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This guidance provides information on comparator products used in studies supporting abridged marketing authorisation applications
Details of the process changes for established medicines, effective from 1 March 2024, which apply specifically to chemical products.
Guidance on Conditional Marketing Authorisations, exceptional circumstances Marketing Authorisations and national scientific advice
Guidance for the pharmaceutical industry on how to apply to vary a veterinary Marketing Authorisation (MA) or Homeopathic Remedy.
Guides councils in how to assess their housing needs.
VAT treatment of transactions in commodities, commodity derivatives and on terminal markets.
This guide is to help you and your business understand how to ensure that content on your service is appropriate for children.
Rules to follow if you put batteries, including batteries in vehicles or appliances, on the UK market for the first time.
How online marketplaces will deal with VAT for goods from overseas that are sold to customers in the UK.
Find out which standards and regulations apply to your product and how to make sure you follow the right procedures.
Guide for businesses on best practice when using non-disclosure clauses in compensation settlement agreements where product safety is a factor.
How UK organisations that supply or import packaging should comply with extended producer responsibility (EPR) for packaging.
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)’
The Capacity Market ensures security of electricity supply by providing a payment for reliable sources of capacity.
Information and guidance on a range of medical devices for users and patients.
Get authorised to declare goods you bring into Northern Ireland 'not at risk’ of moving to the EU, so that the applicable EU rate of duty will not be payable on those goods.
Legal terms for veterinary medicines, marketing of non-medicinal products including medicinal words and phrases, how to complain.
Comply with good manufacturing practice (GMP) and good distribution practice (GDP), and prepare for an inspection.
What you need to do to place a medical device on the Great Britain, Northern Ireland and European Union (EU) markets.
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