Understanding biocompatibility of medical devices

Medical device manufacturers must conduct biological safety (biocompatibility) evaluations for their medical devices to meet regulatory obligations and receive approval to market medical devices. The complexity of this process is increasing due to new regulatory requirements. Do you have an updated strategy for the biological evaluation of your medical device products?

Welcome to join us at the next Medicon Valley MedTech Network meeting to learn more about ISO 10993* and the recent changes in the standard, and understand how to make a biological evaluation of your medical device products.

Tidspunkt

tir 02 okt 18

Arrangør

DTU

Kontaktperson

Hvor

Auditorium, Medicon Village, Lund

Scheelevägen 2,
Lund, 223 63 Sweden