Institutional Research Services
Advarra provides tailored consulting services to revitalize your HRPP, ensuring it meets your unique objectives and thrives in a complex regulatory landscape.
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.
Startup While the definition varies across companies, study startup typically includes the process of identifying and qualifying sites, collecting essential
At institutional research programs around the U.S., there exists a pervasive myth: internal institutional review board (IRB) reviews are free.
Discover strategies for sponsors and CROs to navigate single IRB mandates, from institutional IRB roles to optimizing compliance and efficiency.
The National Institutes of Health (NIH) has chosen Advarra as its exclusive single institutional review board (sIRB) for clinical trials.
Interim staffing offers HRPPs specialized expertise, fresh perspectives, and support for accreditation and structural improvements without disrupting daily operations.
Gene therapy research is at the forefront of a coming boom in the clinical setting. Understand the growth, risks, and regulatory requirements here.
This blog explores how research sites are focusing on their institutional biosafety committee (IBC) programs as part of overall study activation time.
Gene therapy research requires both IRB and IBC oversight—while IRBs protect participants, IBCs ensure community and environmental safety with local site-specific reviews.