LinkedIn Live: Don't Bury Your Head in the Sand: MDR is Here

As CEO and Owner of AKRA TEAM and former Vice President of TÜV SÜD, Dr Bassil Akra has extensive experience in guiding medical device companies through the intricate regulatory landscape.

Dr Akra has played a key role in drafting and implementing major EU regulations, including the MDR as well as In Vitro Diagnostic Regulation (IVDR).

His consultancy, AKRA TEAM, was founded to support the medical device industry in meeting regulatory requirements while prioritizing patient safety.

In this recorded LinkedIn Live, Dr. Akra covers:

• The current state of MDR and why companies must adapt now
• How the MDR will impact innovation and product development in Europe
• The critical role of notified bodies and their differing interpretations of regulations
• How regulatory shifts will affect marketing strategies

You won’t want to miss this opportunity to hear directly from one of the foremost experts in EU medical device regulations!