Office of Research Compliance

• Office of Academic Integrity
• U.S. Food and Drug Administration (FDA)
• Office for Human Research Protections (OHRP)
• (AAHRPP) Association for Accreditation of Human Research Protection Programs, Inc.
• (CITI) Collaborative Institutional Training Initiative Program

• Compliance Home
• Office of Sponsored Programs
• Technology Transfer
• Business Incubator
• Research Office
• WVU Research Portal

IRB Power Point Presentations

• Children, Assent, and Consent Waivers and Waiver of Documentation - Aug 07
• Expedited Procedures - Jun 08
• IDE and HUD - Jun 07
• NHSR, Exempt, and Expedited Research - Apr 08
• Privacy and Confidentiality - Sept 07
• Regulatory Criteria for Approval - Jul 07
• Research with Children - Apr 08
• WVU IRB Training - Dec 09

Introduction to Good Clinical Practice Lectures

• Clinical Trial Process Presentation
• Not research, exempt, or expedited research
• Privacy and Confidentiality, Feb 08
• Investigator-Initiated, Pharma-Sponsored Clinical Trials in Human Subjects