View Information Collection Request (ICR) Package
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Blank fields in records indicate information that was not collected or not collected electronically prior to July 2006.
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:
0938-0581
ICR Reference No:
199212-0938-001
Status:
Historical Active
Previous ICR Reference No:
199206-0938-001
Agency/Subagency:
HHS/CMS
Agency Tracking No:
Title:
CLINICAL LABORATORY IMPROVEMENT AMENDEMENTS (CLIA), APPLICATION FORMS
Type of Information Collection:
Revision of a currently approved collection
Common Form ICR:
No
Type of Review Request:
Regular
OIRA Conclusion Action:
Approved without change
Conclusion Date:
12/23/1992
Retrieve Notice of Action (NOA)
Date Received in OIRA:
12/17/1992
Terms of Clearance:
Approved for use through 12/93 under the following conditions: 1) HCFA incorporates an additional "reason" code on pg. 8 pertaining statutory and regulatory requirements for physician referrals; and 2) No later than 1/93, HCFA presents OMB its plans to collect data on an ongoing basis from laboratories that may have closed due to the regulatory costs of CLIA. These labs may be identified using a combin tion of data sources, including Medicare claims files.
Inventory as of this Action
Requested
Previously Approved
Expiration Date
12/31/1993
12/31/1993
09/30/1993
Responses
320,000
0
320,000
Time Burden (Hours)
826,667
0
826,667
Cost Burden (Dollars)
0
0
0
Abstract:
THESE FORMS (HCFA 114 AND 116) MUST BE COMPLETED BY ENTITIES PERFORMIN LABORATORY TESTING ON HUMAN SPECIMENS FOR HEALTH PURPOSES. THE INFORMATION ON THESE FORMS IS VITAL TO THE CERTIFICATION. WHILE THE HCFA 589 IS COMPLETED ON A VOLUNTARY BASIS, WE ARE URGING ENTITIES TO COMPLETE THIS FORM SO WE WILL HAVE NECESSARY BASELINE INFORMATION.
Authorizing Statute(s):
None
Citations for New Statutory Requirements:
None
Associated Rulemaking Information
RIN:
Stage of Rulemaking:
Federal Register Citation:
Date:
Federal Register Notices & Comments
Did the Agency receive public comments on this ICR?
No
Number of Information Collection (IC) in this ICR:
1
IC Title
Form No.
Form Name
CLINICAL LABORATORY IMPROVEMENT AMENDEMENTS (CLIA), APPLICATION FORMS
HCFA-108, 109
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
320,000
320,000
0
0
0
0
Annual Time Burden (Hours)
826,667
826,667
0
0
0
0
Annual Cost Burden (Dollars)
0
0
0
0
0
0
Burden increases because of Program Change due to Agency Discretion:
No
Burden Increase Due to:
Burden decreases because of Program Change due to Agency Discretion:
No
Burden Reduction Due to:
Short Statement:
Annual Cost to Federal Government:
$0
Does this IC contain surveys, censuses, or employ statistical methods?
No
Is the Supporting Statement intended to be a Privacy Impact Assessment required by the E-Government Act of 2002?
No
Is this ICR related to the Affordable Care Act [Pub. L. 111-148 & 111-152]?
Uncollected
Is this ICR related to the Dodd-Frank Wall Street Reform and Consumer Protection Act, [Pub. L. 111-203]?
Uncollected
Is this ICR related to the American Recovery and Reinvestment Act of 2009 (ARRA)?
Uncollected
Is this ICR related to the Pandemic Response?
Uncollected
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:
12/17/1992
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