Long pages

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

1. (hist) ‎The International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use ‎[9,531 bytes]
2. (hist) ‎Regulation (EU) No 536/2014 ‎[9,410 bytes]
3. (hist) ‎Clinical research regulations in the European Union ‎[7,376 bytes]
4. (hist) ‎Clinical study ‎[7,064 bytes]
5. (hist) ‎Comparison of IRB and IEC requirements ‎[6,418 bytes]
6. (hist) ‎Sub-investigator ‎[6,409 bytes]
7. (hist) ‎Essential documents ‎[6,392 bytes]
8. (hist) ‎Phase I clinical trials ‎[6,174 bytes]
9. (hist) ‎Subject ‎[4,936 bytes]
10. (hist) ‎Clinical research regulations in the United States ‎[4,911 bytes]
11. (hist) ‎Protocol ‎[4,795 bytes]
12. (hist) ‎Placebo ‎[4,709 bytes]
13. (hist) ‎Regulatory authority ‎[4,610 bytes]
14. (hist) ‎Randomization ‎[4,353 bytes]
15. (hist) ‎Standard operating procedures ‎[4,283 bytes]
16. (hist) ‎Phase II clinical trials ‎[4,192 bytes]
17. (hist) ‎Institutional review board ‎[4,142 bytes]
18. (hist) ‎Plain language summary of study results ‎[4,089 bytes]
19. (hist) ‎Clinical research ‎[4,078 bytes]
20. (hist) ‎Quality assurance ‎[3,837 bytes]
21. (hist) ‎Sponsor ‎[3,611 bytes]
22. (hist) ‎Trial site ‎[3,580 bytes]
23. (hist) ‎Sandbox ‎[3,562 bytes]
24. (hist) ‎21 CFR 312 ‎[3,554 bytes]
25. (hist) ‎Abbreviations ‎[3,504 bytes]
26. (hist) ‎Informed consent ‎[3,449 bytes]
27. (hist) ‎Clinical data management ‎[3,202 bytes]
28. (hist) ‎Serious adverse event (serious adverse drug reaction) ‎[3,082 bytes]
29. (hist) ‎Vulnerable subjects ‎[3,053 bytes]
30. (hist) ‎Corrective and Preventive Action ‎[2,979 bytes]
31. (hist) ‎Safety ‎[2,964 bytes]
32. (hist) ‎Source data ‎[2,919 bytes]
33. (hist) ‎Unexpected adverse drug reaction ‎[2,701 bytes]
34. (hist) ‎Impartial witness ‎[2,550 bytes]
35. (hist) ‎Regulatory inspection ‎[2,512 bytes]
36. (hist) ‎Certified copy ‎[2,464 bytes]
37. (hist) ‎Source documents ‎[2,436 bytes]
38. (hist) ‎Codex of clinical research ‎[2,392 bytes]
39. (hist) ‎Phases of clinical trials ‎[2,387 bytes]
40. (hist) ‎Sponsor-investigator ‎[2,386 bytes]
41. (hist) ‎Interim Clinical Trial (Study) Report ‎[2,334 bytes]
42. (hist) ‎Austin Bradford Hill ‎[2,320 bytes]
43. (hist) ‎Quality control ‎[2,311 bytes]
44. (hist) ‎Independent ethics committee ‎[2,289 bytes]
45. (hist) ‎Subject identification code ‎[2,229 bytes]
46. (hist) ‎Direct Access ‎[2,209 bytes]
47. (hist) ‎Independent data-monitoring committee ‎[2,098 bytes]
48. (hist) ‎Well-being ‎[2,039 bytes]
49. (hist) ‎Project:Privacy Policy ‎[2,039 bytes]
50. (hist) ‎Protocol Amendment ‎[1,977 bytes]