Data Management Plan for Clinical Trials
What is a Data Management Plan in Clinical Trials?
A clinical Data Management Plan (DMP) is a document that describes how data is obtained and handled during all the stages of a clinical trial. The DMP includes aspects related to clinical data collection, storage, review, cleaning, validation, export, analysis, and long-term archiving.
Sofpromed’s Data Management Services
Sofpromed is a clinical research organization (CRO) specialized in providing data management services, including the writing of data management plans. 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).