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Who in the pharmaceutical industry can be a Marketing Authorisation Holder, named distributor or local representative and how to make changes to these.
Guidance on Conditional Marketing Authorisations, exceptional circumstances Marketing Authorisations and national scientific advice
Use the rolling review route when you want to submit your eCTD dossier in separate parts for pre-assessment instead of making a full consolidated document submission.
How the MHRA assesses Marketing Authorisation Applications (MAA) for medicines referred under Article 29.
If you're advertising or marketing, including direct marketing, you must be accurate and honest and follow the advertising codes of practice
How to get scientific advice about your licence application from MHRA, including: submitting a request, your meeting with MHRA, fees.
Quality and labelling rules for growing, packing, distributing, importing and selling fresh fruit and vegetables.
Guidance for the pharmaceutical industry on Marketing Authorisations for veterinary medicines in the UK.
How to find export opportunities and overseas customers for your business on great.gov.uk: get help selling online overseas, get help from a trade specialist.
Find a supplier who can provide a specialist, such as a data scientist or developer, for a specific piece of work.
Submissions related to human medicines need to be submitted directly to the MHRA.
Steps to help grow your business - finding finance, mentors, increasing sales and developing products and services
Marketing authorisations granted in 2024
Marketing authorisations (MAs) granted since January 2014.
Guidance on how to license electronic cigarettes and other inhaled nicotine-containing products (NCPs) as medicines in the UK.
How to write requirements for services on the Digital Outcomes and Specialists framework
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.
Service for Marketing Authorisation Holders, Manufacturers and Wholesalers.
How to submit an application, data package and responses for proposed or existing marketing authorisations.
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