Results: 101-120 of 159
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No.Document TitleIDUpdatedHits
101 Reporting to Institutional and External Authorities
291782018-02-073783
102 Review of Data and Safety Monitoring in Research
294972018-02-073625
103 Maintenance of IRB Records
294762018-02-073338
104 ED/SBS IRB Principal Investigator Responsibilities
557692018-02-071935
105 PI Status for UW-Madison hESC Protocols
347052017-12-213007
106 Good Clinical Practice (GCP) Refresher Instructions
624332017-11-173857
107 UW-Madison Guidance for Investigators Requesting to Add hESC Lines to the UW-Madison hESC Registry
347182017-10-252454
108 UW-Madison Policy for Full Committee or Expedited Panel Review of Studies Using Human Embryo and or Human Pluripotent Stem Cells
347162017-10-252429
109 IRB Analysis of Risks and Benefits of Research Guidance
294782017-10-035715
110 OPRR Guidance on 45 CFR 46.101(b)(5): Exemption for Research and Demonstration Projects on Public Benefit and Service Programs
557722017-10-031740
111 IRB Consultants Use and Conflict of Interest
294602017-10-033509
112 Preventing Noncompliance Guidance
693702017-10-034169
113 NIH Genomic Data Sharing Policy for Human Data Guidance
495782017-10-032934
114 UW-Madison HIPAA Program
557702017-10-031902
115 Office for Human Research Protections (OHRP) - IRB Knowledge of Local Research Context
507842017-10-032082
116 FDA IRB Regulations (21 CFR 56)
544892017-10-031968
117 Exceptions to Informed Consent Requirements in Emergency Situations
295622017-10-032682
118 IRB Meetings
294672017-10-033333
119 Use of Human Fetal Tissue in Research
289972017-10-035198
120 Considerations for Accepting or Ceding IRB Review Guidance
566202017-10-032382

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