x

Join Advarra

Learn more about our company team, careers, and values. Join Advarra’s Talented team to take on engaging work in a dynamic environment.

See Jobs

Independent Review Committee Solutions to Protect Participants and Optimize Research Performance

Safeguard participants, research staff, and the community with truly integrated, expert review solutions designed to streamline study conduct.

Your Trusted Partner for Independent Research Oversight

IRB

Institutional review board (IRB)

Rely on the research community’s preferred independent IRB when conducting efficient, responsible research regardless of project scope, therapeutic niche, or number of investigators.

Over 3,500 institutions, academic medical centers, and hospitals rely on Advarra’s IRB.

IBC

Institutional biosafety committee (IBC)

Advance your research by leveraging the world’s largest integrated IRB and IBC service, combined with the most comprehensive Gene Therapy Ready site network.

Advarra provides comprehensive review and oversight of clinical trials involving investigational products containing engineered genetic material.

DMC/DSMB

Data monitoring committee (DMC) / data safety monitoring board (DSMB)

Ensure independent, knowledgeable oversight of interim clinical trial data with a worldwide network of experienced biostatistical and medical professionals.

Advarra has deep expertise in all therapeutic areas, trial designs, and complex biostatistical endpoints.

EAC

Endpoint adjudication committee (EAC)

Secure independent evaluation and adjudication of complex clinical drug and device trial endpoints worldwide.

Whether you need assessment from one medical expert or an EAC, Advarra’s experts understand the various comorbidities and confounding variables present in complex clinical trials.

Expertise for Every Study

 

Every Phase and Type

Each clinical trial phase has its own unique challenges and needs. Device, social behavioral, and post marketing studies have their own dynamics. Advarra has experience with all trial phases, and our IRB roster also includes unique expertise in early phase, device, and minimal risk research.

Every Specialty

Work with research compliance professionals who understand the latest clinical developments, regulatory requirements, and research innovations. From genetic engineering and gene therapy, to oncology basket studies and decentralized trial modalities, Advarra draws upon a broad network of experts to ensure robust oversight.

Every Review

Ensure comprehensive, truly independent ethical and safety oversight with a full suite of review services: IRB, IBC, DMC/DSMB, and EAC. Advarra is the largest integrated independent research oversight services organization.

Read our Related Resources

 
Podcast

James Riddle and Barbara Schneider Delve into the Different Players Involved in Reviewing Clinical Research

August 11, 2021

About the Advarra In Conversations With… The future of healthcare innovation hinges on research and clinical trials. Advarra sits down...

In this podcast episode, we discuss the different clinical research oversight committees and functions to ensure the safety of participants.

Listen Now
Read more
 
E-Learning

IBC Overview eLearning Module

June 3, 2021

Institutional biosafety committee oversight is necessary to ensure the safety of those involved in research with engineered genetic materials.

Read Now
Read more
 
White Paper

What Level of Review Does Your Study Need?

January 15, 2020

The level of IRB review required for research involving human subjects depends on the study’s specific design and the risks involved. Some research must be reviewed by the fully convened ...

Read Now
Read more

Visit the Resource Library