Clinical Trial Technology Solutions for Sites
Our integrated portfolio of cloud-based standardized solutions was built in collaboration with the world’s leading research sites.
Our integrated portfolio of cloud-based standardized solutions was built in collaboration with the world’s leading research sites.
Simplify federal grant submissions with Advarra’s expert IRB support, offering compliance guidance and oversight for both single and multisite studies.
Advarra reviews research in the U.S., Puerto Rico, Canada, and limited minimal risk research outside these regions.
Advarra’s IBC services offer rapid, flexible solutions for IBC review, especially critical for gene therapy and other high-stakes research.
Advarra’s Institutional Review Board (IRB) offers expert guidance, supporting more than 3,500 institutions, academic medical centers, and site networks.
Secure independent evaluation and adjudication of complex clinical trial endpoints.
Leverage Advarra’s expertise in Canada as the only officially recognized IRB/REB, offering extensive site reach and top-notch research ethics services.
As the research community’s preferred sIRB partner, we help you meet regulatory requirements with efficiency and transparency.
Advarra provides accelerated review timelines, specialized support, and intuitive technology tailored to early phase studies.
Advarra University offers a vast catalog of engaging training solutions tailored to research professionals.
Advarra’s GTR Site Network includes 1,500+ vetted sites worldwide, fully prepared to support clinical trials in genetic engineering and advanced therapies.
Advarra’s eSource and EDC Study Design service provides expert support in building protocol calendars and case report forms.