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Details of the system for reporting adverse drug reactions from medicines or adverse incidents with medical devices in the UK
A guide to the legislation enabling drug services and others to supply take home naloxone without a prescription to save a life in an emergency.
UK companies who have their licence to manufacture or wholesale medicines terminated and cancelled.
How to manage and use bed rails safely.
Code of practice on the effective prevention and control of infection by health service providers.
Comply with good manufacturing practice (GMP) and good distribution practice (GDP), and prepare for an inspection.
Apply for changes to your marketing authorisation, including minor variations type IA and IB, major variations type II and extensions.
Guidance for GP practices, hospitals, hospices and medical examiner offices about when to order more MCCDs and what to do with completed MCCDs.
Guidance for medical practitioners completing a medical certificate of cause of death in England and Wales.
How to show the MHRA you're meeting good clinical practice (GCP) standards and what to expect from an inspection.
How to apply for, update and cancel licences for the manufacture, import and wholesale of human and veterinary medicines.
Sets out standards required for NHS organisations concerning patient confidentiality.
How to register on the MHRA portal and use it to apply for and update marketing authorisations and make other applications.
A summary of the types of scientific advice available at the MHRA, the process for getting advice and the fees involved.
Pharmacy (P), prescription-only (POM), and general sale list (GSL) medicines: apply to move your medicine to a different classification.
Who can supply or administer medicines to patients without a doctor under a PGD, which medicines they can supply, and legal requirements for PGDs.
Reporting, investigating and recalling suspected defective medicinal products to the Defective Medicines Report Centre (DMRC).
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 respond to individuals at risk of developing pressure ulcers, prevent harm where they occur and raise a safeguarding concern.
Information on when software applications (apps) are considered to be a medical device and how they are regulated.
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