This on-demand webinar, hosted by Greenlight Guru, explores the criticality of Post-Market Surveillance (PMS) in ensuring the safety and efficacy of medical devices and combination products. Using case studies to illustrate the key elements of an effective PMS system, this webinar highlights the evolving regulatory requirements and offers best practices for MedTech professionals.
Main points covered:
1. Key elements and importance of Post-Market Surveillance for medical devices and combination products.
2. Integrating risk management and usability into PMS.
3. Exploring the differences in PMS requirements in the US and EU.
4. Utilizing PMS for label expansions and leveraging real-world evidence.
5. Addressing future challenges in PMS, including personalized devices and 3D printing.
Target Audience:
• Medical Device Industry Executives
• Quality Professionals and Management
• Regulatory Professionals and Management
• Clinical Affairs Professionals and Management
• R&D Engineers and Management
Access the printable slides for this presentation by visiting:
www.greenlight.guru/webinar/p...
Негізгі бет Ғылым және технология Post-Market Surveillance for Medical Devices & Combination Products
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