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Monitoring Informed Consent, HIPAA and Consent Process

Standard operating procedure of IRB review for informed consent ensures investigator compliance with regulations and Rush policies in human subject research studies. 

The Office of Research Compliance has implemented a complete Informed Consent Quality Improvement Plan, which includes the Informed Consent Form (ICF), the consent process, and consent documentation. The initiative creates many opportunities for research personnel to advance their knowledge and ensure compliance with Rush policy, federal regulations and Good Clinical Practice (GCP).

Learn about informed consent at Rush