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Overview of the Clinical Research Process FDA Regulations and GCP Guidelines Role of the CRA and Key Research Site Personnel Designing a Clinical Study and Protocol Development Data Management The Study Investigational Agent Selecting the Investigative Site Pre-Study Sponsor Activities Study Initiation Adverse Event Monitoring Management of the Clinical Research Site Periodic Site Visits and Specific Monitoring Processes Study Termination Audits Traveling Independent Consulting
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Add Clinical Research Monitor Handbook: Gcp Tools and Techniques, It is the responsibility of the research monitor to manage numerous trials at various centers, as well as keep everyone on schedule. In this completely revised edition, topics covered include designing case report forms, interacting with clinicians and ot, Clinical Research Monitor Handbook: Gcp Tools and Techniques to the inventory that you are selling on WonderClubX
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Add Clinical Research Monitor Handbook: Gcp Tools and Techniques, It is the responsibility of the research monitor to manage numerous trials at various centers, as well as keep everyone on schedule. In this completely revised edition, topics covered include designing case report forms, interacting with clinicians and ot, Clinical Research Monitor Handbook: Gcp Tools and Techniques to your collection on WonderClub |