Institutional Review Board (IRB)

InfoEd Electronic Submission

For IRB Members

HIPAA for Research

Grants and Contracts Office

1. How the Process Works
1. Is it Human Subject Research?
2. Types of Review
3. Periods of Approval
2. Download Forms
1. MSSM Grants and Contracts Office forms
2. MSSM IRB forms
3. HIPAA for Research
3. Preparing Your Application
1. Checklists for Standard Submissions
2. Exempt Projects
3. Expedited Projects
4. Device Studies
1. Device Form
2. Humanitarian Use Device Only Form
5. Disclosing a Potential Conflict of Interest in the Research
6. Emergency Use
   1. Emergency Use Guidance
   2. Emergency Use Form (Unapproved Drug/Biologic)
   3. Emergency Use Form (Unapproved Device)
   4. Emergency Use Consent Form Template
   5. Previous One-Time Emergency Uses
7. "Just In Time" Applications
8. Literature Search Techniques for Determining Drug and Device Safety
9. Research on Human Data (including existing medical records)
1. Guidance
2. Flow Chart
3. Forms for Doing Research on Existing Data
   1. Existing Data Collected during Previous Research
   2. Existing Data Collected during Clinical Care
4. Review of HIV Information
1. Guidance
2. Application Form
10. Pharmacy
    1. Drug/Biologic Information Sheet
    2. Emergency Use Guidance (Unapproved Drugs/Biologics/Devices)
11. Personnel Changes
12. Repository Establishment (Data or Biological Material)
13. Risk/Benefit Analysis
1. Points to Consider
2. Compensation/Treatment Resulting from Injury
14. Research on Human Specimens
1. Forms for Doing Research on Existing Specimens
   1. Collected during Previous Research
   2. Collected during Clinical Care
4. Meeting Dates, Deadlines, and Results
   1. Meeting dates and deadlines
   1. 2009
   2. 2008
   3. 2007
   4. 2006
   5. 2005
   6. 2004
   2. Availability of Meeting Results
   3. FAQs about Continuation Application Submissions
5. Research at Our Affiliates
1. Research Affiliate Locations
1. James J. Peters VA Medical Center
2. Elmhurst Hospital Center
3. Queens Hospital Center
4. Jewish Home and Hospital
6. Doing Research at External Sites
1. Working with other Domestic Sites under active FWAs
2. Working with International Sites
1. Those with an active FWA
2. Those without an active FWA
7. IRB Fees
8. Changing Approved Applications
1. Amending a Submission
2. Protocol Deviations, Exceptions, Violations

Please note that information above is forthcoming.

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