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Register to vote Register by 18 June to vote in the General Election on 4 July.
How we evaluated pre-exposure prophylactic (preventative) treatments for COVID-19.
Details of the process changes for established medicines, effective from 1 March 2024, which apply specifically to chemical products.
Guidance on how to reclassify your medicine and how to name medicines.
Apply for an import certificate to import a medicinal product into the UK for veterinary use.
Report a problem ('adverse incident') with a medical device or medicine to MHRA using the Yellow Card Scheme
The actions to take for sourcing medicines in different circumstances.
The CMU is part of the Medicine, Pharmacy and Industry Group of DHSC which looks at supply and procurement in hospitals.
Information about how to register your homeopathic medicinal product through the Simplified Homeopathic Registration Scheme or the UK Homeopathic National Rules Scheme
You must get permission to export certain drugs and medicines.
Actions that trial sponsors should consider to build resilience into clinical trial design
Guidance on naming human medicines, including Braille requirements for the name on the product label.
Links to EU guidance, as it stood immediately before end of transition period.
Guidance for industry on flexible approaches to regulation we are taking during the COVID-19 outbreak.
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.
Guidance on medicines for food and non-food horses and record keeping requirements including the horse passport.
How to carry out a clinical trial to apply for a marketing authorisation, manage your authorisation and report safety issues.
A summary of recent letters and notifications sent to healthcare professionals about medicines and medical devices.
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
Details of the Yellow Card scheme, which is the system for recording adverse incidents with medicines and medical devices in the UK.
Prescribing or supplying veterinary medicines including requirements for registration and inspection of premises.
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