Medical Device Biocompatibility and Toxicology is a conference dedicated to the revision of ISO 10993, especially Part 1, Part 17, Part 18 and Part 2.
Topics
- ABBOTT - Post Market Changes and the Impact on Biocompatibility
- DEPUY SYNTHES - Overcoming the Contradictions Between FDA Regulation and MDR
- CONVATEC - Reporting the Current Status of the Revision of ISO 10993
- SMITH & NEPHEW - Creating Efficient Biological Evaluation Plans within a Risk Management Process
- MEDTRONIC - Utilizing In-Vitro Testing as an Alternative to In-Vivo Testing
- BOSTON SCIENTIFIC - Dealing the Chemical Characterization and the Toxicological Risk Assessment According to ISO 10993-18 & Upcoming ISO 10993-17
