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On-Demand Webinars

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ISO 10993-1: Key update on the new revision of this critical standard

This webinar delves into the latest updates to ISO 10993-1, the cornerstone standard guiding biocompatibility assessment for medical devices. The...

Reprocessing Rethought: An Open Forum Discussion On Approaches for Cleaning Validations of Single-Use 3D Printed Devices Processed at Healthcare Facilities

The presence of 3D printed single-use devices that require processing (cleaning and disinfection or sterilization) at the healthcare facility prior...

Reprocessing Rethought: An Open Forum Discussion On Novel Decontamination Methods for Reusable Medical Devices

As reusable medical devices have advanced, the importance of effective decontamination methods (cleaning, disinfection, and/or sterilization) has increased to ensure...

Regulatory Insights: The Future of MedTech and Pharma Under the New Administration

The new presidential administration in the United States could significantly impact MedTech and pharmaceutical regulations for manufacturers and product developers....

Navigating the FDA’s Medical Device Presubmission Process

This webinar provides a comprehensive overview of the FDA’s medical device pre-submission process, a critical step for manufacturers seeking to...