A鈥揨 Resources
This A鈥揨 index provides a comprehensive list of resources available through the Office for Human Subject Protection (OHSP), including policies, guidelines, webpages, training materials, templates and reference materials. Links to other research-related institutional offices, support materials, as well as external resources are also provided.
If you have questions or need help accessing these materials, please contact us.
Resources list
A
- Acronyms and abbreviations
- Adverse Events
- Adverse Device Effects
- Ancillary Committee Reviews
- Artificial Intelligence (AI)
D
- Data and Safety Monitoring
- Data Management and Sharing
- OHSP Guideline for Human Genomic Data Sharing and Institutional Certification
- NIH Data Management & Sharing Policy
- Data Security
- Decisional Impairment
- Department & Scientific Review
- Department of Defense
- Deviations
- Devices
- Drugs, Biologics & Supplements
E
- e-Consent
- Educational Research
- Emergency Use
- Exempt Research
F
G
- Genetic Testing
- General Data Protection Regulation (European Union GDPR)
- Genomic Data Sharing Template Language
- Good Clinical Practice (GCP)
H
- HIPAA
-
- The 18 Protected Health Information (PHI) Identifiers
- OHSP Policy 702: HIPAA Privacy Rule
- (including HIPAA Forms for: Reviews Preparatory to Research [25.3]; Research on Decedent’s Information [25.4]; De-identified Information [25.5.1, 25.5.2]; and Limited Data Sets/Data Use Agreements [25.6.1, 25.6.2, 25.6.3])
- HIV Testing
- Home Visits
- Human Research Protection Program (HRPP)
- Human Subject Protection (HSP) Training
I
- Informed Consent
- IRB Fee Schedule
- IRB Membership
- IRB Roster
- OHSP Policy 302: RSRB Membership & Composition
- OHSP Policy 303: Board Member Conflict of Interest
- (**Access is restricted to current RSRB Members only**)
- OHSP Guideline for Board Member Terms of Appointment & Evaluation听
- IRB Scope
-
- IRB Overview
- Getting Started with Your Human Subject Research Guide and Flowchart
- Preparing your IRB Submission
- IRB Exemptions
- IRB Review Process
- IRB Submission Checklist
- Criteria for IRB Approval
- FAQ: What is the difference between a ‘not human subject research’ and ‘exemption’ determination?
- FAQ: What is the difference between exempt and expedited reviews?
- FAQ: What are the IRB’s submission deadlines for convened board review?
- FAQ: What is the difference between the approval and effective date?
- FAQ: When can I close a study with the IRB?
L
O
P
- Participating in Research at the University
- 听Payment
- OHSP Policy 703: Recruitment & Subject Payment
- OHSP Guideline for Subject Payment
- OHSP Guideline for Payment to Subjects to Recruit Other Subjects (Peer Recruiters)
- University Accounts Payable Policies & Procedures
- University Policy on Enrollment Incentive Payments by or to University Clinical Trial Researchers
- 听Placebo
- Pregnant Women
- Prisoners
- Privacy & Confidentiality
- Protocols
R
- Recruitment
- Reliance & Multi-Site Research
- HRP Review Form when Relying on External IRB
- IRB Fee Schedule
- OHSP Policy 504: IRB Reliance and Collaborative Research
- OHSP Guideline for When 天美传媒 is the Reviewing IRB
- OHSP Guideline for When 天美传媒 is the Relying IRB
- OHSP Guideline for Single IRB Plan in an NIH Grant Application
- OHSP Guideline for Review of External (Non-UR) Investigators
- Reportable Events
- Repositories
- OHSP Guideline for Research Involving Repositories (Databases, Repositories & Registries)
- Risk Assessment
S
- Screening & Enrollment
- Secondary Use of Data, Records & Specimens/Chart Reviews
- Social Media
- Study Documentation
- Study Team Members & Responsibilities
T
- Translator Attestation
- Training & Onboarding Resources
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