FREE Webinar – Post Market Clinical Follow-Up

Join us for this free webinar: Post Market Clinical Follow-Up for a Medical Device – How to reach MDR Requirements? December 16, 2020  •  14.00-14.20 CET Learn more about how you can apply a post-market clinical follow-up in order to collect clinical data What is a post-market clinical follow-up (PMCF)? Examples of activities under PMCF How to […]

Emma Pedersen – New director for Biological Evaluations & Toxicology

Say hello to Emma Pedersen! New director for Biological Evaluations & Toxicology at Key2Compliance®. Emma Pedersen comes from 11 years at RISE (Research Institutes of Sweden) working as a research scientist, mainly with biological evaluation of medical devices according to ISO 10993 (including in vitro testing under GLP) and replacement of animal testing methods for […]