You are working to develop life-changing treatments for patients around the world. Chesapeake IRB’s people, process and platform can help by managing regulatory requirements, simplifying reporting and streamlining project communications. Our dedicated study coordinators can spend more time with you because they are supported by the transparency and efficiency of our IRB-Ready® approach, and the Center for IRB Intelligence (CIRBI), our unique, cloud-based submission and review platform.

Communicate Efficiently

The faster you can access information, update records and securely communicate, the more value you can offer research sponsors and study participants. Be prepared with Chesapeake IRB’s fully validated submission and review platform, CIRBI. With CIRBI you can access and manage your project anytime, anywhere.

Conduct More Trials

Agreeing to and preparing to conduct a clinical trial is not a trivial process. Stay in control and able to initiate new research studies at any time with our IRB-Ready® approach. Our team will maintain an ongoing relationship with you, supporting you with earlier recruitment and enrollment and reduced time from site activation to first patient first visit.

Access Your Project Anytime, Anywhere

Throughout the duration of your project, it’s important you keep data security and regulatory compliance in check. Chesapeake IRB’s certified IRB professional team can help you and your staff address your needs with more action and less bureaucracy. And, with CIRBI, you will never lose track of a document. Access the most up-to-date, approved version anytime, anywhere.