Proposed Information Collection Activity; Center for States Evaluation Ancillary Data Collection (0970-0501), 30710-30711 [2020-10906]

Download as PDF 30710 Federal Register / Vol. 85, No. 98 / Wednesday, May 20, 2020 / Notices Center’s programmatic balance and mission; (3) submission of secondary review recommendations to the Center Director of applications to be considered for funding support; (4) review of research portfolios; and (5) review of program proposals. Matters To Be Considered: The open portion of the agenda will include an update on the formation of the BSC, NCIPC Opioid Workgroup, a presentation focused on opportunities for stakeholder engagement on management of acute and chronic pain, and an update on the CDC Opioid Prescribing Estimates Project. All presentations will be followed by discussion by the BSC. The closed portion of the agenda will focus on the secondary peer review of extramural research grant applications received in response to two (2) Notice of Funding Opportunities (NOFOs): RFA–CE20– 001—‘‘Evaluating Practice-Based Programs, Policies, and Practices from CDC’s Rape Prevention and Education (RPE) Program: Expanding the Evidence to Prevent Sexual Violence’’; and RFA– CE20–003—‘‘Research Grants for Preventing Violence and ViolenceRelated Injury’’ (R01). Agenda items are subject to change as priorities dictate. The Director, Strategic Business Initiatives Unit, Office of the Chief Operating Officer, CDC, has been delegated the authority to sign Federal Register notices pertaining to announcements of meetings and other committee management activities, for both the Centers for Disease Control and Prevention and the Agency for Toxic Substances and Disease Registry. Kalwant Smagh, Director, Strategic Business Initiatives Unit, Office of the Chief Operating Officer, Centers for Disease Control and Prevention. [FR Doc. 2020–10891 Filed 5–19–20; 8:45 am] BILLING CODE 4163–18–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Administration for Children and Families Proposed Information Collection Activity; Center for States Evaluation Ancillary Data Collection (0970–0501) Children’s Bureau, Administration on Children, Youth and Families, Administration for Children and Families, HHS. ACTION: Request for public comment. AGENCY: The Administration for Children and Families (ACF) is requesting a 3-year extension of the collection of information under the Center for States Evaluation Ancillary Data Collection (OMB #0970–0501, expiration date 8/31/2020) without changes. SUMMARY: Comments due within 60 days of publication. In compliance with the requirements of Section 3506(c)(2)(A) of the Paperwork Reduction Act of 1995, ACF is soliciting public comment on the specific aspects of the information collection described above. ADDRESSES: Copies of the proposed collection of information can be obtained and comments may be DATES: forwarded by emailing infocollection@ acf.hhs.gov. Alternatively, copies can also be obtained by writing to the Administration for Children and Families, Office of Planning, Research, and Evaluation (OPRE), 330 C Street SW, Washington, DC 20201, Attn: ACF Reports Clearance Officer. All requests, emailed or written, should be identified by the title of the information collection. SUPPLEMENTARY INFORMATION: Description: The Evaluation of the Child Welfare Capacity Building Collaborative, Center for States is sponsored by the Children’s Bureau (CB), ACF. The purpose of this evaluation is to respond to a set of crosscutting evaluation questions posed by CB. This existing information collection is an ancillary part of a larger data collection effort being conducted for the evaluation of the Child Welfare Capacity Building Collaborative (0970–0484 and 0970–0494). This notice details a group of instruments that are specific only to the Center for States. The instruments focus on (1) evaluating an innovative approach to engaging professionals in networking and professional development through virtual conferences, (2) understanding fidelity to and effectiveness of the Center for States’ Capacity Building Model, and (3) capturing consistent information during the updated annual assessment process focused on related contextual issues impacting potential service delivery such as implementation of new legislation. Respondents: Respondents of these data collection instruments will include child welfare agency staff and stakeholders who directly receive services. ANNUAL BURDEN ESTIMATES Total number of respondents Instrument Child Welfare Virtual Conference: Child Welfare Virtual Conference Session Surveys ..... Child Welfare Virtual Conference Focus Group Guide Child Welfare Virtual Conference Interview Guide ....... Child Welfare Virtual Conference Registration Form ... Child Welfare Virtual Conference Exit Survey ............. Tailored Services Capacity Building Approach: Tailored Services Practice Model Survey .................... Assessment Observation— Group Debrief .................. Service Delivery and Tracking and Adjustment Observation—Group Debrief .............................................. Assessment and Service Delivery State Lead Interviews—Supplemental Questions .............................. Assessment questions: Annual Assessment Update (8 systematic questions) Total ....................................................................... VerDate Sep<11>2014 17:51 May 19, 2020 Jkt 250001 PO 00000 Total number of responses per respondent Average burden hours per response Total burden hours Annual burden hours 450 30 20 1000 225 6 1 1 1 1 .08 1 .5 .03 .16 216 30 10 30 36 72 10 3 10 12 130 50 1 1 .12 .25 15.6 12.5 5 4 80 1 .25 20 7 30 1 .5 15 5 54 1 .08 4.32 1 ........................ ........................ ........................ ........................ 