SOP Design, Administration, and Compliance

Ensure Informed Consent Form Compliance with Advarra Professional Services

Guarantee your clinical trial documentation is compliant and easy to understand by utilizing Advarra’s Services for Informed Consent Form (ICF) development, making your study activation process more efficient. Our experts are skilled at crafting ICF documents, providing researchers an ICF that is fully compliant with all applicable regulations while clearly and concisely outlining the protocol for their participating subjects.

Fill out the form to start the conversation

Who should watch?

text goes here

CEU Credits

text goes here

Certificate of Attendance

text goes here

Time: 1 p.m. ET, 12 p.m. CT, 10 a.m. PT
Duration: 1 hour

Get Help Now