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Guidance, application forms and protocols for plant breeders' rights, national listing, seed certification and farmed saved seed.
Get help to classify herbal medicines, vitamins, food preparations, supplements and tonics for import and export.
Search for information about medicines including patient information leaflets (PILs), details on how the medicine can be used (SmPCs) and scientific reports (PARs).
The Brucella Reference Unit (BRU) provides laboratory diagnostic and clinical management services for Brucella species.
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.
The characteristics, diagnosis and management of Candida auris (C. auris).
The New Active Substance Work Sharing Initiative (NASWSI) has successfully approved several medicines through this international collaboration and continues to foster cooperation and strong relationships between its Access partners. The Biosimilar Work Sharing Initiative (BSWSI) builds on this success.
This guide is about infections that occur in people who inject drugs (PWID).
Details of certificates issued under the Special Import System for the top ten veterinary medicines that were imported 1 Jan - 31 Mar 2024.
How to get scientific advice about your licence application from MHRA, including: submitting a request, your meeting with MHRA, fees.
How to apply for national listing of agricultural and vegetable plant varieties in Great Britain and Northern Ireland.
A summary of recent letters and notifications sent to healthcare professionals about medicines and medical devices.
The seeds which must be certified before you can market them, how to get them certified and how to get a licence for your seed business.
Protocols and procedures for testing the value for cultivation or use (VCU) of agricultural crops.
The characteristics, diagnosis, management, surveillance and epidemiology of Pseudomonas aeruginosa.
Check if your import, export or re-export needs a permit or certificate under the Convention on International Trade in Endangered Species of Wild Fauna and Flora (CITES).
Controlled drugs and precursor chemicals licensing fees information for individuals and companies.
How to get plant breeders' rights and what protection it gives your plant varieties.
Directory of current ICH Guidelines which have been implemented by the Medicines and Healthcare products Regulatory Agency.
The MHRA has authorised cabotegravir as 30 mg tablets and as a 600 mg long-acting injection administered every two months
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