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    CLINICAL COMPLIANCE 2012 - Preparing for FDA GCP Inspections ? Essentials for Sponsor Companies

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    Website http://www.complianceonline.com/ecommerce/control/trainingFocus/~product_id=701923?channel=ourglocal | Want to Edit it Edit Freely

    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)

    Call For Papers - CFP

    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.
    Disclaimer: ourGlocal is an open academical resource system, which anyone can edit or update. Usually, journal information updated by us, journal managers or others. So the information is old or wrong now. Specially, impact factor is changing every year. Even it was correct when updated, it may have been changed now. So please go to Thomson Reuters to confirm latest value about Journal impact factor.