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Register to vote Register by 18 June to vote in the General Election on 4 July.
We are seeking views on the UK’s future regime for the exhaustion of intellectual property rights which will underpin the UK’s system of parallel trade.
Guidance on the Genetic Modification Inspectorate (GMI) seed audit programme for companies in England that import, produce or market seed.
What you need to do to comply with regulations on manufactured products you place on the market in Great Britain.
Guidance for the pharmaceutical industry on how to apply to vary a veterinary Marketing Authorisation (MA) or Homeopathic Remedy.
Find out how to work out your annual alcohol production if you’re part of a group, or you merge with, or separate from another business.
How to make a payment to MHRA by credit or debit card or a bank transfer.
This collaboration offers a strategic opportunity for the UK and ROK to establish global leadership in the priority area of Open RAN network power efficiency.
How to apply for accreditation, comply with your accreditation and packaging waste technical information.
The Intellectual Property Office offers different methods of accelerating the processing of your patent application.
Guidance for organisations who may need to report packaging data because they are affected by extended producer responsibility (EPR) for packaging
Quality and labelling rules for growing, packing, distributing, importing and selling fresh fruit and vegetables.
For manufacturers and distributors of intermediate and final feedingstuffs containing a medicinal premix or specified feed additives.
Guidance on plan-making.
Guidance for the veterinary pharmaceutical industry on the production of mock-ups for assessment.
Check the VAT rules for food processing and abattoir services.
How to apply for an authorisation to manufacture authorised veterinary medicines or medicines marketed under the Exemptions for small pet animals.
Producer responsibility laws in the UK cover packaging, electrical and electronic equipment (EEE), batteries and end of life vehicles (ELVs).
Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
Find out what you can do with your goods when they are being processed or repaired using inward processing.
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