Topics Map > Research Policy and Compliance > Human Research Protection Program (HRPP) > HRPP Resources for Researchers
HRPP Guidance, Forms and Resources
Guidance:
- Accessing ARROW and the NetID Process
- Application of Good Clinical Practice at UW-Madison
- Certificate of Confidentiality (CoC) Guidance
- Guidance on External Sharing of Human Subjects Research Data
- Guidance on Receiving Human Subjects Research Data from an External Entity
- List of Approved De-Identified Publicly Available Datasets
- NIH Genomic Data Sharing Policy for Human Data Guidance
- Reportable Abuse and Neglect Guidance
- Preventing Noncompliance Guidance
- Developing an Internal Quality Assurance (QA) Program Guidance
- Investigating the Cause of Noncompliance and Implementing Corrective and Preventive Action (CAPA) Plans Guidance
Forms:
Agencies, Regulations, and Laws Governing Human Participants Research:
- Common Rule and Subparts
- Food and Drug Administration (FDA) and FDA Regulations
- Issues in Human Subjects Research When State Law May Apply
- National Science Foundation (NSF)
- Office for Human Research Protection (OHRP)
- UW–Madison Federalwide Assurance (FWA) & IRB Registration Numbers
- VA Research - Overview
Communications:
UW–Madison Resources:
- HIPAA at UW–Madison
- Research Close-Out Checklist
- Payments to Research Participants Policy
- Data Security, Management, and Retention
- Misconduct in Scholarly Research
- Quality Assurance Committees
UW–Madison Research Services:
- Clinical Research Toolkit (includes checklists and templates for study conduct)
- UW Institute for Clinical & Translational Research (ICTR) Clinical Research Services
- Pharmaceutical Research Center (PRC)
- Research Data Services
- University of Wisconsin Survey Center