Verification and Validation (V&V) of Software in the Medical Devices (Medical Devices)

Venue: Online Event

Location: Palo Alto, California, United States

Event Date/Time: Jun 06, 2012 End Date/Time: Jun 06, 2012
Report as Spam

Description

This 90-minute presentation will cover the FDA Quality System Requirements for software used in medical devices. The presenter will review FDA guidelines on software verification and validation and discuss methods to verify and validate even complex software.

Why Should You Attend:

Software problems are now the third-leading cause for recalls of medical devices. Most recalls are because of incorrect verification and validation for safety. Most of the knowledge on how to do a comprehensive V&V is not widely understood. Software design is a complex set of interactions within the device, with the connecting devices, and with users of the device. Usually multiple factors affect the device performance. Therefore right validation is the key to prevent device recalls.

This 90-minute presentation will cover the FDA Quality System Requirements for software used in medical devices. The presenter will review FDA guidelines on software verification and validation and discuss methods to verify and validate even complex software.

Venue

Online Event
2600 E. Bayshore Road
Palo Alto
California
United States
MORE INFO ON THIS VENUE