Proposed Information Collection Activity; Comment Request, 73196-73197 [2013-29083]

Download as PDF 73196 Federal Register / Vol. 78, No. 234 / Thursday, December 5, 2013 / Notices PURPOSE(S) OF THE MATCHING PROGRAM: The purpose of this computer matching agreement is to establish the conditions, safeguards and procedures under which the CMS and PC@HAC will conduct a computer-matching program to determine entitlement to CHAMPVA benefits. Under the terms of this matching agreement, PC@HAC will provide to CMS a list of social security numbers (SSN) for all CHAMPVA eligible beneficiaries who may also be eligible for Medicare benefits. This information is maintained in PC@HAC’s System of Records (SOR) entitled ‘‘Health Administration Center Civilian Health and Medical Program RecordsVA.’’ CMS agrees to conduct a computer match of the SSNs of beneficiaries provided by PC@HAC against the information found in CMS’s Enrollment Database (EDB) SOR. PC@HAC will receive the results of the computer match in order to determine a beneficiary’s eligibility for care under CHAMPVA. CATEGORIES OF RECORDS AND INDIVIDUALS COVERED BY THE MATCH: ehiers on DSK2VPTVN1PROD with NOTICES DESCRIPTION OF RECORDS TO BE USED IN THE MATCHING PROGRAM: A. Systems of Records 1. Records Maintained by PC@HAC The information used in this matching program is maintained in the PC@HAC system identified as 54VA16, entitled ‘‘Health Administration Center Civilian Health and Medical Program 13:57 Dec 04, 2013 Jkt 232001 INCLUSIVE DATES OF THE MATCH: The CMP shall become effective no sooner than 40 days after the report of the Matching Program is sent to OMB and Congress, or 30 days after publication in the Federal Register, whichever is later. The matching program will continue for 18 months from the effective date and may be extended for an additional 12 months thereafter, if certain conditions are met. [FR Doc. 2013–29066 Filed 12–4–13; 8:45 am] Upon establishment of the CHAMPVA program under Public Law 93–82, CHAMPVA entitlement will be terminated when any individual becomes eligible for Medicare Part A (Hospital Insurance) on a non-premium basis. Public Law 94–581 provided for reinstatement of CHAMPVA as second payer for beneficiaries aged 65 and over who exhausted a period of Medicare Part A (Hospital Insurance). These beneficiaries must also be enrolled in Medicare Part B (Medical Insurance) in order to retain their CHAMPVA entitlement. Public Law 102–190 extended CHAMPVA benefit to age 65 for any beneficiary eligible for Medicare Part A on the basis of disability/end stage renal disease (ESRD) only if that individual is also enrolled in Medicare Part B. Public Law 107–14 provided for extending benefit coverage for beneficiaries over the age of 65 years if the beneficiary is in receipt of Medicare Part A and Medicare Part B. VerDate Mar<15>2010 Records-VA,’’ last published at 68 Fed. Reg. 53784 (September 12, 2003). SSNs of CHAMPVA beneficiaries will be released to CMS pursuant to the routine use number 21 as set forth in the system notice. 2. Records Maintained by CMS The matching program will be conducted with data maintained by CMS in the EDB, System No. 09–70– 0502, published at 73 Fed. Reg. 10249 (February 26, 2008). Matched data will be released to PC@HAC pursuant to the routine use number 2 as set forth in the system notice. BILLING CODE 4120–03–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Administration for Children and Families Proposed Information Collection Activity; Comment Request Proposed Projects Title: Child and Family Services Plan (CFSP), Annual Progress and Services Review (APSR), and Annual Budget Expenses Request and Estimated Expenditures (CFS–101). OMB No.: 0970–0426. Description: Under title IV–B, subparts 1 and 2, of the Social Security Act (the Act), States, Territories, and Tribes are required to submit a Child and Family Services Plan (CFSP). The CFSP lays the groundwork for a system of coordinated, integrated, and culturally relevant family services for the subsequent five years (45 CFR 1357.15(a)(1)). The CFSP outlines initiatives and activities the State, Tribe or territory will carry out in administering programs and services to promote the safety, permanency, and well-being of children and families. By June 30 of each year, States, Territories, and Tribes are also required to submit PO 00000 Frm 00011 Fmt 4703 Sfmt 4703 an Annual Progress and Services Report (APSR) and a financial report called the CFS–101. The APSR is a Yearly report that discusses progress made by a State, Territory or Tribe in accomplishing the goals and objectives cited in its CFSP (45 CFR 1357.16(a)). The APSR contains new and updated information about service needs and organizational capacities throughout the five-year plan period. The CFS–101 has three parts. Part I is an annual budget request for the upcoming fiscal year. Part II includes a summary of planned expenditures by program area for the upcoming fiscal year, the estimated number of individuals or families to be served, and the geographical service area. Part III includes actual expenditures by program area, numbers of families and individuals served by program area, and the geographic areas served for the last complete fiscal year. The Child and Family Services Improvement Act of 2006 amended Title IV–B, subparts 1 and 2, adding a number of requirements that affect reporting through the APSR and the CFS–101. Of particular note, the law added a provision requiring States (including Puerto Rico and the District of Columbia) to report data on caseworker visits (section 424(e) of the Act). States must provide annual