- Tufts University
- Tufts Medical Center
- State
- Federal
- Regulatory and Clinical Research Organizations
- Historical Documents Relating to Human Subject Research
- Tips on Informed Consent
- Office of the Vice Provost
- Social, Behavioral and Educational Research (SBER) IRB (Medford Campus)
- Institutional Animal Care and Use Committee (IACUC)
Tufts Medical Center (Please note: user must be connected to Tufts Medical Center intranet to view website)
- Office for Human Research Protections (OHRP)
- Office for Human Research Protections (OHRP) - Guidance Topics by Subject
- U.S. Food and Drug Administration (FDA)
- Health Insurance Portability and Accountability Act of 1996
- Department of Health and Human Services
- Office of Research Integrity
- FDA Guidance on Financial Disclosure by Clinical Investigator
- FDA Guidance on Recruiting Study Subjects
- FDA Guidance on Screening Tests Prior to Study Enrollment
- FDA Federal Regulations
- Federal Certificate of Confidentiality
- U.S. Census Bureau
- Center for Drug Evaluation and Research
- Code of Federal Regulations
- National Institutes of Health (NIH)
- "Off-Label" Use of Marketed and Investigational Use of Marketed Drugs, Biologics, and Medical Devices
- NIH Human Embryonic Stem Cell Registry
REGULATORY AND CLINICAL RESEARCH ORGANIZATIONS
- Public Responsibility in Medicine and Research (PRIM&R)
- Regulatory Affairs Professionals Society (RAPS)
- Association of Clinical Research Professionals (ACRP)
- The Institutional Review Board - Discussion and News Forum
- Society of Clinical Research Associates (SoCRA)
HISTORICAL DOCUMENTS RELATING TO HUMAN SUBJECTS RESEARCH
