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VIRTUAL Overextended EudraVigilance Medicinal Product Dictionary Training CourseOVERVIEW The submission of data on medicines by marketingauthorisation holders is a legal requirement from Article 57(2)

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How to fill out xevmpd managementasphalion service mini

01

Log in to the xevmpd management system provided by Asphalion.

02

Navigate to the section for filling out the mini form.

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Enter the required information such as product details, substance information, and regulatory authority details.

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Submit the form using the designated method.

Who needs xevmpd managementasphalion service mini?

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Pharmaceutical companies who need to comply with xevmpd regulations.

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Regulatory affairs professionals responsible for submitting information to the EMA.

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What is xevmpd managementasphalion service mini?

Xevmpd managementasphalion service mini is a service provided by Asphalion for managing data related to medicinal products in the European Union.

Who is required to file xevmpd managementasphalion service mini?

Marketing authorization holders (MAHs) are required to file xevmpd managementasphalion service mini.

How to fill out xevmpd managementasphalion service mini?

Xevmpd managementasphalion service mini can be filled out through the Asphalion platform or by submitting the required information directly to the European Medicines Agency (EMA).

What is the purpose of xevmpd managementasphalion service mini?

The purpose of xevmpd managementasphalion service mini is to ensure the accurate and up-to-date reporting of medicinal product data to regulatory authorities in the EU.

What information must be reported on xevmpd managementasphalion service mini?

Information such as product details, manufacturing information, pharmacovigilance contact details, and regulatory submissions must be reported on xevmpd managementasphalion service mini.

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