When Design Input Requirements Go Wrong

This on-demand webinar, hosted by Greenlight Guru, focuses on the critical role of design inputs in the development of medical devices and the common pitfalls encountered in defining design requirements.

Watch now as we delve into the importance of getting design inputs right, which can take up a significant portion of the project timeline, especially for complex designs.

Main points covered:
1. Common mistakes made in defining design requirements (and how to avoid them)
2. Understanding design input requirements according to FDA 21 CFR 820 and ISO 13485:2016
3. The process of effectively defining design inputs
4. Various sources for obtaining design inputs
5. Best practices for mastering design input requirements
6. A real-life case study illustrating these concepts
7. Interactive Q&A session for deeper insights

Target Audience:
• Medical Device Executives
• Regulatory Affairs Professionals and Management
• Quality 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/design-input-requireme…