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Guidance on how to license electronic cigarettes and other inhaled nicotine-containing products (NCPs) as medicines in the UK.
Guidance on infant and follow-on formula, the application form for infant and follow-on formula made from protein hydrolysates, and forms to notify the authority.
Provides advice on the key points to take into account on design.
Advice on ingredients in nicotine-containing liquids in electronic cigarettes and refill containers.
Guidance on the submission, processing and assessment of all completed paediatric studies sponsored by Marketing Authorisation Holders (MAHs)
This study explored the genotoxicity of flubendazole and its main metabolites, and tested a new oral formulation
Definitive fees charged for applications under Schedule 7 of the Veterinary Medicines Regulations 2013.
This study analysed the pediatric ARV market from 2004 to 2012 and assessed pricing trends and associated factors
For the treatment of severe acute malnutrition in children: a noninferiority individually randomized controlled efficacy clinical trial in Malawi
New treatment introduction is complicated by diverse country processes, adoption criteria, and evidence requirements
GALVmed and Animal Husbandry Department, Uttar Pradesh organized this workshop during August 2017 in Lucknow
Information companies placing hazardous mixtures on the UK market (such as manufacturers, importers, downstream users and distributors) should submit to the National Poisons Information Service.
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