Short pages

Showing below up to 50 results in range #1 to #50.

1. (hist) ‎FDA Form 1572 ‎[163 bytes]
2. (hist) ‎Bias ‎[172 bytes]
3. (hist) ‎Compassionate use ‎[365 bytes]
4. (hist) ‎Estimand ‎[367 bytes]
5. (hist) ‎Data and safety monitoring ‎[526 bytes]
6. (hist) ‎Project:Copyrights ‎[577 bytes]
7. (hist) ‎Basic experimental studies involving humans ‎[790 bytes]
8. (hist) ‎45 CFR 46 ‎[808 bytes]
9. (hist) ‎Clinical Trials Information System ‎[950 bytes]
10. (hist) ‎Artificial intelligence ‎[991 bytes]
11. (hist) ‎Functional Service Provision ‎[1,026 bytes]
12. (hist) ‎Audit Certificate ‎[1,032 bytes]
13. (hist) ‎Audit Trail ‎[1,060 bytes]
14. (hist) ‎Coordinating Committee ‎[1,082 bytes]
15. (hist) ‎Audit Report ‎[1,090 bytes]
16. (hist) ‎Investigator's brochure ‎[1,105 bytes]
17. (hist) ‎Applicable Regulatory Requirement(s) ‎[1,113 bytes]
18. (hist) ‎Legally acceptable representative ‎[1,115 bytes]
19. (hist) ‎Case report form ‎[1,123 bytes]
20. (hist) ‎Comparator ‎[1,156 bytes]
21. (hist) ‎Request for Proposal ‎[1,175 bytes]
22. (hist) ‎Clinical trial registry ‎[1,193 bytes]
23. (hist) ‎Original medical record ‎[1,194 bytes]
24. (hist) ‎Investigational product ‎[1,196 bytes]
25. (hist) ‎Approval (in relation to Institutional Review Boards) ‎[1,208 bytes]
26. (hist) ‎Contract Research Organization ‎[1,215 bytes]
27. (hist) ‎Monitoring report ‎[1,267 bytes]
28. (hist) ‎Coordinating Investigator ‎[1,286 bytes]
29. (hist) ‎Project:About ‎[1,318 bytes]
30. (hist) ‎Nonclinical study ‎[1,319 bytes]
31. (hist) ‎ALCOA ‎[1,340 bytes]
32. (hist) ‎Blinding (Masking) ‎[1,344 bytes]
33. (hist) ‎Documentation ‎[1,347 bytes]
34. (hist) ‎Adverse event ‎[1,359 bytes]
35. (hist) ‎Contract ‎[1,374 bytes]
36. (hist) ‎Bioavailability and bioequivalence requirements ‎[1,411 bytes]
37. (hist) ‎Monitoring ‎[1,438 bytes]
38. (hist) ‎Audit ‎[1,442 bytes]
39. (hist) ‎Clinical trial (study) report ‎[1,514 bytes]
40. (hist) ‎Multicentre trial ‎[1,549 bytes]
41. (hist) ‎Compliance ‎[1,610 bytes]
42. (hist) ‎Confidentiality ‎[1,644 bytes]
43. (hist) ‎Opinion (in relation to Independent Ethics Committee) ‎[1,673 bytes]
44. (hist) ‎Good Clinical Practice ‎[1,690 bytes]
45. (hist) ‎Project:Terms of Service ‎[1,728 bytes]
46. (hist) ‎Adverse drug reaction ‎[1,798 bytes]
47. (hist) ‎Controls in clinical trials ‎[1,808 bytes]
48. (hist) ‎FDA Bioresearch monitoring ‎[1,875 bytes]
49. (hist) ‎Investigator ‎[1,887 bytes]
50. (hist) ‎Institution ‎[1,973 bytes]