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ANNEX I LIST OF THE INVENTED NAMES, PHARMACEUTICAL FORMS, STRENGTHS OF THE MEDICINAL PRODUCTS, ROUTE OF ADMINISTRATION, MARKETING Authorization HOLDERS, PACKAGING AND PACKAGE SIZES IN THE MEMBER STATES
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The annex i list is a list of items or documents that provide additional information or details about a particular subject.
The annex i list is typically required to be filed by individuals, organizations, or entities that are subject to specific regulations or reporting requirements.
The process to fill out the annex i list may vary depending on the specific requirements set forth by the governing authority. Generally, it involves gathering the necessary information or documents and completing the designated form or template.
The purpose of the annex i list is to provide additional information or details that may be necessary for compliance, evaluation, documentation, or other specific purposes.
The specific information that must be reported on the annex i list will depend on the applicable regulations or requirements. It may include details about certain items, documentation, certifications, or any other relevant information.
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