EU MDR – Understanding the Medical Device Regulation and European Market Requirements

This webinar introduces the European Union Medical Device Regulation (EU MDR) and its implications for medical device manufacturers seeking access to the European market. Participants will explore the regulation’s key requirements, medical device classification, conformity assessment, CE marking, and post-market surveillance obligations.

By the end of this webinar, participants will be able to:

• Understand the purpose and scope of EU MDR.
• Identify the major changes and requirements introduced by the regulation.
• Understand medical device classification and conformity assessment requirements.
• Recognize key regulatory and compliance considerations for accessing the European market.

Agenda

• Introduction to EU MDR
• Scope and key regulatory requirements
• Medical device classification
• Conformity assessment and CE marking
• Post-market surveillance and compliance
• Q&A

Target Audience

This webinar is recommended for:

• Medical device manufacturers
• Regulatory Affairs professionals
• Quality Management professionals
• Medical device consultants
• Medical device importers and distributors
• Organizations preparing for EU market compliance

Language: Arabic

Cost: No Charge