Learn how to comply with European medical device requirements with our Essentials of European Medical Device Regulatory Affairs training course. You will get a comprehensive overview of the industry in an interactive environment which will be ideal for anyone starting a career in regulatory affairs.
By attending this training course on 29 November 2024, either in-person in Berlin or online, you will:
✅ Develop a broad understanding of the regulatory affairs profession within the medical devices industry
✅ Learn from expert speakers while gaining a clear and concise understanding of the industry
✅ Build a network that will support you for the rest of your career
✅ Earn 6 CPD hours
This course is led by Theresa Jeary from the British Standards Institute BSI-KSA and Angela Stokes from Sharp Regulatory Consulting Limited, both of whom bring a wealth of industry knowledge and experience that will enhance your learning.
Book now 👉 https://www.topra.org/TOPRA/TOPRA_Member/Events/Event_Display.aspx?EventKey=MDBAS1124&Category=BASIC
This course is part of our range of Basics training courses which are aimed at those wanting to take their first steps in regulatory affairs or from other disciplines who require an overview.
Discounted rates are available for those working for regulatory or government agencies, academic institutions, charities, patient groups, or in full time education.
