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FAQ
Frequently Asked Questions

  1. What type of new study application should I submit?
  2. When is the next application submission deadline?
  3. What do I need to submit to the IRB with my application?
  4. Do I need to complete research education, or “be certified,” to conduct human subject research?
  5. If my research is federally funded do I need to submit a copy of the grant to the IRB office?
  6. When can we start our research?
  7. How long do we need to keep our research study records?
  8. Why was review of our study delayed?
  9. I’m writing a case report; does it need IRB review and approval?
  10. Where can I get a copy of the IRB roster for our study sponsor?

1.   What type of new study application should I submit?

The first step is for the PI to determine if the study is minimal risk or greater than minimal risk. The type of review is based on risk – minimal risk or greater than minimal risk – to the study participants. If the study qualifies for exemption, an Exempt Status Application is to be completed and submitted to the IRB office. If the study qualifies for expedited review an Expedited Review Application is to be completed and submitted to the IRB office. If the study is greater than minimal risk a Convened Committee Review Application is to be completed and submitted to the IRB office.


2.    When is the next application submission deadline?

IRB meeting dates and submission deadlines are posted online. Typically, the deadline date for new submissions is the 1st Wednesday of the month and the IRB meets on the 4th Wednesday of the month. Both dates are subject to change. We do not have deadlines for the submission of exempt and expedited new studies; they are reviewed in the IRB office in the order of receipt.


3.    What do I need to submit to the IRB with my application?

The original signed hard copy documents are to be submitted to the IRB office. They can be sent by interdepartmental mail or dropped of at the IRB office. To help facilitate and expedite the review process, the documents should also be emailed to Ida Rego, the IRB Administrator.


4.    Do I need to complete research education, or “be certified,” to conduct human subject research?

Yes, all research team members must complete human subject training. CHA defines “research team members” as people who contribute to the design, conduct, or reporting of a research study, have direct contact with study participants, contribute to the research in a substantive way, have contact with a study participant’s identifiable data or biological samples (e.g., tissue, blood, urine, plasma, saliva), or uses participants’ personal information. Please refer to the research education webpage for more information.

Principal Investigators and research team members must complete a mandatory training program prior to beginning research and must undergo continuing education every 3 years. The CHA research education requirements are detailed online. Each individual is to keep a copy of his/her documentation of completion from the “CITI gradebook.”

Principal Investigators are to retain a copy of education certificates for all research team members; these documents are subject to audit. A copy does not need to be submitted to the IRB office.


5.    If my research is federally funded do I need to submit a copy of the grant to the IRB office?

Yes, if the CHA researcher is the primary grant recipient a complete copy of the grant, not including the budget, is to be submitted to the IRB office. If CHA is a sub-contract or sub-award site of a federal grant, a copy of the grant does not need to be submitted to the IRB. Please call the IRB office with questions related to funding information that needs to be submitted with an IRB application.


6.    When can we start our research?

Research, including advertising, etc., cannot begin until the PI receives the signed approval letter from the CHA IRB.


7.    How long do we need to keep our research study records?

In general, most study records need to be kept for 7 years after a study is terminated with the IRB in order to comply with Massachusetts laws on contract and tort claim requirements. The Department of Health and Human Services regulations specify that records must be kept for 3 years after completion of all research activities. If a study is regulated by the US Food and Drug Administration (drug/device/biologic study) research records must be kept for 2 years after a marketing application is approved. The Health Insurance Portability and Accountability Act requires records to be retained for up to 6 years after the last subject has completed study activity.


8.   Why was review of our study delayed?

We have come up with a helpful list of common issues that unnecessarily delay IRB review and approval and suggestions on how to avoid delays.


9.    I’m writing a case report; does it need IRB review and approval?

A case report or a case series is a retrospective analysis of 1, 2, or 3 clinical cases intended to broaden information for medical or educational purposes. Generally, reporting on up to 3 cases does not strictly meet the federal definition of research.

CHA does not require IRB review and approval if 3 or fewer patients’ records will be accessed; however, the HIPAA Privacy Rule applies. Please see the CHA policy statement about case reports for more detailed information and specifics about requirements.


10.    Where can I get a copy of the IRB roster for our study sponsor?

CHA doesn’t provide a list of IRB member names. Instead the institution has a statement of attestation that CHA has a FWA, which can be printed and given to the sponsor.

IRB Office Contact
Ida Rego

IRB office: (617) 806-8702
IRB office fax: (617) 806-8710

IRB office physical location:
1035 Cambridge Street , Suite 27A
Cambridge, MA 02141

IRB office mailing address:
Cambridge Health Alliance
Institutional Review Board Office
1493 Cambridge Street
Cambridge, MA 02139
IRB Leadership Contact
We can be reached through the IRB office at (617) 806-8702:

J. Glover Taylor
Institutional Official
Chief Compliance Officer

Jennifer A. Graf
Manager, Human Research Protection Program and Research Integrity

Lior Givon, MD, PhD
IRB Chair

Sarah E. Nelson, PhD
IRB Vice-Chair