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What you need to do to comply with regulations on manufactured goods you place on the Northern Ireland market.
Guidance for suppliers and dealers.
What you need to know about and do to comply with the law and keep consumers safe.
How to renew marketing authorisations for products granted through different routes and at different times.
A new pathway supporting innovative approaches to the safe, timely and efficient development of medicines to improve patient access.
How a marketing authorisation holder should report a defect with a veterinary medicine.
If your business sells amateur plant protection products (PPPs) in Great Britain, register to comply with regulations.
The legal requirements to advertise and promote your medicine including the Blue Guide which interprets the law in more detail.
Find out how to apply VAT to charges for postage, delivery services and how to treat direct marketing services involving distribution of printed matter.
There are changes to the legislation of Reference Medicinal Products (RMPs) used to support abridged marketing authorisation applications
How the MHRA assesses Marketing Authorisation Applications (MAA) for medicines referred under Article 29.
The rules about product labelling - including special rules for retailers and manufacturers in different business sectors (like food, jewellery and toys)
Search for information about medicines including patient information leaflets (PILs), details on how the medicine can be used (SmPCs) and scientific reports (PARs).
Find out about the Fruit and Vegetables Aid Scheme.
What you need to do as a food and drink business to work with the EU.
Details of the process changes for established medicines, effective from 1 March 2024, which apply specifically to chemical products.
What you need to do to comply with regulations on manufactured goods you place on the EU market.
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