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A summary of recent letters and notifications sent to healthcare professionals about medicines and medical devices, and information about the publication of two recent Device Safety Information pages. The article also includes information on a recent National Patient Safety Alert...
The actions to take for sourcing medicines in different circumstances.
Latest FCDO travel advice for Western Sahara including on entry requirements, safety and security and local laws and customs.
Guidance for industry on flexible approaches we are taking on good distribution practices.
Biheldon cat and dog wormers seized at East Midlands Airport.
Guidance on applications and licences for manufacturers & wholesalers, suspended and revoked licences, registrations, exporting medicines, defective medicinal products and fees.
Safety leaflet on topical corticosteroids and withdrawal reactions to help patients and their carers to use these medicines safely.
How the MHRA makes decisions on what is a medicinal product (borderline products).
Guidance for the pharmaceutical industry on Marketing Authorisations for veterinary medicines in the UK.
Guidance for UK wholesalers and manufacturers on how to import human medicines including unlicensed medicines, how to apply for a licence and how much it costs.
How to apply for, update and cancel licences for the manufacture, import and wholesale of human and veterinary medicines.
How to comply with the requirements on promoting medicines to the public and to prescribers and suppliers of medicines.
Placing a veterinary medicine on the market, including non-medicinal products, medicinal words and phrases, how to obtain advice, report non-compliance.
Kieron Banks (34) was sentenced today at the Nightingale Court in Wolverhampton for the illegal possession and intent to supply prescription-only medication valued at over £2m following investigations by the Medicines and Healthcare products Regulatory Agency (MHRA).
An overview of the process including submitting or fast-tracking an application, naming your medicine and paying fees.
Information about new applications, post-licensing, advertising, product information and fees.
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.
Guidance on how to license electronic cigarettes and other inhaled nicotine-containing products (NCPs) as medicines in the UK.
Information for patients, healthcare professionals and developers of new medicines
How to renew marketing authorisations for products granted through different routes and at different times.
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