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Annex I List of the names, pharmaceutical forms, strengths of the veterinary medicinal products, animal species, route of administration, and marketing authorization holders in the Member States1/29MemberMarketingStateauthorisationEU/EEAholderAustriaZoetis
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Start by gathering all the necessary information and documents related to the items that need to be included in the Annex I list.
02
Make sure you have a clear understanding of the purpose and requirements of the Annex I list.
03
Begin by entering the necessary details of each item in the list, such as the item's name, description, quantity, and any other relevant information.
04
Double-check the accuracy of the information provided for each item before moving on to the next one.
05
If required, attach any supporting documents or references to each item in the list.
06
Review the completed Annex I list to ensure all the required information has been included and is correct.
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Submit the filled-out Annex I list to the designated authorities or as per the given instructions.

Who needs annex i list of?

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The Annex I list is needed by individuals or organizations who are required to provide a comprehensive inventory of specific items. This can include government agencies, research institutions, import/export businesses, or any other entity that needs to keep track of particular items in a formal and organized manner.
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Annex I list of refers to a specific inventory or register required for compliance, typically related to environmental regulations or financial reporting.
Entities or individuals involved in activities that fall under the regulatory framework associated with Annex I are required to file this list.
To fill out the Annex I list, follow the prescribed format, provide all necessary details, and ensure accuracy in reporting the required information.
The purpose of the Annex I list is to maintain transparent reporting and monitoring of activities that are subject to regulatory oversight.
The information reported typically includes details about the activities, substances involved, quantities, and any relevant compliance data.
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