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  • Comply with good manufacturing practice (GMP) and good distribution practice (GDP), and prepare for an inspection.

  • Sets out medicines that cannot be exported from the UK or hoarded because they are needed for UK patients.

  • 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.

  • A wholesale dealer in Great Britain may import Qualified Person certified medicines from the European Economic Area if certain checks are made by the ‘Responsible Person (import)’

  • 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.

  • Details of the organisations that are currently approved to undertake conformity assessments on medical devices.

  • How to register as a manufacturer, importer or distributor of active substances.

  • Sets out medicines that can be moved to Northern Ireland to meet patient need.

  • 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.

  • Reporting, investigating and recalling suspected defective medicinal products to the Defective Medicines Report Centre (DMRC).

  • Information for wholesale dealer licence holders about the medicines put on the UK market for UK patients that they cannot export or hoard.

  • An interpretation of the good manufacturing practice (GMP) requirements for specials manufacturers.

  • The locations for a Marketing Authorisation Holder (MAH) and a Qualified Person responsible for Pharmacovigilance (QPPV)

  • Approved countries for batch testing and importation of medicines

  • Information about how approved bodies help regulate medical devices and how to apply for approval.

  • What you need to do to supply authorised medicines from Great Britain to Northern Ireland.

  • Apply for and maintain registrations for the brokering of human medicines.