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Find out how to account for VAT schemes on business gifts, samples and promotional schemes.
Explainer on product information templates to be used by applicants and Marketing Authorisation Holders (MAHs) of veterinary medicines.
How to get scientific advice about your licence application from MHRA, including: submitting a request, your meeting with MHRA, fees.
Explainer for the pharmaceutical industry on the ongoing implementation of the Veterinary Medicines Regulation relating to applications and authorisations for veterinary medicines.
Information for ECTs on professional development training and support based on the early career framework (ECF). This is part of your 2-year induction.
Find out how to prove the originating status of your goods and check if you can claim preferential tariff treatment.
Get help to classify pharmaceutical products used to treat or prevent diseases or ailments (in humans or animals), including comparators used in clinical trials and placebos.
Check when packaging is classified as a finished plastic packaging component, and what is meant by substantial modifications, to find out if you must register for the tax.
Check what classifies as plastic, recycled plastic and packaging components, and if the packaging you manufacture or import is subject to the tax.
How to use Method 1 to work out the customs value of your imported goods if you're an importer or clearing agent.
This toolkit is for Innovation Passport holders following the Innovative Licensing and Access Pathway (ILAP) and provides activities to support the design and development of medicines.
Find out what goods you do not value when when working out the VAT due on import to the UK.
How product specific rules are used to identify the country of origin when importing or exporting between the UK and EU.
Guidance for organisations who may need to report packaging data because they are affected by extended producer responsibility (EPR) for packaging
Supplier declarations are where your UK supplier provides you with information needed to prove the origin of your goods for preferential rates of duty between the UK and other countries.
Guidance for the veterinary pharmaceutical industry on the production of mock-ups for assessment.
Guide to licensing procedure and other restrictions for export of controlled dual-use items, software and technology, goods for torture and radioactive sources.
A guide to documenting how you’ve collected your packaging data, known as your ‘methodology’. Online marketplaces affected by extended producer responsibility (EPR) for packaging must submit a methodology.
Information on how to submit an expression of interest (EoI) to take part in DCMS' Growing Place-based Giving Programme.
Use the case studies to help you decide when your goods may (or may not) go beyond insufficient production.
Don’t include personal or financial information like your National Insurance number or credit card details.
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