View Information Collection Request (ICR) Package
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Please note that the OMB number and expiration date may not have been determined when this Information Collection Request and associated Information Collection forms were submitted to OMB. The approved OMB number and expiration date may be found by clicking on the Notice of Action link below.
View ICR - OIRA Conclusion
OMB Control No:
0920-0931
ICR Reference No:
202405-0920-005
Status:
Active
Previous ICR Reference No:
202109-0920-008
Agency/Subagency:
HHS/CDC
Agency Tracking No:
0920-0931
Title:
Blood Lead Surveillance System (BLSS)
Type of Information Collection:
Extension without change of a currently approved collection
Common Form ICR:
No
Type of Review Request:
Regular
OIRA Conclusion Action:
Approved without change
Conclusion Date:
07/01/2024
Retrieve Notice of Action (NOA)
Date Received in OIRA:
05/28/2024
Terms of Clearance:
Previous Terms of Clearance/Comments continue. Dissemination of the aggregate data set and statistics generated from the aggregate data set will always be accompanied by an appropriate description of any limitations/caveats.
Inventory as of this Action
Requested
Previously Approved
Expiration Date
07/31/2027
36 Months From Approved
07/31/2024
Responses
305
0
277
Time Burden (Hours)
1,338
0
1,226
Cost Burden (Dollars)
0
0
0
Abstract:
This ICR covers 2 information collections, one for childhood blood lead surveillance by NCEH and another for adult blood lead surveillance by NIOSH. This joint ICR includes 2 data collection systems that provide a coordinated, comprehensive, and systematic public health approach to the surveillance and monitoring of blood lead levels (BLLs) for children < 16 years old and for occupationally exposed adults ≥ 16 years old in the U.S. The goal of the NCEH CLPPP is to promote primary prevention of exposure to lead in children, and, as a secondary prevention strategy, to promote blood lead testing and surveillance of BLLs in children to ensure that there is a comprehensive system in place for the identification, referral, case management, and follow-up evaluation of lead-exposed children. This Non-Substantive Change Request is submitted to remove "NIOSH" from the ICR title, as the collection is led by NCEH. There is no change to the burden or data collection instruments.
Authorizing Statute(s):
PL:
Pub.L. 111 - 148 4002
Name of Law: Patient Protection and Affordable Care Act
PL:
Pub.L. 114 - 322 2204
Name of Law: Water Infrastructure Improvements for the Nation (WIIN) Act
PL:
Pub.L. 91 - 596 20
Name of Law: 1970 Occupational Safety and Health Act
US Code:
42 USC 241
Name of Law: Research and investigations generally
Citations for New Statutory Requirements:
None
Associated Rulemaking Information
RIN:
Stage of Rulemaking:
Federal Register Citation:
Date:
Not associated with rulemaking
Federal Register Notices & Comments
60-day Notice:
Federal Register Citation:
Citation Date:
88 FR 82897
11/27/2023
30-day Notice:
Federal Register Citation:
Citation Date:
89 FR 46117
05/28/2024
Did the Agency receive public comments on this ICR?
Yes
Number of Information Collection (IC) in this ICR:
4
IC Title
Form No.
Form Name
ABLES Aggregate Records Form
0920-0931
ABLES Aggregate Records Form
ABLES Case Records Form
0920-0931
ABLES Case Records Form
CBLS Aggregate Records Forms
0920-0931
Childhood Blood Lead Surveillance (CBLS) Aggregate Records Forms
CBLS Variables -Text Files
0920-0931
Submission Format for Childhood Blood Lead Surveillance (CBLS) Data Files
ICR Summary of Burden
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
305
277
0
28
0
0
Annual Time Burden (Hours)
1,338
1,226
0
112
0
0
Annual Cost Burden (Dollars)
0
0
0
0
0
0
Burden increases because of Program Change due to Agency Discretion:
Yes
Burden Increase Due to:
Miscellaneous Actions
Burden decreases because of Program Change due to Agency Discretion:
No
Burden Reduction Due to:
Short Statement:
This is an extension of a previously approved collection requesting 3 years of approval for 1,338 per year.
Annual Cost to Federal Government:
$13,042,000
Does this IC contain surveys, censuses, or employ statistical methods?
Yes
Part B of Supporting Statement
Does this ICR request any personally identifiable information (see
OMB Circular No. A-130
for an explanation of this term)? Please consult with your agency's privacy program when making this determination.
Yes
Does this ICR include a form that requires a Privacy Act Statement (see
5 U.S.C. §552a(e)(3)
)? Please consult with your agency's privacy program when making this determination.
Yes
Is this ICR related to the Affordable Care Act [Pub. L. 111-148 & 111-152]?
Yes
Is this ICR related to the Dodd-Frank Wall Street Reform and Consumer Protection Act, [Pub. L. 111-203]?
No
Is this ICR related to the American Recovery and Reinvestment Act of 2009 (ARRA)?
No
Is this ICR related to the Pandemic Response?
No
Agency Contact:
Odion Clunis 770 488-0045 lta2@cdc.gov
Common Form ICR:
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:
(a) It is necessary for the proper performance of agency functions;
(b) It avoids unnecessary duplication;
(c) It reduces burden on small entities;
(d) It uses plain, coherent, and unambiguous language that is understandable to respondents;
(e) Its implementation will be consistent and compatible with current reporting and recordkeeping practices;
(f) It indicates the retention periods for recordkeeping requirements;
(g) It informs respondents of the information called for under 5 CFR 1320.8 (b)(3) about:
(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;
(h) It was developed by an office that has planned and allocated resources for the efficient and effective management and use of the information to be collected.
(i) It uses effective and efficient statistical survey methodology (if applicable); and
(j) It makes appropriate use of information technology.
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.
Certification Date:
05/28/2024
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