Results: 1-20 of 65

No.Document TitleIDUpdatedViews
1Devices Implanted or Applied to Subjects Guidance195552023-03-025911
2Identification of Suicidality or Major Depression Guidance195562023-03-027934
3Guidance on FDA Regulation of Medical Mobile Apps417712023-03-0210769
4Protocol Guidance188422023-03-0223872
5Emergency, Expanded Access for an Investigational Medical Product (One Patient)987002023-03-023090
6Continuing Review: UW-Madison Purview Enrollment Guidance195592023-03-027889
7Data Safety Monitoring Plans (DSMP) Guidance195382023-03-0217372
8Understanding the NIH Genomic Data Sharing (GDS) Policy772762023-03-027898
9Guidance on Exemption Categories under the Revised Common Rule790522023-03-027961
10Do I need to get consent for my exempt study?550392023-03-0211689
11Sending or Receiving Specimens/Data/Images Guidance188802023-03-0212993
12Guidance Regarding Research that Involves the Collection of Information about Illegal Substance or Alcohol Abuse273602023-03-0210913
13Case Reports and Case Series Guidance188662023-03-0241758
14Information for New Investigators234262023-03-0255485
15Application Type Guidance195342023-03-0215554
16VA Research: Health Sciences IRBs Policy for IRB Review of Human Subjects Research that Falls Under VA Purview554292023-03-027776
17International Research Guidance188772023-02-288815
18Investigational Software Guidance305142023-02-2810649
19MRIs and Pregnancy Status Guidance188782023-02-287218
20Using Specimens/Information from Decedents: The Common Rule and FDA Regulations274172023-02-287571
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