FDA Requests Comments Regarding Info Collected from Entry Respondents

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December 02, 2013

Recently, the Food and Drug Administration (FDA) published a notice in the Federal Register requesting comments concerning a collection of data retrieved from import entry respondents.  Topics include: 1) Whether the mandatory information for FDA-regulated products being imported into the U.S. is necessary and/or practical 2) The accuracy of FDA’s methodology of estimated amount of burden on importers 3) How the information collected can be enhanced and 4) Other ways to reduce burden for respondents.

Comments are due January 27, 2014, and can be submitted either electronically or written.  Please submit online comments at http://www.regulations.gov.  Written comments can be submitted to Division of Dockets Management, Food and Drug Administration, 5630 Fishers Lance, Rm. 1061, Rockville, MD 20852.

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