GxP Services
Advarra’s GxP services offer tailored support for every trial phase, ensuring seamless execution from startup to closeout for global therapeutic delivery.
Advarra’s GxP services offer tailored support for every trial phase, ensuring seamless execution from startup to closeout for global therapeutic delivery.
Advarra provides tailored consulting services to revitalize your HRPP, ensuring it meets your unique objectives and thrives in a complex regulatory landscape.
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.