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No.Document TitleIDUpdatedHits
1 Do I need to get consent for my exempt study?
550392020-09-166928
2 Guidance on Research vs. Quality Improvement and Program Evaluation
333862020-09-0482615
3 Remote Study Activities Guidance
1025802020-08-28992
4 Sending or Receiving Specimens/Data/Images Guidance
188802020-05-209866
5 Documenting Consent Electronically or for Remote Subjects Guidance
767262020-04-2429416
6 Guidance on Exemption: Not Human Subjects Research
195372020-03-2726195
7 Application Type Guidance
195342020-03-1912945
8 Emergency Use of Test Articles and of Humanitarian Use Devices Policy
554752020-03-184012
9 Emergency Use/Expanded Access
990332020-03-18845
10 Expanded Access of Investigational Medical Product Requests (Non-emergency)
989662020-03-18411
11 Emergency, Expanded Access for an Investigational Medical Product (One Patient)
987002020-03-18465
12 Information for New Investigators
234262020-03-1150241
13 Expedited Change of Protocol Guidance
188502020-03-0312756
14 Principal Investigator Changes and Personnel Updates Guidance
188522020-02-2619523
15 Release of Grant Funds When IRB Review for a Study is Ceded to an External IRB
268242020-02-216163
16 Processing the Departure of a Principal Investigator Guidance
775922020-02-182207
17 Understanding the NIH Genomic Data Sharing (GDS) Policy
772762020-02-184065
18 Protocol Guidance
188422020-02-1719978
19 Guidance on Making Editorial Changes to Subject-Facing Study Materials
949292020-02-07868
20 Scientific Review Requirement
188442019-12-058664

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