Center for Information & Study on Clinical Research Participation (CISCRP)

CISCRP is a global nonprofit that supports life sciences companies with specialized, participant-facing services that enhance trust, comprehension, and transparency in clinical research. Our services include: Trial Results Summaries (PLS), Protocol Synopses, Plain Language Summaries of Publications, Informed Consent Templates, Visual Aids, Trial Registry Listings, Participant Advisory Boards (PABs), Journey Mapping Workshops, Global Surveys, Interviews, and Communication Cards. We work closely with Clinical Operations, Medical Affairs, Patient Engagement, and Medical Writing teams to help meet growing global regulatory expectations—particularly the EU’s plain language summary mandate—and align with best practices in participant communication. Active in 35+ countries and across 60+ therapeutic areas, our work fuels our mission: to make clinical trial participation more accessible, respectful, and informed worldwide.