This on-demand webinar, hosted by Greenlight Guru, focuses on the crucial role of risk management in the medical device product lifecycle. The webinar provides actionable insights into how to effectively apply risk management best practices at every stage of the product lifecycle, from concept to obsolescence.
Main points covered:
1. Integrating Risk Management in all phases of the Product Lifecycle.
2. The evolving nature of the Risk Management File throughout the lifecycle.
3. The necessity of a closed-loop approach in Product Surveillance for safety assurance.
4. Maintaining ongoing Risk Management to balance the benefits and risks of the Medical Device.
5. Open Q&A session addressing specific concerns and strategies.
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:
[ Ссылка ]
