Involving study participants as partners in research requires a proactive and transparent system that builds participant rapport and engagement. To meet participant expectations, Chesapeake IRB supports many forms of research and participant outreach programs. These programs involve study participants both as individuals and as members of a community.
In addition, we provide tools and hands-on support to sponsors, CROs, institutions and researchers to ensure the protection of all participants. We believe in the importance of providing study participants and advocacy groups with the best information available, helping them decide if a clinical study is right for them.
We’ve trained our people and designed our process and platform to assist stakeholders so that they can help their participants understand clinical research and more securely access and share information. We are continuously evolving our processes to exceed customer expectations as well as to adhere to and advance applicable regulatory, legal and ethical requirements.