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Register to vote Register by 18 June to vote in the General Election on 4 July.
Submission dates and how the submissions using the EC decision reliance procedure work.
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.
Guidance for the pharmaceutical industry on Marketing Authorisations for veterinary medicines in the UK.
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 the decentralised and mutual recognition reliance procedure (MRDCRP) for marketing authorisation applications including information on how to apply.
If you're advertising or marketing, including direct marketing, you must be accurate and honest and follow the advertising codes of practice
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 how to apply for an authorisation to place a veterinary medicine on the UK market or part of, or to expire one.
Details of the process changes for established medicines, effective from 1 March 2024, which apply specifically to chemical products.
How to renew marketing authorisations for products granted through different routes and at different times.
Quality and labelling rules for growing, packing, distributing, importing and selling fresh fruit and vegetables.
Steps to help grow your business - finding finance, mentors, increasing sales and developing products and services
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.
How to get scientific advice about your licence application from MHRA, including: submitting a request, your meeting with MHRA, fees.
This guidance covers ‘grandfathering’ and managing the lifecycle changes of medicinal products.
How the MHRA processes variations to Marketing Authorisations (MAs)
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.
How to submit an application, data package and responses for proposed or existing marketing authorisations.
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