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What you need to do to comply with regulations on manufactured products you place on the market in Great Britain.
Find out what a composite food product is, and the rules you need to follow to export or move these products from Great Britain to the EU and Northern Ireland.
Find out the information you must give to customers on food products and how to give it.
Check what you need to do to sell cosmetic products in Great Britain.
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.
How product specific rules are used to identify the country of origin when importing or exporting between the UK and EU.
How the MHRA makes decisions on what is a medicinal product (borderline products).
The guide, toolkit and further information for GB authorities with responsibility for consumer product safety.
Explainer on product information templates to be used by applicants and Marketing Authorisation Holders (MAHs) of veterinary medicines.
A new pathway supporting innovative approaches to the safe, timely and efficient development of medicines to improve patient access.
How to display the legal name for your food product.
If you're advertising or marketing, including direct marketing, you must be accurate and honest and follow the advertising codes of practice
Find out what a composite product is, and how to import or move composite products from the EU and Northern Ireland to Great Britain.
What you need to do to export or move food, drink and agricultural products.
Get help classifying computers, inkjet and toner cartridges and their components.
Use these general provisions to help you determine the origin of your products.
Guidance for the veterinary pharmaceutical industry on the production and submission of the Summary of Product Characteristics (SPCs) and product literature mock-ups.
How to submit a cosmetic product notification to the Office for Product Safety and Standards (OPSS).
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.
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