Online Resources
Online Resources Heading link
UIC Resources
Department of Health and Human Services (DHHS) - Research with Human Subjects
Food and Drug Administration (FDA)
- Food and Drug Administration (FDA)
- FDA Good Clinical Practice (GCP) Program
- 21 CFR 50 – Protection of Human Subjects
- 21 CFR 54 – Financial Disclosure by Clinical Investigators
- 21 CFR 56 – Institutional Review Boards
- 21 CFR 312 – Investigational New Drug Application
- Investigational New Drug (IND) Application
- Pre-IND Consultation Process
- 21 CFR 600 – Biological Products
- 21 CFR 812 – Investigational Device Exemptions
- Information Sheet Guidance for IRBs, Clinical Investigators, and Sponsors
Office for Civil Rights (OCR)
National Institutes of Health (NIH)
- National Institutes of Health (NIH)
- Inclusion of Women and Minorities as Subjects in Clinical Research
- Inclusion of Women and Minorities as Participants in Research Involving Human Subjects – Policy Implementation
- Inclusion of Children – Policy Implementation
- Research Involving Individuals with Questionable Capacity to Consent
European Union (EU) General Data Protection Regulation (GDPR)
Other Resources
- ClinicalTrials.gov
- Chicago Public School (CPS) Research Information
- Public Responsibility in Medicine & Research (PRIM&R)
- Ethical and Legal Aspects of Human Subjects Research in Cyberspace