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Register to vote Register by 18 June to vote in the General Election on 4 July.
This is a study for the Department for Digital, Culture, Media & Sport on online advertising issues and self-regulatory initiatives.
An overview of the process including submitting or fast-tracking an application, naming your medicine and paying fees.
Business plans - download free templates and get help writing a business plan
Submissions related to human medicines need to be submitted directly to the MHRA.
How to submit an application, data package and responses for proposed or existing marketing authorisations.
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.
Processes for marketing authorisations granted before 31 December 2020, or submitted or ongoing from 1 January 2021.
Guidance on how to license electronic cigarettes and other inhaled nicotine-containing products (NCPs) as medicines in the UK.
Your purchasing strategy must show you’ve considered commercial and technology aspects, and contractual limitations.
This guidance is designed to help UKHSA customers and partners to navigate engaging and working with us and to signpost upcoming events and opportunities.
How to request and manage school-led initial teacher training (ITT) places for School Direct.
How to use an interrupted time series to evaluate your digital health product.
The MHRA will review applications for orphan designation at the time of a marketing authorisation (MA) or variation application.
Form for a business to register seed marketing operations.
This guidance outlines how to create and implement a cloud strategy, and when to consider a single, hybrid or multi-cloud solution.
Sources of advice and financial support for UK farmers exporting agricultural products to the EU and beyond
The approach the MHRA intends to take for products approved or pending in decentralised procedure (DCP) or mutual recognition procedures (MRP).
A new pathway supporting innovative approaches to the safe, timely and efficient development of medicines to improve patient access.
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