Erik Vollebregt

medical devices mdr ivdr in vitro diagnostics ivd software medtech ivds privacy mhealth ehealth eu data protection clinical trial clinical data clinical evaluation medical device gdpr cybersecurity eudamed apps ce marking ivd directive notified bodies molecular diagnostics economic operators product liability europe clinical research security personal data transparency recast 3d printing healthcare hcp compliance sunshine supply chain distribution biotechnology and pharmaceuticals medisch hulpmiddel post marketing surveillance medicinal products advertising packaging pregnancytesting self-test certification exemption corona covid-19 mergers and acquisitions m&a class i qms prrc ivdd ziekenhuizen european law performance evaluation tissue samples raps general data protection regulation sterilization reusable medical devices hospital reprocessing custom made devices additive manufacturing conformity assessment classification connected health telemedicine patient data outsourcing reporting networks wearables health data confidentiality revision unique device identifier udi medicinal devices biofabrication atmp regulatory health market surveillance mobile health fcpa bribery genetics imports dia euromeeting importer distributor regulation stem cell cell cell therapy biotechnology software as a service social media subcontracting pms ipad app combination products who borderline products borderline world health organization netherlands germany marketing uk diet food food information food supplements en 62304