Clinical Research Support
Office for Human Research Studies (OHRS)
Partners Policy and Guidance Links
- Office for Human Research Studies (OHRS)
- Contacts
- Information for Sponsors
- Submitting A New Protocol
- Single Patient IND/Emergency Use of a Test Article
- Consent Documents
- After Initial Submission Forms
- HIPAA
- Information Sheets
- Resources for Biospecimen and Biobanking Research
- ANPRM
- FDA Guidance
- External Regulatory Guidance
- OHRS News Updates
- Oncology Protocol System and OHRS Submit
- Presentation and Training Materials
- Partners Policy and Guidance Links
- Quality Assurance Office for Clinical Trials (QACT)
- Clinical Trials Education Office (CTEO)
- Clinical Investigations Leadership Committee (CLC)
- Clinical Research Unit (CRU)
- Protocol Review and Monitoring System (PRMS)
- OnCore
- Office for Human Research Studies (OHRS)
