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

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Category FDA GXP Compliance - Medical Devices

Deadline: December 11, 2014 | Date: December 11, 2014

Venue/Country: Tampa, U.S.A

Updated: 2014-12-02 22:20:50 (GMT+9)

Call For Papers - CFP

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.

Learning Objectives:

To educate attendees on the vital reasons for risk management and the key role it plays in the product life cycle

To demonstrate the requirements of ISO 14971, how they reflect FDA concerns

To clarify how risk management impacts international standards, such as IEC 60601, and how to conform to risk management requirements

To provide practical application experience and skills in the process and tools of risk management, enabling attendees to be effective risk managers

Who will benefit:

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.