Advanced Biocompatibility

Information från Medico Industien - vår systerförening i Danmark.

The recent release of ISO 10993-1:2018 and the upcoming Medical Device Regulation (MDR) General Safety and Performance Requirements (GSPR) bring new challenges for medical device manufacturers.
This course is structured to be hands-on and is designed for those who have a working knowledge of biocompatibility and are looking to update and sharpen their skills, in light of new updates and developments.

Led by a trainer from Namsa with substantial experience in biocompatibility, chemical characterization and sterilization validation, the course will also be augmented with a Q&A session (via teleconference) from a certified toxicologist, as well as case studies provided both by the trainers and by notable Danish medical device manufacturers. 

For more information and registration >>


Sveavägen 63, Stockholm

Box 3601
103 59 Stockholm

Telefon 08-586 246 00 (vxl)


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