Assisted Reproductive Technology (ART) Program Reporting System

ICR 200211-0920-002

OMB: 0920-0556

Federal Form Document

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ICR Details
0920-0556 200211-0920-002
Historical Active 200204-0920-004
HHS/CDC
Assisted Reproductive Technology (ART) Program Reporting System
Extension without change of a currently approved collection   No
Regular
Approved without change 01/13/2003
Retrieve Notice of Action (NOA) 11/26/2002
CDC has increased the burden estimate by 56,067 hours. In the future, CDC should take care to ensure that the burden estimate reported to OMB is an accurate reflection of the burden imposed on the respondents.
  Inventory as of this Action Requested Previously Approved
01/31/2006 01/31/2006 01/31/2003
400 0 400
63,400 0 7,333
1,000 0 1,000

The Centers for Disease Control and Preventive (CDC) is seeking approval of a reporting system for the Assisted Reproductive Technology (ART) Program. The reporting system has been designed in collaboration with the Society for Assisted Reproductive Technology (SART) to comply with the requirements of Section 2(a) of Pub. L. 102-493 (known as the Fertility Clinic Success Rate and Certification Act of 1982 [FCSRRCA], 42 U.S.C. 263a-1(a)). This Act requires that each ART program shall annually report to the Secretary through the CDC - (1) pregnancy success rates achieved by such ART program, and...

None
None


No

1
IC Title Form No. Form Name
Assisted Reproductive Technology (ART) Program Reporting System

  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 400 400 0 0 0 0
Annual Time Burden (Hours) 63,400 7,333 0 56,067 0 0
Annual Cost Burden (Dollars) 1,000 1,000 0 0 0 0
Yes
No

$0
No
No
Uncollected
Uncollected
Uncollected
Uncollected

  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.
11/26/2002


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