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Federal Register / Vol. 86, No. 24 / Monday, February 8, 2021 / Notices Lack of consistency for what supplies to include in an emergency supply kit:
While the public can access information on what contents are likely important to include in emergency supply kits, there is a lack of information as to whether there is a standard set of supplies that is consistently needed across disaster types Lack of a standard tool for evaluation of emergency supply kit use and effectiveness Lack of information on how emergency supply kit items are used during or following disasters:
Currently we lack detailed information on how households use emergency supply kit items during or following disasters and what, if any, are barriers to their use Lack of information on effectiveness of emergency supply kits in preventing adverse outcomes: To our knowledge, there is no information on whether the use of emergency supply items prevents adverse health outcomes. Among individuals with
health conditions, it remains unclear whether preparing an emergency supply kit with adequate medications and medical supplies prevents the worsening of conditions or the need for emergency medical services Lack of data to support emergency supply kit recommendations: It is unclear whether having essential supplies improves self-sufficiency and lessens the need for outside assistance This general lack of research on the efficacy and use of emergency supply kits impedes our ability to make datadriven recommendations regarding emergency supply kit promotion. The cross-sectional disaster survey and focus groups on the publics knowledge, preparedness, and use of emergency supply kits will identify and inform public health officials about the most useful items to include in an emergency supply kit, ideally across two different types of disasters.
Survey participants will be selected via address-based sampling in the
defined geographic area impacted by the disaster and given the choice to complete the survey via paper i.e., Teleform or online via a web-based instrument. Survey participants will also be recruited using an existing, nonprobability web panel and be directed to the online, web-based instrument to create a larger, more costeffective dataset. Focus group participants will be randomly selected among survey respondents and/or recruited via targeted social media e.g., Facebook, Craigslist to provide context and enhancement to the survey.
The estimated annualized burden is 384 hours. The estimated burden is based on conducting the survey at one site per year, taking 15 minutes per respondent via the web or 30 minutes via paper survey, and up to two focus groups in each site taking approximately five minutes for the focus group screener and two hours for the focus group. There is no cost to respondents other than their time.

ESTIMATED ANNUALIZED BURDEN HOURS
Form name
General public

Web survey
Paper survey
Focus group screener
Focus group

Jeffrey M. Zirger, Lead, Information Collection Review Office, Office of Scientific Integrity, Office of Science, Centers for Disease Control and Prevention.
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and Prevention 30 Day2120OS

Agency Forms Undergoing Paperwork Reduction Act Review
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Number of respondents
Type of respondents
In accordance with the Paperwork Reduction Act of 1995, the Centers for Disease Control and Prevention CDC
has submitted the information collection request titled COVID19
Pandemic Response, Laboratory Data Reporting to the Office of Management and Budget OMB for review and approval. CDC previously published a Proposed Data Collection Submitted
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for Public Comment and Recommendations notice on June 5th, 2020 to obtain comments from the public and affected agencies. CDC
received two comments related to the previous notice. This notice serves to allow an additional 30 days for public and affected agency comments.
CDC will accept all comments for this proposed information collection project.
The Office of Management and Budget is particularly interested in comments that:
a Evaluate whether the proposed collection of information is necessary for the proper performance of the functions of the agency, including whether the information will have practical utility;
b Evaluate the accuracy of the agencies estimate of the burden of the proposed collection of information, including the validity of the methodology and assumptions used;
c Enhance the quality, utility, and clarity of the information to be collected;

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Average burden per response in hours 15/60
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d Minimize the burden of the collection of information on those who are to respond, including, through the use of appropriate automated, electronic, mechanical, or other technological collection techniques or other forms of information technology, e.g., permitting electronic submission of responses; and e Assess information collection costs.
To request additional information on the proposed project or to obtain a copy of the information collection plan and instruments, call 404 6397570.
Comments and recommendations for the proposed information collection should be sent within 30 days of publication of this notice to www.reginfo.gov/public/
do/PRAMain. Find this particular information collection by selecting Currently under 30-day ReviewOpen for Public Comments or by using the search function. Direct written comments and/or suggestions regarding the items contained in this notice to the Attention: CDC Desk Officer, Office of Management and Budget, 725 17th
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