Jan 12

Online Event

This webinar is focused on understanding the requirements of the Medical Device Directives, their linkage to the EU Clinical Trial Directive, and the requirements of CE Marking and ISO Certification on commercializing products. The training will be discussing the recently implememented and currently planned changes to the Medical Device Directives across the EU. It includes specific insight from direct involvement and work within the EU and the Commission's major improvement objectives to their system today. Specific targeted areas for change are discussed as well as the likely implementation timetable.