Wenche Groennvold


Wenche Groennvold work as a senior regulatory associate medical device at Link Medical Research AS, a European CRO based in Norway.  She has 15 years of experience working in the medical device industry in Sweden, Norway and Switzerland with companies like Vascutek Ltd (now Terumo Vascutek), Philips, Sonosite and St.Jude Medical. She has a BSc in occupational therapy from the University College of Oslo and a master degree in Clinical Research Management from the University of Liverpool.

Her focus and special interest the last few years has been on clinical research and the new European Medical Device Regulation and in December 2015 she completed her 9 month long master thesis about the new European medical device regulations impact on clinical investigation for manufacturers of implantable medical devices.