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Safety leaflet on topical corticosteroids and withdrawal reactions to help patients and their carers to use these medicines safely.
The way you apply to licence biological products has changed
Get help to classify herbal medicines, vitamins, food preparations, supplements and tonics for import and export.
This environmental resource guide seeks to support the rollout of digital infrastructure in England, by providing greater awareness of climate adaptation, environmental improvements (biodiversity gains), and low carbon considerations. The guide is based on England jurisdiction, but has direct relevance...
How the MHRA makes decisions on what is a medicinal product (borderline products).
Information on taking, submitting and processing samples which potentially contain monkeypox virus.
Guidance for industry on flexible approaches to regulation we are taking during the COVID-19 outbreak.
Labelling rules for businesses in Great Britain (England, Scotland and Wales) and retailers in Northern Ireland, for certain agri-food products moved under the Northern Ireland Retail Movement Scheme.
How to submit a cosmetic product notification to the Office for Product Safety and Standards (OPSS).
How to package medicines for sale and what information you must provide to consumers and healthcare professionals.
Find out which regulations apply to your products and where to go for further information on how to comply with them.
Details of the process changes for established medicines, effective from 1 March 2024, which apply specifically to chemical products.
Guidance on PPE, face coverings, face visors, and hand cleaning and sanitising products, for the protection of consumers during the COVID-19 pandemic.
Advice and guidance on the health needs of migrant patients for healthcare practitioners.
Check the tariff classification for surface-active preparation for washing the skin and the hair (gel 2-in-1).
Things to consider when buying and using products.
Marketing Authorisation Holders should review their manufacturing processes to identify and, if found, to mitigate the risk of nitrosamine impurities being present.
The review of the safety of isotretinoin has concluded.
Comply with good pharmacovigilance practice and prepare for an inspection.
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