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The Medicines and Healthcare products Regulatory Agency (MHRA) has today (11 March 2024) approved the medicine quizartinib (Vanflyta) to be used alongside chemotherapy as first line treatment for adults who have acute myeloid leukaemia (AML).
How lead providers of post-16 education and training should request approval to subcontract 16 to 19 provision which involves distance learning.
The conditions you must meet to apply for and use Approved Importer status to commercially import dogs, cats and ferrets into England from Belarus, Poland, Romania or Ukraine.
Form for approval to process animal by-products (ABPs) at your processing facility.
Guide to submitting research applications to the Administration of Radioactive Substances Advisory Committee (ARSAC).
Evaluation of the Department for Education impact assessment for New approval process for prospective adopters and legislation on referrals to the Adoption Register
Form for a compost or biogas plant to apply for approval to treat animal by-products or catering waste.
Apply to get a certificate to prove a load compartment follows a design you've had approved to be used under the TIR scheme for international border crossings.
How we will transition from the existing funding approval process to the new process, and how existing post-16 qualification offers will change.
The Medicines and Healthcare products Regulatory Agency (MHRA) has today (7 March 2024) approved the medicine rozanolixizumab (Rystiggo) to treat adults with generalised myasthenia gravis, an autoimmune disease that causes muscle weakness, which can affect multiple muscle groups throughout the...
You need approval from the Heath and Safety Executive (HSE) Chemicals Regulation Directorate (CRD) to sell, distribute or store new pesticides in the UK
Weights and Measures Act 1985 and subsequent Deregulation Order 1999 (as amended).
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