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On-Demand Webinars

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Reprocessing Considerations during Design Development for Reusable Medical Devices

Reusable medical devices are medical devices intended for repeated use on patients. These devices range from simple, non-invasive types, such...

Sterilization by Filtration: Validating Filtration for an Aseptic Process

This presentation explores the validation of sterilization by filtration as a critical step in aseptic pharmaceutical processing. Sterile filtration ensures...

Beyond Biocompatibility: 10993-1 & FDA Expectations for Particulate Evaluation in Vascular Devices

Recent updates to ISO 10993-1 and evolving FDA feedback are raising the bar for particulate evaluation in vascular medical devices....

A Dive into Disinfection Validations of Non-critical Devices

This discussion swims through topics related to disinfection validations of non-critical devices. Including selecting the appropriate level of disinfection, methods...

DAY 1 – Big Changes in Medical Device Biocompatibility: Updates Coming to ISO 10993-1

This three-day webinar series explores major changes coming to medical device biocompatibility standards. Day 1 covers critical updates to ISO...