The University of Toledo

Federal Information and Industry Links

OHRP Guidance Topics

407 Review Process Adverse Events (see also Unanticipated Problems) AIDS Assurance FAQs Biological Specimens (see also Coded Private Information) Children Certificate of Confidentiality Clinical Trial Websites (see also IRBs) Coded Private Information (see also Biological Specimens) Common Rule Compliance Oversight Conflict of Interest Consent (see also Informed Consent) Continuing Review Databases and Data Storage Decision Charts Emergency Research Engagement in Research Exculpatory Language Exempt Research/Exemptions Expedited Review Fetal Tissue Frequently Asked Questions (FAQs) FWA HHS Funding/Support HIV/AIDS Human Subjects Incident Reporting Individual Investigator Agreement Informed Consent Informed Consent FAQ's Investigator Responsibilities FAQs In Vitro Medical Devices    IRBs IRB Registration FAQs

Federal Drug Administration http://www.fda.gov/

Bioethics Resources http://www.genome.gov/10001744

National Cancer Institute http://www.nci.nih.gov/aboutnci

National Institutes of Health http://www.nih.gov/