Our consultants have extensive experience in computer systems development, with the majority of that being in the pharmaceutical industry in regulated environments. They have played key roles in all aspects of the software development life cycle, from project management, requirements analysis and system design, to implementation, systems integration and both user and system testing.

  • Clinical Studies DBMS / Data Collection and Reporting
  • Adverse Event Coding and Tracking
  • Clinical Drug Supplies Inventory
  • Records Management / Archival
  • Drug Safety Protocol Management
  • Pathology / Clinical Pathology Data Collection and Reporting
  • Toxicology / Teratology Data Collection and Reporting
  • Laboratory Information Management Systems (LIMS)
  • Chromatography Data Acquisition / Management
  • Contract Laboratory Tracking
  • Stability Test Scheduling and Results Reporting
  • Drug Formulation and Packaging Libraries
  • Animal Facility Management
  • Quality Assurance Audit Tracking
  • Employee Training Records Database