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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).