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Marketing standards for poultry meat producers, manufacturers, retailers and distributors.
Guidance for prescribing vets on the use of the cascade.
Check the tariff classification for preparations put up for retail sale.
How to package medicines for sale and what information you must provide to consumers and healthcare professionals.
Links to EU guidance, as it stood immediately before end of transition period.
Information on the implementation of labelling and packaging requirements for medicinal products for human use under the Windsor Framework.
We’re responsible for handling applications for the discharge of patients detained in psychiatric hospitals. We also handle applications to change community treatment orders and the conditions placed on a ‘conditional discharge’ from hospital. Who we are We are part of...
Information for 16 to 19 providers delivering CDF industry placement(s) for academic year 2020 to 2021.
Safety leaflet on opioid medicines to help patients and their families reduce the risks of harm.
An interim position paper on the safety of hydroxyanthracene derivatives for use in food by the Committee on Carcinogenicity of Chemicals in Food, Consumer Products and the Environment
Guidance for pharmacists on prescriptions issued in EU countries, Norway, Iceland, Liechtenstein and Switzerland.
Recent updates regarding regulated qualifications.
Evidence reviews conducted by the Clinical and Public Health Response Evidence Review team and the Science Evidence Review team within UKHSA.
Advice for medical professionals to follow when assessing drivers with psychiatric disorders.
The MHRA is continuing to accept Active Substance Master Files (ASMFs) and Certificates of Suitability (CEPs)
UK Health Security Agency (UKHSA) proficiency testing (PT) samples for food microbiology in freeze-dried format.
This note is part of the statutory guidance under s215 of the HRA 2008 (from 1 April 2024)
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