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ANNEX I LIST OF THE NAMES, PHARMACEUTICAL FORMS, STRENGTHS OF THE MEDICINAL PRODUCTS, ROUTE OF ADMINISTRATION, AND MARKETING Authorization HOLDERS IN THE MEMBER STATES AND NORWAY AND ICELAND 1 Member

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h-art31-767-en - ec europa is a specific form or document required for reporting certain information to the European Commission, often related to financial or administrative activities.

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Entities and individuals engaged in activities that fall under the relevant regulations or funding schemes set by the European Commission are required to file this form.

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The information that must be reported includes personal or organizational details, financial data, project progress, and any other information required by the regulatory framework.

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