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Guidance on the collection, verification, and reporting of safety events in clinical trials of an investigational medicinal product.
This notice explains how the rules are applied to this quota and how to apply for a licence.
Check if you can apply for authorised use to reduce your payments when you import goods for a specific use. This can include repairs, maintenance or processing.
Find out how to declare that your goods have been put to their authorised use, destroyed or re-exported.
Read the Council Directive 2003/48/EC of 3 June 2003 on taxation of savings income in the form of interest payments.
Check the tariff classification for preparations put up for retail sale.
Guidance for veterinary medicines manufacturers and wholesale dealers in GB on selling and supplying products placed on the EU and UK markets before 1 January 2021 and the evidence you may need to provide.
Guidance on labelling for medicinal products used in clinical trials.
Information to help you protect, manage and enforce your intellectual property (IP) rights in Brazil.
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