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Comply with good manufacturing practice (GMP) and good distribution practice (GDP), and prepare for an inspection.
Guidance for industry on flexible approaches we are taking on good distribution practices.
This guidance demonstrates stakeholders, including the government, working together to address supply issues.
The Good Manufacturing Practice (GMP) and Good Distribution Practice (GDP) Consultative Committee discusses the manufacture and wholesale distribution of medicines.
Advice on writing clear notices and maximising replies to your FSNs.
For MAHs, manufacturers, wholesalers, retailers (including vets) and feed businesses on the manufacture and movement of veterinary medicines in relation to the NI Protocol and Brexit.
Guidance for the pharmaceutical industry on who can be a Marketing Authorisation Holder, named distributor or local representative and how to make changes to these.
How to apply for, update and cancel licences for the manufacture, import and wholesale of human and veterinary medicines.
How marketing authorisation holders should provide educational materials to MHRA for assessment and approval prior to launching their products on the UK market.
Music industry voluntary code that is a commitment to standards of good practice in relation to music streaming.
What you need to do to supply authorised medicines from Great Britain to Northern Ireland.
Registers of authorised manufacturers, wholesale dealer sites and retailers.
Register as a manufacturer, importer or distributor of active substances.
Apply for and maintain registrations for the brokering of human 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)’
Information on good laboratory, manufacturing and distribution practice, good pharmacovigilance practice (GPvP), out-of-specification investigations, inspection metrics and fees.
How to show MHRA you're meeting good clinical practice (GCP) standards and what to expect from an inspection.
An external quality assessment (EQA) scheme for laboratories routinely testing for a range of food-borne pathogens and indicator organisms.
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