CRF Design for Clinical Trials

What is CRF Design in Clinical Trials?

CRF design consists of writing the specifications of a case report form (CRF), which is a set of forms used to collect data in a clinical trial. The CRF design describes the data collection forms and fields that will be used to enter clinical data, including form names, field texts, and input types. This CRF specification will then be utilized to implement the Electronic Data Capture (EDC) system.

Sofpromed’s Data Management Services

Sofpromed is a clinical research organization (CRO) specialized in providing data management services, including CRF design. Our clinical data management capabilities include:

• Writing of Data Management Plan (DMP)
• Writing of Data Validation Plan (DVP)
• Case Report Form (CRF) design
• EDC system implementation
• Clinical data cleaning 

Sofpromed’s CRO services are focused on phase I-IV clinical trials and post-marketing studies across multiple therapeutic areas (oncology, cardiovascular, metabolic, central nervous system, dermatology, infectious, and respiratory diseases, among others).