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Friday, November 12, 2010, Part II Department of Health and Human Services Food and Drug Administration McDonald on DSK2BSOYB1PROD with PROPOSALS2 21 CFR Part 1141 Required Warnings for Cigarette
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What is 21 cfr part 1141?
21 CFR Part 1141 refers to the regulations set by the U.S. Food and Drug Administration (FDA) regarding the Mandatory Reporting of Adverse Events for Tobacco Products.
Who is required to file 21 cfr part 1141?
Manufacturers, importers, and retailers of tobacco products are required to file 21 CFR Part 1141.
How to fill out 21 cfr part 1141?
To fill out 21 CFR Part 1141, you need to provide the required information on adverse events associated with tobacco products using the reporting forms specified by the FDA. These forms can be submitted electronically or by mail.
What is the purpose of 21 cfr part 1141?
The purpose of 21 CFR Part 1141 is to ensure that adverse events related to tobacco products are reported to the FDA, enabling them to take necessary actions to protect public health.
What information must be reported on 21 cfr part 1141?
21 CFR Part 1141 requires the reporting of information such as the type of tobacco product involved, the adverse event description, the affected individual's demographics, and the product manufacturer's contact information.
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