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UKHSA Chief Executive Professor Dame Jenny Harries visits Manchester and Liverpool to launch campaign as measles cases continue to rise.
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.
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.
The Media Literacy Programme Fund awards grant funding to organisations undertaking media literacy activity that tackles the media literacy challenges in the Online Media Literacy Strategy.
A research paper from the CMA
Guidance on applying to renew a marketing authorisation (MA) for a veterinary medicine.
Apply for changes to your marketing authorisation, including minor variations type IA and IB, major variations type II and extensions.
Guidance for the pharmaceutical industry on Marketing Authorisations for veterinary medicines.
Find out how to apply VAT to charges for postage, delivery services and how to treat direct marketing services involving distribution of printed matter.
Service for Marketing Authorisation Holders, Manufacturers and Wholesalers.
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.
Case study on how the advertising industry initiated a system of self-regulation in non-broadcast media in 1962, followed by co-regulation with…
Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
How to renew marketing authorisations for products granted through different routes and at different times.
Create hard copy and social media marketing materials using our Get into Teaching branded templates.
How the MHRA assesses Marketing Authorisation Applications (MAA) for medicines referred under Article 29.
Using an ecological momentary assessment to evaluate your digital health product.
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