YORIK DRAFT – EMA IDMP Roadmap: Updates, Requirements and Impact on Industry (Session 1 of 2)

By the end of 2024, EMA updated the IDMP guidance and the Product Management Service (PMS) implementation guide after the achievement of some milestones including PMS go live. The EMA IDMP project is intricately linked to SPOR, XEVMPD and SIAMED databases and to the different EMA platforms demanding the active cooperation of industry and NCAs.

 

In this session, you will receive information about:

  • Latest IDMP updates on PMS & the impact on industry
  • The prerequisites and actions needed to fulfil the EMA IDMP requirements Guidance update
  • Use of the union list of critical medicines & new shortages platform ESMP
  • The concept of PMS as a unique source of data
  • IDMP timeline including the industry actions
  • Requirements from MAHs to complete
  • Practical implementation impacts

 

The EMA IDMP project is alive and the IDMP compliance will become more complex, requiring data readiness and optimisation of the established processes to face the current deadlines and follow the next implementation steps.

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