MHRA Cancels Consultation with Carl Phillips Regarding Electronic Cigarettes
The UK Medicines and Healthcare products Regulatory Agency, the United Kingdom's version of the FDA, wants to classify electronic cigarettes as a drug device. To that end they had scheduled a consultation meeting where they hoped to gain support from expert testimony for their recent proposal of giving e-cigarette manufacturers just two weeks to license the product as a drug under their jurisdiction, a process which usually takes two years.
