About

Services:

Heartland IRB, a commercial IRB, provides ethical review and support in accordance with research standards established by the National Institute of Health (NIH), Federal Drug Administration (FDA), and the Association for the Accreditation of Human Research Protection Program, Inc. (AAHRPP).  

Heartland IRB reviews in compliance with other applicable federal and state laws and regulations governing IRBs and research with humans.  

FDA-regulated studies are reviewed in accordance with the regulations outlined in the Title 21 of the Code of Federal Regulations (CFR) Parts 50-56, and Good Clinical Practices (GCP), as applicable.  

Non-FDA regulated studies are reviewed under the provisions Title 45 CFR 46, and Good Clinical Practices (GCP), as applicable.