Studies of Adverse Reproductive Outcomes in Female Occupational Groups

Forms and Documents

Document Name	Status

No forms / supporting documents in this ICR. Check IC Document Collections.

IC Document Collections

IC ID	Document Title	Status
6779	Studies of Adverse Reproductive Outcomes in Female Occupational Groups	Migrated

ICR Details

OMB Control No: 0920-0367	ICR Reference No: 199612-0920-002
Status: Historical Active	Previous ICR Reference No: 199505-0920-002
Agency/Subagency: HHS/CDC	Agency Tracking No:
Title: Studies of Adverse Reproductive Outcomes in Female Occupational Groups
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: 01/30/1997
	Date Received in OIRA: 12/02/1996
Terms of Clearance: OMB approves this study as amended by the correspondences of January 10 and 29, 1997. In particular, OMB emphasizes the significance of CDC's receipt of the Department's Assurance of Confidentiality under Section 308(d) of the Public Health Service Act. CDC must maintain the confidentiality assurance for the life of the project and must not conduct any aspect of this study without it. With respect to the additional studies CDC proposed to conduct under the same approval, OMB determines that the agency's request is not permissable under the PRA. Only after adhering to the PRA's requirements, including seeking public comment and receiving OMB approval, is CDC permitted to conduct other studies of reproductive outcomes in female occupational groups.

	Inventory as of this Action	Requested	Previously Approved
Expiration Date	01/31/2000	01/31/2000	08/31/1998
Responses	6,200	0	7,400
Time Burden (Hours)	6,200	0	1
Cost Burden (Dollars)	0	0	0

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Abstract: The reproductive health of a group of female workers exposed to a particular environmental chemical or agent will be compared to the reproductive health of a group of working women with no occupational exposure to known or suspected reproductive toxicants.

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Authorizing Statute(s): None

Citations for New Statutory Requirements: None

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Associated Rulemaking Information
RIN:	Stage of Rulemaking:	Federal Register Citation:	Date:

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Federal Register Notices & Comments

Did the Agency receive public comments on this ICR? No

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Number of Information Collection (IC) in this ICR: 1

IC Title	Form No.	Form Name
Studies of Adverse Reproductive Outcomes in Female Occupational Groups

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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	6,200	7,400	0	-1,200	0	0
Annual Time Burden (Hours)	6,200	1	0	6,199	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:

Burden decreases because of Program Change due to Agency Discretion: No

Burden Reduction Due to:

Short Statement:

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Annual Cost to Federal Government: $0

Does this IC contain surveys, censuses, or employ statistical methods? Yes Part B of Supporting Statement

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

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Common Form ICR:  No

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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: 12/02/1996

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