The Center for Information and Study on Clinical Research Participation (CISCRP) is a first-of-its-kind 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.

Target audience

Patients, Caregiver (inc. family members), Healthcare professionals, General Public

Types

Other

Formats

Online Pre-recorded Webinar, Online e-learning, Video, Other

Levels

Beginner, Intermediate, Advanced

Language

English

Accessibility

Easy read

Certification

No

Patients involved

Yes

PFMD last access

28 Nov 2020

Organizations

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

Patient Advocacy Organization