Single Institutional Review Board (sIRB) Services Info Sheet
As the research community’s preferred sIRB partner, we help you meet regulatory requirements with efficiency and transparency.
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.
Site Technology Advarra Cloud Automate, connect, and expedite processes across the clinical trial lifecycle. Advarra Cloud is a next-generation platform
Advarra’s eConsent system is designed to enhance participant engagement while ensuring regulatory compliance through 21 CFR Part 11 standards.
Leverage the only Research Evaluation System designed with guidance from the National Cancer Institute (NCI) and the National Institutes of Health (NIH).
Ensure compliance with Medicare billing regulations through expert, customized coverage analysis integrated with your CTMS.
Effortlessly manage study timelines and ensure protocol compliance with custom-built calendars tailored to your clinical trial’s specific needs.
Boost patient safety and elevate the quality of care with BioPoint, a comprehensive software suite tailored for Veterans Administration and surgical facilities.
Reach funding goals faster with expert budget negotiation tailored to clinical trials, reducing your workload and speeding up timelines.