The Center for Information and Study on Clinical Research Participation (CISCRP) is a first-of-its-kind 501(c) 3 nonprofit organization 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.
For Patients, Caregivers, & the Public
CISCRP offers a portfolio of services to support patient engagement, clinical research education, and clinical trial participation for study volunteers, clinical research stakeholders, and sponsor organizations. As an independent, neutral, non-profit organization dedicated to patient outreach and education, CISCRP is uniquely positioned to assist with a variety of activities including developing lay language clinical trial summaries, organizing and running patient advisory boards, conducting research to better understand public perceptions about research, and finding clinical trials.
The CISCRP store includes brochures, videos, books, posters and other materials that you may order and provide to your clients and patients to help them understand clinical research. CISCRP also has many opportunities for professionals to stay involved in clinical research.