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Guidance for the pharmaceutical industry on Marketing Authorisations for veterinary medicines.
Guidance on how to license electronic cigarettes and other inhaled nicotine-containing products (NCPs) as medicines in the UK.
Pharmacy, prescription-only (POM), and general sale list (GSL) medicines: apply to move your medicine to a different classification.
This guidance provides information on comparator products used in studies supporting abridged marketing authorisation applications
This is a work sharing model for the co-ordinated assessment of a generic application that has been filed with multiple Access Consortium agencies.
A wholesale dealer in Great Britain may import Qualified Person certified medicines from the European Economic Area if certain checks are made by the ‘Responsible Person (import)’
Guidance for UK wholesalers and manufacturers on how to import human medicines including unlicensed medicines, how to apply for a licence and how much it costs.
The eMIT provides information about prices and usage for generic drugs and pharmaceutical products.
How to apply for, update and cancel licences for the manufacture, import and wholesale of human and veterinary medicines.
The actions to take for sourcing medicines in different circumstances.
Check if you can claim a VAT refund using the DIY housebuilders scheme, if you’re converting an existing building into a dwelling.
An overview of the process including submitting or fast-tracking an application, naming your medicine and paying fees.
How to package medicines for sale and what information you must provide to consumers and healthcare professionals.
Check if you can claim a VAT refund using the DIY housebuilders scheme, if you’re building a new house.
Find out when it's possible to get zero-rated supplies on medical and research goods and services that have been funded by charities.
Draft European Commission regulation setting the rules for applications on the use of generic descriptors under health and nutrition claims.
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