130 Frm 00029 Fmt 4703 Sfmt 4703 E:\FR\FM\20MYN1.SGM 20MYN1 Federal Register / Vol. 85, No. 98 / Wednesday, May 20, 2020 / Notices Comments: 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. Authority: Section 203 of Section II: Adoption Opportunities of the Child Abuse Prevention and Treatment Act (CAPTA) (42 U.S.C. 5113). Molly B. Jones, ACF/OPRE Certifying Officer. [FR Doc. 2020–10906 Filed 5–19–20; 8:45 am] BILLING CODE 4184–01–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Food and Drug Administration [Docket No. FDA–2013–N–1155] Agency Information Collection Activities; Submission for Office of Management and Budget Review; Comment Request; Food Labeling Regulations 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. DATES: Submit written comments (including recommendations) on the collection of information by June 19, 2020. ADDRESSES: To ensure that comments on the information collection are received, OMB recommends that written comments be submitted to https:// www.reginfo.gov/public/do/PRAMain. Find this particular information collection by selecting ‘‘Currently under Review—Open for Public Comments’’ or by using the search function. All comments should be identified with the OMB control number 0910–0381. Also include the FDA docket number found SUMMARY: VerDate Sep<11>2014 17:51 May 19, 2020 Jkt 250001 in brackets in the heading of this document. FOR FURTHER INFORMATION CONTACT: Domini Bean, Office of Operations, Food and Drug Administration, Three White Flint North, 10A–12M, 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: Food Labeling Regulations OMB Control Number 0910–0381— Revision This information collection supports our food labeling regulations and associated Agency guidance. Under the authority of sections 4, 5, and 6 of the Fair Packaging and Labeling Act (FPLA) (15 U.S.C. 1453, 1454, and 1455) and sections 201, 301, 402, 403, 409, 411, 701, and 721 of the Federal Food, Drug, and Cosmetic Act (FD&C Act) (21 U.S.C. 321, 331, 342, 343, 348, 350, 371, and 379e), we have issued regulations regarding the labeling of food. The regulations are codified in parts 101, 102, 104, and 105 (21 CFR parts 101, 102, 104, and 105) and implement statutory provisions that a food product shall be deemed to be misbranded if, among other things, its label or labeling fails to bear certain required information concerning the food product, is false or misleading in any particular, or bears certain types of unauthorized claims. While part 101 sets forth general food labeling provisions, requirements pertaining to the common or usual name for nonstandardized foods; guidelines for nutritional quality to prescribe the minimum level or range of nutrient composition appropriate for a given class of food; and requirements for foods for special dietary use are found in parts 102, 104, and 105, respectively. The disclosure requirements, along with the reporting and recordkeeping provisions, are necessary to ensure the safety of food products produced or sold in the United States and enable consumers to be knowledgeable about the foods they purchase. Nutrition labeling provides information for use by consumers in selecting a nutritious diet. Other information enables consumers to comparison shop. Ingredient information also enables consumers to avoid substances to which they may be sensitive. Petitions or other requests submitted to us provide the basis for us to permit new labeling statements or to grant exemptions from certain labeling PO 00000 Frm 00030 Fmt 4703 Sfmt 4703 30711 requirements. Recordkeeping requirements enable us to monitor the basis upon which certain label statements are made for food products and whether those statements are in compliance with the requirements of the FD&C Act or the FPLA. Specifically, the regulations set forth the general content and format requirements for food packaging, including nutrition and ingredient information. Additional regulations provide for nutrient content claims. To assist respondents in this regard, we developed the document entitled ‘‘Guidance for Industry: Notification of a Health Claim or Nutrient Content Claim Based on an Authoritative Statement of a Scientific Body.’’ The guidance is available from our website at: https://www.fda.gov/regulatoryinformation/search-fda-guidancedocuments/guidance-industrynotification-health-claim-or-nutrientcontent-claim-based-authoritativestatement. The guidance communicates our recommendations regarding food labeling claims associated with regulations found in §§ 101.13, 101.14, 101.54, 101.69, and 101.70. It was developed to assist respondents in satisfying criteria found or discussed in these regulations regarding the submission of notifications for certain health claims and identifies information to include and information we will evaluate in determining compliance with statutory requirements (e.g., supporting literature; discussion of analytical methodology or methodologies used in support of a particular claim). The regulations also include provisions applicable to the labeling of dietary supplements. To assist respondents in this regard and in understanding provisions under the Dietary Supplement and Nonprescription Drug Consumer Protection Act (Pub. L. 109–462), we developed the guidance entitled ‘‘Questions and Answers: Labeling of Dietary Supplements as Required by the Dietary Supplement and Nonprescription Drug Consumer Protection Act.’’ The guidance is available from our website at: https:// www.fda.gov/regulatory-information/ search-fda-guidance-documents/ guidance-industry-questions-andanswers-regarding-labeling-dietarysupplements-required-dietary. The guidance communicates the following information: (1) What ‘‘domestic address’’ means for purposes of the dietary supplement labeling requirements in section 403(y) of the FD&C Act; (2) FDA’s recommendation for the use of an introductory statement E:\FR\FM\20MYN1.SGM 20MYN1

