Proposed Information Collection Activity; Comment Request, 48089-48090 [2017-22294]

Download as PDF 48089 Federal Register / Vol. 82, No. 198 / Monday, October 16, 2017 / Notices or follow any new or changed items and extant sections, which are topically related. Researchers also conduct this testing to identify redundant and overlapping questions. Extant sections of the questionnaire unrelated to new items do not require testing. The demographic questions on the core Individuals who participate in fieldtesting are drawn from a different sample than individuals who participate in the BRFSS surveys. Participation is voluntary and there is no cost to participate. The average time burden per response will be 22 minutes. The total time burden across all respondents will be approximately 241,518 hours. BRFSS survey are included on each field test. CDC will submit change requests to OMB annually to gain approval to implement modifications identified in field tests. Researchers typically conduct field tests in a single state with appropriate computer-assisted telephone interview (CATI) capability. ESTIMATED ANNUALIZED BURDEN HOURS Number of respondents Number of responses per respondent Average burden per response (in hours) Total burden (in hours) Type of respondents Form name U.S. General Population ................... Landline Screener ............................ Cell Phone Screener ........................ Field Test Screener .......................... BRFSS Core Survey ........................ 375,000 292,682 900 480,000 1 1 1 1 1/60 1/60 1/60 15/60 6,250 4,878 15 120,000 BRFSS Optional Modules ................ Field Test Survey ............................. 440,000 500 1 1 15/60 45/60 110,000 375 ........................................................... ........................ ........................ ........................ 241,518 Annual Survey Respondents (Adults >18 Years). Field Test Respondents (Adults >18 Years). Total ........................................... Leroy A. Richardson, Chief, Information Collection Review Office, Office of Scientific Integrity, Office of the Associate Director for Science, Office of the Director, Centers for Disease Control and Prevention. [FR Doc. 2017–22317 Filed 10–13–17; 8:45 am] BILLING CODE 4163–18–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Centers for Disease Control and Prevention [30Day–17–1083] Agency Forms Undergoing Paperwork Reduction Act Review—Evaluation of the National Tobacco Prevention and Control Public Education Campaign; Correction Centers for Disease Control and Prevention (CDC), Department of Health and Human Services (HHS). ACTION: Notice; correction. AGENCY: The Centers for Disease Control and Prevention (CDC) published a document in the Federal Register of October 3, 2017, concerning request for comments on Agency Forms Undergoing Paperwork Reduction Act Review—Evaluation of the National Tobacco Prevention and Control Public Education Campaign. The document provided the incorrect proposed project type (Revision). FOR FURTHER INFORMATION CONTACT: Leroy Richardson, 1600 Clifton Road, MS D–74, Atlanta, GA 30333; telephone (404) 639–4965; email: omb@cdc.gov. Correction In the Federal Register of October 3, 2017, in FR Doc. 2017–21122, on page 46059, in the first column (Proposed Project), correct the proposed project type to read: Evaluation of the National Tobacco Prevention and Control Public Education Campaign (OMB Control Number 0920–1083, Expiration 09/30/2017)—Reinstatement with Change—National Center for Chronic Disease Prevention and Health Promotion (NCCDPHP), Centers for Disease Control and Prevention (CDC). Dated: October 10, 2017. Leroy A. Richardson, Chief, Information Collection Review Office, Office of Scientific Integrity, Office of the Associate Director for Science, Office of the Director, Centers for Disease Control and Prevention. [FR Doc. 2017–22256 Filed 10–13–17; 8:45 am] BILLING CODE 4163–18–P ethrower on DSK3G9T082PROD with NOTICES SUMMARY: VerDate Sep<11>2014 16:59 Oct 13, 2017 Jkt 244001 DEPARTMENT OF HEALTH AND HUMAN SERVICES Administration for Children and Families Proposed Information Collection Activity; Comment Request Title: Community-Based Family Resource and Support Grants (Name PO 00000 Frm 00040 Fmt 4703 Sfmt 4703 changed to Child Abuse Prevention Program—OIS notified 6/2007). OMB No.: 0970–0155. Description: The Program Instruction, prepared in response to the enactment of Community-Based Child Abuse Prevention (CBCAP) program, as set forth in Title II of the Child Abuse Prevention and Treatment Reauthorization Act of 2010 (Pub. L. 111–320) or CAPTA, provides direction to the states and territories to accomplish the purposes of (1) supporting community-based efforts to develop, operate, expand, and where appropriate to network, initiatives aimed at the prevention of child abuse and neglect, and to support networks of coordinated resources and activities to better strengthen and support families to reduce the likelihood of child abuse and neglect, and; (2) fostering an understanding, appreciation, and knowledge of diverse populations in order to be effective in preventing and treating child abuse and neglect. This Program Instruction contains information collection requirements that are found in CAPTA and pursuant to receiving a grant award. The information submitted will be used by the agency to ensure compliance with the statute, complete the calculation of the grant award entitlement, and provide training and technical assistance to the grantee. Respondents: State Governments. E:\FR\FM\16OCN1.SGM 16OCN1 48090 Federal Register / Vol. 82, No. 198 / Monday, October 16, 2017 / Notices