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Register to vote Register by 18 June to vote in the General Election on 4 July.
Guidance on how to reclassify your medicine and how to name medicines.
Details of the process changes for established medicines, effective from 1 March 2024, which apply specifically to chemical products.
Dermipred tablets seized at East Midlands Airport.
Directory of current ICH Guidelines which have been implemented by the Medicines and Healthcare products Regulatory Agency.
Information and documents on Public Health England’s review of the evidence for dependence on, and withdrawal from, prescribed medicines.
The CMU is part of the Medicine, Pharmacy and Industry Group of DHSC which looks at supply and procurement in hospitals.
You must get permission to export certain drugs and medicines.
Information about how to register your homeopathic medicinal product through the Simplified Homeopathic Registration Scheme or the UK Homeopathic National Rules Scheme
Guidance for prescribing vets on the use of the cascade.
Links to EU guidance, as it stood immediately before end of transition period.
Guidance on naming human medicines, including Braille requirements for the name on the product label.
The actions to take for sourcing medicines in different circumstances.
Actions that trial sponsors should consider to build resilience into clinical trial design
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.
How to carry out a clinical trial to apply for a marketing authorisation, manage your authorisation and report safety issues.
Guidance for industry on flexible approaches to regulation we are taking during the COVID-19 outbreak.
A summary of recent letters and notifications sent to healthcare professionals about medicines and medical devices.
Details of the Yellow Card scheme, which is the system for recording adverse incidents with medicines and medical devices in the UK.
How to obtain an authorisation to wholesale veterinary medicines.
How to apply for an authorisation to manufacture authorised veterinary medicines or medicines marketed under the Exemptions for small pet animals.
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