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Departments, agencies and public bodies
News stories, speeches, letters and notices
Detailed guidance, regulations and rules
Reports, analysis and official statistics
Consultations and strategy
Data, Freedom of Information releases and corporate reports
How the MHRA processes variations to Marketing Authorisations (MAs)
Decisions made by MHRA on adverts reported to have breached the legislation on advertising medicines.
Quality and labelling rules for growing, packing, distributing, importing and selling fresh fruit and vegetables.
Case study on how the advertising industry initiated a system of self-regulation in non-broadcast media in 1962, followed by co-regulation with…
How to use a behaviour change techniques review to evaluate your digital health product.
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.
Find out how to account for VAT schemes on business gifts, samples and promotional schemes.
Guidance for the pharmaceutical industry on Marketing Authorisations for veterinary medicines.
Culture Secretary Lucy Frazer's speech on the strength of the UK's advertising industry at the Ad Association's LEAD conference.
A research paper from the CMA
This playbook explains how we use social media at GDS. In it, we share our best practice, what we've learned and what we're planning to do.
This guide is to help you and your business understand how to ensure that content on your service is appropriate for children.
This page provides a guide for those interested in key upcoming digital regulatory activity being explored, developed or implemented by government. It covers a range of governance activities, from legislative change to the development of co-regulatory and self-regulatory frameworks.
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 the MHRA assesses Marketing Authorisation Applications (MAA) for medicines referred under Article 29.
Rules on labelling food, feed and seed as organic or using organic production terms if you produce, prepare, store, import, export or sell organic food in the UK.
How to get scientific advice about your licence application from MHRA, including: submitting a request, your meeting with MHRA, fees.
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