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No.Document TitleIDUpdatedHits
1 Recruitment Registry, Data Repository, and Tissue Repository Guidance
673872021-01-156763
2 Documenting Consent Electronically or for Remote Subjects Guidance
767262020-12-0340396
3 Control of Test Articles Used in Research Policy
588602020-11-303731
4 Review of FDA-Regulated Research Policy
588592020-11-306384
5 Emergency Use of Test Articles and of Humanitarian Use Devices Policy
554752020-11-304629
6 Humanitarian Use Device Policy
551562020-11-305064
7 VA Research: Policy for IRB Review of Human Subjects Research that Falls Under VA Purview
554292020-11-306030
8 Policy and Guidance
188372020-11-3037446
9 Guidance for X-Ray Radiation Use in Research Studies for Non-Healing Arts Purposes
448302020-11-196109
10 Remote Study Activities Guidance
1025802020-10-211671
11 Do I need to get consent for my exempt study?
550392020-09-168704
12 Guidance on Research vs. Quality Improvement and Program Evaluation
333862020-09-0486384
13 Sending or Receiving Specimens/Data/Images Guidance
188802020-05-2010566
14 Guidance on Exemption: Not Human Subjects Research
195372020-03-2727579
15 Application Type Guidance
195342020-03-1913624
16 Emergency Use/Expanded Access
990332020-03-181410
17 Expanded Access of Investigational Medical Product Requests (Non-emergency)
989662020-03-18804
18 Emergency, Expanded Access for an Investigational Medical Product (One Patient)
987002020-03-181015
19 Information for New Investigators
234262020-03-1151779
20 Expedited Change of Protocol Guidance
188502020-03-0313552

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