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On-Demand Webinars

Learn from our experts on industry topics.

SVP Packaging – NB Persepective on CE-marked Medical Devices versus Article 117 MDR Combination Products

This presentation will provide an overview of considerations regarding biological risks from primary packaging materials for CE marking of combination...

US Drug Delivery Combination Product Regulatory

This presentation will include a short summary of the types of Drug Delivery Combination products codified by US FDA regulation,...

Overcoming a Cytotoxicity Failure

Every medical device needs to have proven biocompatibility to protect users from potential biological risks arising from its intended use....

A Structured Approach to Selection of Container Closure Materials for Small Volume Parenterals – Pipe Dream or Necessity?

This presentation will provide reasons why material selection for small volume parenteral container closures should be built upon well-defined attributes...

Reprocessing Validations: Flexible Endoscopes and AAMI ST91

The new revised AAMI ST91:2021 not only discusses flexible and semi-rigid endoscope processing in healthcare facilities but also the requirements...