Make compliance your success factor – a conference for QA/RA professionals
Join our Medical Device Quality Assurance and Regulatory Affairs conference: An international conference on medical device pre- and post-market strategies to maintain safety and effectiveness throughout the medical device product life cycle.
We will outline strategies, evaluate and demonstrate device safety and effectiveness during the entire product life cycle, starting from user needs, through design, manufacturing, and a proactive post-market surveillance, in close collaboration with your key stakeholders.
Date: 26-27 October 2022
Venue: Lund, Sweden
WHAT
- A conference with a real life cycle approach, on medical device quality and regulatory processes
- An opportunity to deepen your understanding on responsibilities of, and relationships between, economic operators
- Presentations, interactions, and workshops that will give new insights and tools, for your daily work
WHY
- Stay in top of the latest interpretations of the regulations
- Listen and learn from some of the most experienced experts within the industry
- Broaden your understanding, learn new skills and expand your professional network
WHO
Professionals working with:
- Product safety, as Quality or Regulatory Design and development
- Clinical/ performance evaluations
- Post-market-clinical follow-up activities
- Process development
- Quality Assurance/Regulatory Affairs
This conference will include:
2 Days of networking, expert speakers and workshops
Organized by:
