With the recent approval of the National Institutes of Health’s policy, “Use of a Single Institutional Review Board (sIRB) of Record for Multi-Site Research,” you may be wondering how you will manage your IRB oversight in the changing research environment and spend time on what’s really important: protecting the rights and welfare of research participants and executing your study.
Chesapeake IRB is a trusted risk-management partner to institutions, hospital systems and academic medical centers. Our policies and procedures are at the forefront of industry best practices, and our people, processes and platform provide transparency into your investigator’s projects, allowing you to stay in control and monitor what is happening across all studies at your institution in real time. We can support and audit everything from single investigational sites to multiple hospital and clinic locations.
Spend less time on paperwork and more time focusing on your participants while expanding and supporting your research programs in new ways. With the right support from our IRB professionals, IRB-Ready® approach and powerful IRB platform, your team of investigators can conduct research with greater efficiency and security.
CIRBI, our paperless, cloud-based IRB submission and review platform, enables you to create shared workspaces with customizable settings for relevant stakeholders in your institution, supporting efficiencies across your entire research enterprise.