Advarra Launches Study Design Solution, Powered by Braid, to Improve Operational Efficiency in Clinical Trials — Read the Press Release

Phase I Contact Us

Explore IRB review essentials for Phase I research, including protocol expectations and critical informed consent topics for successful approval.

NIH sIRB Docs Contact Us

Simplify your grant application with sIRB support documents tailored to meet requirements for NIH and other federally funded multisite research.

IRB Roster Contact Us

Access the latest IRB roster with ease via CIRBI’s reference materials or request a copy to be sent directly to your email.

IRB Contact Us

Learn more about Advarra’s IRB services or log in to CIRBI for study-specific updates and streamlined information requests.

Biopoint Tracker Demo Request

Enhance resource efficiency and patient access with Biopoint Tracker, a versatile tracking solution for surgery, pharmacy, radiology, and more.

Biopoint Patient ID Demo Request

Improve patient safety and staff satisfaction with a specialized identification system crafted for Veterans Administration healthcare settings.

Biopoint BPOC Demo Request

Biopoint BPOC ensures seamless electronic medication administration and record continuity during VA system or network outages.

Person signing informed consent form

Informed Consent Forms

Simplify study activation with expertly crafted informed consent forms that ensure compliance and clear communication for research participants.

Stock imagery of computer with graphs and data visualizations

Institutional Research Contact Request

Optimize workflows and boost efficiency with Advarra’s comprehensive services, from IRB reviews to specialized consulting and professional support.

Coworkers investigating gene therapy research data nd computer code

GTR List Request

Discover 1,500+ vetted sites worldwide ready for gene therapy and mRNA trials, offering streamlined startup and proven research capabilities.

Scroll to Top