Premarket Review of New and Modified Tobacco Products 2013

  • 24 Oct 2013
  • Webinar

Description

Topics
  • Section 910 New Tobacco Product Application
  • Premarket Review of New and Modified Tobacco Products
  • Section 905(j)(3) Minor Modification Exemption
  • Section 905(j) Substantial Equivalence Report
  • What E-Cigarettes and Other Tobacco Products Can Expect
  • Section 911 Modified Risk Tobacco Product Application
Who should Attend
  • Regulatory Compliance Associates and Managers
  • General Counsel and Management of tobacco companies, e-cigarette companies, etc
  • Regulatory affairs professionals and scientists who work in this area
  • Medical professionals, public health and consumer advocates, and other individuals working in the smoking control/ harm reduction area
  • Suppliers to Tobacco Industry
  • Manufacturers and importers of e-cigarettes and other novel tobacco products

Past Events

Important

Please, check "Premarket Review of New and Modified Tobacco Products" official website for possible changes, before making any traveling arrangements

Event Categories

Government & Global Issues: Law & Regulations
Health & Medicine: Healthcare
Science: Life Sciences & Biology

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