Research Ethics
- International Ethical Guidelines for Biomedical Research Involving Human Subjects
- Belmont Report
- Declaration of Helsinki
- Ethical Guidelines for Biomedical Research on Human Subjects - Indian Council of Medical Research New Delhi
- Nuremberg Code
- Canadian Tri-Council Policy Statement: Ethical Conduct for Research Involving Humans
- Ethical and Legal Aspects of Human Subject Research on the Internet
- ACCP White Paper: Ethical Issues Related to clinical Pharmacy Research
- ICH Harmonized Tri Partite Guideline: Guidelines for Good Clinical Practice
Other Resources
- Federal Policy on Research Misconduct
- Health Hippo - Collection of Policy and Regulatory Materials
- Guidance and Information Sheets on Good Clinical Practice in FDA-Regulated Clinical Trials
- Educational Materials About Good Clinical Practice and Clinical Trials
- Office of Research Integrity
- Office of Research Administration forms
- Guidance on Continuing Review
- Frequently Asked Questions - Humanitarian Device Exemptions
- Categories of Research that may be Reviewed by the IRB through an Expedited Review Procedure
- Guidance on Reviewing and Reporting Unanticipated Problems Involving Risks to Subjects or Others and Adverse Events
- Informed Consent
Seton is proud to have four hospitals – the only hospitals in Central Texas - that have earned the