PharmaCRO is the most competent and experienced CRO company to help with successful clinical trials and product registrations.



We are able to help starting from the development stages of the Protocol/CRF until the completion of the clinical trials such as Data Management and Statistical Analysis. In order to ensure transparent and accurate analysis during the course of data management and statistical analysis, we comply with clinical trial plan and SOPs to provide thorough planning and accurate analysis results.

Our service includes

Data Management

  • Data Management Plan (DMP)
  • CRF Development
  • Data Validation Specification(DVS)
  • Database Buildup and Validation
  • Query Management
  • Medical coding
  • Database Quality Check
  • Database Lock

Statistical Analysis

  • Sample size Calculation
  • Randomization Management
  • Statistical Analysis Plans
  • Statistical Analysis Reports