If you missed Eurofins Medical Device Testing’s live design & development conference track at MD&M East, or just want to view it again, you can now view our six sessions on-demand to help ensure your medical device design verification plan meets FDA expectations, new EU regulations, and the new ISO 10993-1 guidance.

  • Changes in Europe’s Medical Device Regulation: Consequences for Manufacturers

  • Developing Test Strategies Per the New ISO 10993-1: Current Status & Upcoming Changes

  • Chemical Characterization: The Starting Point for Biological Evaluations

  • Biocompatibility Basics: Making Sense of the Annex A Matrix

  • Developing a Testing Plan for Medical Device Design Verification

  • Endotoxin Testing: Make Sure FDAs New Guidance Doesn’t Delay Your Product Launch

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on-demand sessions.