Medical Director

Some Typical Challenges

How IRIS can help

Resources stretched too thin

Tools to prioritise projects across all therapeutic areas/business units

Lack of clarity on project priorities

Ready access to project priorities across all therapeutic areas/business units

Meeting launch readiness expectations

Clearly defined process for product launches (i.e. New Indication, Line Extension, New Chemical Entity etc.)

Focusing clinical trials programme on high priority launches

Visibility and tracking of all milestones from study startup to close-out

Risk of low compliance and frustrating manual process of promotional material approval

Up to 66% reduction in promotional material approval whilst ensuring high compliance

The IRIS Advantage

  • Deliver more effective, higher quality and trouble-free product launches with ease
  • Improve management of Executive team expectations
  • Manage Global expectations on Clinical Trial performance
  • Managing and tracking turnaround time for Regulatory submissions
  • Ensure resources are working effectively on the right projects