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Guidance on how to license electronic cigarettes and other inhaled nicotine-containing products (NCPs) as medicines in the UK.
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.
Apply for changes to your marketing authorisation, including minor variations type IA and IB, major variations type II and extensions.
How to use a patient-reported outcomes and experiences study to evaluate your digital health product.
If you're advertising or marketing, including direct marketing, you must be accurate and honest and follow the advertising codes of practice
Submission dates and how the submissions using the EC decision reliance procedure work.
How veterinary medicines can be advertised.
Using an ecological momentary assessment to evaluate your digital health product.
Guidance for manufacturers, importers and distributors.
If you put EEE on the UK market you must follow rules on both the EEE you sell and the EEE that becomes waste (WEEE).
The eMIT provides information about prices and usage for generic drugs and pharmaceutical products.
This section provides best practice guidance on ways to encourage and provide access to local authority land, buildings and other assets for digital deployment.
Guidance on the decentralised and mutual recognition reliance procedure (MRDCRP) for marketing authorisation applications including information on how to apply.
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.
Guidance on Conditional Marketing Authorisations, exceptional circumstances Marketing Authorisations and national scientific advice
Find out how to account for VAT schemes on business gifts, samples and promotional schemes.
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