Policies and Regulations
Read more about the university, statewide, national and international policies that govern our Human Research Protection Program at Rutgers.
Accordion Content
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90.2.11 Policy for Human Subjects Protection and the Institutional Review Board (From the Rutgers Policy Library)
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Clinical Trials Registration and Results Reporting Policy [Rutgers University] (PDF)
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Family Educational Rights and Privacy Act (FERPA) and Student Privacy
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Standards for Privacy of Individually Identifiable Health Information (PDF)
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Students’ Rights and Disclosure of Directory Information (Related to FERPA)
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- Access to Medical Research Act (PDF)
- Age of Majority 9:17B-3 (PDF)
- Human Stem Cell Research NJSA C.26:2Z-1
- Limitation of Guardian Power for Eligible Elderly Persons
- Minors in Adult Circumstances (NJ Dept of Children & Families Policy Manual)
- New Jersey Genetic Privacy Act (PDF)
- Patient Rights 30:4-24.2 (PDF)
- Research Involving Death Records / Certificates N.J.A.C. 8:2A-2.2 (PDF)
- Research Involving Emergency Medical Services N.J.A.C. 8:41-5.1 (PDF)
- Research with Prisoners [NJAC Title 10A; Chapters 1-10 NJ Dept of Corrections: Research]
- School Surveys and Parental Consent (2002)
- Title 9 - CHILDREN--JUVENILE AND DOMESTIC RELATIONS COURTS Section 9:6-8.10 - Report of Abuse
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- APA Ethical Principles of Psychologists and Code of Conduct
- Additional Safeguards for Children in Clinical Investigations [FDA Subpart D]
- Code of Federal Regulations - Title 45 CFR Part 46
- Code of Federal Regulations - Title 21 CFR Part 50
- Code of Federal Regulations - Title 21 CFR Part 56
- Code of Federal Regulations - Title 21 CFR Part 312
- Code of Federal Regulations - Title 21 CFR Part 600
- Code of Federal Regulations - Title 21 CFR Part 812
- Clinregs (Online Database of Country-Specific Clinical Research Regulatory Information)
- Declaration of Helsinki
- Device Advice: Comprehensive Regulatory Assistance
- Family Educational Rights and Privacy Act (FERPA) (Privacy of Student Education Records)
- FDA Guidance for IRBs and Clinical Investigators
- Genetic Information Nondiscrimination Act (GINA) Genetic Research (PDF)
- Genetic Privacy Act & Commentary
- Index, Information for FDA-Regulated Industry
- Information for Health Professionals
- NIH - Certificates of Confidentiality Kiosk
- NIH FAQs Regarding Human Participant Research
- NIH Further Guidance on a Data and Safety Monitoring for Phase I and Phase II Trials
- NIH Policy - Required Education in the Protection of Human Research Participants
- NIH Policy for Data and Safety Monitoring
- Office for Human Research Protections (OHRP) - Policy Guidance
- Protection of Pupil Rights Amendment (PPRA)
- Regulations for Drugs
- Regulations for Medical Devices
- Regulations for Vaccines, Blood & Biologics
- Regulations: FDA CFR Title 21 - Food and Drugs: All Parts 1 to 1499 Search
- Significant Differences Between HHS and FDA Regulation
- The Belmont Report
- The Menlo Report - Ethical Principles Guiding Information and Communication Technology Research (August 2012)
- The Nuremberg Code