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Data, Freedom of Information releases and corporate reports
Professor Dame Angela McLean’s review on pro-innovation regulation for advanced manufacturing and the government response.
A bold plan for reform of DFID’s work with suppliers.
How test manufacturers or distributors can apply for approval of their tests to sell on the UK market.
Brian Holliday will support work investigating the pro-innovation regulation of advanced manufacturing, one of the Chancellor’s five key growth areas.
How to register your medical devices with the Medicines and Healthcare products Regulatory Agency (MHRA) for the markets in Great Britain and Northern Ireland
Advice on writing clear notices and maximising replies to your FSNs.
Information about when you need to submit substantial amendments to a clinical trial including changes to the trial sponsor or legal representative, Investigational medicinal product certification and importation.
The Department for Business and Trade has announced the 10 SME winners of the 2024 Made in the UK, Sold to the World Awards.
Comply with good manufacturing practice (GMP) and good distribution practice (GDP), and prepare for an inspection.
Finding the right advice and advisor is the first step in making the best decisions for your invention or business.
How to apply for simultaneous review of veterinary medicine submissions to the Australian Pesticides and Veterinary Medicines Authority (APVMA) and the VMD.
Find out if a business is, or has been, authorised by the Financial Conduct Authority to provide claims management services
The start of an anti-dumping and countervailing duties exemption review for a Canadian exporting producer of biodiesel.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
A review that examines the risks of modern slavery within NHS supply chains and provides recommendations to mitigate these risks.
How to package medicines for sale and what information you must provide to consumers and healthcare professionals.
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