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No.Document TitleIDUpdatedHits
1 Control of Test Articles Used in Research Policy
588602020-11-303353
2 Review of FDA-Regulated Research Policy
588592020-11-305805
3 Emergency Use of Test Articles and of Humanitarian Use Devices Policy
554752020-11-304221
4 Humanitarian Use Device Policy
551562020-11-304629
5 VA Research: Policy for IRB Review of Human Subjects Research that Falls Under VA Purview
554292020-11-305660
6 Policy and Guidance
188372020-11-3036552
7 Guidance for X-Ray Radiation Use in Research Studies for Non-Healing Arts Purposes
448302020-11-195714
8 Remote Study Activities Guidance
1025802020-10-211245
9 Documenting Consent Electronically or for Remote Subjects Guidance
767262020-10-2133841
10 Do I need to get consent for my exempt study?
550392020-09-167520
11 Guidance on Research vs. Quality Improvement and Program Evaluation
333862020-09-0483997
12 Sending or Receiving Specimens/Data/Images Guidance
188802020-05-2010072
13 Guidance on Exemption: Not Human Subjects Research
195372020-03-2726676
14 Application Type Guidance
195342020-03-1913151
15 Emergency Use/Expanded Access
990332020-03-181068
16 Expanded Access of Investigational Medical Product Requests (Non-emergency)
989662020-03-18548
17 Emergency, Expanded Access for an Investigational Medical Product (One Patient)
987002020-03-18620
18 Information for New Investigators
234262020-03-1150695
19 Expedited Change of Protocol Guidance
188502020-03-0313022
20 Principal Investigator Changes and Personnel Updates Guidance
188522020-02-2619871

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