Post-Market Surveillance and Vigilance for Medical Devices
Venue: TOPRA Office, 3 Harbour Exchange, London, UK.
Start: Wednesday 23 Oct 2024 13:30
End: Friday 25 Oct 2024 15:30
This event is brought to you by TOPRA.
Learn about the key terminology and core concepts of vigilance and Post Market Surveillance (PMS) in our Post Market Surveillance and Vigilance for Medical Devices Masterclass.
Led by industry experts, this masterclass will give you practical insights into how these processes are applied and integrated throughout the life cycle of a medical device, with a strong focus on meeting European requirements. You will also learn how to critically appraise and make recommendations on the implementation of a PMS system.
By attending on 23-25 October 2024 in London, UK and online you’ll learn to:
✅ Assess communications and legal documentation from authorities, notified bodies, and other stakeholders.
✅ Develop an understanding of European legislation, guidance, and documentation relating to surveillance and vigilance for medical devices.
✅ Understand how to navigate complex issues and make well-informed decisions, even when faced with incomplete data.
✅ Effectively communicate your conclusions clearly to specialist and non-specialist audiences.
✅ Develop a network to support you for the rest of your career.
✅ Earn 15 CPD hours.
This programme will be led by several experts including Stephan Buttron of Buttron Consulting, Grant Castle of Covington & Burling LLP, Adrian Keene of North American Science Associates (NAMSA) and Jenny Young-Gough of JYG Consulting.
Whether you're advancing your career in regulatory affairs or looking to deepen your understanding, this masterclass will equip you with the essential knowledge for navigating EU compliance and regulations.
This course is part of our range of masterclasses and is Module 16 in our MSc programme. Our masterclasses are developed and delivered by a faculty of expert speakers and validated by the University of Hertfordshire.
Discounted rates are available for TOPRA MSc students, those working for regulatory or government agencies, academic institutions, charities, patient groups, or in full time education.