Join us for a webinar that will provide an overview of the changes to an important Medical device Risk management standard, ISO 14971:2019. And learn how it can help in the current situation.
Objectives:
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Understand the key elements required for the management of risk as specified in ISO 14971:2019
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Understand the relationship between risk management and regulatory requirements
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Understand the relationship between risk management and quality management system requirements
Agenda:
- Introduction
- Understand the key elements required for the management of risk as specified in ISO 14971:2019 and changes from ISO 14971:2007
- Understand the relationship between risk management and regulatory requirements
- Understand the relationship between risk management and quality management system requirements
- What can SGS do to help?
- Questions
Target Audience:
Medical device manufacturers registered with SGS, and other medical device manufacturers
Date/Time: May 19, 2020 | 11:00-12:00 pm EST
Cost: No Charge
Language: English
Presenter: Greg Jones – SGS Technical Director Medical Devices NAM
For more information, please contact:
Kimberlyn Sanchez
Marketing
t: +1 201 508 3000
400 Broadacres Drive,
Suite 200, 2nd Floor,
Bloomfield, New Jersey, 07003,
United States