One of the new requirements has the device manufacturer update the clinical evaluation (and its documentation) with data obtained from the post-market surveillance.
Live webinar on Integrating Clinical Evaluation and Risk Management By Compliance2go
10 May 2012, Houston, Texas, United Kingdom
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Online
Online, 10777 Westheimer Suite 1100, Houston, Texas, 77042, United Kingdom
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Compliance2go
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Miss Trisha Paul
10777 Westheimer Suite 1100, Houston, Texas, 77042, United States of America
1.877.782.4696
Contact us by email
10777 Westheimer Suite 1100, Houston, Texas, 77042, United States of America
1.877.782.4696
Contact us by email
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