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What do you do when you:
- Have an illiterate subject, and you don’t know how to obtain consent and follow the regulations
- Want to submit a protocol and don’t know if the safety monitoring will be deemed adequate by the IRB
- Have a question about modifying research in response to the coronavirus disease (COVID-19) outbreak
- Have a vaccine trial under development that will need IBC review
Fill out this form to gain trusted advice from our experts about human subject protections, biosafety, and other research compliance issues.
Please note: Protocol-specific questions for studies overseen by Advarra should be submitted through your IRB/IBC contact person, not through this form.
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, or other similar regulatory determination; nor should they be construed as an assurance of how the IRB, IBC, 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.