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Regulatory Compliance Experts can act as "3rd Party Agents" to help meet market approval requirements and stay-in-business. This statement of work is to advocate, educate, and assist business owners and operators of domestic tobacco product establishments to file with the FDA, in compliance with the Tobacco Control Act, including:• Who should make establishment registration and product listing submissions;• What information to include in the submissions;• When to submit the information; and• How to submit the informationThe failure to register, the failure to provide any information, or the failure to provide a notice required is prohibited. A tobacco product is deemed "misbranded" if it was manufactured, prepared, or processed in an establishment not duly registered, or if it was not included in a product listing as required. Violations are subject to regulatory and enforcement action.All electronic nicotine delivery systems or ENDS (including e-cigarettes, vape pens, personal vaporizers, etc.) are subject to the new regulations. ENDS products also include both the e-liquid and aerosolizing apparatus, whether sold as a unit or separately.Please contact us for more information:Tom Navarro, RACIndependent Regulatory Affairs Project Management ConsultantRegulatory Compliance Experts LLCSan Francisco Bay AreaRA Operations, Labeling & SubmissionsCynthia CabreraExpert Vapor Industry ConsultantThe Cating Group Miami/Fort Lauderdale Area Monica SchickCEO, North Guide SolutionsGreater Los Angeles AreaQuality Consultant Dedicated to Small Businesses Success in the E-Liquid Sector
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