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Register to vote Register by 18 June to vote in the General Election on 4 July.
Guidance for the pharmaceutical industry on how to apply to vary a veterinary Marketing Authorisation (MA) or Homeopathic Remedy.
This guidance covers ‘grandfathering’ and managing the lifecycle changes of medicinal products.
Get help to classify textiles and which headings and codes to use.
How to use an interrupted time series to evaluate your digital health product.
How to get a parallel import licence for your medicine in the UK, including pharmacovigilance requirements and submitting your application.
Apply for changes to your marketing authorisation, including minor variations type IA and IB, major variations type II and extensions.
When and how you need to register your item or apply for an exemption certificate to deal in ivory.
How a product complies with EU safety, health and environmental requirements, and how to place a CE marking on your product.
Get help to classify articles of leather and other items in chapter 42 of the tariff for import and export.
Find out when you can zero rate books and other forms of printed matter.
Submit a return (EX606) to declare duty on wine, cider and other fermented products (formally made-wine) each month.
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.
Get help to classify various items of iron and steel, primarily those classified under chapter 72.
How to use a before-and-after study to evaluate your digital health product.
Guide to licensing procedure and other restrictions for export of controlled dual-use items, software and technology, goods for torture and radioactive sources.
Statements delivered by Simon Manley, the UK's Permanent Representative to the WTO and UN, on 22nd and 23rd May 2024 at the WTO in Geneva.
Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
Ensuring you get what you pay for.
How to use an N-of-1 study to evaluate your digital health product.
How to get scientific advice about your licence application from MHRA, including: submitting a request, your meeting with MHRA, fees.
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