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Register to vote Register by 18 June to vote in the General Election on 4 July.
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 if the goods you're declaring to inward or outward processing are classed as sensitive goods.
Advice for manufacturers of Class I medical devices for placing products on the UK market
A guide to collecting data about your packaging. This is for UK organisations affected by extended producer responsibility (EPR) for packaging.
What you need to do to comply with regulations on manufactured products you place on the market in Great Britain.
This guidance explains the legal framework for labelling and packaging as described in UK legislation and gives best practice for producing medicines labelling and packaging.
How you must label fluorinated gas (F gas) products you produce, import, or install.
You must batch and label the beef and veal you sell or supply according to specific rules, which vary from product to product.
A guide to the international regulations on the transportation of dangerous goods by air, sea, road, rail or inland waterway.
Information on the implementation of labelling and packaging requirements for medicinal products for human use under the Windsor Framework.
Find out if your product or service is eligible for an EU Ecolabel and how to apply for one.
Find out about applying for the Spirit Drinks Verification Scheme, how to submit brand information, fees and making sure your production process is compliant.
Requirements for importers, retailers and wholesalers selling and labelling wine in Great Britain, including labelling laws for wine imports into England from 1 January 2024.
What happens if an inspector finds you are breaking regulations on compulsory beef labelling.
Rapid evidence assessment on labelling schemes and implications for consumer IoT security - PETRAS IoT Hub
Apply for changes to your marketing authorisation, including minor variations type IA and IB, major variations type II and extensions.
Placing a veterinary medicine on the market, including non-medicinal products, medicinal words and phrases, how to obtain advice, report non-compliance.
Get help to classify articles of leather and other items in chapter 42 of the tariff for import and export.
How to conform with the legal requirements for placing medical devices on the market.
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