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Timely Implementation Strategies for Complying with New Regulations and Guidelines

April 10, 2018
  • London, United Kingdom

Join your colleagues at CBI’s very timely, one day summit on Medical Devices Regulation and MedTech Europe Code of Ethical Business Practices. You won’t want to miss this excellent opportunity to learn more about the latest 2017 changes and impact on the medical technology industry in Europe. Find out more about the key challenges and how companies are currently planning for implementation and compliance.

Key Attendee Benefits:

  • Hear Best Practices for Mitigating Risks with Third Parties
    While Complying with the MedTech Europe Code of
    Ethical Business Practices Guidelines
  • Understand the Upcoming MDR
  • Evaluate How Medical Device Manufacturers are Getting
    Their Devices Certified Through Their Notified Bodies,
    While Remaining Compliant With the New Regulation
  • Discuss Challenges of Remaining Efficient While
    Becoming Compliant with New Regulations
  • Learn How the New Rules Affect the Responsibilities of
    the Players in the Supply Chain