Medical Device Risk Management A to Z - Best Practices for Effectiveness and Efficiency: 2-day In-person Seminar

FDA views risk management as an essential process both during inspections and in the review of pre-market submissions. Effective risk management has become critical to medical device manufacturers and this interactive two day seminar is aimed at providing medical device professionals with the tools necessary for effective risk management implementation in device manufacturing and marketing.

• Project managers
• Quality managers and staff
• R & D managers and staff
• Regulatory and compliance managers and staff
• Anyone with risk management responsibilities

Use coupon code 232082 and get 10% off on registration.