Clinical Trial Terminology

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Across
  1. 5. This document describes every step of the study and contains answers to many study-related questions
  2. 6. When data is missing, vague, or incomplete a CRA may issue one of these.
  3. 13. Forgetting to complete a required procedure or conducting a visit out of window may result in one of these
  4. 14. The point at which a subject is officially enrolled into a study
  5. 15. None of these criteria can be met in order for a subject to enroll
  6. 16. This is collected by the coordinator and entered into the EDC by one of Optimed’s data managers
  7. 18. Like an ICF, but for minors
  8. 19. The service that Optimed sites use to compensate study participants
Down
  1. 1. The one-stop-spot for all your regulatory needs
  2. 2. This must be obtained prior to performing and study related procedures
  3. 3. All of these criteria must be met before a subject can enroll
  4. 4. Fill out one of these at every visit in which labs are collected. Make sure to include a copy with your samples!
  5. 7. A cooler sounding name for the doctor overseeing the clinical trial
  6. 8. Another name for a clinical research associate (CRA)
  7. 9. Medications are considered this term if they are being taken at the time of consent, or started after consenting
  8. 10. Subjects receive one of these after completing study visits
  9. 11. This phase of clinical research is also called “post market surveillance”
  10. 12. The period in which medical history is reviewed and eligibility is determined
  11. 17. Complete study visits and answer internal queries on this site