FDA Seeks Comments on Information Collections Related to Tobacco, Dietary Supplements
The FDA is seeking public comments on information collections related to the following forms:
Sign up for a free preview to unlock the rest of this article
If your job depends on informed compliance, you need International Trade Today. Delivered every business day and available any time online, only International Trade Today helps you stay current on the increasingly complex international trade regulatory environment.
- Form FDA 3852, the "Report of Tobacco Product Removals Subject to Tax for Tobacco Product User Fee Assessment," which facilitates the collection of data from domestic manufacturers and importers to calculate tobacco product user fee assessments.
- Form FDA 3955, which allows respondents to submit information electronically to the Food Applications Regulatory Management System. The FDA uses this information to evaluate whether statements made for dietary ingredients or dietary supplements are permissible under the Federal Food, Drug, and Cosmetic Act.
- Form FDA 3500A, which importers and manufacturers use to submit medical device reports and report adverse events involving medical devices to the FDA.
Comments on all three proposed information collection extensions are due by Aug. 28.