Medical Device Risk Management A to Z - Best Practices for Effectiveness and Efficiency

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Category Medical Device;

Deadline: September 10, 2015 | Date: September 10, 2015-September 11, 2015

Venue/Country: Chicago, U.S.A

Updated: 2015-08-24 21:11:39 (GMT+9)

Call For Papers - CFP

Learning Objectives:

Upon completion of the course, the participants will have learned how to implement good risk management principles into medical products manufacturing operations such as medical devices, combination products, and pharmaceuticals:

Understand what are the current issues and recommended solutions

How to implement the ISO 14971 framework

Use a Traceability Report for improved risk management operations

How to Use Standards to Facilitate Product-to-Market Achievements

Who will benefit:

The course is designed for manufacturing professional employees that must interface with or implement product risk management activities in a medical product manufacturing operation.

Product Risk Managers

Quality Assurance

Regulatory Affairs

Research & Development

Project Managers

Operations Managers

Note:

Use coupon code NB5SQH8N and get 10% off on registration, Valid till Dec 31st 2015.

For Registration:

http://www.complianceonline.com/iso-14971-medical-device-risk-management-a-to-z-best-practices-seminar-training-80076SEM-prdsm?channel=ourglocal