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01-Jul-2019 - 05-Jul-2019

The Medical Device Summer School - From Concept to CE Marking

  • Location:
    • Thurloe Place
    • London
    • Greater London
    • SW7 2RS
    • United Kingdom
  • View on a map

Course overview

This comprehensive course has been designed to map the processes from device concept to marketing and show how regulatory, quality, clinical and other aspects of device development are joined into a continuous process. It will commence with a general introduction as to what devices are and how they are developed, and continue with lectures, workshops and case studies covering each process appliatble to device development, marketing and eventually the post market procedures. There will be ample time for informal discussions alongide the presentations and workshops.

Bringing a Medical Device to the market place is a complex and lengthy procedure which requires experience, knowledge and specialist skills. The contribution to a successful market placement comes from many different skilled individuals and organisations. Those contributing towards the placing of devices on the market should be aware of all the stages involved and be able to relate their responsibilities to the needs of other professionals, scientists, clinicians and regulatory and quality experts.

This comprehensive course has been designed to map the processes from device concept to marketing and show how regulatory, quality, clinical and other aspects of device development are joined into a continuous process. It will commence with a general introduction as to what devices are and how they are developed, and continue with lectures, workshops and case studies covering each process applicable to device development, marketing and eventually the post market procedures. There will be ample time for informal discussions alongside the presentations and workshops.

Benefits of attending this five day course

  • Understand the Procedures for Taking a Medical Device to the Market Place
  • Learn what Regulations Control the Manufacture and Marketing of Devices in the EU
  • Be Prepared for the Changes to the Requirements and the Impact of the MDR
  • Gain an Insight into Different Aspects of the Process for Obtaining the CE Mark for a Device
  • Discover a Holistic Approach to Device Development and Marketing
  • Participate in Workshops and Learn from Other People’s Experiences
  • Understand how Other Professionals Affect the Process for Bringing a Device to Market
  • Network with Participants from Organisations Similar to Your Own