Alternatives to PMCF Clinical Investigations

This on-demand webinar, hosted by Greenlight Guru, focuses on exploring alternatives to Post-Market Clinical Follow-up (PMCF) clinical investigations for medical device regulatory compliance in the EU.
Watch this video to gain valuable insights on accommodating clinical data to meet PMCF requirements under the EU MDR.
Main points covered:
1. Different alternatives to a full-scale PMCF clinical investigation.
2. Criteria for selecting an alternative method for PMCF.
3. Guidance on choosing the most suitable alternative for a specific medical device.
4. Strategies to ensure compliance with the EU MDR using alternative PMCF methods.
5. Practical advice on implementing these alternatives effectively.
Target Audience:
• Medical device manufacturers with products in the EU market
• Professionals aiming to market medical devices in Europe
• Regulatory affairs and compliance specialists
• Clinical operations and quality management personnel
Access the printable slides for this presentation by visiting:
www.greenlight...