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Dr. Derek Beauchamp, a Senior Technical Director at Avomeen, discusses the FDA's premarket tobacco application (PMTA) along with the testing and data required to complete the application in this on-demand webinar. Better understand the PMTA, including what tobacco and electronic nicotine device (ENDS) products require a premarket tobacco application, and what companies are required to submit a PMTA for their e-liquids and vape products. Learn what FDA requires to be included in a PTMA submission, and the costs of completing a full PMTA for one SKU. The PMTA is an investment, so how are products identified and selected for premarket tobacco applications? We explore ways to mitigate risk and assess whether a specific e-liquid or ENDS device has a higher probability of obtaining premarket authorization and approval. Come away with an understanding of your options to mitigate risk and inform product selection, including deformulation (reverse engineering) of vape products, e-liquid and vape flavor screening, including screening for Harmful and Potentially Harmful Constituents (HPHCs), and ENDS device screening. Case studies provide real-world examples of other ENDS companies who undertook similar strategies to help you determine what the right path is for your product. For more information about the PMTA and e-liquid testing, visit https://www.avomeen.com/industries/co....