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VDEC responds strategically to AMR pathogens and new emerging threats (fungi, viruses, and bacteria), by determining the most appropriate research goals to combat these pathogens
The UK government has introduced the Northern Ireland MHRA Authorised Route (NIMAR). This new route for supply became operational 1 January 2022.
General advice on due diligence - electronic cigarettes devices and refill containers.
Briefing for local authorities on the increasing role of community pharmacy in public health, working with councils and other community partners.
Guidance on labelling requirements pertinent to the type of medicinal product and its supply status, as defined in UK legislation.
The Defence and Security Accelerator (DASA) is running a Market Exploration to explore the Non-Compressible Haemorrhage (NCH) environment. To understand who is doing work in this area and possible novel solutions of treatmen…
Device-specific guidance for manufacturers on reporting adverse incidents under the vigilance system.
The UK Good Laboratory Practice Monitoring Authority (UK GLPMA) recognises that there are potential challenges COVID-19 will present to members of the GLP monitoring programme.
How to test and report levels of nicotine uptake when submitting a notification of intent to market e-cigarette and vape products.
A unique initiative which aims to accelerate the time to patient care for transformative medicines and medicine-device combinations.
The types of emissions a manufacturer or importer of e-cigarettes should notify us about.
From discovery to real-world impact, VDEC equips scientists with the expertise and facilities to navigate each step in the development of vaccines and therapeutics.
The MHRA is ready to provide any assistance for clinical trials applications submitted for COVID-19
Information for manufacturers and users of medical devices containing plastic with DEHP phthalates.
Information for pharmaceutical wholesalers explaining the main changes the Windsor Framework introduces to the packaging for all medicines licensed in the UK, effective from 1 January 2025.
Information and advice on submitting a dermatological product to the Advisory Committee for Borderline Substances (ACBS).
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