4,4'-Methylenedianiline General Industry 29 CFR 1910.1050

OMB Control No: 1218-0184	ICR Reference No: 200611-1218-001
Status: Historical Active	Previous ICR Reference No: 200309-1218-006
Agency/Subagency: DOL/OSHA	Agency Tracking No: 1218-0184(2006)
Title: 4,4'-Methylenedianiline General Industry 29 CFR 1910.1050
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: 02/15/2007
Retrieve Notice of Action (NOA)	Date Received in OIRA: 12/21/2006
Terms of Clearance:

	Inventory as of this Action	Requested	Previously Approved
Expiration Date	02/28/2010	36 Months From Approved	02/28/2007
Responses	583	0	581
Time Burden (Hours)	293	0	295
Cost Burden (Dollars)	19,312	0	19,000

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Abstract: The purpose of this Standard and its information collection requirements is to provide protection for employees from adverse health effects associated with occupational exposure to MDA. Employers must monitor exposure, keep employee exposures within the permissible exposure limits, provide employees with medical examinations and training, and establish and maintain employee exposure-monitoring and medical records.

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Authorizing Statute(s): US Code: 29 USC 655 Name of Law: The Occupational Safety and Health Act    US Code: 29 USC 651 Name of Law: The Occupational Safety and Health Act    US Code: 29 USC 657 Name of Law: The Occupational Safety and Health Act

Citations for New Statutory Requirements: None

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Associated Rulemaking Information
RIN:	Stage of Rulemaking:	Federal Register Citation:	Date:
	Not associated with rulemaking

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Federal Register Notices & Comments
60-day Notice:	Federal Register Citation:	Citation Date:
	71 FR 51639	08/30/2006
30-day Notice:	Federal Register Citation:	Citation Date:
	71 FR 76363	12/20/2006
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 4,4'-Methylenedianiline General Industry 29 CFR 1910.1050

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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	583	581	0	0	2	0
Annual Time Burden (Hours)	293	295	0	0	-2	0
Annual Cost Burden (Dollars)	19,312	19,000	0	0	312	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: The Agency is requesting an adjustment decrease of two hours from 295 hours to 293 hours. The two-hour reduction is the result of decreasing the number of employees submitting records (from three sets of records to one set of records) to NIOSH under “Transfer of records (§1910.1050(n)(7)).” There is an overall increase in capitol costs of $312 (from $19,000 to $19,312) resulting from the following: an increase of $300 for two additional medical examinations; a $37 increase due to rounding, and a decrease of $25 due to reducing the number of employers mailing records to NIOSH.

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Annual Cost to Federal Government: $53

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

Agency Contact: Jamaa Hill 202-693-1965 [email protected]

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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: 12/21/2006

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