Post-Design Medical Device Risk Management - Webinar by GlobalCompliancePanel 2010
September 7, 2010(Ended)
Online Webinar
In this presentation we will explore the requirements for
post-design risk management and determine how to apply the
requirements. The presentation is conceived as a practical
demonstration of how to meet post-design requirements of ISO 14971. We
will review the production and post-production requirements of ISO
14971 as stated in Clause 9 and interpret their meaning for the medical
device industry. The presentation will use practical examples of the
application and use of risk management information as well as determine
when risk management files need to be updated. We will also review the
requirements for Management Review of risk management activities in the
post-design portion of the product lifecycle, and present examples of
how to meet these requirements.
Why Should You Attend: Medical device companies have done some form of design risk management for many years, although with the introduction of ISO 14971, the techniques have evolved and improved. The area of Post-design Risk Management is new to the medical device world with the introduction of ISO 14971. Companies are attempting to interpret and apply these new requirements with mixed results. In addition are the changing requirements of regulatory bodies in the postmarket phase of the device lifecycle.
Prices *
245 US Dollar (Early registration date: September 6, 2010)
Exhibition
No exhibition
Organization
Categories
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Important
Please, check the conference website for possible changes, before you make any traveling
arrangements
* Prices are for evaluation only.
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