Showing below up to 50 results in range #1 to #50.
- Sandbox (20 revisions)
- Codex of clinical research (20 revisions)
- Abbreviations (17 revisions)
- Clinical study (13 revisions)
- Investigator (9 revisions)
- Regulation (EU) No 536/2014 (9 revisions)
- Phase I clinical trials (9 revisions)
- Clinical research (8 revisions)
- Adverse event (8 revisions)
- Adverse drug reaction (8 revisions)
- Case report form (7 revisions)
- Audit (7 revisions)
- Project:Terms of Service (7 revisions)
- Clinical research regulations in the United States (7 revisions)
- FDA Bioresearch monitoring (6 revisions)
- Ethics committee (6 revisions)
- Quality assurance (6 revisions)
- Institution (6 revisions)
- Protocol Amendment (6 revisions)
- Independent data-monitoring committee (6 revisions)
- Data and safety monitoring (6 revisions)
- Regulatory authority (6 revisions)
- Compliance (6 revisions)
- 21 CFR 312 (6 revisions)
- Good Clinical Practice (6 revisions)
- Blinding (Masking) (5 revisions)
- Regulatory inspection (5 revisions)
- Clinical trial (5 revisions)
- Applicable Regulatory Requirement(s) (5 revisions)
- Source data (5 revisions)
- Institutional review board (5 revisions)
- The International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use (5 revisions)
- Standard operating procedures (5 revisions)
- Independent ethics committee (5 revisions)
- Clinical data management (5 revisions)
- Protocol (5 revisions)
- Approval (in relation to Institutional Review Boards) (5 revisions)
- Subject (5 revisions)
- Phases of clinical trials (5 revisions)
- Essential documents (5 revisions)
- ALCOA (4 revisions)
- Certified copy (4 revisions)
- Comparison of IRB and IEC requirements (4 revisions)
- Audit Report (4 revisions)
- Plain language summary of study results (4 revisions)
- Amendment (4 revisions)
- Comparator (4 revisions)
- Corrective and Preventive Action (4 revisions)
- Project:About (4 revisions)
- Clinical trial registry (4 revisions)