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Guidance on how to license electronic cigarettes and other inhaled nicotine-containing products (NCPs) as medicines in the UK.
How to use a behaviour change techniques review to evaluate your digital health product.
Review of how the legislation has been implemented.
How to register your medical devices with the Medicines and Healthcare products Regulatory Agency (MHRA) for the markets in Great Britain and Northern Ireland
MHRA review of levothyroxine products in response to concerns about potential inconsistencies of different products.
The CMA has opened an investigation into Unilever UK Limited’s compliance with consumer protection law.
The Medicines and Healthcare products Regulatory Agency regulates medicines, medical devices and blood components for transfusion in the UK. MHRA is an executive agency, sponsored by the Department of Health and Social Care .
Guidance on the 150-day assessment timeline for high-quality marketing authorisation applications including information on how to apply.
Information on the VMD’s PIR of the Animals & Animal Products Regulation of 2015 and questionnaire link.
When military end-use export controls apply and to which destinations.
This is the 12th review of controls on imports of animals and animal products (April 2014 to March 2016).
How to make sure that your products are properly checked for conformity and your technical documents are managed correctly.
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