Info Sheet

Advarra’s institutional review board (IRB) can support local ethics committee reviews and confirm compliance with U.S. regulations.

Download the info sheet to learn about Advarra’s manual data migration services for various technology platforms.

Advarra provides flexible solutions that help accelerate the initial IRB review process and make it more efficient.

Advarra ReadyQMS, a quality management system for biopharmaceutical companies, reduces risk and ensures regulatory compliance.

Designing your data monitoring committee to provide the appropriate oversight to support participant safety and statistical evaluations.

Advarra's endpoint adjudication services secure independent evaluation and adjudication of complex clinical trial endpoints.

Simplify oversight and expand remote consenting capabilities with Advarra’s 21 CFR Part 11 compliant electronic consent management system.

Equip your team and staff with the knowledge and tools to navigate Advarra technology in their day-to-day operations.

Obtaining the effective informed consent for individuals participating in a clinical trial is paramount to ethical research.

February 18, 2021

November 13, 2020

What is an IBC? How long does an IBC review take? Read our IBC 101 handout to get answers to some of your most frequently asked questions.

Download our info sheet to learn how Advarra can revitalize your human research protection program (HRPP) with customized consulting support