Pre-Market Medical Device Studies and GCP - Strategies for Success

This on-demand webinar, hosted by Greenlight Guru, focuses on strategies for success in pre-market medical device studies by adhering to Good Clinical Practice (GCP) guidelines. Discover the best practices for designing and conducting clinical trials that meet regulatory standards and ensure the safety and efficacy of your medical device.

Main points covered:
1. Overview of Good Clinical Practice (GCP) guidelines
2. Key considerations for designing pre-market medical device studies
3. Strategies for ensuring compliance with regulatory requirements
4. Best practices for managing clinical trials and data integrity
5. Case studies and lessons learned from successful pre-market studies

Target Audience:
• Clinical Research Professionals
• Regulatory Affairs Specialists
• Medical Device Manufacturers
• Quality Assurance Managers

Access the printable slides for this presentation by visiting: https://www.greenlight.guru/webinar/p...