Institutions

SUPPORTING RESEARCH AT INSTITUTIONS

Chesapeake IRB serves as a trusted risk-management partner to institutions wishing to expand their research portfolio built on a fully electronic platform that gives the institutions full visibility into their outsourced IRB.

The relationship between the institution and Chesapeake IRB are comprehensive and transparent because Chesapeake IRB’s policies and procedures are based on an academic medical center model coupled with industry best practices.

Founding IRB members included individuals from large teaching institution, community hospitals, and experts in a wide range of therapeutic areas as well as regulatory and ethical issues.  Chesapeake IRB continues to provide thought leadership as the research enterprise evolves to integrate various human research protections models with the goal of conducting efficient and timely research.

Contact us to discuss how our fully electronic, FDA 21 CFR Part 11 compliant, platform (CIRBI) can competitively position your institution and investigators to be sought after for multicenter trials.

CIRBI SUBMISSIONS

SUBMISSION GUIDE

FEE SCHEDULE

  • Our 100% web-based, electronic submission platform, CIRBI, simplifies and streamlines the submission process.
  • A CIRBI User Guide is provided to assist you with your CIRBI submissions.
  • Request a copy of our current fee schedule.

FAQ’S

USEFUL LINKS

CONTACT US

  • Answers to our clients’ frequently asked questions.
  • Links to useful information.
  • Contact Chesapeake IRB.

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