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How to ensure the products you make or import comply with the law and are safe for consumers to use.
Guidance providing practical information for placing construction products on the Northern Ireland market and unfettered access provisions.
Find out which types of food are zero-rated and which are standard-rated for VAT purposes.
Information on OPSS product safety alerts, reports and recalls for unsafe products and resources for consumers, businesses and regulators.
How to get scientific advice about your licence application from MHRA, including: submitting a request, your meeting with MHRA, fees.
Product security factsheet accompanying the Product Security and Telecommunications Infrastructure Bill, outlining the problems the Bill will address and how.
How to apply to protect a food, drink or agricultural product name under the UK GI schemes.
Search for information about medicines including patient information leaflets (PILs), details on how the medicine can be used (SmPCs) and scientific reports (PARs).
Our primary purpose is to protect people and places from product-related harm, ensuring consumers and businesses can buy and sell products with confidence. Office for Product Safety and Standards is part of the Department for Business and Trade .
Uses of fluorinated gases (F gases) that are banned or will be banned in the future.
Get help to classify herbal medicines, vitamins, food preparations, supplements and tonics for import and export.
Papers from the Office for Product Safety and Standards.
Guidance for suppliers and dealers.
Guidance for the veterinary pharmaceutical industry on the production of mock-ups for assessment.
Licences and authorisations to import genetic material, research and diagnostic samples, trade samples and display items, and some live animals and animal products.
The Medicines and Healthcare products Regulatory Agency regulates medicines, medical devices and blood components for transfusion in the UK. MHRA is an executive agency, sponsored by the Department of Health and Social Care .
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
How to access public data from the Companies House register using our data products.
Find out the rules to establish the country of origin of imported and exported goods and to help identify goods which qualify for lower or no Customs Duty.
Directory of current ICH Guidelines which have been implemented by the Medicines and Healthcare products Regulatory Agency.
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