Generic Clearance for the Collection of Qualitative Feedback on Agency Service Delivery

ICR 201612-0920-007

OMB: 0920-1009

Federal Form Document

ICR Details
0920-1009 201612-0920-007
Historical Active 201405-0920-002
HHS/CDC 21359
Generic Clearance for the Collection of Qualitative Feedback on Agency Service Delivery
Revision of a currently approved collection   No
Regular
Approved with change 02/28/2017
Retrieve Notice of Action (NOA) 12/12/2016
Previous Terms continue: OMB approves this collection for a period of three years. To request approval of information collections under this generic approval, the agency must do the following: 1) Unless an agency is using multiple modes of collection (e.g., paper forms and electronic submissions), provide a Generic Clearance Submission Template for each Instrument; 2) If the agency is using multiple modes of collection (e.g., paper forms and electronic submissions), the same Generic Clearance Submission Template may be used for both instruments; 3) each Generic Clearance Submission Template must be uploaded as a Supplementary document using a naming convention that allows the public to identify the associated instrument; 4) submit no more than five Generic Submission Templates with each request. No payment or other form of remuneration will be provided to respondents for GenICs submitted under this generic. Focus groups and cognitive laboratory studies are the exceptions and will contain a comprehensive justification for why the incentive is necessary within the submitted sub-study.
  Inventory as of this Action Requested Previously Approved
02/29/2020 36 Months From Approved 03/31/2017
61,920 0 228,000
18,315 0 104,250
0 0 0

This collection of information is necessary to enable the Agency to garner customer and stateholder feedback in an efficient, timely manner, in accordance with our commitment to improving service elivery. The information collected from our customers and stakeholders will help ensure that users have an effective, efficient, and satisfying experience with the Agency's programs. The responsible unit is the National Center for Injury Prevention and Control within the Centers for Disease Control and Prevention.

EO: EO 12862 Name/Subject of EO: Setting Customer Service Standards
  
None

Not associated with rulemaking

  79 FR 24432 04/30/2014
81 FR 89465 12/12/2016
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 61,920 228,000 0 -166,080 0 0
Annual Time Burden (Hours) 18,315 104,250 0 -85,935 0 0
Annual Cost Burden (Dollars) 0 0 0 0 0 0
No
Yes
Miscellaneous Actions
Based on the number of burden hours actually used during the initial approval period and the number of respondents involved in this and other expiring collections, we are requesting a decrease in the number of respondents and burden hours.

$55,000
Yes Part B of Supporting Statement
No
No
No
No
Uncollected
Renita Macaluso 770 488-6458 arp5@cdc.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.
12/12/2016


© 2024 OMB.report | Privacy Policy