Clinical Trial, Phase I ×
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Table of contents
  1. 1. Clinical Trial
  2. 2. Routine Documentation
  3. 3. Registry/Cohort Study
  4. 4. Quality Assurance
  5. 5. Data Standard
  6. 6. Patient-Reported Outcome
  7. 7. Medical Specialty
Selected data models

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- 1/23/21 - 1 form, 13 itemgroups, 85 items, 1 language
Itemgroups: Administrative Data, Type of Report, Randomisation, Serious Adverse Event Entry, Intensity Changes, Serious Adverse Event, Seriousness of Adverse Event, Medications relevant to SAE, Medical Conditions/Risk Factors relevant to SAE, Diagnostic test results relevant to SAE, Rechallenge, Investigational Product, General narrative comments, Non Clinical