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Livre Blanc
Navigating IDMP Through the Extended EudraVigilance Medicinal Product Dictionary (XEVMPD)
Harnessing expertise, strategies and best practices for successful implementation.
Jul 26, 2024
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  • Navigating IDMP Through the Extended EudraVigilance Medicinal Product Dictionary (XEVMPD)
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The pharmaceutical industry faces significant challenges in implementing the Identification of Medicinal Products (IDMP) standards. Our white paper, "Navigating IDMP Through XEVMPD," offers comprehensive insights, strategies, and best practices for successful IDMP implementation. Authored by our regulatory experts, it delves into the complexities of IDMP, including data management, compliance, and leveraging technological advancements. The paper highlights the importance of the Extended Eudravigilance Medicinal Product Dictionary (XEVMPD) and its role in ensuring data quality and regulatory compliance. It also addresses the global implementation of IDMP standards and the transition to the new ISO IDMP-compatible data submission format.

A notable case study with Swedish Orphan Biovitrum AB (Sobi) demonstrates how IQVIA's expertise supports IDMP readiness. The collaboration focuses on data enrichment, PMS implementation, and ensuring compliance with ISO IDMP standards.

Discover how IQVIA's expertise can support your organization in achieving IDMP readiness, enhancing product information quality, and navigating the evolving regulatory landscape.

Download the white paper now to stay ahead in the pharmaceutical industry's regulatory compliance journey.

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Automate and standardize your regulatory management, from correspondence and commitments to registration and tracking.

Safety & Regulatory Compliance

Meet the challenge of changing stakeholder demands and increasing cost constraints with IQVIA's integrated technology services and analytics-driven offerings.

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