A new report from ECigIntelligence provides a succinct summation of the Food and Drug Administration (FDA)’s process for moving from its proposed deeming regulations to a set of final, approved rules regarding e-cigarettes in the USA.
The report includes an overview of the process that lays out the various steps and requirements in a simple and understandable format.
It also includes a summation of the various information requests the FDA has asked for as part of its public consultation on e-cigarettes.
The report is a must for anyone planning to be involved in the American e-cigarette sector over the next few years.
- FDA’s 9-step regulatory process
- Public comment
- Information requests on e-cigarettes
- FDA Case studies
- Impact of public consultation submissions
- Summary: extension of public consultation
ECigIntelligence does not provide legal, strategic or investment advice. Tamarind Media Limited, the publisher of ECigIntelligence, does not accept any liability or responsibility for information or views published.
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