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