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Get help to classify pharmaceutical products used to treat or prevent diseases or ailments (in humans or animals), including comparators used in clinical trials and placebos.
How the MHRA makes decisions on when a product is a medical device (borderline products), and which risk class should apply to a medical device.
Guidance for manufacturers, importers and distributors.
Substances that are classed as persistent organic pollutants (POPs) and when you're allowed to use them.
Get help to classify herbal medicines, vitamins, food preparations, supplements and tonics for import and export.
Get help to classify cigarettes, cigars, raw tobacco, smoking tobacco, tobacco for heating and nicotine substitutes for import and export.
Get help to classify organic chemicals that contain certain permitted additives or can be dissolved in water, for import and export.
Guidance for the veterinary pharmaceutical industry on the production of mock-ups for assessment.
Get help to classify electrical equipment such as communication equipment, cameras, and their parts and accessories.
What you need to do to comply with regulations on manufactured products you place on the market in Great Britain.
Find out which regulations apply to your products and where to go for further information on how to comply with them.
Product security factsheet accompanying the Product Security and Telecommunications Infrastructure Bill, outlining the problems the Bill will address and how.
A new pathway supporting innovative approaches to the safe, timely and efficient development of medicines to improve patient access.
How to make sure that your products are properly checked for conformity and your technical documents are managed correctly.
How to register your medical devices with the Medicines and Healthcare products Regulatory Agency (MHRA) for the markets in Great Britain and Northern Ireland
Get help to classify various items of iron and steel, primarily those classified under chapter 72.
Find out if you need to use the UKCA (UK Conformity Assessed) marking on products you manufacture or handle.
Licences and authorisations to import genetic material, research and diagnostic samples, trade samples and display items, and some live animals and animal products.
Find out which types of food are zero-rated and which are standard-rated for VAT purposes.
How to get scientific advice about your licence application from MHRA, including: submitting a request, your meeting with MHRA, fees.
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