• Data Safety Monitoring Plan
  (this link requires Adobe® Acrobat Reader to view)
• Guidelines for Resubmission of Protocol / Informed Consent Document
  (this link requires Microsoft® Word to view)
• NIH Glossary
• Office for Human Research Protections (OHRP)
• Policies and Procedures Section 5, page 66 (Investigator Responsibilities)
  (this link requires Adobe® Acrobat Reader to view)
• Policies and Procedures Section 15, page 103 (Conflict of Interest)
  (this link requires Adobe® Acrobat Reader to view)
• Unanticipated Problems Involving Risks
  (this link requires Microsoft® Word to view)
• U.S. Food & Drug Administration

Tissue Studies

All studies using human tissue must be submitted to the Research Review Committee and then the IRB for review and approval. Additional infromation is available in the Institutional Review Board/Ethics section of the FCCC library.

For more information, please call the IRB office at 215-214-3754