data on 1) the percentage of children in foster care under the responsibility of the State who were visited on a monthly basis by the caseworker handling the case of the child; and 2) the percentage of the visits that occurred in the residence of the child. In addition, by June 30, 2008, States must set target percentages and establish strategies to meet the goal that; by October 1, 2011; at least 90 percent of the children in foster care are visited by their caseworkers on a monthly basis and that the majority of these visits occur in the residence of the child (section 424(e)(2)(A) of the Act). Respondents: States, Territories, and Tribes must complete the CFSP, APSR, and CFS–101. Tribes and territories are exempted from the monthly caseworker visits reporting requirement of the APSR. There are approximately 180 Tribal entities that are eligible for IV–B funding. There are 52 States (including Puerto Rico and the District of Columbia) that must complete the CFSP, APSR, and CFS–101. There are a total of 232 possible respondents. E:\FR\FM\05DEN1.SGM 05DEN1 Federal Register / Vol. 78, No. 234 / Thursday, December 5, 2013 / Notices 73197 ANNUAL BURDEN ESTIMATES Number of respondents Instrument Number of responses per respondent Average burden hours per response Total burden hours APSR ............................................................................................................. CFSP ............................................................................................................. CFS–101, Parts I, II, and III .......................................................................... Caseworker Visits .......................................................................................... 232 232 232 52 1 1 1 1 76.58 120.25 4.38 99.33 17,766.56 27,898 1,016.16 5,165.16 Estimated Total Annual Burden Hours: .................................................. ........................ ........................ ........................ 51,845.88 In compliance with the requirements of Section 506(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, 370 L’Enfant Promenade SW., Washington, DC 20447, 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. Robert Sargis, Reports Clearance Officer. [FR Doc. 2013–29083 Filed 12–4–13; 8:45 am] ehiers on DSK2VPTVN1PROD with NOTICES BILLING CODE 4184–01–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Food and Drug Administration [Docket No. FDA–2013–N–0823] Agency Information Collection Activities; Submission for Office of Management and Budget Review; Comment Request; Over-the-Counter Drugs; Labeling Requirements 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: Fax written comments on the collection of information by January 6, 2014. ADDRESSES: 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 0910–0340. Also include the FDA docket number found in brackets in the heading of this document. SUMMARY: FDA PRA Staff, Office of Operations, Food and Drug Administration, 1350 Piccard Dr., PI50–400B, Rockville, MD 20850, PRAStaff@fda.hhs.gov. SUPPLEMENTARY INFORMATION: In compliance with 44 U.S.C. 3507, FDA has submitted the following proposed collection of information to OMB for review and clearance. FOR FURTHER INFORMATION CONTACT: Over-the-Counter Drugs; Labeling Requirements—(OMB Control Number 0910–0340)—Extension In the Federal Register of March 17, 1999, (64 FR 13254) (the 1999 labeling VerDate Mar<15>2010 13:57 Dec 04, 2013 Jkt 232001 PO 00000 Frm 00012 Fmt 4703 Sfmt 4703 final rule), we amended our regulations governing requirements for human drug products to establish standardized format and content requirements for the labeling of all marketed over-thecounter (OTC) drug products in part 201 (21 CFR part 201). The regulations in part 201 require OTC drug product labeling to include uniform headings and subheadings, presented in a standardized order, with minimum standards for type size and other graphical features. Specifically, the 1999 labeling final rule added new § 201.66 (21 CFR 201.66) to part 201. Section 201.66 sets content and format requirements for the Drug Facts portion of labels on OTC drug products. On June 20, 2000 (65 FR 38191), we published a Federal Register final rule that required all OTC drug products marketed under the OTC monograph system to comply with the labeling requirements in § 201.66 by May 16, 2005, or sooner (65 FR 38191 at 38193). Currently marketed OTC drug products are already required to be in compliance with these labeling requirements, and thus will incur no further burden to comply with Drug Facts labeling requirements in § 201.66. Modifications of labeling already required to be in Drug Facts format are usual and customary as part of routine redesign practice, and thus do not create additional burden within the meaning of the Paperwork Reduction Act of 1995 (the PRA). Therefore, the burden to comply with the labeling requirements in § 201.66 is a one-time burden applicable only to new OTC drug products introduced to the marketplace under new drug applications, abbreviated new drug applications, or an OTC drug monograph, except for products in ‘‘convenience size’’ packages.1 New OTC drug products 1 In a final rule published in the Federal Register of April 5, 2002 (67 FR 16304), the Agency delayed the compliance dates for the 1999 labeling final rule for all OTC drug products that: (1) Contain no more than two doses of an OTC drug; and (2) because of their limited available labeling space, would require more than 60 percent of the total surface area available to bear labeling to meet the requirements E:\FR\FM\05DEN1.SGM Continued 05DEN1

