Human Research Protections Office (HRPO)
Federal or Other Funded Research
All applications for sponsored projects to be conducted under the auspices of the School of Medicine must be approved by the Dean's Office before being submitted to UMB Campus Office for Research & Development for institutional sign-off. Applications should be delivered to room 14-021 Bressler Research Building no less than one week before the sponsor's deadline. All routed applications must include: completed routing form, cover pages, budget page, project narrative (DRAFT versions are acceptable), details of animal & human subject usage if applicable (eg. Sections e & f on PHS form 398).
For protocols that are Federal or Other Funded the following tools should be used to assist in developing and conducting your research:
- Continuing Review Table to Report SAE's (MSWord)
- BRAAN Protocol Format (PDF)
- Data and Safety Monitoring Plan (MSWord)
- General Requirements for Informed Consent (PDF)
- HIPAA Authorization Form (MSWord)
- Human Subjects Training Assurance (MSWord)
- Inclusion/Exclusion Checklist (MSWord)
- Instructions for Completing Routing Form (MSWord)
- IRB Regulatory Compliance Letter (PDF)
- New Protocol Checklist (MSWord)
- Sample Letter of Invitation-Phone Interview (MSWord)
- Sample Letter of Invitation-Survey (MSWord)
- QI Self Assessment Tools (MSWord)
- Evaluation to Sign Consent Form (PDF)
- Tools & Tips for Writing a Clear and Appropriate Informed Consent Document (PDF)
- Tips to Help Avoid a Protocol Bounce Back (MSWord)
- Obtaining Human Research Data Under HIPAA (PDF)
- Delegation of Responsibility Log (MSWord)
- Tips for Submitting Renewals (PDF)
- Economic Interest Disclosure (MSWord)
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