27FEB2025 Webinar – Distributor Requirements – EU MDR

Date:?Thursday, February 27^th

Time: 5pm (GMT+1hr / CET / French time) / 8am (USA Pacific Standard Time)

Join us for an engaging and informative webinar on Medical Device Regulation and Invitro Device Regulation impact on Distributors!

Whether you’re a professional looking to expand your knowledge on the topic or learn real solutions that have been implemented, this session will provide valuable insights, expert and experienced advice, and practical solutions that have proven to work through multiple audits and companies across multiple notified bodies.

What to Expect:

• Deep dive into relevant aspects of MDCG 2021-23 Guidance for notified bodies, distributors and importers on certification activities, ?Article 14 ? General Obligations of Distributors, and Article 16 ? ?Cases in which obligations of manufacturers apply to importers, distributors or other persons?
• Gain insight into a phased implementation approach and lessons learned from real-world examples and case studies
• Review requirements and responsibilities for the Economic Operators that provide import and distribution services for the European Union (EU).
• Learn about solutions to facilitate improving at your own pace
• Interactive Q&A session with our panelists
• Actionable tips and tools to apply to your work
• Expert speakers from quality/regulatory and technical lead that supported MDR certification for multiple quality systems for both EU and non-EU based medical device manufacturers and distributors.

Who Should Attend:

• Distributor personnel responsible to handle field actions on behalf of manufacturers
• Quality or Regulatory personnel that interact with distributors and importers

Don?t miss this opportunity to expand your knowledge, network with like-minded individuals, and stay ahead of the curve!

This purchase is not transferable to another individual or company