Each training provider is responsible for reviewing the official statutes, regulations, and guidance from the appropriate regulatory authority to ensure their curriculum is accurate and compliant.
NIDA, Food and Drug Administration) in addition to NCI and FIC
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The person using the device inhales the vapor, thus vaping
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Our work for the Tobacco and E-Vapor industries include: Assisting manufacturers and importers of tobacco products in navigating complicated FDA requirements including premarket review procedures, manufacturing establishment registration, product and ingredient listing, labeling, advertising and warning requirements, retailer and distributor compliance, and product testing and toxicity analysis Helping companies resolve Warning Letters and implement corrective actions to ensure youth access is prevented and that marketing is targeted to adult consumers Assisting companies and trade associations in drafting and submitting comments to FDA proposed rules and draft guidance, as well as filing Citizens Petitions Guiding manufacturers on environmental compliance, including with state and federal hazardous waste disposal requirements, and regularly prepare Environmental Assessments to be included in tobacco product premarket applications Ensuring that our clients comply with safety and disclosure requirements as their products are shipped and distributed Advising on state and local laws, including sales restrictions, age-limits, flavor bans, and licensing and PACT Act reporting requirements Tracking tobacco legislative and regulatory developments around the world, including in North America, Europe, the Middle East, and Asia Helping to deal with government and non-governmental scrutiny and handling enforcement and litigations proceedings when they arise Keller and Heckmans Tobacco and E-Vapor practice hosts the highly regarded annual E-Vapor and Tobacco Law Symposium
