Best Practices When Validating Reusable Devices
The advancement of reusable medical devices has significantly transformed the medical device industry, bringing about changes in...
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Thermal Disinfection & Steam Sterilization Validation for Reusable Devices
Join hosts Jason Pope and Lise Vanderkelen in this informative webinar that will delve into the essential...
Cleaning Validations for Reusable Devices A Road Trip to the EU and US Market
Reprocessing validations for reusable medical devices have often been neglected, but recent regulatory developments have brought their...
Reprocessing Validations of Reusable Medical Devices
Reprocessing validations of reusable medical devices have often been neglected, with their importance underestimated until recently. However,...
If Something Looks Clean, Is It Really Clean? Cleaning Validations for Reusable Devices
Reprocessing validations of reusable medical devices have often been overlooked. However, the upcoming Medical Device Regulation (MDR)...
DISINFECTION VALIDATION: How to Classify and Validate Your Medical Device Disinfection Process
Reprocessing reusable medical devices involves cleaning, disinfecting, and sterilizing them to ensure they are safe and effective...
Considerations for Third-Party Reprocessing of Single-Use Medical Devices
Reusing single-use devices that have been safely reprocessed by a third-party reprocessor offers significant benefits for healthcare...
Chemical Disinfection Validations for Reusable Devices
Chemical disinfection validations for reusable devices are critical to ensure the safety and efficacy of medical devices...
Successful Medical Device Cleaning Validations: What You Need to Know
Validating cleaning instructions for a tray of reusable orthopedic devices is an essential milestone on the path...
Single Use & Newly Manufactured Device Cleaning Validations
Performing a cleaning validation during the initial phase of a device’s lifecycle is crucial for manufacturers to...