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This guidance explains how you can apply common security standards in your organisation to secure email.
How to renew marketing authorisations for products granted through different routes and at different times.
Guidance on the decentralised and mutual recognition reliance procedure (MRDCRP) for marketing authorisation applications including information on how to apply.
How the MHRA assesses Marketing Authorisation Applications (MAA) for medicines referred under Article 29.
How to create a Driver and Vehicle Standards Agency (DVSA) email alerts account and update your subscription preferences.
How the MHRA processes variations to Marketing Authorisations (MAs)
Verify or change the email address we use for your customs messages and notifications.
How to buy assisted digital and digital inclusion services through the Digital Training and Support framework.
This guidance covers ‘grandfathering’ and managing the lifecycle changes of medicinal products.
Business customers can apply to access our electronic services through the portal or Business Gateway.
Learn about about importing and exporting goods.
Guidance for the pharmaceutical industry on how to apply to vary a veterinary Marketing Authorisation (MA) or Homeopathic Remedy.
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.
Guidance on setting up and securing email in government organisations.
Details of the process changes for established medicines, effective from 1 March 2024, which apply specifically to chemical products.
Guidance on how to license electronic cigarettes and other inhaled nicotine-containing products (NCPs) as medicines in the UK.
Learn more about Making Income Tax and VAT Digital if you’re an agent or a business.
How to send your information to Companies House using our online services.
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