellent choice for complex and critical monitoring tasks in GxP environments. Features Temperature range: -85°C to 140°C Available sensors: Single, Dual, and 5-Channel Sensor length: 1,000 mm (40") Sensor tip diameter: 2.4 mm Sensor tip length: 25 mm (0.98") Applications Steam sterilizers Steam in Place (SIP) Waterfall sterilizers Incubators Stability chambers Freezers Refrigerators Freeze dryers/Lyophilization Bioreactors and vessels Specifications Specifications Flexible Sensor Type Single, Dual and 5-Channel Sensor Length 40" inches 1000 mm Tip Diameter 0.095"; 2.4mm Measurement Range -85°C to 140°C Accuracy -85°C to 140°C, ±0.1°C Kaye ValProbe RT Generic Specifications Logger Dimensions Hight: 1,9'' / Diameter 1,4'' 48mm / 36mm Logger Material Stainless Steel 316L and Peek Battery Field replaceable - 3.6V Lithium Sampling Rate Starting at 1 sec Data Storage 100.000 Samples retained in non-volatile memory Real-Time Clock Accuracy < 15sec/day Kaye ValProbe RT Generic Specifications Calibration NVLAP (NVLAP LAB CODE 200913-0)/DAkkS Calibration Verification Automated User Verification capability Sensing Element Precision Platinum RTD Environmental Temperature -85°C to 140°C Environmental Pressure 0-5bar absolute Environmental Humidity 0-100% condensing Regulatory Compliance UL and CE Enquire Now Fill out the form below and together we will find a perfect customised solution tailored for your business. * First name * Email * Phone * State How can we help? Submit