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Data, Freedom of Information releases and corporate reports
Information for people who wish to apply to release a vaccine or a blood product to market in the UK.
How to use a behaviour change techniques review to evaluate your digital health product.
Guidance on the 150-day assessment timeline for high-quality marketing authorisation applications including information on how to apply.
The Lambert toolkit is for universities and companies that wish to undertake collaborative research projects with each other.
How to choose the right tools to measure your service: features, cost, security, support.
Find out if simplified expenses suits your business. Compare what expenses you can claim using simplified expenses with what you can claim by working out the actual costs.
This guidance is designed to help UKHSA customers and partners to navigate engaging and working with us and to signpost upcoming events and opportunities.
How to comply with the requirements on promoting medicines to the public and to prescribers and suppliers of medicines.
Find out if you need to use the UKCA (UK Conformity Assessed) marking on products you manufacture or handle.
How we work with buyers and suppliers to improve the way technology is bought across government and the public sector.
The IPO's IP for business tools, training and guidance can help you create value from your ideas, turning inspiration into sustainable business success.
How a product complies with EU safety, health and environmental requirements, and how to place a CE marking on your product.
Marketing authorisations granted in 2024
How veterinary medicines can be advertised.
A list of upcoming webinars on the UK’s approach to product marking and placing products on the market in Great Britain and Northern Ireland.
Resources for regulators.
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