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Sets out medicines that cannot be exported from the UK or hoarded because they are needed for UK patients.
Comply with good manufacturing practice (GMP) and good distribution practice (GDP), and prepare for an inspection.
How to apply for, update and cancel licences for the manufacture, import and wholesale of human and veterinary medicines.
Pharmacy (P), prescription-only (POM), and general sale list (GSL) medicines: apply to move your medicine to a different classification.
You must get permission to export certain drugs and medicines.
Details of the organisations that are currently approved to undertake conformity assessments on medical devices.
What you need to do to supply authorised medicines from Great Britain to Northern Ireland.
A wholesale dealer in Great Britain may import Qualified Person certified medicines from the European Economic Area if certain checks are made by the 바카라 사이트˜Responsible Person (import)바카라 사이트™
Information relating to parallel imports and the implementation of the Windsor Framework.
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.
Sets out medicines that can be moved to Northern Ireland to meet patient need.
Information relating to the disapplication of falsified medicines under UK Law.
How to register as a manufacturer, importer or distributor of active substances.
Helping interpret the Human Medicines (Amendment) Modular Manufacture and Point of Care regulations 2025.
Information on sourcing medicines that can be supplied by wholesale distributor authorisation (WDA) holders based in the UK.
Outlining the principles for the management and oversight of the import of investigational medicinal products (IMPs) to Great Britain from listed countries.
The UK government has introduced the Northern Ireland MHRA Authorised Route (NIMAR). This new route for supply became operational 1 January 2022.
Actions QPs, RPis and RPs need to take following agreement of the Windsor Framework
An interpretation of the good manufacturing practice (GMP) requirements for specials manufacturers.
Reporting, investigating and recalling suspected defective medicinal products to the Defective Medicines Report Centre (DMRC).
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