The FDA’s Premarket Tobacco Product Application (PMTA) pathway is extremely complex and potentially very expensive. Elixa Health believes FDA will allow marketing of vape products for those who successfully scientifically address the elements of the PMTA for each individual product to prove its appropriateness for the protection of public health. Our team has in-house professionals committed to creatively tell your product’s story and ensure the long-term prosperity for the small and medium sized businesses of the vape industry.