Introduction

Learn how define the residual risk of your device and how to streamline the verification process by employing a risk based approach.

Adjusting the verification process to account for the criticality of the verified items can drastically reduce the overall cost and time for verification activities. By implementing a risk based verification approach activities at the end of the device development can be streamlines and the time to market can be shortened without compromising the safety or effectiveness of the medical device.

Venue

online training webinar

online training webinar, 1000 N West Street, Suite 1200, Wilmington, 19801, United States

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• Venue information More information about the venue

Organised by

globalcompliancepanel

Contact information

webinar web
1000 N West Street, Suite 1200, 1000 N West Street, Wilmington, Zip 19801, United States of America
08004479407
Contact us by email

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