Topics Map > Research Policy and Compliance > Human Research Protection Program (HRPP)
Results: 41-60 of 99
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No.Document TitleIDUpdatedHits
41 Maintenance of IRB Records
294762018-02-072291
42 ED/SBS IRB Principal Investigator Responsibilities
557692018-02-07967
43 Contact Information for Reporting Suggestions and Concerns
568892017-11-202232
44 Good Clinical Practice (GCP) Refresher Instructions
624332017-11-171642
45 UW HRPP Quality Assurance
462602017-11-171620
46 Cross-Campus Human Research Protection Program (HRPP) Committee Charter
297912017-10-092959
47 OHRP & FDA Expedited Review Guidance
550202017-10-03930
48 OHRP Guidance on Engagement of Institutions in Human Subjects Research
497932017-10-031225
49 IRB Meetings
294672017-10-032261
50 Compliance with Human Research Protections in Sponsored Research
295542017-10-031690
51 HRPP and IRB Resources
291642017-10-031837
52 Office for Human Research Protections (OHRP) - IRB Knowledge of Local Research Context
507842017-10-031104
53 IRB Review of Study Resources
291672017-10-031828
54 Retention of IRB Records
294772017-10-033365
55 Developing an Internal Quality Assurance (QA) Program Guidance
695542017-10-031392
56 Considerations for Accepting or Ceding IRB Review Guidance
566202017-10-031261
57 Expert Review
294512017-10-032787
58 Monitoring the Consent Process
295632017-10-032076
59 UW-Madison HIPAA Program
557702017-10-031040
60 Campus IT Policies
507612017-10-031016

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