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Departments, agencies and public bodies
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Data, Freedom of Information releases and corporate reports
The medicines regulators from Australia, Canada, Singapore, Switzerland and the United Kingdom (Access Consortium) have discussed the continued need for COVID-19 medicines that are safe, effective and of high quality
Guidance for prescribing vets on the use of the cascade.
An overview of the process including submitting or fast-tracking an application, naming your medicine and paying fees.
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.
Information on carrying medicine containing controlled drugs for individual travellers entering or leaving the UK.
How to comply with the exemption from the Veterinary Medicines Regulations that allow certain animal medicines to be sold without an authorisation.
A summary of recent letters and notifications sent to healthcare professionals about medicines and medical devices.
Guidance for veterinary medicines manufacturers and wholesale dealers in GB on selling and supplying products placed on the EU and UK markets before 1 January 2021 and the evidence you may need to provide.
From brussels sprouts to dodgy diet products, these tips from the MHRA will help you stay safe during the festive season and beyond
The Medicines and Healthcare products Regulatory Agency (MHRA), working with law enforcement partners, seized more than 15.5 million doses of illegally traded medicines with a street value of more than £30 million during 2023.
Guidance on naming human medicines, including Braille requirements for the name on the product label.
List of sites granted a manufacturer or wholesale dealer licence
medac GmbH (t/a medac Pharma LLP) is recalling the product for the batch specified in this notification due to particles detected during long-term stability tests.
How to carry out a clinical trial to apply for a marketing authorisation, manage your authorisation and report safety issues.
Information on granted EAMS scientific opinions, including the public assessment report and treatment protocols.
Guidance for industry on flexible approaches we are taking on good distribution practices.
These temporary good manufacturing practice (GMP) flexibilities will be allowed to address the current exceptional circumstances
This guidance demonstrates stakeholders, including the government, working together to address supply issues.
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