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Document Number EMO 0122Version 2.0EMVO: EMUS Master Data Guide Effective Date 19JUN2018Page No 0 of 1Master Data GuideFilename: EMO 0122 EMUS Master Data Guide as published.docx Copyright EMO, 2018
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The EMVS master data guide is typically needed by pharmaceutical companies or entities involved in the manufacturing, distribution, or selling of medicinal products within the European Union (EU). It is used to provide accurate and up-to-date information about the master data related to medicines, including product details, packaging information, and authorization status. Regulatory authorities, wholesalers, healthcare professionals, and other stakeholders may also require access to this guide for various purposes.
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EMVS Master Data Guide is a document that provides instructions and guidelines for submitting master data to the European Medicines Verification System (EMVS).
Manufacturers, Marketing Authorization Holders, and Parallel Distributors are required to file EMVS Master Data Guide.
EMVS Master Data Guide can be filled out electronically through the EMVS portal using the specified format and templates provided.
The purpose of EMVS Master Data Guide is to ensure accurate and timely submission of product master data to facilitate the verification of the authenticity of medicinal products.
EMVS Master Data Guide requires information such as product code, batch number, expiration date, and serial number of medicinal products.
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