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Business rates information letters are issued by the Department for Levelling Up, Housing and Communities at regular intervals throughout the year.
Submission dates and how the submissions using the EC decision reliance procedure work.
Use this form to confirm that your limited liability partnership (LLP) details are up to date.
How to conform with the legal requirements for placing medical devices on the market.
This page provides practical information to help you make the most of your IP when doing business in Kazakhstan.
Comply with good manufacturing practice (GMP) and good distribution practice (GDP), and prepare for an inspection.
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)’
How to show MHRA you're meeting good clinical practice (GCP) standards and what to expect from an inspection.
Class and permitted use of passenger ships, cargo ships, tankers, tugs, tenders, fishing boats, yachts, commercial vessels, and the required certificates.
Check the regulations on aircraft parts imported with a certificate of airworthiness.
How to make sure that your products are properly checked for conformity and your technical documents are managed correctly.
Definitive fees charged for applications under Schedule 7 of the Veterinary Medicines Regulations 2013.
Information for manufacturers.
Check if you need a tuberculosis (TB) test to support your visa application and find an approved clinic in your country
How to legally run a business that deals with the wholesale of animal medicines (veterinary medicinal products) and the WDA Register.
Guidance for manufacturers and distributors of premixtures and feedingstuffs containing veterinary medicines or specified feed additives.
The Foreign, Commonwealth & Development Office (FCDO) provides lists of English-speaking lawyers abroad to help British nationals find the legal support they need.
If the UKCA marking applies to products you manufacture or supply, you will have specific obligations and responsibilities for compliance, depending on your role.
Details of General Licences issued by OFSI
Guidance on applying to renew a marketing authorisation (MA) for a veterinary medicine.
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