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Annex I
List of the names, pharmaceutical form, strength of the medicinal product,
route of administration, Marketing Authorization Holders in the Member
States1Member Telemarketing authorization/EEAholderAustriaAstraZeneca
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Begin filling out the form by entering your personal or organizational details in the designated fields.
04
Carefully review the list of items or entities that need to be included in the annex i list.
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For each item or entity, provide all the necessary information such as name, description, quantity, and relevant details.
06
Ensure that all the information provided is accurate and up to date.
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If required, attach any supporting documents or evidence that validate the inclusion of certain items or entities in the annex i list.
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Specific industries or activities that involve controlled substances, sensitive information, or restricted goods may have a legal obligation to maintain and submit an annex i list.
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The exact requirements for who needs the annex i list can vary depending on the laws, regulations, or policies of the specific jurisdiction.
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What is annex i list of?
Annex I list refers to a detailed document that specifies controlled substances, items, or activities that require regulatory compliance.
Who is required to file annex i list of?
Entities or individuals involved in the production, distribution, or handling of substances or activities listed in Annex I are required to file the list.
How to fill out annex i list of?
To fill out Annex I, you must provide accurate information regarding the items, quantities, and relevant details as specified by the regulatory authority, ensuring all sections are completed.
What is the purpose of annex i list of?
The purpose of Annex I is to monitor and regulate the handling of specific substances or activities to ensure compliance and safety.
What information must be reported on annex i list of?
The report must include details such as item descriptions, quantities, handling procedures, and stakeholders involved in the activities.
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