Visioner les webinars

2015 webinars

  • FDIS ISO 13485 Update
  • Software regulation
  • ASEAN MDD
  • Product responsibilities
  • MDR product reclassification
  • Clinical evaluation and investigations
  • Person Responsible for Regulatory Compliance
  • IVD Field Safety Notices
  • Audits Inopinés – Retour d'expérience (FR)
  • Mise à jour réglementaire DDM et DMIA (FR)
  • Medical Device Single Audit Program















Do you understand how software is regulated? 20 Nov 2015




Will your product be reclassified under the new MDR? 09 Sept 2015