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Representative Matters Regulatory Advised clients on FDA compliance, including: Ingredient, additive, and harmful and potentially harmful constituent (HPHC) testing and disclosure requirements Health document submissions Manufacturing facility registration and product listing (TRLM/FURLS) Good Manufacturing Practice guidance Substantial equivalency determinations and exemptions Premarket Tobacco Product Applications Environmental Assessments for premarket applications Tobacco Product Master Files Modified Risk Tobacco Product Applications Labeling and warning requirements Retailer compliance issues Tobacco product testing requirements E-liquid and aerosol toxicity analyses and risk assessments Advised coalition of e-vapor and e-liquid manufacturers through the PMTA process, filing over 350 applications with FDA ahead of the September 9, 2020 deadline Advised clients on import and export of tobacco products under U.S

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