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Product Management Services (PMS) is a software platform built on the ISO Identification of Medicinal Products standards (ISO IDMP), and it will replace the existing Extended EudraVigilance Medicinal Product Dictionary (XEVMPD) in the near future. It contains more fields for industry to complete than XEVMPD, and one of its features is that it groups several products from XEVMPD, namely those with different pack size information, under a single PMS ID. We can help you submit accurate data to PMS and ensure correct extraction from XEVMPD.
Submit your mandatory data ahead of the deadlines
For products on the Union List of Critical Medicines (ULCM), submission is mandatory by 30 June 2026 for all non-centrally authorised medicinal products, and by 31 December 2026 for all other non-centrally authorised products. We help you meet these deadlines with complete and correct submissions.
Complete the editable PMS fields
At present, two fields are available for editing by industry users: structured pack size information and Manufacturer Business Operations (MBOs). We assist you in enriching your products progressively as these fields become available.
Ensure your XEVMPD data is correct
Because PMS data originates from XEVMPD, errors in your existing XEVMPD submissions carry through. We verify that data submitted to PMS and data extracted from XEVMPD is accurate, giving you a reliable foundation.
Enable downstream applications
Once your information is correct in PMS, it can be processed in other applications such as ESMP, IRIS, the electronic Application Form, and others. We make sure your PMS data is ready to flow through to these systems successfully.
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