Results: 1-20 of 81

No.Document TitleIDUpdatedViews
1Clinical Trials Registration & Results Reporting340442024-06-0459114
2Certificate of Confidentiality (CoC) Application Help360922024-05-0714666
3Good Clinical Practice (GCP) Training Guidance and Instructions611352024-01-1124095
4HRPP Guidance, Forms and Resources341022023-09-2722136
5UW Post-Approval Monitors468582023-08-095931
6UW–Madison Federalwide Assurance (FWA) & IRB Registration Numbers340482022-10-2615336
7Post Approval Monitoring Program Services628712022-04-184974
8Post-Approval Monitoring Program462612022-04-1115311
9Instructions for Linking Previous CITI Training to Your NetID327242022-01-2863570
10Contact Information for Reporting Suggestions and Concerns568892022-01-288559
11Issues in Human Subjects Research When State Law May Apply295462022-01-2721039
12Instructions for Completing CITI Refresher Training608382021-10-2027627
13Investigating the Cause of Noncompliance and Implementing Corrective and Preventive Action (CAPA) Plans Guidance695642021-08-0916821
14Preventing Noncompliance Guidance693702021-08-0911402
15Developing an Internal Quality Assurance (QA) Program Guidance695542021-08-0910900
16Recruitment of Research Participants Guidance295602021-02-0316307
17Human Subjects Research Protection Program (HRPP) Policy Index341012020-11-3053685
18Reporting of Suggestions and Concerns Regarding HRPP Performance and Function557992020-11-306090
19Use of Human Fetal Tissue in Research289972020-11-2510810
20Unanticipated Problems295062020-11-259445
1  2  3  4  5  Next

Not finding what you are looking for? Suggest a new document be created, or try adjusting your search criteria.