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Register to vote Register by 18 June to vote in the General Election on 4 July.
Guidance for suppliers and dealers.
Search for information about medicines including patient information leaflets (PILs), details on how the medicine can be used (SmPCs) and scientific reports (PARs).
What you need to know about and do to comply with the law and keep consumers safe.
Guidance for manufacturers, importers and distributors on the Product Security and Telecommunications Infrastructure Act 2022 and Regulations 2023.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
Search reports on business payment practices: when invoices are paid, payment terms and practices
Product security factsheet accompanying the Product Security and Telecommunications Infrastructure Bill, outlining the problems the Bill will address and how.
We advance prosperity by ensuring no viable UK export fails for lack of finance or insurance, doing that sustainably and at no net cost to the taxpayer.
Explainer on product information templates to be used by applicants and Marketing Authorisation Holders (MAHs) of veterinary medicines.
Sources of advice and financial support for UK farmers exporting agricultural products to the EU and beyond
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.
What you need to do to comply with regulations on manufactured goods you place on the Northern Ireland market.
How a product complies with EU safety, health and environmental requirements, and how to place a CE marking on your product.
Find out the information you must give to customers on food products and how to give it.
A new pathway supporting innovative approaches to the safe, timely and efficient development of medicines to improve patient access.
Get help to classify electrical equipment such as communication equipment, cameras, and their parts and accessories.
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.
How to get scientific advice about your licence application from MHRA, including: submitting a request, your meeting with MHRA, fees.
Things to consider when buying and using products.
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