🚬FDA Request for Comments on Tobacco User Fees Information Collection
Agency Information Collection Activities; Proposed Collection; Comment Request; Tobacco Products, User Fees, Requirements for the Submission of Data Needed To Calculate User Fees for Domestic Manufacturers and Importers of Tobacco Products
Summary
The Food and Drug Administration (FDA or Agency) is announcing an opportunity for public comment on the proposed collection of certain information by the Agency. Under the Paperwork Reduction Act of 1995 (PRA), Federal Agencies are required to publish notice in the Federal Register concerning each proposed collection of information, including each proposed extension of an existing collection of information, and to allow 60 days for public comment in response to the notice. This notice solicits comments on "Tobacco Products, User Fees, Requirements for the Submission of Data Needed to Calculate User Fees for Domestic Manufacturers and Importers of Tobacco Products."
Agencies
- Health and Human Services Department
- Food and Drug Administration
Business Impact
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The document outlines new regulatory requirements for domestic manufacturers and importers of tobacco products regarding user fees and data submission, indicating compliance obligations that could impact operational costs and processes. Business owners in the tobacco industry must prepare for these changes, potentially increasing their regulatory burden and financial overhead.