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Register to vote Register by 18 June to vote in the General Election on 4 July.
Steps to help grow your business - finding finance, mentors, increasing sales and developing products and services
Guidance for manufacturers, importers and distributors on the Product Security and Telecommunications Infrastructure Act 2022 and Regulations 2023.
Use form ALVS1 if the Automatic Licence Verification System cannot process an automatic release on CHIEF or the Customs Declaration Service.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
Guidance for manufacturers, importers and distributors.
What you need to do to comply with regulations on manufactured goods you place on the Northern Ireland market.
A wholesale dealer in Great Britain may import Qualified Person certified medicines from the European Economic Area if certain checks are made by the ‘Responsible Person (import)’
Details of the process changes for established medicines, effective from 1 March 2024, which apply specifically to chemical products.
Guidance on Conditional Marketing Authorisations, exceptional circumstances Marketing Authorisations and national scientific advice
The rules about product labelling - including special rules for retailers and manufacturers in different business sectors (like food, jewellery and toys)
Find out what a composite product is, and how to import or move composite products from the EU to Great Britain.
The final report recommends the introduction of a small suite of simple savings and protection insurance products. HM Treasury has reviewed progress made one year on from the final report.
Search for information about medicines including patient information leaflets (PILs), details on how the medicine can be used (SmPCs) and scientific reports (PARs).
Explainer on product information templates to be used by applicants and Marketing Authorisation Holders (MAHs) of veterinary medicines.
Things to consider when buying and using products.
How to create a model of how your digital health product works and choose measures for your evaluation.
How to register your medical devices with the Medicines and Healthcare products Regulatory Agency (MHRA) for the markets in Great Britain and Northern Ireland
The CMA investigated the anticipated acquisition by Theramex HQ UK Limited of the European Rights to Viatris’ Femoston and Duphaston Products.
How to make sure that your products are properly checked for conformity and your technical documents are managed correctly.
Guidance for the pharmaceutical industry on how to apply to vary a veterinary Marketing Authorisation (MA) or Homeopathic Remedy.
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