Get free answers to your most pressing research questions in 1 business day.
What do you do when you:
- Have an illiterate subject, and you don’t know how to obtain consent and follow the regulations
- modifying research in response to an unexpected disruption in ongoing research
- Have a vaccine trial under development that will need IBC review
- Unsure whether your research qualifies for an IRB exemption
Fill out this form to gain trusted advice from our IRB and IBC experts about human subject protections, biosafety, and other research compliance issues.
For general inquiries about working with Advarra, submit your question here.
Please Note: Protocol-specific questions for studies overseen by Advarra should be submitted through your IRB/IBC contact person, not through this form. If the Ask Advarra team is unable to answer your question, we will let you know and attempt to connect you with a resource who can help.
Please note: Protocol-specific questions for studies overseen by Advarra should be submitted through your IRB/IBC contact person, not through this form.
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Questions submitted to this site are subject to the following terms and conditions: The responses provided through the Ask Advarra service are the professional view and opinion of the Advarra team member(s) responding to the inquiry and are not binding. Responses are not legal advice; nor do they represent in any way an IRB, IBC, DMC, or other similar regulatory determination; nor should they be construed as an assurance of how the IRB, IBC, DMC, or other board may vote on a particular matter. Advarra does not link or refer individuals to clinical trials; nor will we provide medical advice. Advarra will do its best to provide answers to questions submitted but reserves the right to determine to not answer certain questions. Any question submitted to this site may be made publicly available.
Questions submitted to this site are subject to the following terms and conditions: The responses provided through the Ask Advarra service are the professional view and opinion of the Advarra team member(s) responding to the inquiry and are not binding. Responses are not legal advice; nor do they represent in any way an IRB, IBC, DMC, or other similar regulatory determination; nor should they be construed as an assurance of how the IRB, IBC, DMC, or other board may vote on a particular matter. Advarra does not link or refer individuals to clinical trials; nor will we provide medical advice. Advarra will do its best to provide answers to questions submitted but reserves the right to determine to not answer certain questions. Any question submitted to this site may be made publicly available.
