MARS (Medical Automated Regulatory System)

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What does it allows the system to do?

  • Manage end-to-end aggregate reporting process from automated scheduling to automated authoring, distribution and submission tracking of reports.
  • Centralized tracking and dissemination of SUSAR information eliminating manual steps thereby reducing the chance for delays or errors.
  • One stop shop to identify, track and measure drug safety activities and deliverables.
  • Manage up-to-date regulations in a collaborative environment with ability to assess impact of regulations across drug safety business processes.

Who manages this applications access?

This is managed by the IT Service Desk.