Pulmonary Function Testing Course Approval Program, 29 CFR 1910.1043

Forms and Documents

Forms and supporting documents for this ICR

Document	Type	Status	Availability
Form 1 Annual Report	Form and Instruction	Modified	Available
Form 4 NIOSH-Approved Spirometry Refresher Course Application	Form and Instruction	Modified	Available
Form 3 NIOSH-Approved Spirometry Testing Course Application	Form and Instruction	Modified	Available
Form 2 NIOSH -Approved Spirometry Course Sponsorship Renewal Application	Form and Instruction	Modified	Available
0920-0138 Part B.doc	Supporting Statement B	Uploaded 2011-07-11	Available
0920-0138 Part A.doc	Supporting Statement A	Uploaded 2011-07-11	Available

IC Document Collections

Information collection document groups

IC ID	Collection	Type	Status	Form
6649	Pulmonary Function Testing Course Approval Program Annual Report	Form and Instruction	Modified	Annual Report
184872	Request for Course Change Sample	Other-Email	Modified
184871	Refresher Course Application	Form and Instruction	Modified	NIOSH-Approved Spirometry Refresher Course Application
184870	Initial Application	Form and Instruction	Modified	NIOSH-Approved Spirometry Testing Course Application
184869	Renewal Application	Form and Instruction	Modified	NIOSH -Approved Spirometry Course Sponsorship Renewal Application

ICR Details

OMB Control No: 0920-0138	ICR Reference No: 201107-0920-003
Status: Historical Active	Previous ICR Reference No: 200805-0920-006
Agency/Subagency: HHS/CDC	Agency Tracking No:
Title: Pulmonary Function Testing Course Approval Program, 29 CFR 1910.1043
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: 08/08/2011
Retrieve Notice of Action (NOA)	Date Received in OIRA: 07/19/2011
Terms of Clearance:

table that charts list comparision

	Inventory as of this Action	Requested	Previously Approved
Expiration Date	08/31/2014	36 Months From Approved	08/31/2011
Responses	73	0	73
Time Burden (Hours)	196	0	197
Cost Burden (Dollars)	0	0	0

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Abstract: NIOSH maintains a Pulmonary Function Testing Course Approval Program. The program consists of an application submitted by potential sponsors (universities, hospitals, and private consulting firms) who seek NIOSH approval to conduct courses, and if approved, notification to NIOSH of any course or faculty changes during the approval period, which is limited to five years. Submissions are required for NIOSH to evaluate a course and determine whether it meets the criteria in the Standard and whether technicians will be adequately trained as mandated under the Standard. The estimated annual burden to respondents is 196 hours.

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Authorizing Statute(s): PL: Pub.L. 91 - 596 20 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:
	76 FR 24028	04/29/2011
30-day Notice:	Federal Register Citation:	Citation Date:
	76 FR 39878	07/07/2011
Did the Agency receive public comments on this ICR? No

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Number of Information Collection (IC) in this ICR: 5

table that charts list of burden

IC Title	Form No.	Form Name
Initial Application	3	NIOSH-Approved Spirometry Testing Course Application
Pulmonary Function Testing Course Approval Program Annual Report	1	Annual Report
Refresher Course Application	4	NIOSH-Approved Spirometry Refresher Course Application
Renewal Application	2	NIOSH -Approved Spirometry Course Sponsorship Renewal Application
Request for Course Change Sample

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ICR Summary of Burden

table that charts list 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	73	73	0	0	0	0
Annual Time Burden (Hours)	196	197	0	-1	0	0
Annual Cost Burden (Dollars)	0	0	0	0	0	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: Yes

Burden Reduction Due to: Miscellaneous Actions

Short Statement: The average burden per response in the initial application has decreased from 4 to 3.5. This is due to the fact that all applications and supporting documentation are now submitted electronically; some were previously submitted as hard copies. This reduces the time for preparing the materials for mailing.

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Annual Cost to Federal Government: $7,958

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? Yes

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? 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: 07/19/2011

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