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Federal Register / Vol. 86, No. 27 / Thursday, February 11, 2021 / Notices development, validation, or appropriate use of innovative Lyme disease diagnostic tests, and what factors are most critical to ensure their success?
This information will inform the development of the HHS Lyme Innovation initiative and the LymeX
public-private partnership to create meaningful incentives to develop or validate new diagnostic tests for Lyme disease.
Kristen Honey, Senior Advisor to the Assistant Secretary for Health ASH, Office of the Assistant Secretary for Health, U.S. Department of Health and Human Service.
FR Doc. 202102796 Filed 21021; 8:45 am BILLING CODE 415028P

DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Document Identifier OS0990xxxx
Agency Information Collection Request. 60-Day Public Comment Request Office of the Secretary, HHS.
Notice.

AGENCY:
ACTION:

In compliance with the requirement of the Paperwork Reduction Act of 1995, the Office of the Secretary OS, Department of Health and Human Services, is publishing the following summary of a proposed collection for public comment.
DATES: Comments on the ICR must be received on or before April 12, 2021.
ADDRESSES: Submit your comments to Sherrette.Funn@hhs.gov or by calling 202 7957714.
FOR FURTHER INFORMATION CONTACT:
When submitting comments or requesting information, please include the document identifier 0990-New-60D, and project title for reference, to Sherrette Funn, Reports Clearance Officer, Sherrette.funn@hhs.gov, 202
7957714.
SUMMARY:

Interested persons are invited to send comments regarding this burden estimate or any other aspect of this collection of information, including any of the following subjects: 1 The necessity and utility of the proposed information collection for the proper performance of the agencys functions; 2 the accuracy of the estimated burden; 3 ways to enhance the quality, utility, and clarity of the information to be collected; and 4 the use of automated collection techniques or other forms of information technology to minimize the information collection burden.
Title of the Collection: Family Planning Annual Report 2.0.
Type of Collection: New.
Abstract: The Office of Population Affairs OPA, within the Office of the Assistant Secretary for Health, seeks approval for a new encounter level data collection for the Family Planning Annual Report FPAR. Currently collected in aggregate under OMB No.
09900221, this new data collection, FPAR 2.0, will collect information at the encounter level and build on the existing data collection and reporting system. This annual reporting requirement is for competitively awarded grants authorized and funded by the Title X Family Planning Program.
Need and Proposed Use of the Information: The Office of Population Affairs OPA Title X Family Planning Program is the only federal grant program dedicated solely to providing comprehensive family planning and related preventive health services.
Annual submission of the FPAR is required of all Title X family planning services grantees for purposes of monitoring and reporting program performance 45 CFR part 74 and 45
CFR part 92. The FPAR is the only source of annual, uniform reporting by all grantees funded under Section 1001
of the Title X Public Health Service Act.
Similar to the previous FPAR, FPAR 2.0

SUPPLEMENTARY INFORMATION:

will provide consistent, national-level data on the Title X Family Planning program and its users. OPA will be able to assemble and analyze comparable and relevant program data to answer questions about the characteristics of the population served, the provision and use of services, and the impact of the program on certain family planning outcomes. FPAR 2.0 will also collect a standard set of data elements pertaining to users and encounters, such as user demographics, service delivery, family planning intentions and methods, and other indicators, which allow for comparisons over time at all levels of the program e.g., national, regional, state, and grantee. Encounter level data collected through FPAR 2.0 will ultimately improve the quality of data reported to OPA and reduce reporting burden by grantees. Additionally, the more granular data collected with FPAR
2.0 will help contribute to a learning healthcare environment by greatly expanding the options for data analysis and reportingfor example, through interactive data dashboards and visualizations, customized tabulations and reports, and application of analytics and statistical analyses on the encounter-level data files.
Information from FPAR 2.0 is important to OPA for many reasons, and will be used to:
1 Monitor compliance with statutory requirements, regulations, and operational guidance.
2 Comply with accountability and federal performance requirements for Title X family planning funds.
3 Guide strategic and financial planning, to monitor performance, to respond to inquiries from policymakers and Congress about the program, and to estimate program impact.
Type of respondent: Annual reporting;
respondents are all grantees that receive Title X funding from OPA.

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ANNUALIZED BURDEN HOUR TABLE
Average burden per response
Respondents if necessary
FPAR 2.0

Grantees

74

1

36

2,664

Total

1

2,664

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Number of respondents
Number of responses per respondents
Forms if necessary
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Total burden hours