Reporting

The reporting module of ACM Global Central Laboratory Information Management System (LIMS) provides a fully automated reporting procedure to investigators, trial monitors and clinical project managers –as soon as the Senior Scientists have authorised the laboratory results.

Customized reports are designed on a study-specific basis.

  1. project managers
  2. trial monitors
  3. investigators

Flexible and multiple reporting formats are available:

  • Individual or Cumulative reporting
  • SI units or Conventional units
  • Standardized reporting format

Delta flagging –eg significant changes from previous visits

Clinical Insight
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