Lead in General Industry (29 CFR 1910.1025)

Forms and Documents

Document Name	Status
SS_1218-0092(07-22-09).pdf Supporting Statement A	2009-07-24
Section 657.doc Supplementary Document	2009-07-07
Section 6551.doc Supplementary Document	2009-07-07
Section651.doc Supplementary Document	2009-07-07
Rules of agency practice and procedures.pdf Supplementary Document	2009-07-07
Access to employee exposure and medical records.pdf Supplementary Document	2009-07-07
1910134(2009).pdf Supplementary Document	2009-07-07
Lead in GI Standard 1910.1025.pdf Supplementary Document	2009-07-07
60-day notice 2009.pdf Supplementary Document	2009-07-07

IC Document Collections

IC ID	Document Title	Status
14001	Lead in General Industry (29 CFR 1910.1025)	Modified

ICR Details

OMB Control No: 1218-0092	ICR Reference No: 200907-1218-001
Status: Historical Active	Previous ICR Reference No: 200603-1218-002
Agency/Subagency: DOL/OSHA	Agency Tracking No: 1218-0092(2009)
Title: Lead in General Industry (29 CFR 1910.1025)
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: 10/13/2009
	Date Received in OIRA: 07/29/2009
Terms of Clearance:

	Inventory as of this Action	Requested	Previously Approved
Expiration Date	10/31/2012	36 Months From Approved	10/31/2009
Responses	4,219,272	0	4,068,503
Time Burden (Hours)	1,225,255	0	1,242,562
Cost Burden (Dollars)	143,566,299	0	139,869,000

---

Abstract: The purpose of this standard and its information collection requirements is to provide protection for employees from the adverse effects associated with occupational exposure to the carcinogen lead. Employers must monitor exposure to lead, provide medical surveillance, train employers about the hazards of lead, and establish and maintain accurate records of employee exposure to lead. These records will be used by employers, employees, physicians, and the Government to ensure that employees are not being harmed by exposure to lead.

---

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

Citations for New Statutory Requirements: None

---

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

---

Federal Register Notices & Comments
60-day Notice:	Federal Register Citation:	Citation Date:
	74 FR 23209	05/18/2009
30-day Notice:	Federal Register Citation:	Citation Date:
	74 FR 37732	07/29/2009
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
Lead in General Industry (29 CFR 1910.1025)

---

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	4,219,272	4,068,503	0	0	150,769	0
Annual Time Burden (Hours)	1,225,255	1,242,562	0	0	-17,307	0
Annual Cost Burden (Dollars)	143,566,299	139,869,000	0	0	3,697,299	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 a -17,307 hour decrease, from 1,242,562 hours to 1,225,255 hours. The decrease is primarily due to the reduction in the number of facilities (from 62,357 to 61,405) and exposed employees (from 887,113 to 871,974). Additionally, although there is a reduction in the number of facilities and exposed employees as stated above, the cost estimate to perform medical surveillance has increased from $61.50 to $65.37 and medical examinations increased from $210 to $223 resulting in a cost increase of $3,697,299.

---

Annual Cost to Federal Government: $3,030

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)? No

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: 07/29/2009

---