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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.
What denatured alcohol is, and how you apply for authorisation to produce, stock, distribute, sell or use it.
Information on waste batteries excluded from the regulations, definitions and battery types.
How to assess household and non-household packaging from 2024 onwards if you’re a UK organisation affected by extended producer responsibility (EPR) for packaging.
Find out about clearance applications and how to apply to HMRC for advance confirmation of an exempt distribution when a company purchases its own shares.
Licence and registration application information for companies that deal in precursor chemicals.
Who in the pharmaceutical industry can be a Marketing Authorisation Holder, named distributor or local representative and how to make changes to these.
A guide to collecting data about your packaging. This is for UK organisations affected by extended producer responsibility (EPR) for packaging.
Obligated packaging producers must register and meet their waste packaging recycling responsibilities.
For manufacturers and distributors of intermediate and final feedingstuffs containing a medicinal premix or specified feed additives.
Register as a manufacturer, importer or distributor of active substances for use in veterinary medicines.
How UK organisations that supply or import packaging should comply with extended producer responsibility (EPR) for packaging.
How to apply for, update and cancel licences for the manufacture, import and wholesale of human and veterinary medicines.
The process to convert Parallel Distribution Notices (PDNs) into Parallel Import Licences (PILs)
Registers of authorised manufacturers, wholesale dealer sites and retailers.
Register as a manufacturer, importer or distributor of active substances.
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