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
• 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:

• Advance Directive for Research Participation Form
• A Minor’s Right to Consent to Treatment and Authorize Disclosure of PHI
• Request for PI Status Form
• Request for Personally Identifiable Information from Student Education Records for Research Purposes

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
• [Link for document 18470 is unavailable at this time]

Communications:

• UW-Madison HRPP Newsletter

UW–Madison Resources:

• Research Close-Out Checklist
• Misconduct in Scholarly Research
• Quality Assurance Committees

Ethical Guidelines:

• Belmont Report
• Declaration of Helsinki