CISCRP is an independent nonprofit organization that provides patient engagement and clinical research communication services, including plain language clinical trial summaries, patient advisory boards, community engagement programs, and research on participant perspectives. These services help organizations increase understanding, trust, and participation in clinical research.
We strive to educate and help patients, their family members, and members of the general public that are interested in clinical research understand the process and what it means to be a clinical research participant.
We help professionals better understand the needs of trial participants with facts and figures, polls, surveys and other resources, while promoting a greater awareness of clinical trials.
Our team of experienced professionals is committed to providing high-quality services to the clinical research community. We are dedicated to helping our clients achieve their research goals.
CISCRP’s experienced team is skilled at engaging patients and their support network to obtain meaningful insights for sponsors – including but not limited to pharmaceutical, biotechnology, and medical device companies; contract research organizations; academic and for-profit institutions; foundations; and nonprofit organizations.
We work with research sponsors from around the world to prepare and communicate clinical trial results summaries and clinical research information to patients and their families in plain, easy-to-understand language.
We specialize in engaging with the public to spread awareness on the importance of clinical research participation. Through our community programs and educational materials, organizations have the opportunity to strengthen their engagement with patients and the public.
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