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Register to vote Register by 18 June to vote in the General Election on 4 July.
How a product complies with EU safety, health and environmental requirements, and how to place a CE marking on your product.
Find out what to do when you transport goods under a transit movement into or through the UK from common transit countries.
How to ensure the products you make or import comply with the law and are safe for consumers to use.
Marketing Authorisation Holders should review their manufacturing processes to identify and, if found, to mitigate the risk of nitrosamine impurities being present.
Find out what to do when you transport goods out of the UK under a transit movement to common transit countries.
What you need to do to comply with regulations on manufactured products you place on the market in Great Britain.
How to create a model of how your digital health product works and choose measures for your evaluation.
How you import from and export to Côte d’Ivoire (Ivory Coast).
Get help to classify various items of iron and steel, primarily those classified under chapter 72.
Labelling rules for businesses in Great Britain (England, Scotland and Wales) and retailers in Northern Ireland, for certain agri-food products moved under the Northern Ireland Retail Movement Scheme.
How to make an import declaration and get goods through the UK border.
How the MHRA makes decisions on when a product is a medical device (borderline products), and which risk class should apply to a medical device.
Customs and security requirements for rail freight movements entering or leaving the UK.
Get help to classify pharmaceutical products used to treat or prevent diseases or ailments (in humans or animals), including comparators used in clinical trials and placebos.
Use these general provisions to help you determine the origin of your products.
How to make export declarations and get goods through the UK border
How to get scientific advice about your licence application from MHRA, including: submitting a request, your meeting with MHRA, fees.
This guidance covers ‘grandfathering’ and managing the lifecycle changes of medicinal products.
Find out which sanitary protection products you can supply at the zero rate of VAT.
How to begin with evaluating a digital health product, including when to evaluate, budgeting and getting support.
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