Sponsors / CROs

QUALITY IRB SERVICES THAT YOU CAN COUNT ON

Chesapeake IRB understands that the partners you select for the research your company sponsors can both facilitate timely initiation of, and mitigate risks in, your research.  At Chesapeake IRB, a dedicated Project Coordinator is assigned to each project to ensure that a clear line of communication is established.  A “kick-off” meeting is also held prior to the review of your study to ensure that project expectations are discussed.

We built our fully electronic, FDA 21 CFR Part 11 compliant, platform to facilitate the timely submission of investigator information which inturn results in faster study start-up resulting in quicker subject enrollment.

Contact us to discuss how we can help the efficient and timely initiation of your research program.

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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