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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
Marketing standards for poultry meat producers, manufacturers, retailers and distributors.
Guidance for UK companies on winning business from international aid and development projects.
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.
Marking, labelling and marketing standards you must follow to import and export plant seeds, food and manufactured goods.
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)’
Find a supplier who can provide user research participants to test your service with.
How the MHRA makes decisions on when a product is a medical device (borderline products), and which risk class should apply to a medical device.
The New Active Substance Work Sharing Initiative (NASWSI) has successfully approved several medicines through this international collaboration and continues to foster cooperation and strong relationships between its Access partners. The Biosimilar Work Sharing Initiative (BSWSI) builds on this success.
From 13 May 2024 we are introducing a change to the procedure for new Marketing Authorisation (MA) applications, where a joint assessment of labels is requested.
Form for a business to register seed marketing operations.
Guidance for veterinary medicines manufacturers and wholesale dealers in GB on selling and supplying products placed on the EU and UK markets before 1 January 2021 and the evidence you may need to provide.
Growth Hubs are local public/private sector partnerships led by the Local Enterprise Partnerships (LEPs). They join up national and local business support so it is easy for businesses to find the help they need.
When you must report the amount of electrical and electronic equipment (EEE) you place on the market and how to do it.
Processes for marketing authorisations granted before 31 December 2020, or submitted or ongoing from 1 January 2021.
Use this form to notify the IPO of marketing authorisation for a medicinal or plant protection product, granted after your application for an SPC for that product.
How to use a cost benefit analysis to evaluate your digital health product.
Understand and avoid all types of anti-competitive and cartel activity including price-fixing, collusion, bid-ridding and sharing markets. Know how to report concerns to the CMA.
Find out what you should consider before using an umbrella company to make sure it complies with the tax rules.
The MHRA will review applications for orphan designation at the time of a marketing authorisation (MA) or variation application.
How to transfer the ownership of a marketing authorisation including the form you need to complete.
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