Bloodborne Pathogens Standard (29 CFR 1910.1030)

Forms and Documents

Forms and supporting documents for this ICR

Document	Type	Status	Availability
DSG-7197 - 1218-0180 - Bloodborne Pathogens Standard ICR Spreadsheet Tables.pdf	Supplementary Document	Uploaded 2021-06-11	Available
SS_1218-0180_ Bloodborne Pathogens_07-20-21_ROCIS.docx	Supporting Statement A	Uploaded 2021-07-20	Repair queued
86 FR 19904.pdf	Supplementary Document	Uploaded 2021-06-10	Missing upstream
Public Law 106-430.pdf	Supplementary Document	Uploaded 2021-06-10	Repair queued
29 CFF 1904.33 Electronic Code of Federal Regulations (eCFR) 04.16.21.pdf	Supplementary Document	Uploaded 2021-06-10	Repair queued
29 CFF 1904.8 Electronic Code of Federal Regulations (eCFR) 04.16.21.pdf	Supplementary Document	Uploaded 2021-06-10	Repair queued
29 CFF 1913.10 Electronic Code of Federal Regulations (eCFR) 04.16.21.pdf	Supplementary Document	Uploaded 2021-06-10	Repair queued
29 CFF 1910.1020 Electronic Code of Federal Regulations (eCFR) 04.16.21.pdf	Supplementary Document	Uploaded 2021-06-10	Repair queued
29 CFF 1910.1030 Electronic Code of Federal Regulations (eCFR) 04.16.21.pdf	Supplementary Document	Uploaded 2021-06-10	Missing upstream
OSH Act Section 8 USC 657.pdf	Supplementary Document	Uploaded 2018-09-19	Repair queued
OSH Act Section 6 USC 655 (2).pdf	Supplementary Document	Uploaded 2018-09-19	Repair queued
OSH Act Section 2 USC 651 (2).pdf	Supplementary Document	Uploaded 2018-09-19	Repair queued

IC Document Collections

Information collection document groups

IC ID	Collection	Type	Status	Form
14124	Bloodborne Pathogens Standard (29 CFR 1910.1030)		Modified

ICR Details

OMB Control No: 1218-0180	ICR Reference No: 202105-1218-005
Status: Received in OIRA	Previous ICR Reference No: 201809-1218-019
Agency/Subagency: DOL/OSHA	Agency Tracking No: 1218-0180(2021)
Title: Bloodborne Pathogens Standard (29 CFR 1910.1030)
Type of Information Collection: Extension without change of a currently approved collection	Common Form ICR:  No
Type of Review Request: Regular	Date Submitted to OIRA: 07/27/2021

table that charts list comparision

	Requested	Previously Approved
Expiration Date	36 Months From Approved	08/31/2021
Responses	26,841,471	26,656,386
Time Burden (Hours)	5,720,498	5,687,682
Cost Burden (Dollars)	52,516,112	51,817,985

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Abstract: The Bloodborne Pathogen Standard is an occupational safety and health standard that prevents occupational exposure to bloodborne pathogens. The standard's information collection requirements are essential components that protect workers from occupational exposure. The information is used by employers and workers to implement the protection required by the Standard. OSHA compliance officers will use some of the information in their enforcement of the Standard.

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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

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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:
	86 FR 19904	04/15/2021
30-day Notice:	Federal Register Citation:	Citation Date:
	86 FR 40212	07/27/2021
Did the Agency receive public comments on this ICR? Yes

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

table that charts list of burden

IC Title	Form No.	Form Name
Bloodborne Pathogens Standard (29 CFR 1910.1030)

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ICR Summary of Burden

table that charts list of burden

	Total Request	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	26,841,471	26,656,386	0	0	185,085	0
Annual Time Burden (Hours)	5,720,498	5,687,682	0	0	32,816	0
Annual Cost Burden (Dollars)	52,516,112	51,817,985	0	0	698,127	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 increase of 32,816.66 burden hours (from 5,687,682.00 hours to 5,720,498.67). This increase is a result of updated data showing an increase in the number of facilities (from 700,724 to 701,563) and employees (from 8,399,358 to 8,425,607) affected by the Standard. The operation and maintenance cost increased $698,127.50, from $51,817,985.00 to $52,516,112.50, due to the increase in medical costs (administration of the Hepatitis B Vaccine and the PEP treatment). This increase is also a result of updated data showing an increase in the number of facilities and employees affected by the Standard.

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Annual Cost to Federal Government: $0

Does this IC contain surveys, censuses, or employ statistical methods? No

Does this ICR request any personally identifiable information (see OMB Circular No. A-130 for an explanation of this term)? Please consult with your agency's privacy program when making this determination.     No

Does this ICR include a form that requires a Privacy Act Statement (see 5 U.S.C. §552a(e)(3))? Please consult with your agency's privacy program when making this determination.     No

Is this ICR related to the Affordable Care Act [Pub. L. 111-148 & 111-152]? No

Is this ICR related to the Dodd-Frank Wall Street Reform and Consumer Protection Act, [Pub. L. 111-203]? No

Is this ICR related to the American Recovery and Reinvestment Act of 2009 (ARRA)? No

Is this ICR related to the Pandemic Response? No

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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: 07/27/2021

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