Although the effective date of the Regulation (EU) 2017/745 has been delayed to 26 May 2021, medical device companies are still facing major changes. However, the regulation represents not only a compliance challenge but also a huge chance for a company-wide approach. If you want to know what companies need to do to become EU MDR compliant, this webcast fits perfectly.

The 45 minutes presentation deals with the main topics of the regulation and the latest updates and developments. The webcast will focus on device registration, Unique Device Identification (UDI) data management, product labeling and the handling of master data. Learn why an integrated, model-driven, and flexible Master Data Management (MDM) platform can provide the functionality needed to meet compliance requirements.

After the presentation you will have the opportunity in the Q&A session to raise your questions to the expert.

TARGET GROUP

UDI Team Members
Product Labeling Team Members
Global Strategy Business Managers
Regulatory Affairs/Operation Leaders
Product Managers and Business Analysts
Manufacturing, Operations, and Supply Chain Leaders
Quality Leaders
Medical Device IT Support Personnel

LEARNINGS

Holistic overview of the latest developments of EU MDR
Compliance challenges of the medical device industry
Learning for your daily business
Harmonization of substrate and printer