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Guidance on managing and using bed rails safely.
Comply with good manufacturing practice (GMP) and good distribution practice (GDP), and prepare for an inspection.
Details of the Yellow Card scheme, which is the system for recording adverse incidents with medicines and medical devices in the UK.
Code of practice on the effective prevention and control of infection by health service providers.
How to get the new MCCD if your organisation uses the current MCCD.
Pharmacy, prescription-only (POM), and general sale list (GSL) medicines: apply to move your medicine to a different classification.
Sets out standards required for NHS organisations concerning patient confidentiality.
How to show MHRA you're meeting good clinical practice (GCP) standards and what to expect from an inspection.
Apply for changes to your marketing authorisation, including minor variations type IA and IB, major variations type II and extensions.
How to apply for, update and cancel licences for the manufacture, import and wholesale of human and veterinary medicines.
Current list of organisations that will receive the new medical certificate of cause of death (MCCD), which must be used from 9 September 2024.
Guidance on manufacturing, importing, distributing and supplying specially manufactured or ordered products, including cannabis-based products for medicinal use in humans (CBPMs), known as 'specials'
How to apply for a traditional herbal registration (THR) to market a herbal medicine in the UK.
Information on when software applications are considered to be a medical device and how they are regulated.
How to get scientific advice about your licence application from MHRA, including: submitting a request, your meeting with MHRA, fees.
Who can supply and or administer specific medicines to patients without a doctor under a PGD and which medicines can be administered.
Guidance for UK wholesalers and manufacturers on how to import human medicines including unlicensed medicines, how to apply for a licence and how much it costs.
UK companies who have their licence to manufacture or wholesale medicines terminated and cancelled.
How the death certification process in England and Wales will change from 9 September 2024, including the introduction of medical examiners.
Detailed guidance on advertising and promoting medicines.
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