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What You Will Learn:
Learn about the application of Risk Management to Medical Devices. Find out how to conduct a Risk Analysis on known Medical Device using templates. Become familiar with related topics such as Risk Evaluation and Risk Control.
Who Should Attend:
Managers and Technical staff of Medical Devices organizations who are in charge of certifying and qualifying their products. Also, people who wish to learn how Risk Management applies to their product.
This Seminar is closely related to ISO 13485 for Medical Devices.
Duration:
One day Seminar, also available on-site
CEU: 0.8 units
Check our training schedule for seminars
About the Seminars (Hours, Fee Structure, Location, How to register)
Seminar Outline:
- Overview of ISO 14971:2000
- Application of Risk Management including Risk Analysis, Risk Evaluation, Risk Control
- Brief outline of Risk Analysis Methods
- Conducting a Risk Analysis on a known Medical Device using templates
Please call or e-mail today at (416) 667-9119 or info@grt77.com for information and further details.
G.R. Technologies
1110 Finch Ave. West, Suite 516
Toronto, Ontario
M3J 2T2
E-mail: info@grt77.com
Tel: (416) 667-9119
Fax: (416) 667-1288