Date: 8 May 2025
Time: 16:00h - 17:00h CET
Location: Virtual
Language: English
Introduction
The latest UK Post-Market Surveillance Regulations will have significant implications for your business. Join our webinar by industry experts Dennis Sarwin and Melissa Smits to explore the purpose of the new regulations, the key changes, and the differences and impact on CE-marked medical devices in the UK.
The webinar consists of a 45-minute presentation and a live Q&A. Questions for the Q&A session can be sent in through the registration form, by email at marketing@qservegroup.com or during the webinar.
Learning Objectives
- Learn about the new UK PMS requirements
- Learn about the impact of the new regulations on your post-market procedures, vigilance procedures and your CE-marked medical devices in the UK
Who should attend the webinar?
The webinar is essential for professionals in the medical device and in-vitro diagnostic industry who want to sell or already sell their products in the UK.
- Regulatory Affairs Specialists & Managers
- Post-Market Surveillance Teams
- Quality Assurance & Compliance Officers
Qserve Speaker