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This guidance covers ‘grandfathering’ and managing the lifecycle changes of medicinal products.
Protocols and procedures for testing the distinctiveness, uniformity and stability (DUS) of certain agricultural and vegetable plants.
The epidemiology, symptoms, diagnosis and management of human T-cell lymphotropic virus types 1 and 2 (HTLV-1 and HTLV-2).
Guidance for the veterinary pharmaceutical industry on the production and submission of the Summary of Product Characteristics (SPCs) and product literature mock-ups.
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.
Check the tariff classification for peptide nisin standardised with sodium chloride
This guidance specifies the standards for the continuous monitoring and sampling of stack emissions.
The penalties if you are caught taking or dealing drugs - drug classification, fines and prison sentences
Dose of nicotine delivered & uptake and consistency of dose.
Advice and guidance on the health needs of migrant patients for healthcare practitioners.
Covering thalidomide, lenalidomide, and pomalidomide: temporary guidance for pregnancy prevention arrangements for patients taking them during COVID-19
Details of certificates issued under the Special Import System for the top ten veterinary medicines that were imported 1 Oct - 31 Dec 2023.
How catch limits are set and how to get involved in setting them. This includes current catch limits and closed fishing areas.
Urgent public health message: UKHSA has been notified about an outbreak of food botulism in France involving a small number of British nationals.
Details of certificates issued under the Special Import System for the top ten veterinary medicines that were imported 1 Jan - 31 Mar 2024.
Apply to manufacture Extemporaneous preparations, Autogenous vaccines, authorisations for Equine Stem Cell Centre (ESCCA) or Non-Food Animal Blood Bank (NFABBA).
How to use a multiphase optimisation strategy (MOST) to evaluate your digital health product.
Decision on application for authorisation under UK REACH.
Guidance for industry on flexible approaches we are taking on good distribution practices.
How the MHRA makes decisions on what is a medicinal product (borderline products).
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