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From 1 January 2014 herbal smoking products will have Tobacco Products Duty charged on them unless they are to be used exclusively for medical purposes.
Product Safety Report for Wau Wa Eczema Herbal Cream presenting a serious chemical risk.
An overview of the process including submitting or fast-tracking an application, naming your medicine and paying fees.
This report makes recommendations on whether to regulate practitioners of herbal medicine and the products they use to keep the public safe.
Guidance on how to license electronic cigarettes and other inhaled nicotine-containing products (NCPs) as medicines in the UK.
There are changes to the legislation of Reference Medicinal Products (RMPs) used to support abridged marketing authorisation applications
The MHRA is undertaking a public consultation on proposals to end the 'sell through' of unlicensed herbal remedies legally on market at April 2011.
This guidance provides information on comparator products used in studies supporting abridged marketing authorisation applications
Apply for changes to your marketing authorisation, including minor variations type IA and IB, major variations type II and extensions.
How DNA molecular approaches can be used to identify and detect species in herbal medicinal products.
Pharmacy, prescription-only (POM), and general sale list (GSL) medicines: apply to move your medicine to a different classification.
Information for patients, healthcare professionals and developers of new medicines
How to prepare for implementation and compliance of the Safety Features Regulation.
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