ANNUAL BURDEN ESTIMATES Number of respondents Instrument Application ....................................................................................................... Annual Report .................................................................................................. Estimated Total Annual Burden Hours: 3,328. In compliance with the requirements of Section 3506(c)(2)(A) of the Paperwork Reduction Act of 1995, the Administration for Children and Families is soliciting public comment on the specific aspects of the information collection described above. Copies of the proposed collection of information can be obtained and comments may be forwarded by writing to the Administration for Children and Families, Office of Planning, Research, and Evaluation, 330 C Street SW., Washington, DC 20201, Attn: ACF Reports Clearance Officer. Email address: infocollection@acf.hhs.gov. All requests should be identified by the title of the information collection. The Department specifically requests comments on (a) whether the proposed collection of information is necessary for the proper performance of the functions of the agency, including whether the information shall have practical utility; (b) the accuracy of the agency’s estimate of the burden of the proposed collection of information; (c) the quality, utility, and clarity of the information to be collected; and (d) ways to minimize the burden of the collection of information on respondents, including through the use of automated collection techniques or other forms of information technology. Consideration will be given to comments and suggestions submitted within 60 days of this publication. Mary Jones, ACF/OPRE Reports Clearance Officer. [FR Doc. 2017–22294 Filed 10–13–17; 8:45 am] ethrower on DSK3G9T082PROD with NOTICES BILLING CODE 4184–29–P 52 52 DEPARTMENT OF HEALTH AND HUMAN SERVICES Food and Drug Administration [Docket No. FDA–2014–D–0329] Agency Information Collection Activities; Submission for Office of Management and Budget Review; Comment Request; Guidance for Industry on Fees for Human Drug Compounding Outsourcing Facilities Under the Federal Food, Drug, and Cosmetic Act AGENCY: Food and Drug Administration, HHS. ACTION: Notice. The Food and Drug Administration (FDA) is announcing that a proposed collection of information has been submitted to the Office of Management and Budget (OMB) for review and clearance under the Paperwork Reduction Act of 1995. SUMMARY: Fax written comments on the collection of information by November 15, 2017. DATES: To ensure that comments on the information collection are received, OMB recommends that written comments be faxed to the Office of Information and Regulatory Affairs, OMB, Attn: FDA Desk Officer, Fax: 202– 395–7285, or emailed to oira_ submission@omb.eop.gov. All comments should be identified with the OMB control number 0910–0776. Also include the FDA docket number found in brackets in the heading of this document. ADDRESSES: FOR FURTHER INFORMATION CONTACT: Domini Bean, Office of Operations, Food and Drug Administration, Three White Flint North, 10A63, 11601 Landsdown St., North Bethesda, MD 20852, 301–796–5733, PRAStaff@ fda.hhs.gov. In compliance with 44 U.S.C. 3507, FDA has submitted the following proposed collection of information to OMB for review and clearance. SUPPLEMENTARY INFORMATION: VerDate Sep<11>2014 16:59 Oct 13, 2017 Jkt 244001 PO 00000 Frm 00041 Fmt 4703 Sfmt 4703 Number of responses per respondent 1 1 Average burden hours per response 40 24 Total burden hours 2,080 1,248 Guidance for Industry on Fees for Human Drug Compounding Outsourcing Facilities Under Sections 503B and 744K of the FD&C Act OMB Control Number 0910–0776—Extension This information collection supports the Agency’s guidance on fees for human drug compounding outsourcing facilities under the Federal Food, Drug, and Cosmetic Act (the FD&C Act). On November 27, 2013, the President signed the Drug Quality and Security Act (DQSA) (Pub. L. 113–54) into law. The DQSA added a new section, 503B (21 U.S.C. 353B), to the FD&C Act, creating a category of entities called ‘‘outsourcing facilities.’’ Outsourcing facilities, as defined in section 503B(d)(4) of the FD&C Act, are facilities that meet certain requirements described in section 503B, including registering with FDA as an outsourcing facility and paying associated fees. Drug products compounded in an outsourcing facility can qualify for exemptions from the FDA approval requirements in section 505 of the FD&C Act (21 U.S.C. 355), and the requirement to label products with adequate directions for use under section 502(f)(1) of the FD&C Act (21 U.S.C. 352(f)(1)), if the requirements in section 503B of the FD&C Act are met. The guidance is intended for entities that compound human drugs and elect to register as outsourcing facilities under section 503B of the FD&C Act. Once an entity has elected to register as an outsourcing facility, it must pay certain fees to be registered as an outsourcing facility. The guidance describes the types and amounts of fees that outsourcing facilities must pay, the adjustments to fees required by law, the way in which outsourcing facilities may submit payment to FDA, the consequences of outsourcing facilities’ failure to pay fees, and the way an outsourcing facility may qualify as a small business to obtain a reduction in fees. In the Federal Register of June 15, 2017 (82 FR 27493), we published a 60day notice requesting public comment on the proposed extension of this collection of information. No comments were received. We therefore estimate the burden associated with the information collection as follows: E:\FR\FM\16OCN1.SGM 16OCN1

