About

The Center for Information and Study on Clinical Research Participation (CISCRP) is a first-of-its-kind nonprofit organization, founded in 2003, dedicated to educating and informing the public, patients, medical/research communities, the media, and policy makers about clinical research and the role each party plays in the process.

As part of its mission, CISCRP provides a variety of award-winning resources, programs and services that are designed to assist clinical research stakeholders in understanding public and patient attitudes and experiences in research as well as improving volunteer participation experiences and satisfaction.

CISCRP collaborates with a wide variety of patient advocacy groups, disease-specific organizations, sponsors, sites, and CROs in order to successfully serve communities with our education and outreach programs.