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Product Recall for Swirl Plus 500ml and 30ml Mouthwash presenting a microbiological risk.
Check the tariff classification for surface-active preparation for washing the skin and the hair (gel 2-in-1).
Batches of some products made by Legency Remedies Pvt Ltd have been found to contain a bacteria called Ralstonia pickettii (R. pickettii). All potentially affected batches are being recalled following an MHRA investigation.
Find out the information you must give to customers on food products and how to give it.
This document details the service standards of the Veterinary Medicines Directorate (VMD)
Guidance for the pharmaceutical industry on Marketing Authorisations for veterinary medicines.
Information and documents related to the Disrespect NoBody campaign, which helps young people understand what a healthy relationship is.
Guidance on mouth care for patients with confirmed or suspected COVID-19 who are non-ventilated, ventilated and those having step down or end of life care.
These temporary good manufacturing practice (GMP) flexibilities will be allowed to address the current exceptional circumstances
The Medicines and Healthcare products Regulatory Agency regulates medicines, medical devices and blood components for transfusion in the UK. MHRA is an executive agency, sponsored by the Department of Health and Social Care .
How to account for VAT on goods and services provided by registered health professionals, including doctors, dentists, nurses and pharmacists.
Competent authorities of exporting countries should use the relevant model health certificate as a template to create a version exporters can apply for to export other animal by-products to Great Britain, the Channel Islands or Isle of Man.
Advice and guidance on the health needs of migrant patients for healthcare practitioners
OPSS is leading a fresh campaign to raise awareness among parents and carers about potential hazards to children associated with swallowing small magnets, button batteries, loose/small toy parts and imitation food.
Details of the process changes for established medicines, effective from 1 March 2024, which apply specifically to chemical products.
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