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No.Document TitleIDUpdatedHits
1 Guidance on Research vs. Quality Improvement and Program Evaluation
333862020-09-0484590
2 Information for New Investigators
234262020-03-1150946
3 Use of Email for Research Purposes Guidance
717452018-03-1343561
4 IRB QI/Program Evaluation Self-Certification Tool Guidance
372642018-12-1243242
5 Guidance Regarding Types of Supporting Materials that Require IRB Review and Approval
274882017-10-0239948
6 Case Reports and Case Series Guidance
188662019-08-2238179
7 Policy and Guidance
188372020-11-3036817
8 Documenting Consent Electronically or for Remote Subjects Guidance
767262020-12-0336162
9 Deception in Research Guidance
682862016-11-2131340
10 Guidance on Research Involving Surveys, Interviews, and Focus Groups
417692019-01-2427831
11 Guidance on Exemption: Not Human Subjects Research
195372020-03-2726933
12 Summary of Investigator Responsibilities
188812019-05-0722354
13 Guidance for the Submission of Investigator's Drug Brochures (IDBs) and Package Inserts
192542018-07-2721763
14 Protocol Guidance
188422020-02-1720511
15 Principal Investigator Changes and Personnel Updates Guidance
188522020-02-2620041
16 Data Safety Monitoring Plans (DSMP) Guidance
195382017-01-3014462
17 Vulnerable Populations Guidance
642182017-06-0613969
18 Guidance on Presenting Changes of Protocol to IRB
215932017-12-1313526
19 Application Type Guidance
195342020-03-1913290
20 Expedited Change of Protocol Guidance
188502020-03-0313168

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