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news.UK-based Pharma eReport's Centrality EudraVigilance Medicinal Product Dictionary (EVMPD/XEVMPD) software suite is now available following changes from the European Medicines Agency (EMA).
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EVMPD compliance solution has been fully tested to compliantly generate valid, syntactically-correct XML data.
Centrality software allows Marketing Authorisation Holders (MAHs) to easily convert existing medicinal product information into an XML Schema Definition (XSD) compliant format.
The Centrality platform is available as a secure, on-demand cloud-based application accessed via a standard web browser, or it can be installed as a standalone software application.
Pharma eReport CEO Marco Rubinstein said the schema-derived nature of Centrality platform means that any EMA specification changes and, indeed, any intermediate schemes ahead of the planned ISO IDMP (Identification of Medicinal Products) standard can be quickly and seamlessly incorporated into the platform.