In Vitro Diagnostic Medical Device Regulation (IVDR) Introduction eLearning Course

Details
Available Offerings

Objectives

This course will provide participants with an overview of the critical changes in relation to EU In Vitro Diagnostic Regulation, along with the implementation timescales.

Audience

This course is intended for, but not limited to, regulatory personnel, managers, CEO, CFO, or any medical device or IVD field personnel who want to learn about the new regulations

Click here to view available offerings

Online

Identifier{A40AC657-38C7-4334-B2DD-963948D20826}LanguageEnglish