Webinar: Federal, State and Self-Regulation of E-cigarettes

InstantGMP Vape, Vape Mentors and EAS Consulting are teaming up to present Dealing with the Man: Federal, State and Self-Regulation of E-cigarettes. The webinar will take place on Tuesday, July 28th at 1 PM ET.

 The
FDA released its initial proposals for regulating e-cigarettes on April
24th, 2014. The rules would “deem” e-cigarettes as tobacco products and
regulate them as such. States have also changed the outlook of the
industry by passing their own laws.

Industry experts knew these laws would eventually come into play and showed a commitment to quality and safety with self-regulation.
AEMSA (American E-liquid Manufacturing Association) created a set of
standards for manufacturing vape products. InstantGMP sought to help
those committed to quality with the creation of InstantGMP Vape,
software that guides e-liquid creators through Good Manufacturing
Practices.

In
this webinar, regulatory experts from InstantGMP will share updates on
the regulatory landscape of the e-liquid industry and steps you can take
on how to prepare. Topics covered include:

  • Current State of FDA Deeming Regulation
  • Common state regulations
  • Self-regulation
  • Quality, Brand Image and Protection
  • Resources available to vape businesses
The
webinar will last about an hour, with time available for questions.
This is a great opportunity to gain valuable insight from compliance
experts. The InstantGMP team has over 40 years of experience with FDA
regulations and Good Manufacturing Practices. – See more at:
http://www.instantgmp.com/_blog/InstantGMP_Blog/post/webinar-tips-for-gmp-compliant-master-batch-records/#sthash.uQngvFWz.dpuf

We hope to customize the webinar to reflect the state regulations and concerns of the attendees, so be sure to include the address of your business when you register. The webinar will last about an hour with time for questions at the end. This is a great opportunity to get insights on current and upcoming vape legislation from regulatory experts.

The
webinar will last about an hour, with time available for questions.
This is a great opportunity to gain valuable insight from compliance
experts. The InstantGMP team has over 40 years of experience with FDA
regulations and Good Manufacturing Practices. – See more at:
http://www.instantgmp.com/_blog/InstantGMP_Blog/post/webinar-tips-for-gmp-compliant-master-batch-records/#sthash.uQngvFWz.dpuf

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