Are you ready to delve beyond the textbook scenarios and explore the tangible challenges and opportunities of Post-Market Surveillance (PMS)?
We’ll take you through the complex world of PMS and Post-Market Clinical Follow-Up (PMCF), breaking down what regulators really expect today. But it’s not just about overcoming challenges; it’s about seizing the opportunities that PMS presents. Discover how a well-executed PMS system can become a powerful tool for enhancing device safety, improving product design, company´s benefits and, ultimately, ensuring patient satisfaction.
Join Laura Eder, our expert in Medical Device vigilance, and equip yourself with firsthand knowledge to master your PMS strategy with confidence. She will go over:
- Real-World Challenges: Understanding the practical challenges of implementing PMS under the new MDR, with a focus on actual case studies and experiences.
- Seizing Opportunities: Uncovering how to turn PMS challenges into opportunities to improve processes, enhancing device safety and strengthening market presence.
- Maximizing Impact: Learning how a well-implemented PMS can transform patient care and set new standards in the medical device industry.
Registrations are open. You can register here: POST-MARKETING SURVEILLANCE SYSTEM WEBINAR
For further information, you can contact us at: [email protected]
