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Clinical Data Management (CDM)

DataClin has the expertise and knowledge of this critical phase in clinical research, which leads to generation of high-quality, reliable, and statistically sound data from clinical trials.

DataClin Team have records of achievement in producing a drastic reduction in time from CRF development to database lock. Our clients stay ahead of the competition by means of faster publications/product commercialization.

Our team is actively involved in all stages of clinical trial right from inception to completion with an adequate process knowledge that helps maintain the quality standards of our processes, which are assessed for quality at regular intervals during a trial.

Our Service includes:
  • CRF design
  • CRF annotation
  • CRF specifications
  • CRF completion guidelines
  • Database design
  • Database validation
  • Medical coding
  • Preparation for SAE reconciliation support
  • Medical / Safety review(s)
  • Cleaning and discrepancies management
  • Audit
  • Database lock
  • Lab data management