Agencies

[Federal Register Volume 82, Number 198 (Monday, October 16, 2017)]
[Notices]
[Pages 48089-48090]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2017-22294]


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DEPARTMENT OF HEALTH AND HUMAN SERVICES

Administration for Children and Families


Proposed Information Collection Activity; Comment Request

    Title: Community-Based Family Resource and Support Grants (Name 
changed to Child Abuse Prevention Program--OIS notified 6/2007).
    OMB No.: 0970-0155.
    Description: The Program Instruction, prepared in response to the 
enactment of Community-Based Child Abuse Prevention (CBCAP) program, as 
set forth in Title II of the Child Abuse Prevention and Treatment 
Reauthorization Act of 2010 (Pub. L. 111-320) or CAPTA, provides 
direction to the states and territories to accomplish the purposes of 
(1) supporting community-based efforts to develop, operate, expand, and 
where appropriate to network, initiatives aimed at the prevention of 
child abuse and neglect, and to support networks of coordinated 
resources and activities to better strengthen and support families to 
reduce the likelihood of child abuse and neglect, and; (2) fostering an 
understanding, appreciation, and knowledge of diverse populations in 
order to be effective in preventing and treating child abuse and 
neglect. This Program Instruction contains information collection 
requirements that are found in CAPTA and pursuant to receiving a grant 
award. The information submitted will be used by the agency to ensure 
compliance with the statute, complete the calculation of the grant 
award entitlement, and provide training and technical assistance to the 
grantee.
    Respondents: State Governments.

[[Page 48090]]



                                             Annual Burden Estimates
----------------------------------------------------------------------------------------------------------------
                                                                     Number of    Average burden
                   Instrument                        Number of     responses per     hours per     Total burden
                                                    respondents     respondent       response          hours
----------------------------------------------------------------------------------------------------------------
Application.....................................              52               1              40           2,080
Annual Report...................................              52               1              24           1,248
----------------------------------------------------------------------------------------------------------------

    Estimated Total Annual Burden Hours: 3,328.
    In compliance with the requirements of Section 3506(c)(2)(A) of the 
Paperwork Reduction Act of 1995, the Administration for Children and 
Families is soliciting public comment on the specific aspects of the 
information collection described above. Copies of the proposed 
collection of information can be obtained and comments may be forwarded 
by writing to the Administration for Children and Families, Office of 
Planning, Research, and Evaluation, 330 C Street SW., Washington, DC 
20201, Attn: ACF Reports Clearance Officer. Email address: 
infocollection@acf.hhs.gov. All requests should be identified by the 
title of the information collection.
    The Department specifically requests comments on (a) whether the 
proposed collection of information is necessary for the proper 
performance of the functions of the agency, including whether the 
information shall have practical utility; (b) the accuracy of the 
agency's estimate of the burden of the proposed collection of 
information; (c) the quality, utility, and clarity of the information 
to be collected; and (d) ways to minimize the burden of the collection 
of information on respondents, including through the use of automated 
collection techniques or other forms of information technology. 
Consideration will be given to comments and suggestions submitted 
within 60 days of this publication.

Mary Jones,
ACF/OPRE Reports Clearance Officer.
[FR Doc. 2017-22294 Filed 10-13-17; 8:45 am]
 BILLING CODE 4184-29-P