Investigators and study personnel should be familiar with the following policies that relate to human subject protections. (Policies are in PDF.)

• Authority of the Human Subjects Protection Office, Policy 2004-02
• Clinical Research / Trials Budget Review, Policy 2006-07
• Clinical Research Trials Facility Discount for Hospital-Based Outpatient Programs, Policy 2010-01
• Clinical Research Trials Patient Billing Compliance, Policy 2006-08
• Clinical Trials Under Contract – Administrative Requirements, Policy 2007-06
• Confidentiality, Policy 2002-43
• Conflicts of Interest in Research Policy, 2006-01
• Data Ownership Policy, 2003-42
• Electronic Communication of Confidential Data, Policy 2011-004
• Information Security:  Anti-Virus and Software Update, Policy 2005-10
• Information Security:  Data Authentication, Physical Safeguards, Policy 2011-01
• Information Security:  Risk Assessment, Policy 2005-08
• Information Technology Security:  Systems Access Control, Policy 2011-03
• IRB Approval of Human Research Conducted by Subcontractors, Policy 2004-04
• Manufacturing of Drugs, Devices or Biologics for Human Research, Policy 2005-12
• Mobile Computing Device (MCD) Security, Policy 2008-03
• Review and Approval of Research Involving Human Subjects, Policy 2002-42
• Review of Alleged Misconduct of Research
• Rules of Conduct, Policy 2002-03
• Written Agreements for Sponsored/Funded Research Involving Human Subjects, Policy 2004-05