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Clinical Resources
  • Subject Management + Site Activities
    • Adverse Events and Serious Adverse Event Management
    • Data Management (CRFS and Source)
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    • Site Monitor Visits
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Subject Management + Site Activities

Contents
  • Adverse Events and Serious Adverse Event Management
  • Data Management (CRFS and Source)
  • Informed Consent In Research
  • Participant Retention Planning
  • Recruitment of Research Study Participants
  • Screening Practices
  • Screening and Preparing for a Study Visit
  • Site Monitor Visits
  • Study Implementation / In-Service Training
University Approvals + Institutional Requirements Adverse Events and Serious Adverse Event Management

 

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