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Document Number EMVO00122Version v7.0EMVS Master Data Guide Approval Date 24 Nov 2022Page No 1 of 33EMVS MASTER DATA GUIDEConfidentiality level: Public Copyright EMVO, 2022 Uncontrolled when printedDocument Number EMVO00122Version v7.0EMVS Master Data Guide Approval Date 24 Nov 2022Page No 2 of 33Revision History Version DateVersion Author13/6/20171.014/6/20182.0Paul Mills Stefan Artlich Grant Courtney Anci Kvarnstrm Paul Mills28/11/20183.0Paul Mills16/OCT/20194

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Gather all necessary documents related to the data you need to input.

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Who needs emvs master data guide?

01

Pharmaceutical companies managing market authorization.

02

Distributors and wholesalers involved in the supply chain.

03

Pharmacists and healthcare professionals tracking medication safety.

04

Regulatory authorities monitoring compliance with safety standards.

05

Technology providers facilitating the implementation of EMVS.

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What is emvs master data guide?

The EMVS Master Data Guide is a comprehensive document that provides instructions and guidelines for maintaining and submitting master data related to medicines in the European Medicines Verification System (EMVS).

Who is required to file emvs master data guide?

All stakeholders involved in the pharmaceutical supply chain, including manufacturers, wholesalers, and retailers, are required to file the EMVS Master Data Guide to ensure compliance with the regulations.

How to fill out emvs master data guide?

To fill out the EMVS Master Data Guide, stakeholders should gather the necessary product information, follow the structured guidelines provided in the document, and accurately complete each section before submission to the relevant authorities.

What is the purpose of emvs master data guide?

The purpose of the EMVS Master Data Guide is to facilitate the accurate reporting and verification of medicinal products in the EU, ultimately enhancing patient safety and combating counterfeit medicines.

What information must be reported on emvs master data guide?

The information that must be reported includes product identifiers, packaging details, company information, and any unique attributes related to the specific medicinal product being registered under the EMVS.

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