CISCRP is an independent, non-profit organization dedicated to improving patient engagement and understanding in clinical research. We offer a broad range of services—from creating plain language trial summaries and community engagement programs to organizing patient advisory boards and conducting research on public perceptions of clinical trials—helping sponsor organizations and stakeholders better support and engage patients.
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 Research Services 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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