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Departments, agencies and public bodies
News stories, speeches, letters and notices
Detailed guidance, regulations and rules
Reports, analysis and official statistics
Consultations and strategy
Data, Freedom of Information releases and corporate reports
How to begin with evaluating a digital health product, including when to evaluate, budgeting and getting support.
The MHRA will review applications for orphan designation at the time of a marketing authorisation (MA) or variation application.
How the MHRA makes decisions on what is a medicinal product (borderline products).
Legal standards for labelling and composition of food products such as bottled water, milk and meat.
Ensuring you get what you pay for.
Waste electrical and electronic equipment (WEEE) - retailer and wholesaler responsibilities, waste collection and compliance schemes.
What animal by-products (ABPs) are, how to set up a site that uses them safely, the paperwork you need, and how to dispose of them.
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.
Explainer for the pharmaceutical industry on the ongoing implementation of the Veterinary Medicines Regulation relating to applications and authorisations for veterinary medicines.
Find out what a composite food product is, and the rules you need to follow to export or move these products from Great Britain to the EU and Northern Ireland.
If you buy or sell second-hand vehicles, find out how other products and circumstances affect the scheme and how you account for VAT. (VAT Notice 718)
Current issues relating to imports and exports of animals and animal products.
The way you apply to licence biological products has changed
A wholesale dealer in Great Britain may import Qualified Person certified medicines from the European Economic Area if certain checks are made by the ‘Responsible Person (import)’
How to use a cost benefit analysis to evaluate your digital health product.
Submissions related to human medicines need to be submitted directly to the MHRA.
Apply for a Temporary Work – Government Authorised Exchange (GAE) visa for work experience, training, research or fellowship - eligibility, extend or switch, family members
Guidance for manufacturers, importers and distributors.
How to use a quasi-experimental 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
Don’t include personal or financial information like your National Insurance number or credit card details.
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