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"What to consider when developing a clinical strategy for CE marking of a new medical device" by Nancy Boodhun, NAMSA

About Nancy: Nancy has over 17 years of experience of clinical research gained through in-house roles for medical device manufacturers. She currently holds the position of Clinical & Consulting Specialist at NAMSA, where she is able to transfer her knowledge to clients considering their clinical strategy and study execution for new product developments and post market requirements.

Please register via our Eventbrite link: https://oxmcefmay2018.eventbrite.co.uk