2nd Annual Medical Devices Regulations & Safety 2024
- 05th — 06th December, 2024
CLIN-r+ are delighted to announce their participation at the 2nd Annual Medical Devices Regulations & Safety 2024 Conference!
Our Director of Clinical and Regulatory Affairs, Jacqueline van Druten will be discussing the Ace your submission – Focus on EU MDR Clinical Evaluation Conformity routes. What you need to know for your legacy and new products:
Day 2 – 15:35 – 16:00 Ace your submission – Focus on EU MDR Clinical Evaluation Conformity routes. What you need to know for your legacy and new products.
The panel will include MedTech regulatory expert Jacqueline van Druten (MICR.CIM.RD) Clinical Regulatory Affairs director from CLIN-r+ and other industry though leaders to discuss this topic and help you build an understanding around the key strategic plans needed to unlock the potential of your MEDTech innovation.
We always enjoy a catch-up and chat, and you are also welcome to make an appointment with us in advance to discuss your regulatory or clinical affairs needs to obtain your MDR CE mark or your GREEN transistion. During the event, we will be offering clients a free 40-minute consultation (at the event or virtually) to discuss your most pressing EU MDR Clinical Regulatory questions.
Note: Limited seats and only one session per company.
More about 2nd Annual Medical Devices Regulations & Safety 2024 Conference:
We are thrilled to bring together industry leaders, regulatory experts, and stakeholders for two days of insightful discussions, collaborative learning, and networking opportunities. Throughout the conference, attendees will gain valuable insights into the latest regulatory updates, emerging safety standards, and innovative strategies for compliance.
From risk management methodologies to quality assurance best practices, our diverse range of sessions will equip you with the knowledge and tools needed to navigate the complex landscape of medical device regulations. Join us as we explore the future of medical device safety and regulation together!
Key poins:
• Updates on medical device regulations and safety standards. • Discussions on improving safety practices.
• Strategies for navigating regulatory complexities.
• Effective risk mitigation techniques.
• Ensuring product integrity through quality assurance.
• Exploring the impact of emerging technologies on regulations. • Networking opportunities and collaboration for industry pro- fessionals and regulators.
Download 2nd Annual Medical Devices Regulations & Safety 2024 Conference Official Brochure!
