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Guidance for holders of Marketing Authorisations approved in Northern Ireland or the EU/EEA member states who want to bring a product to market in Great Britain.
Use this form to notify the IPO of marketing authorisation for a medicinal or plant protection product, granted after your application for an SPC for that product.
Marketing standards for hops producers, manufacturers, retailers and distributors.
Form for a business to register seed marketing operations.
Explainer for the pharmaceutical industry on the ongoing implementation of the Veterinary Medicines Regulation relating to applications and authorisations for veterinary medicines.
Marketing Authorisation Holders should review their manufacturing processes to identify and, if found, to mitigate the risk of nitrosamine impurities being present.
How to change the ownership from one marketing authorisation (MA) holder to another.
This guidance covers ‘grandfathering’ and managing the lifecycle changes of medicinal products.
This toolkit is for Innovation Passport holders following the Innovative Licensing and Access Pathway (ILAP) and provides activities to support the design and development of medicines.
The Defence and Security Accelerator (DASA) conducts Market Explorations to determine future activities.
From 13 May 2024 we are introducing a change to the procedure for new Marketing Authorisation (MA) applications, where a joint assessment of labels is requested.
How to apply for marketing authorisation via this new procedure.
Declaration for approval under Commission Regulation 1019/2002.
Marketing standards for poultry meat producers, manufacturers, retailers and distributors.
Don’t include personal or financial information like your National Insurance number or credit card details.
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