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US: e-cigarette regulation

Published: 17th June 2024 | No. pages: 14
$1,750.00

Description

Due to the deeming regulations, e-cigarettes are included within the category of tobacco products at the federal level in the US, so federal law applies.

A premarket tobacco product application (PMTA) must be submitted to the US Food and Drug Administration (FDA) for each e-cigarette product.

There has been increased regulatory and policy pressure at the federal level, specifically about the PMTA process, which was considered to be slow and allowed illegal products to stay in the market unregulated.

There have been a huge number of PMTA denials, and it is not likely for any flavoured vape product to receive a marketing granted order (MGO).

This report provides analysis of the current regulatory regime for e-cigarettes in the US, covering all aspects from labelling and product restrictions, to retail and advertising regulations.

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  • A clear and detailed understanding of current regulatory requirements affecting this sector in a specific jurisdiction, enabling you to be confident your business and your products are compliant.
  • The ability to plan ahead for specific regulatory changes.
  • Strategic understanding of the policy climate within the jurisdiction, enabling you to forecast how it might affect business development.
  • Sources of further information, for example links to full texts of legislation and contact details for relevant government offices.

Table of contents

  1. Executive summary
  2. Outlook
  3. US: the basics
  4. National regulatory framework
  5. Age restrictions
  6. Product restrictions
  7. Labelling and packaging
  8. Barriers to market entry
  9. Obligation to notify
  10. Retail channel restrictions
  11. Public usage
  12. Advertising and marketing
  13. Taxation
  14. Enforcement
  15. Relevant laws
  16. Relevant bodies

Methodology

Our research is completely independent and original. It is conducted by ECigIntelligence’s multilingual legal analysis team, all specialists in this sector, and goes through a rigorous review and editing process before publication. Research draws on multiple sources, including: online and offline resources and data, specialist legal software, our own extensive databases and report archives, interviews with key stakeholders and government officials, and collaboration with local legal firms and on-the-ground professionals in the jurisdictions covered.

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Description

Due to the deeming regulations, e-cigarettes are included within the category of tobacco products at the federal level in the US, so federal law applies.

A premarket tobacco product application (PMTA) must be submitted to the US Food and Drug Administration (FDA) for each e-cigarette product.

There has been increased regulatory and policy pressure at the federal level, specifically about the PMTA process, which was considered to be slow and allowed illegal products to stay in the market unregulated.

There have been a huge number of PMTA denials, and it is not likely for any flavoured vape product to receive a marketing granted order (MGO).

This report provides analysis of the current regulatory regime for e-cigarettes in the US, covering all aspects from labelling and product restrictions, to retail and advertising regulations.

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    “ US: e-cigarette regulation ”