Data Management

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Data Management

Rare disease drug development provides unique issues and challenges in data management. Key among them is the smallness of the number of patients in the study, meaning all efficacy and safety data points must be of immaculate quality in order to establish the evidence of efficacy and safety required by regulatory agencies.

Through strategic relationships with our Data Management partners, our rare disease data mangers and team can help before your study starts, during your study, and after your study ends. Contract with us per hour, per deliverable, per dedicated time fixed rate. You’ll love our pricing.

Services Before Clinical Trial or Observational Study Starts
  • eCRF development
  • Database build
  • Edit checks planning
  • Data Management planning
Services During Clinical Trial or Observational Study
  • Data review and issues resolution to ensure data quality
  • Edit checks conduct
  • DSMB data support
Services After Database Lock or End of Observational Study
  • Close-out activities
  • Data integration support