Erik Vollebregt

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