Join our exclusive webinar tailored for medical device manufacturers in the Middle East region, focusing on the pivotal transition from the Medical Device Directive (MDD) to the Medical Device Regulation (MDR). This transition marks a significant shift in the regulatory landscape for medical devices in Europe, impacting manufacturers globally. 

Objective

This webinar aims to demystify the MDR transition process, highlighting key changes and strategies for compliance. Attendees will gain valuable insights into the MDR’s requirements, timeline, and impact on their operations. SGS experts will bring a wealth of experience in medical device regulations, ensuring an informative session for all participants. 

 Agenda

• Overview of MDR: Understanding its scope and objectives. 
• Transitioning from the MDD to the MDR
• Key Changes: Key regulatory changes and their impact on manufacturers.
• MDR Transition Timeline: Critical deadlines and milestones for compliance. 
• MDR in SGS: How SGS can support your transition and compliance efforts. 
• Key Stages for Transition: Practical steps for manufacturers to achieve compliance with the MDR.

Background 

The Medical Device Regulation (MDR) introduces more stringent clinical and post-market surveillance requirements, expanding the scope of covered devices and tightening the rules on device classification. Transitioning from the MDD to the MDR is not just a regulatory formality; it's a necessity for market access and continued compliance.

Target Audience: This webinar is specifically designed for professionals involved in the medical device industry in Pakistan, including regulatory affairs specialists, quality assurance managers, and senior management of medical device manufacturing companies. 

Language: English
Cost: No Charge

Can't make a live session? Register now and receive a complimentary recording after the live event. For further information, please contact: me.mkg@sgs.com.

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