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Across
  1. 7. The first disease of clinical trial
  2. 8. The act by a regulatory authority(ies) of conducting an official review of documents, facilities, records, and any other resources
  3. 9. A document that describes the objective(s), design, methodology, statistical considerations, and organization of a trial
  4. 11. the hospitals and other medical institutions
  5. 13. A systematic and independent examination of trial-related activities
  6. 14. The act of overseeing the progress of a clinical trial and making sure it is conducted in accordance with the guidelines
  7. 16. A person,the subject or the subject’s legally acceptable representative cannot read, and who reads the informed consent form and any other written information supplied to the subject.
  8. 17. a small change, improvement, or addition that is made to a document
  9. 19. It is an acronym entailing the various principles of recording on paper or electronically
  10. 20. A process by which a subject voluntarily confirms his or her willingness to participate in a particular trial
  11. 22. Notification
  12. 23. The action of checking or proving the validity or accuracy of something
  13. 24. It is a type of immunotherapy and works by helping your immune system to kill cancer cells
  14. 25. A book that gives instructions about how to do something
  15. 26. The most influential documents in the history of clinical research (ten principles)
Down
  1. 1. Any untoward medical occurrence in a patient
  2. 2. A sedative drug discovered at the end of the 50s
  3. 3. An independent body constituted of medical professionals and non-medical members
  4. 4. A person responsible for the conduct of the clinical trial at a trial site
  5. 5. International ethical and scientific quality standard
  6. 6. a sign, symptom, or medical condition that leads to the recommendation of a treatment, test, or procedure
  7. 10. electronic devices which automatically monitor and record environmental parameters over time
  8. 11. A company, institution, or organization that takes responsibility for the initiation, management, and/or financing of a clinical trial.
  9. 12. Original documents, data, and records
  10. 15. To give permission to go ahead with (a project)
  11. 18. The process of assigning trial subjects to treatment or control groups
  12. 21. The ability to produce a desired or intended result