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What you need to do if you sell or store tobacco products in the UK.
Explainer for the pharmaceutical industry on the ongoing implementation of the Veterinary Medicines Regulation relating to applications and authorisations for veterinary medicines.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
Guidance for the veterinary pharmaceutical industry on the production and submission of the Summary of Product Characteristics (SPCs) and product literature mock-ups.
How to comply with the requirements on promoting medicines to the public and to prescribers and suppliers of medicines.
This toolkit is for Innovation Passport holders following the Innovative Licensing and Access Pathway (ILAP) and provides activities to support the design and development of medicines.
How to use a quasi-experimental study to evaluate your digital health product.
How to use a cost utility analysis to evaluate your digital health product.
How a product complies with EU safety, health and environmental requirements, and how to place a CE marking on your product.
Work out the VAT liability of goods and services supplied by health and care institutions and providers of non residential care to children.
Product security factsheet accompanying the Product Security and Telecommunications Infrastructure Bill, outlining the problems the Bill will address and how.
Your purchasing strategy must show you’ve considered commercial and technology aspects, and contractual limitations.
How to export or move fish for human consumption from the UK.
How to import plants, fruit, vegetables, cut flowers, trees, seeds and used agricultural machinery from non-EU countries to Great Britain (England, Scotland and Wales).
Using an ecological momentary assessment to evaluate your digital health product.
What you need to know about and do to comply with the law and keep consumers safe.
How to use a combination of quantitative and qualitative data to evaluate your digital health product.
Guidance for manufacturers, importers and distributors.
Guidance for manufacturers, importers and distributors on the Product Security and Telecommunications Infrastructure Act 2022 and Regulations 2023.
An independent tribunal responsible for handling appeals against decisions made by the Secretary of State for Health and Social Care from pharmaceutical companies.
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