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Register to vote Register by 18 June to vote in the General Election on 4 July.
Find out about applying for the Spirit Drinks Verification Scheme, how to submit brand information, fees and making sure your production process is compliant.
Check the tariff classification for flavour pods.
An overview of the changes made to the Railways (Interoperability) Regulations 2011 that came into force on 1 January 2021.
How to apply for an exemption to use a restricted substance to manufacture electrical and electronic equipment.
Guidance for those conducting research and development on genetic resources.
How to register your medical devices with the Medicines and Healthcare products Regulatory Agency (MHRA) for the markets in Great Britain and Northern Ireland
Lists of standards that businesses can use to show their products, services or processes comply with essential requirements of legislation.
Guidance for industry on flexible approaches to regulation we are taking during the COVID-19 outbreak.
Non-nuclear radioactive substances regulation (RSR), when you need a permit, types of permits, how to apply, change (vary), transfer or surrender your permit.
Guidance and regulatory advice on how to apply for licences issued under ASPA and how your compliance with ASPA and your licence conditions will be assessed.
For manufacturers and distributors of intermediate and final feedingstuffs containing a medicinal premix or specified feed additives.
Check if you can make a declaration by conduct or orally if you’re claiming Returned Goods Relief or Temporary Admission for reusable packaging.
Apply to be a waste electrical and electronic equipment (WEEE) producer compliance scheme and operate legally under your approval.
How to make sure an application relating to an authorisation for a veterinary medicine is complete and will pass validation.
Information about the EU Regulations and their implementation in Northern Ireland
Licences and authorisations to import genetic material, research and diagnostic samples, trade samples and display items, and some live animals and animal products.
What you need to know before you can place a medical device on the Great Britain market with a UKCA mark.
There are changes to the legislation of Reference Medicinal Products (RMPs) used to support abridged marketing authorisation applications
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