Workshop: Medicinal licensing of vaping products and the potential implications for public health

Currently, the only medicines available for physicians to prescribe to help smokers quit smoking are nicotine replacement therapies and pharmacological treatments, which generally have modest efficacy. E-cigarettes are able to provide nicotine in a means and quantity similar to smoking and are potentially more efficacious than NRT or other licensed medications. Therefore, making e-cigarettes available on prescription, alongside their availability as consumer goods, is a potential mechanism by which the population-level harm reduction potential of vaping products can be enhanced. Having medicinally-licensed products available may also have knock-on effects for consumer vaping products, particularly in improving both physicians’ and public perceptions of the benefits and risks of vaping products. The short presentations and panel discussion workshop will explore medicinal licensing of e-cigarettes, focussing particularly on the following: “Do we actually need medicinally licensed vaping products?” | “Regulatory requirements for medicinal licensing in the UK, the USA, and elsewhere” | “Barriers to gaining a medicinal license” | “Benefits from public health and physicians’ perspectives” | “Manufacturers’ perspectives – why bother?” | “How regulators, the academic community, and industry, can work together for the benefit of public health.”

Host

Ian Fearon

Ian Fearon

Host

Scott Leischow

Scott Leischow

Speaker

Martin Cullip

Martin Cullip

Speaker

Jasjit Ahluwalia

Jasjit Ahluwalia

Speaker

Brian Quigley

Brian Quigley

Speaker

Mark Dickinson

Mark Dickinson