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    HEALTH CARE 2011 - Successful Site Qualification Preparation Tools

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    Website http://complianceonline.com/ecommerce/control/trainingFocus/~product_id=702136?channel=ourglocal | Want to Edit it Edit Freely

    Category Clinical Trial Site Qualification;Site Preparation Tools;Site Documents;CRO Communication

    Deadline: November 14, 2011 | Date: November 14, 2011

    Venue/Country: Palo Alto, U.S.A

    Updated: 2011-09-30 18:55:19 (GMT+9)

    Call For Papers - CFP

    This webinar on Clinical Trial Site Qualification will cover the tools and techniques you need to know to get your clinical research site qualified for studies.

    Why Should You Attend:

    The key to securing a study is to be prepared for the Site Qualification Visit. Sponsors/CROs invest a lot of time and money qualifying Sites for studies. It is the responsibility of the Sponsors/CROs to ensure Sites are knowledgeable, staffed, have patient population and, most important, committed to the study. Organized, professional, and prepared Sites have a 90% chance of being recommended for a study. It is imperative that all Research staff read the protocol and ask questions to convey Site commitment.

    This webinar will review the steps of site qualification visits (whether phone or on-site), help you better understand the essential methods that will determine whether or not your Site will secure a study. We will discuss the importance of each preparation tool and why every tool can help reach your study goals.This webinar on Clinical Trial Site Qualification will cover the tools and techniques you need to know to get your clinical research site qualified for studies.


    Keywords: Accepted papers list. Acceptance Rate. EI Compendex. Engineering Index. ISTP index. ISI index. Impact Factor.
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