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MASTER CLINICAL STUDY AGREEMENT THIS MASTER CLINICAL STUDY AGREEMENT is made and entered into as of the 22nd day of July 2003 (the “Effective Date “), by and among Wyeth Pharmaceuticals Inc.,
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This master clinical study is a comprehensive research study that serves as a reference guide for all ongoing clinical studies within a certain organization or institution.
The principal investigator or the lead researcher of a clinical study is required to file this master clinical study.
The master clinical study must be filled out by providing detailed information on all ongoing clinical studies, including study protocols, participants, outcomes, and any adverse events.
The purpose of this master clinical study is to centralize and organize information on all ongoing clinical studies within a specific organization, making it easier to track progress and ensure compliance with regulations.
Information that must be reported on this master clinical study includes study title, principal investigator, study objectives, participant information, study status, and any adverse events or protocol deviations.
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