How Advarra Helps Institutions
Institutions, universities, academic medical centers, hospitals, and healthcare systems all play a critical role in clinical research. In the evolving research ecosystem, study timeline expectations are accelerating, and research priorities are shifting.
Meanwhile, resources are stretched thin, and compliance issues can threaten further funding opportunities. Expand your team’s bandwidth throughout the research lifecycle with Advarra’s integrated solutions. Advarra knows institutions.
Formed in 2017, by the merger of two leading IRBs, Advarra has been reviewing research since 1983. We’ve worked with every major sponsor and CRO, and we understand the industry demands. We’ve also worked with thousands of unique institutions that serve distinct local populations. Our services and solutions are customized to your team’s needs and local requirements.
Keep on track with a clinical trial management system, also known as a CTMS, and stay organized with our eRegulatory management system. By sending your studies to an independent oversight committee, you can ensure timely reviews and appropriate participant protections. This frees up resources to focus on critical local activities.
Advarra’s professional services offer specialized clinical research capabilities, tailored to optimize research productivity and alleviate administrative burdens. Our research professionals can support your team both on-site and remotely, bringing necessary skills and experience to your projects.
Our global consulting experts can help you evaluate, develop and implement improvements to your research administration, compliance and operations. We can increase bandwidth by adding experienced practitioners to your team or by managing your local IRB office.
Our eConsent platform can assist with your virtual or hybrid studies by engaging participants and supporting decentralized, remote trial practices. Increase your team’s bandwidth and keep research moving with Advarra.