Results : 21-40 of 155
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No.Document TitleIDUpdatedHits
21 Good Clinical Practice (GCP) Training Guidance and Instructions
611352022-04-1518259
22 Instructions for Completing CITI Refresher Training
608382021-10-2026135
23 All Campus Animal Planning and Advisory Committee Meeting Schedule
597322022-07-065257
24 Reportable Abuse and Neglect Guidance
591102017-10-034341
25 Institutional Conflict of Interest (ICOI) Procedures
585762019-10-014577
26 Institutional Conflict of Interest (ICOI) Policy
585202019-10-017289
27 UW Human Research Protection Program Newsletter - Fall 2015
568972020-04-023638
28 Contact Information for Reporting Suggestions and Concerns
568892022-01-286496
29 Considerations for Accepting or Ceding IRB Review Guidance
566202017-10-034706
30 Human Research Protection Program Newsletter
565352020-04-024446
31 Reporting of Suggestions and Concerns Regarding HRPP Performance and Function
557992020-11-304775
32 OPRR Guidance on 45 CFR 46.101(b)(5): Exemption for Research and Demonstration Projects on Public Benefit and Service Programs
557722017-10-033734
33 UW-Madison HIPAA Program
557702017-10-033792
34 ED/SBS IRB Principal Investigator Responsibilities
557692018-02-074007
35 Additional Requirements When Conducting Human Subjects Research with Department of Energy (DOE) Support
555892019-08-055804
36 Additional Requirements When Conducting Human Subjects Research with Environmental Protection Agency (EPA) Support
555332019-08-195588
37 Additional Requirements When Conducting Human Subjects Research with Department of Education (ED) Support
548022019-08-056145
38 Additional Requirements When Conducting Human Subjects Research with Department of Justice (DOJ) Support
547972019-08-056141
39 FDA IRB Regulations (21 CFR 56)
544892017-10-033976
40 Common Rule (45 CFR 46)
544882017-10-034464

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