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Deep expertise in coding and trial programming

Data Management

Deep expertise coding and designing trial research data systems. Find out more about our expertise in data management

  • Case report form (CRF) design and development
  • Comprehensive database design and validation
  • Query generation and resolution
  • Medication dictionary coding
  • Safety Adverse Events (SAE) reconciliation and discrepancy management
  • Quality Control (QC) throughout clinical trial
  • Data consolidation and conversion
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Suite 1230
St. Petersburg, Florida 33701

CRC is well-positioned to conduct clinical studies at any stage, Phase I-IV.

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