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Advice and guidance on the health needs of migrant patients for healthcare practitioners.
How to register your medical devices with the Medicines and Healthcare products Regulatory Agency (MHRA) for the markets in Great Britain and Northern Ireland
Use the case studies to help you decide when your goods may (or may not) go beyond insufficient production.
Apply to manufacture Extemporaneous preparations, Autogenous vaccines, authorisations for Equine Stem Cell Centre (ESCCA) or Non-Food Animal Blood Bank (NFABBA).
Kyowa Kirin Limited has notified MHRA that the priming instructions in the current PIL for Tostran 2% gel require updating.
Check what processes are considered as insufficient production under the Trade and Cooperation Agreement.
The agreement for a first-of-a-kind test rig will provide critical data for the design and development of Spherical Tokamak for Energy Production (STEP).
Get help to classify herbal medicines, vitamins, food preparations, supplements and tonics for import and export.
Information about how industry placements for T Levels work and how employers can get involved.
Guidance for manufacturers, importers and distributors.
The figures you’ll need and how to use them to work out your discounted duty rates.
An overview of capital funding for post-16 education providers, the type of funding available, what it can be used for and when to apply.
Questionnaire for patients with Shiga toxin-producing E.coli (STEC), for reporting and surveillance.
Find out about applying for the Spirit Drinks Verification Scheme, how to submit brand information, fees and making sure your production process is compliant.
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