Efficient data management accelerates the clinical trial process and ensures data consistency and accuracy. Symyoo’s data management (DM) team has gained extensive knowledge through the management of vast amounts of data generated by clinical trials. Symyoo’s DM team performs the tasks from case report form (CRF) design to database lock and archiving and guarantees the timely delivery and maximum quality and integrity of clinical data, with quality assurance ensured by validation and verification procedures at every step of the process. Symyoo’s DM team provides project-specific data collection instruments either as paper or electronic CRFs.


  • Design/Development of CRFs
  • Data Management Plan (DMP) Development
  • Database Structure Development
  • Data Validation Specification (DVS) Development
  • Data Entry Screen (DES) Development
  • Data Entry and Validation
  • Medical Coding (MedDRA, ATC Code, etc.)
  • Serious Adverse Event (SAE) Reconciliation
  • Database Quality Control
  • Database Lock
  • Data Transfer
  • Data Back-Up & Archiving