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Register to vote Register by 18 June to vote in the General Election on 4 July.
How to show MHRA you're meeting good clinical practice (GCP) standards and what to expect from an inspection.
An overview of the process including submitting or fast-tracking an application, naming your medicine and paying fees.
Marking, labelling and marketing standards you must follow to import and export plant seeds, food and manufactured goods.
How the MHRA processes variations to Marketing Authorisations (MAs)
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.
How to apply for marketing authorisation via this new procedure.
Details of the process changes for established medicines, effective from 1 March 2024, which apply specifically to chemical products.
This study uses microdata on Indian manufacturing plants
Comply with good manufacturing practice (GMP) and good distribution practice (GDP), and prepare for an inspection.
This guidance outlines how to create and implement a cloud strategy, and when to consider a single, hybrid or multi-cloud solution.
The King's Awards for Enterprise - how to enter, online entry forms, guidance notes, deadline, nominations, award categories
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.
Your purchasing strategy must show you’ve considered commercial and technology aspects, and contractual limitations.
Guidance on how to license electronic cigarettes and other inhaled nicotine-containing products (NCPs) as medicines in the UK.
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.
How to change the ownership from one marketing authorisation (MA) holder to another.
How to submit an application, data package and responses for proposed or existing marketing authorisations.
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.
The MHRA will review applications for orphan designation at the time of a marketing authorisation (MA) or variation application.
How to make sure that your products are properly checked for conformity and your technical documents are managed correctly.
Don’t include personal or financial information like your National Insurance number or credit card details.
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