Generic Clearance for Quantitative Testing for the Development of FDA Communications (CFSAN)

ICR 201812-0910-007

OMB: 0910-0865

Federal Form Document

ICR Details
0910-0865 201812-0910-007
Historical Active
HHS/FDA CFSAN
Generic Clearance for Quantitative Testing for the Development of FDA Communications (CFSAN)
New collection (Request for a new OMB Control Number)   No
Regular
Approved with change 02/08/2019
Retrieve Notice of Action (NOA) 02/05/2019
FDA will submit individual collections under this generic clearance to OMB. Individual collections will also undergo review by FDA’s Research Involving Human Subjects Committee (RIHSC), senior leadership in the Center for Food Safety and Applied Nutrition, and Paperwork Reduction Act (PRA) specialists. FDA will prepare a report during the OMB collection renewal summarizing the number of hours used, as well as the nature and results of the activities completed under this clearance.
  Inventory as of this Action Requested Previously Approved
02/28/2022 36 Months From Approved
93,744 0 0
10,498 0 0
0 0 0

This ICR supports the creation of an information collection for the development of a “Generic Clearance for Quantitative Testing for the Development of FDA Communications.” The generic studies covered by this request will be used to quantitatively test FDA communications and educational messages related to FDA-regulated food and cosmetic products, dietary supplements, and animal food and feed as they are being developed and before they are released to the public. Data will be collected using consumer panels or mall intercepts for surveys and experimental studies.

US Code: 21 USC 393 Name of Law: FFDCA
  
None

Not associated with rulemaking

  83 FR 44888 09/04/2018
83 FR 67300 12/28/2018
No

  Total Approved Previously Approved Change Due to New Statute Change Due to Agency Discretion Change Due to Adjustment in Estimate Change Due to Potential Violation of the PRA
Annual Number of Responses 93,744 0 0 93,744 0 0
Annual Time Burden (Hours) 10,498 0 0 10,498 0 0
Annual Cost Burden (Dollars) 0 0 0 0 0 0
Yes
Miscellaneous Actions
No
This is a new information collection request.

$939,150
Yes Part B of Supporting Statement
    No
    No
No
No
No
Uncollected
Ila Mizrachi 301 796-7726 ila.mizrachi@fda.hhs.gov

  No

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.
02/05/2019


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