ComplianceOnline, Online Event
2012-09-11
Why Should You Attend: Understanding risk management in medical devices is a must do for any professional serving medical industry in any format. It tends to improve product reliability and durability and by that minimize warranty costs, recalls, bad press and more. ISO 14971 promotes good practices and processes necessary to ensure proper risk management is put in place - and it is effective.
During this 120-minute session, the presenters - Jasmin NUHIC and Salim Khan - will share their experiences and insight gained from implementing risk management processes in medical device companies. You will learn from real-life examples, as well as from the research they have conducted in the area of risk management for medical devices. The discussion will be highly interactive and participants can ask specific questions related to the company/environment they serve. Areas Covered in the Seminar: - FDA and ISO 14971.
- Risk Management Process.
- Risk Analysis.
- Risk Evaluation.
- Risk Control.
- Overall Residual Risk Evaluation.
- Production and Post-Production.
- Questions and answers and give opportunity to ask specific questions related to the company/environment you serve.
Event Details: Date: September 11, 2012 Time: 09:00 AM-11:00 AM PDT Cost: $299 per attendee per computer terminal Registration: SIgn-Up on-line now. Add to your shopping cart. |
|