21CFR Part 11 and Harmonization with 21 CFR Part 812 for Medical Device Trials August 23, 2012

This webinar will review the dynamic changes in the conduct of clinical trials that extend beyond the GxP area with the use of lab information systems requiring computer validation, Software Development Life Cycle (SDLC) considerations with an emphasis on Medical Device trials.

Why Should You Attend:

This session will review the dynamic changes in the conduct of clinical trials that extend beyond the GxP area with the use of lab information systems requiring computer validation and Software Development Life Cycle (SDLC) considerations. Participants will gain valuable insight into the regulatory requirements and how device trials have traditionally differed from pharmaceutical clinical trials.

Event Details:
Date: August 23, 2012
Time: 10:00 AM -11:00 AM PDT
Cost: $249 per attendee per computer terminal
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Official Website: http://www.complianceonline.com/ecommerce/control/trainingFocus/~product_id=702412?channel=yahooevent