How does an e-vapor business navigate the FDA’s approval process? On August 8, 2016, the Food and Drug Administration’s “Deeming Rule” took effect, starting a two-year period where every manufacturer of e-cigarettes, e-liquid, and other vapor products would have to get permission from the FDA to keep their products on the market. You’ve heard some statistics on this podcast trying to quantify the regulatory burden, which could be anywhere from a few hundred thousand to millions of dollars per product. But what does that actually look like in the real world? Chris Howard and Jeff Sanderson from E-Alternative Solutions discuss the impact and what they’re doing to get their Cue product through the FDA’s process.
#344: TikTok and the First Amendment
#343: China and National Security
#342: Save the Children (From State Social Media Laws)
#341: The FTC Tries to Shape the Market
#340: Making Sense of the SCOTUS Internet Speech Cases
#339: Will Tech Swallow the Fourth Amendment?
#338: Gonzalez v. Google
#337: China and Domestic Surveillance
#336: Tech Illiteracy on the Right
#335: Is Screen Time Bad for Kids?
#334: Snake Oil Salvation: Malcom Kyeyune on the New Internet Counterculture
#333: The FCC in Space
#332: Facial Recognition Technology
#331: Section 230’s Long Path to SCOTUS
#330: The FTC & FCC in Court
#329: Will Rinehart’s Wild Weird Brain
#328: What’s the Deal with European Antitrust?
#327: The Collapse of Complex Societies
#326: Content Moderation Potpourri
#325: Live: Quinta Jurecic on Jan. 6, Social Media, and the Great Rage
Join Podbean Ads Marketplace and connect with engaged listeners.
Advertise Today
Create your
podcast in
minutes
It is Free
Insight Story: Tech Trends Unpacked
Zero-Shot
Fast Forward by Tomorrow Unlocked: Tech past, tech future
Black Wolf Feed (Chapo Premium Feed Bootleg)
Bannon`s War Room