The Dutch clinical research Foundation's annual congress 2018 will be all about the implementation of the Medical Device Regulation (MDR) and its influence on Medical Device research in the Netherlands. Some experienced speakers will take you on a journey and show you how the Netherlands wants to maintain its leading position as a high-quality research country at Europes top level.
This congress in intended for members of Ethics Committees, Clinical Research Associates, Research Nurses, Trial Managers, Researchers and Medical Specialists, Patient Organizations, Pharmacists, Government Representatives and Hospital Lawyers.
Factory CRO's director Clinical Operations Niels van Tienen will be a guest speaker at the workshop sharing his expertise about the impact of the MDR on research with Medical Devices. Please join us there, click here to get in contact!
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Join us and prepare yourself together with Dutch Clinical Research experts for the MDR implementation in 2020