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Annet Visscher

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Adverse Event reporting in Medical Device Clinical Trials under the MDR
20210413 nvfg acs iso14155 13_apr2021
EU Clinical Investigations Taipei 2018
Globalization of Clinical Trials: Mutual acceptance of Medical Device data
Premarket Clinical Evaluation under the EU MDR proposal
Medical Devices Postmarket Surveillance in Europe updated
ACS IIT 24_nov2013
Medical Devices Postmarket Surveillance 14 jul13