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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.
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