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Declaration relating to the exceptional market conditions in the pigmeat sector in England by the Secretary of State for Environment, Food and Rural Affairs.
The Communities and Local Government Select Committee Report on retail markets recognised the need to share good practice, and recommended that…
An overview of the process including submitting or fast tracking an application, naming your medicine and paying fees.
What you need to do to place a medical device on the Great Britain, Northern Ireland and European Union (EU) markets.
What you need to do to comply with regulations on manufactured goods you place on the Northern Ireland market.
What you need to do to comply with regulations on manufactured products you place on the market in Great Britain.
This is the first report from a programme of research to evaluate Growth and Innovation Fund investments.
What you need to do to comply with regulations on manufactured goods you place on the EU market.
Comply with good manufacturing practice (GMP) and good distribution practice (GDP), and prepare for an inspection.
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.
Outlines guiding principles for parties to follow when submitting technical economic analysis to the CMA as part of an inquiry.
A new pathway supporting innovative approaches to the safe, timely and efficient development of medicines to improve patient access.
Guidance providing practical information for placing construction products on the GB market.
Find out if you will need to use the new UKNI marking and how to use it.
Guidance for the pharmaceutical industry on Marketing Authorisations for veterinary medicines.
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