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Register to vote Register by 18 June to vote in the General Election on 4 July.
Guidance for EU exporters, exporters from rest of the world and UK importers, on how to import groupage or mixed load consignments of animal products into Great Britain (England, Scotland and Wales).
What you need to do to comply with regulations on manufactured goods you place on the Northern Ireland market.
How to change the specification of a product name registered under the UK GI schemes, and object to a substantial change.
What you need to do to export or move animal bones, protein and other by-products.
Uses of fluorinated gases (F gases) that are banned or will be banned in the future.
Exporters of groups of products of animal origin (POAO) to the EU and Northern Ireland can join the groupage export facilitation scheme (GEFS) to use 30-day support attestations.
How to object to an application to register for UK geographical indication (GI) protection, change or cancel a product specification and how to appeal against a decision.
Who in the pharmaceutical industry can be a Marketing Authorisation Holder, named distributor or local representative and how to make changes to these.
Guidance for industry on flexible approaches to regulation we are taking during the COVID-19 outbreak.
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.
Your purchasing strategy must show you’ve considered commercial and technology aspects, and contractual limitations.
How to import plants, fruit, vegetables, cut flowers, trees, seeds and used agricultural machinery from non-EU countries to Great Britain (England, Scotland and Wales).
Reported problems with the supply of an animal medicine and the date when the issue is expected to be resolved.
The rules about product labelling - including special rules for retailers and manufacturers in different business sectors (like food, jewellery and toys)
Guidance for the pharmaceutical industry on Marketing Authorisations for veterinary medicines in the UK.
Apply for changes to your marketing authorisation, including minor variations type IA and IB, major variations type II and extensions.
Guidance to aid producers of e-cigarettes and refill containers to prepare notifications for their products.
Find out if you need to use the UKCA (UK Conformity Assessed) marking on products you manufacture or handle.
The guide, toolkit and further information for GB authorities with responsibility for consumer product safety.
Use a separate statement of objection form for each Moldovan geographical indication (GI) product name you object to.
Don’t include personal or financial information like your National Insurance number or credit card details.
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