Source: FDA, 6/24/16

FDA has released “Timing and Tips - Newly Deemed Tobacco Product Applications,” the latest in its series of webinars to help industry understand a recently finalized rule extending FDA’s authority to all tobacco products.
This new webinar outlines when manufacturers should submit applications for the premarket review of their products and the compliance periods for each premarket pathway. It also provides a list of helpful reminders for submitting product review applications.

The new “deeming” rule extends FDA’s authority to products such as e-cigarettes, cigars, hookah tobacco, and pipe tobacco, among others. The compliance webinars are designed to help regulated tobacco retailers, importers, and manufacturers understand the steps they must take to comply with the rule. Check out the full series on the FDA Tobacco Compliance Webinar webpage.

For more information, click here.