Results: 61-75 of 75
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No.Document TitleIDUpdatedHits
61 Audio Recordings, Video Recordings, Photographs Guidance
195522017-06-065700
62 What Happens After an Application Is Submitted to the Health Sciences or Minimal Risk IRB: Scientific Review
238062017-02-275813
63 Guidance Regarding Drug Shortages and Substitutions that Occur During the Conduct of Research Studies
251912017-02-134026
64 Data Safety Monitoring Plans (DSMP) Guidance
195382017-01-3014462
65 Guidance Regarding Research that Involves the Collection of Information about Illegal Substance or Alcohol Abuse
273602017-01-238244
66 Outline of the Endorsement Process
195312017-01-125211
67 Guidance for Analysis Centers
188652017-01-095541
68 What Happens After a New Application Is Submitted to the Health Sciences or Minimal Risk IRB: IRB Administrative Review and IRB Pre-Review
238092017-01-037564
69 Timeframe for Submission of Changes of Protocol to the IRB
251932016-12-226270
70 Endorsement and Approval of VA Research
195302016-12-195936
71 Changes to Eliminate Immediate Hazards to Subjects Guidance
188492016-12-169092
72 Protocol Development Activities (PDA) Guidance
188402016-12-139226
73 Deception in Research Guidance
682862016-11-2131340
74 Registry-Repository Overview Table
673882016-10-042908
75 Devices Implanted or Applied to Subjects Guidance
195552015-12-114309

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