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A new pathway supporting innovative approaches to the safe, timely and efficient development of medicines to improve patient access.
Find out how you can import goods with a specific authorised use and pay less duty.
A form of IP that extends the protection of patented active ingredients present in pharmaceutical or plant protection products.
Comply with good manufacturing practice (GMP) and good distribution practice (GDP), and prepare for an inspection.
Find out what repairs or processing you can do to your goods in a customs warehouse without authorisation, this is known as usual forms of handling.
Find out what you can do with your goods when they are being processed or repaired using outward processing.
If you import, manufacture, process, distribute or sell plant protection products (PPPs) for professional use in Great Britain, register to comply with regulations.
Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
This guidance provides information on comparator products used in studies supporting abridged marketing authorisation applications
The rules for manufacturing mercury added products in Great Britain, as well as importing and exporting them between Great Britain and non-EU countries.
This collaboration offers a strategic opportunity for the UK and ROK to establish global leadership in the priority area of Open RAN network power efficiency.
Sources of advice and financial support for UK farmers exporting agricultural products to the EU and beyond
Get help to classify herbal medicines, vitamins, food preparations, supplements and tonics for import and export.
How a product complies with EU safety, health and environmental requirements, and how to place a CE marking on your product.
Safety leaflet on topical corticosteroids and withdrawal reactions to help patients and their carers to use these medicines safely.
The MHRA has authorised cabotegravir as 30 mg tablets and as a 600 mg long-acting injection administered every two months
How to get a marketing authorisation for an Advanced Therapy Medicinal Product (ATMP) so it can be sold and/or supplied in Great Britain.
If you’re a business, organisation or sole trader that uses PPPs and adjuvants professionally in Great Britain, register to comply with regulations.
How to assess household and non-household packaging from 2024 onwards if you’re a UK organisation affected by extended producer responsibility (EPR) for packaging.
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