Agencies

[Federal Register Volume 85, Number 98 (Wednesday, May 20, 2020)]
[Notices]
[Pages 30710-30711]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2020-10906]


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DEPARTMENT OF HEALTH AND HUMAN SERVICES

Administration for Children and Families


Proposed Information Collection Activity; Center for States 
Evaluation Ancillary Data Collection (0970-0501)

AGENCY: Children's Bureau, Administration on Children, Youth and 
Families, Administration for Children and Families, HHS.

ACTION: Request for public comment.

-----------------------------------------------------------------------

SUMMARY: The Administration for Children and Families (ACF) is 
requesting a 3-year extension of the collection of information under 
the Center for States Evaluation Ancillary Data Collection (OMB #0970-
0501, expiration date 8/31/2020) without changes.

DATES: Comments due within 60 days of publication. In compliance with 
the requirements of Section 3506(c)(2)(A) of the Paperwork Reduction 
Act of 1995, ACF is soliciting public comment on the specific aspects 
of the information collection described above.

ADDRESSES: Copies of the proposed collection of information can be 
obtained and comments may be forwarded by emailing 
[email protected]. Alternatively, copies can also be obtained 
by writing to the Administration for Children and Families, Office of 
Planning, Research, and Evaluation (OPRE), 330 C Street SW, Washington, 
DC 20201, Attn: ACF Reports Clearance Officer. All requests, emailed or 
written, should be identified by the title of the information 
collection.

SUPPLEMENTARY INFORMATION: 
    Description: The Evaluation of the Child Welfare Capacity Building 
Collaborative, Center for States is sponsored by the Children's Bureau 
(CB), ACF. The purpose of this evaluation is to respond to a set of 
cross-cutting evaluation questions posed by CB. This existing 
information collection is an ancillary part of a larger data collection 
effort being conducted for the evaluation of the Child Welfare Capacity 
Building Collaborative (0970-0484 and 0970-0494). This notice details a 
group of instruments that are specific only to the Center for States. 
The instruments focus on (1) evaluating an innovative approach to 
engaging professionals in networking and professional development 
through virtual conferences, (2) understanding fidelity to and 
effectiveness of the Center for States' Capacity Building Model, and 
(3) capturing consistent information during the updated annual 
assessment process focused on related contextual issues impacting 
potential service delivery such as implementation of new legislation.
    Respondents: Respondents of these data collection instruments will 
include child welfare agency staff and stakeholders who directly 
receive services.

                                             Annual Burden Estimates
----------------------------------------------------------------------------------------------------------------
                                                   Total number   Average burden
           Instrument              Total number    of responses      hours per     Total burden    Annual burden
                                  of respondents  per respondent     response          hours           hours
----------------------------------------------------------------------------------------------------------------
Child Welfare Virtual
 Conference:
    Child Welfare Virtual                    450               6             .08             216              72
     Conference Session Surveys.
    Child Welfare Virtual                     30               1               1              30              10
     Conference Focus Group
     Guide......................
    Child Welfare Virtual                     20               1              .5              10               3
     Conference Interview Guide.
    Child Welfare Virtual                   1000               1             .03              30              10
     Conference Registration
     Form.......................
    Child Welfare Virtual                    225               1             .16              36              12
     Conference Exit Survey.....
Tailored Services Capacity
 Building Approach:
    Tailored Services Practice               130               1             .12            15.6               5
     Model Survey...............
    Assessment Observation--                  50               1             .25            12.5               4
     Group Debrief..............
    Service Delivery and                      80               1             .25              20               7
     Tracking and Adjustment
     Observation--Group Debrief.
    Assessment and Service                    30               1              .5              15               5
     Delivery State Lead
     Interviews--Supplemental
     Questions..................
Assessment questions:
    Annual Assessment Update (8               54               1             .08            4.32               1
     systematic questions)......
                                 -------------------------------------------------------------------------------
        Total...................  ..............  ..............  ..............  ..............             130
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[[Page 30711]]

    Comments: 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.

    Authority:  Section 203 of Section II: Adoption Opportunities of 
the Child Abuse Prevention and Treatment Act (CAPTA) (42 U.S.C. 
5113).

Molly B. Jones,
ACF/OPRE Certifying Officer.
[FR Doc. 2020-10906 Filed 5-19-20; 8:45 am]
BILLING CODE 4184-01-P