SupportingStatement_B_23November_1

Information Collection Request

Respiratory Protective Devices--42 CFR 84--Regulation

Revision (0920-0109)

SUPPORTING STATEMENT

PART B

U.S. DEPARTMENT OF HEALTH AND HUMAN SERVICES

Centers for Disease Control and Prevention

National Institute for Occupational Safety and Health

John Sporrer

National Personal Protective Technology Laboratory

P.O. Box 18070

626 Cochrans Mill Road, Mail Stop P-05

Pittsburgh, PA 15236

(412) 386-6435

[email protected]

November 1, 2023

B. Collections of Information Employing Statistical Methods

B1. Respondent Universe and Sampling Methods

B2. Procedures for the Collection of Information

B3. Methods to Maximize Response Rates and Deal with No Response

B4. Tests of Procedures or Methods to be Undertaken

B5. Individuals Consulted on Statistical Aspects and Individuals Collecting and/or Analyzing Data

Proposed Project

Respiratory Protective Devices—42 CFR part 84—Regulation—(0920– 0109)—Extension—National Institute for Occupational Safety and Health (NIOSH), of the Centers for Disease Control and Prevention (CDC).

B. Collections of Information Employing Statistical Methods

1. Respondent Universe and Sampling Methods

The proposed information collection activity is a request for a benefit, and no sampling is performed.

2. Procedures for the Collection of Information

The Standard Application for Respirator Certification is attached.

Forms for information collection from the human participants are attached.

3. Methods to Maximize Response Rates and Deal with No Response

Response is a request for benefits. The application is readily and freely available.

4. Tests of Procedures or Methods to be Undertaken

The information collection is the minimum to adequately evaluate the request for respirator approval.

Human participant information collection is the minimum to adequately evaluate the respirator performance requirements.

5. Individuals Consulted on Statistical Aspects and Individuals Collecting and/or Analyzing Data

Each SAF response is entered into a digital system by the CDC NIOSH NPPTL Records Room personnel. Once entered in the system, subtasks are automatically assigned to appropriate Institute personnel. Information may be maintained on CDC MUST drives, CDC NIOSH DEIMS, and eventually the CDC NIOSH Respirator Approval System and Edge Computing Platform.

Respirator performance data is entered into a digital system by the NPPTL test personnel. Once entered in the system, the data is part of the project and can be reviewed by appropriate Institute personnel.