Venue: LINK Medical ApS Office, Vimmelskaftet 47. 1. Sal, 1161 København K, Denmark
Time: 14:00 - 17:30
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CHECK EVENT LINK FOR NEW DATE TO BE CONFIRMED
RBM is a regulatory requirement when performing clinical trials. This requirement is an enhanced concept and requires a change in the mindset for the implementation of updated and new processes when conducting clinical studies. The responsibility for these processes always lies with the sponsor, irrespectively if the task in itself is delegated to an outside vendor.
Come listen to Gunnar Danielsson Senior Regulatory Advisor, and Philip Lange Møller, two former GCP Inspectors, talk about risk based quality management and monitoring. At this seminar you will learn:
To read about the speakers and register please Go to the event page
Registration closes April 25th or when it’s fully booked.