Our award-winning program will help your organization provide plain language trial results summaries efficiently, with exceptional care and quality. CISCRP can assist your organization in preparing for and complying with European Union Clinical Trials Regulation (EU CTR) trial results requirements.
Many clinical trial sponsors have turned to CISCRP for assistance in creating plain language summaries for every clinical trial in an efficient and scalable way. CISCRP brings over 15 years of expertise and experience preparing thousands of plain language trial results summaries for each of our engagements.
Our large and growing health communications team is made up of exceptional project managers, medical writers, editors, and graphic designers trained in health literacy best practices who can deliver high-quality summaries while meeting deadlines. In addition, our team is familiar with the clinical research process and gathers input on our summaries from a review panel comprised of a diverse community of patients, patient advocates, the public, and health care professionals.
CISCRP’s internationally recognized solution produces the highest quality content that is well-organized, easy to navigate, visually appealing, and compliant with global regulatory requirements, including Annex V of the 2014 EU Clinical Trials Regulation.
Exceptional plain language communications guided by and for patients and the public
Materials available in print, digital, video, and audio formats
Unequaled expertise, experience, and leadership
