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Documents, certificates, letters and notes available at the British Embassy Baku.
Service for Marketing Authorisation Holders, Manufacturers and Wholesalers.
Check the regulations on aircraft parts imported with a certificate of airworthiness.
Pharmacovigilance system requirements
How to object to the registration of a lasting or enduring power of attorney - including forms and fees
How to check if your criminal record will affect your licence application, and the information you need to provide for our criminality checks.
Use form C88 (status) as proof of authorisation to import or export for the country of destination.
Look up a trade mark to see if something identical or similar to your brand is already registered.
Reclaim VAT you've paid on goods and services bought in the UK to use in your business if you’re registered as a business outside the UK.
The process of taking or giving evidence from abroad for UK court cases and rules on which countries allow it.
Carry out checks on your overseas customers and find out what records you’ll need to keep if you’re approved for the Fulfilment House Due Diligence Scheme.
Explainer for the pharmaceutical industry on the implementation of the Veterinary Medicines Regulation relating to Pharmacovigilance.
Information to help you protect, manage and enforce your intellectual property (IP) rights in China.
You must include the appropriate legal basis for your application when you apply to MHRA for a marketing authorisation.
Guidance for UK businesses on rules for selling services to Lithuania.
How to apply for an exemption to use a restricted substance to manufacture electrical and electronic equipment.
Guidance for the pharmaceutical industry on Marketing Authorisations for veterinary medicines.
Definitive fees charged for applications under Schedule 7 of the Veterinary Medicines Regulations 2013.
How to register, make changes to your registration, view your account and submit returns online
Guidance for organisations involved in any aspect of the pharmaceutical lifecycle or GLP studies regulated by MHRA, covering the approval of paper documents when working from home
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