In accordance with 5 CFR 1320, the information collection is approved for a period of two years. The agency must submit all final instruments to OMB in both English and Spanish prior to impementation. This may be done as a non-material change.
Inventory as of this Action
Requested
Previously Approved
04/30/2014
36 Months From Approved
7,821
0
0
826
0
0
0
0
0
FDA conducts research and educational and public information programs relating to food safety pursuant to its broad statutory authority set forth in section 903(b)(2) of the Federal Food, Drug and Cosmetic Act (FFDCA) (21 U.S.C. 393(b)(2). FDA needs an understanding of how different population groups perceive and behave in terms of food label understanding and use, nutrition, and health, to inform possible measures that the Agency may take to help consumers make informed dietary choices. FDA is aware of no consumer research on a nationwide level, of the impact of language and accculturation ( change in behavior and values by immigrants when they come in contact with a new group , nation or culture )on Hispanics` dietary choices and label use.
On behalf of this Federal agency, I certify that the collection of information encompassed by this request complies with 5 CFR 1320.9 and the related provisions of 5 CFR 1320.8(b)(3).
The following is a summary of the topics, regarding the proposed collection of information, that the certification covers:
(i) Why the information is being collected;
(ii) Use of information;
(iii) Burden estimate;
(iv) Nature of response (voluntary, required for a benefit, or mandatory);
(v) Nature and extent of confidentiality; and
(vi) Need to display currently valid OMB control number;
If you are unable to certify compliance with any of these provisions, identify the item by leaving the box unchecked and explain the reason in the Supporting Statement.