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Category Good clinical practices compliance; FDA GCP requirements; FDA GCP inspections; quality improvement methods; clinical trial compliance; clinical research compliance
Deadline: January 27, 2012 | Date: January 27, 2012
Venue/Country: Palo Alto, U.S.A
Updated: 2011-12-26 17:03:18 (GMT+9)
This webinar on FDA GCP inspections will provide practical information on how to utilize quality improvement methods to effectively prepare for FDA GCP inspections.
Why Should You Attend:GCP inspections, particularly those involving FDA investigators, are often seen as an intimidating and adversarial experience, as opposed to a useful process for improving quality and ensuring compliance. However, there are steps you can take to make the process less stressful, and to avoid the most common issues arising during these inspections.
Keywords: Accepted papers list. Acceptance Rate. EI Compendex. Engineering Index. ISTP index. ISI index. Impact Factor.
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