This generic
clearance for FDA/CFSAN is approved for 2 years under the following
conditions: (1) For individual "tests," FDA shall submit a generic
IC in ROCIS along with: (a) an abbreviated supporting statement in
the template agreed to by OMB and FDA (including a statement of
need, intended use of information, description of respondents,
date(s) and location(s), collection procedures, justification for
any proposed incentive, and estimated burden); (b) participant
screeners, and (c) instruments/moderator guides. (2) OMB will
respond with clearance or questions within 10 working days. (3) OMB
and FDA will jointly evaluate the generic clearance in 18-months;
FDA will provide a summary of each collection approved under the
generic clearance (e.g., use of information) and an overview of the
studies likely to be submitted in the next 18-months. (4) FDA will
not use this information gained from this collection for policy
formation, nor will it release the information to the public.
Inventory as of this Action
Requested
Previously Approved
06/30/2014
36 Months From Approved
75,200
0
0
4,758
0
0
0
0
0
Under section 903 (b)(2) of the
Federal Food, Drug and Cosmetic Act ( FFDCA)( 21 U.S.C. 393 (b)(2),
the Food and Drug Administration ( FDA) is authorized to conduct
research relating to foods and to conduct educational and public
information programs relating to the safety of the Nation`s food
supply. FDA is proposing to survey U.S. consumers using a web-based
panel of U.S. households to collect information on consumers "real
time" knowledge, perceptions, beliefs, and self- reported behaviors
for up to five foodborne illness outbreaks or food recalls a year.
Collecting information quickly during a foodborne illness outbreak
or food recall is important because erroneous perceptions or
misinterpreted information about outbreak or recall can impede
consumer adoption of recommended protective behaviors.
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.