OMB.report

Federal forms, ICRs, and supporting documents

Information Collection Request

Standard on 4,4'-Methylenedianiline (MDA) for General Industry (29 CFR 1910.1050)

ICR 201604-1218-004 · OMB 1218-0184 · Historical Active

Forms and Documents
DocumentTypeStatusAvailability
Final-SS-MDA-1218-0184.docx Supporting Statement A Uploaded 2016-05-11 Repair queued
29 cfr 1910.1200 eCFR — Code of Federal Regulations.pdf Supplementary Document Uploaded 2016-05-11 Repair queued
29 cfr 1910.134 eCFR — Code of Federal Regulations.pdf Supplementary Document Uploaded 2016-05-11 Available
eCFR-1910-1050(GEN.-INDUSTRY).docx Supplementary Document Uploaded 2016-04-27 Available
60-DayFRNotice 1218-0184.pdf Supplementary Document Uploaded 2016-04-27 Available
OSH Act Section 8 USC 657.pdf Supplementary Document Uploaded 2016-04-27 Available
OSH Act Section 6 USC 655.pdf Supplementary Document Uploaded 2016-04-27 Repair queued
OSH Act Section 2 USC 651.pdf Supplementary Document Uploaded 2016-04-27 Repair queued
IC Document Collections
IC IDCollectionTypeStatusForm
14132 4,4'-Methylenedianiline (MDA) for General Industry (29 CFR 1910.1050) Modified
ICR Details
1218-0184 201604-1218-004
Historical Active 201303-1218-001
DOL/OSHA 1218-0184(2016)
Standard on 4,4'-Methylenedianiline (MDA) for General Industry (29 CFR 1910.1050)
Extension without change of a currently approved collection   No
Regular
Approved without change 07/19/2016
Retrieve Notice of Action (NOA) 06/03/2016
  Inventory as of this Action Requested Previously Approved
07/31/2019 36 Months From Approved 07/31/2016
574 0 659
334 0 370
24,180 0 27,982
The purpose of this Standard and its information collection requirements is to provide protection for workers from adverse health effects associated with occupational exposure to Methylenedianiline (MDA) in General Industry. Employers must monitor worker exposures within the permissible exposure limits, provide workers with medical examinations and training, and establish and maintain worker exposure-monitoring and medical records.
US Code: 29 USC 657 Name of Law: The Occupational Safety and Health Act
   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
  
None
Not associated with rulemaking
  81 FR 12966 03/11/2016
81 FR 35804 06/03/2016
No
1
IC Title Form No. Form Name
4,4'-Methylenedianiline (MDA) for General Industry (29 CFR 1910.1050)
  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 574 659 0 0 -85 0
Annual Time Burden (Hours) 334 370 0 0 -36 0
Annual Cost Burden (Dollars) 24,180 27,982 0 0 -3,802 0
No
No
The Agency is requesting an adjustment decrease in burden hours from 370 hours to 334 hours. The decrease is the result of a slight decrease in the number of impacted secondary-use plants and a reduction in workers receiving initial medical examinations, receiving exposure monitoring training, and requesting access to records. There is an overall adjustment decrease in capital costs of $3,802 (from $27,982 to $24,180) resulting from a decrease in the cost to analyze a sample of airborne MDA from $119 to $87 each. However, the cost of a medical exam increased from $187 to $207.
$0
No
No
No
No
No
Uncollected
Doris Edwards 202 693-2045 [email protected]
  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.
06/03/2016