Results : 21-40 of 150
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No.Document TitleIDUpdatedHits
21 FDA IRB Regulations (21 CFR 56)
544892017-10-034651
22 Considerations for Accepting or Ceding IRB Review Guidance
566202017-10-035532
23 OPRR Guidance on 45 CFR 46.101(b)(5): Exemption for Research and Demonstration Projects on Public Benefit and Service Programs
557722017-10-034373
24 UW-Madison Policy for Full Committee or Expedited Panel Review of Studies Using Human Embryo and or Human Pluripotent Stem Cells
347162017-10-255060
25 UW-Madison Guidance for Investigators Requesting to Add hESC Lines to the UW-Madison hESC Registry
347182017-10-255275
26 PI Status for UW-Madison hESC Protocols
347052017-12-215439
27 ED/SBS IRB Principal Investigator Responsibilities
557692018-02-074858
28 De-Identified Publicly Available Datasets Guidance
294652018-02-0710890
29 Reporting Research Misconduct
344862018-03-098574
30 Procedure for Dealing with Misconduct in Scholarly Research
344852018-03-098629
31 Stem Cell Ethics and Policy Training
332852018-04-0555095
32 Responsible Conduct of Research
344832018-04-0610717
33 Equitable Selection of Research Participants Guidance
295592018-04-0912381
34 Request for Approval to Serve as PI
347062018-06-055061
35 Conflict of Interest Training Course
329862018-06-2636708
36 Sub-recipients for PHS Funded Research
355382018-08-068145
37 Management Plan Notification Letter Example
356322018-08-067100
38 Reviewer's Tools
342112018-08-066481
39 Misconduct in Scholarly Research
344842018-08-1615493
40 Obligations and Protections for Graduate Students and Postdoctoral Research Associates in Reporting Wrong Doing, Non-Compliance or Research Misconduct
849242018-08-203795

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