Agencies

[Federal Register Volume 78, Number 234 (Thursday, December 5, 2013)]
[Notices]
[Pages 73196-73197]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2013-29083]


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DEPARTMENT OF HEALTH AND HUMAN SERVICES

Administration for Children and Families


Proposed Information Collection Activity; Comment Request

Proposed Projects

    Title: Child and Family Services Plan (CFSP), Annual Progress and 
Services Review (APSR), and Annual Budget Expenses Request and 
Estimated Expenditures (CFS-101).
    OMB No.: 0970-0426.
    Description: Under title IV-B, subparts 1 and 2, of the Social 
Security Act (the Act), States, Territories, and Tribes are required to 
submit a Child and Family Services Plan (CFSP). The CFSP lays the 
groundwork for a system of coordinated, integrated, and culturally 
relevant family services for the subsequent five years (45 CFR 
1357.15(a)(1)). The CFSP outlines initiatives and activities the State, 
Tribe or territory will carry out in administering programs and 
services to promote the safety, permanency, and well-being of children 
and families. By June 30 of each year, States, Territories, and Tribes 
are also required to submit an Annual Progress and Services Report 
(APSR) and a financial report called the CFS-101. The APSR is a Yearly 
report that discusses progress made by a State, Territory or Tribe in 
accomplishing the goals and objectives cited in its CFSP (45 CFR 
1357.16(a)). The APSR contains new and updated information about 
service needs and organizational capacities throughout the five-year 
plan period. The CFS-101 has three parts. Part I is an annual budget 
request for the upcoming fiscal year. Part II includes a summary of 
planned expenditures by program area for the upcoming fiscal year, the 
estimated number of individuals or families to be served, and the 
geographical service area. Part III includes actual expenditures by 
program area, numbers of families and individuals served by program 
area, and the geographic areas served for the last complete fiscal 
year.
    The Child and Family Services Improvement Act of 2006 amended Title 
IV-B, subparts 1 and 2, adding a number of requirements that affect 
reporting through the APSR and the CFS-101. Of particular note, the law 
added a provision requiring States (including Puerto Rico and the 
District of Columbia) to report data on caseworker visits (section 
424(e) of the Act). States must provide annual data on 1) the 
percentage of children in foster care under the responsibility of the 
State who were visited on a monthly basis by the caseworker handling 
the case of the child; and 2) the percentage of the visits that 
occurred in the residence of the child. In addition, by June 30, 2008, 
States must set target percentages and establish strategies to meet the 
goal that; by October 1, 2011; at least 90 percent of the children in 
foster care are visited by their caseworkers on a monthly basis and 
that the majority of these visits occur in the residence of the child 
(section 424(e)(2)(A) of the Act).
    Respondents: States, Territories, and Tribes must complete the 
CFSP, APSR, and CFS-101. