Bryan Haynes will moderate a panel entitled FDA implementation of Tobacco Product Pathways.  Panelists, which include the Director of the FDA’s Center for Tobacco Products Office of Science, will discuss the FDA’s implementation of tobacco product review pathways including premarket tobacco applications and modified risk tobacco product applications, as well as impacts on consumers, manufacturers, and tobacco harm reduction efforts.  Panelists will also address opportunities to clarify the implementation of these pathways, including the current status of substantial equivalence applications and the need for a clear set of achievable requirements for product review submissions.

We look forward to seeing our clients and friends at the conference.