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Federal Register / Vol. 86, No. 36 / Thursday, February 25, 2021 / Notices participate in the survey. We anticipate that approximately 20% of SSPs will decline to complete the survey, yielding approximately 320 completed surveys per year. However, given that this is the first survey of SSPs funded by CDC and that the COVID19 pandemic makes it challenging to predict future response rates, we are requesting enough burden hours to allow 100% of SSPs to respond to the survey. We estimate that it will take 35 minutes to complete the survey, regardless of how the respondent
described above, we are requesting enough burden hours to allow 100% of SSPs to respond to this question. We estimate that it will take two minutes to respond to this question.
OMB approval is requested for three years. The survey will be administered annually using the most updated national directory of SSPs during each survey administration. Participation is voluntary and there are no costs to respondents other than their time.

chooses to complete it i.e., selfadministered online or intervieweradministered by phone or videoconferencing. SSPs that do not respond to the initial survey invitation will be given reminders to complete the survey over the duration of the survey implementation period. The final reminder will include a link to a single question for SSPs that choose not to complete the survey about why they declined to complete the survey. Given the uncertainties in response rates
ESTIMATED ANNUALIZED BURDEN HOURS
Number of responses per respondent
Number of respondents
Average burden per response in hours
Total burden in hours
Type of respondent
Form
All participating SSPs

400

1

35/60

233

Non-responding SSPs

National Syringe Services Program Evaluation Survey.
Non-Response Survey Item

400

1

2/60

13

Total

246

Jeffrey M. Zirger, Lead, Information Collection Review Office, Office of Scientific Integrity, Office of Science, Centers for Disease Control and Prevention.
FR Doc. 202103924 Filed 22421; 8:45 am BILLING CODE 416318P

DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and Prevention 60Day211266; Docket No. CDC2021
0014

Proposed Data Collection Submitted for Public Comment and Recommendations Centers for Disease Control and Prevention CDC, Department of Health and Human Services HHS.
ACTION: Notice with comment period.
AGENCY:

The Centers for Disease Control and Prevention CDC, as part of its continuing effort to reduce public burden and maximize the utility of government information, invites the general public and other Federal agencies the opportunity to comment on a proposed and/or continuing information collection, as required by the Paperwork Reduction Act of 1995.
This notice invites comment on a proposed information collection project titled HIV prevention among Latina transgender women who have sex with men: Evaluation of a locally developed intervention. The collection is part of a research study designed to evaluate
SUMMARY:

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the efficacy of a locally developed and culturally congruent two-session Spanish-language small-group intervention, ChiCAS Chicas Creando Acceso a la Salud Chicas: Girls Creating Access to Health, which provides combination HIV prention services to adult Hispanic/Latina transgender women at high risk for HIV infection.
DATES: CDC must receive written comments on or before April 26, 2021.
ADDRESSES: You may submit comments, identified by Docket No. CDC2121
0014 by any of the following methods:
Federal eRulemaking Portal:
Regulations.gov. Follow the instructions for submitting comments.
Mail: Jeffrey M. Zirger, Information Collection Review Office, Centers for Disease Control and Prevention, 1600
Clifton Road, NE, MSD74, Atlanta, Georgia 30329.
Instructions: All submissions received must include the agency name and Docket Number. CDC will post, without change, all relevant comments to Regulations.gov.
Please note: Submit all comments through the Federal eRulemaking portal regulations.gov or by U.S. mail to the address listed above.
FOR FURTHER INFORMATION CONTACT: To request more information on the proposed project or to obtain a copy of the information collection plan and instruments, contact Jeffrey M. Zirger, Information Collection Review Office, Centers for Disease Control and Prevention, 1600 Clifton Road NE, MS
D74, Atlanta, Georgia 30329; phone:
4046397570; Email: omb@cdc.gov
PO 00000

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Under the Paperwork Reduction Act of 1995 PRA
44 U.S.C. 35013520, Federal agencies must obtain approval from the Office of Management and Budget OMB for each collection of information they conduct or sponsor. In addition, the PRA also requires Federal agencies to provide a 60-day notice in the Federal Register concerning each proposed collection of information, including each new proposed collection, each proposed extension of existing collection of information, and each reinstatement of previously approved information collection before submitting the collection to the OMB for approval. To comply with this requirement, we are publishing this notice of a proposed data collection as described below.
The OMB is particularly interested in comments that will help:
1. 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;
2. Evaluate the accuracy of the agencys estimate of the burden of the proposed collection of information, including the validity of the methodology and assumptions used;
3. Enhance the quality, utility, and clarity of the information to be collected; and 4. 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
SUPPLEMENTARY INFORMATION:

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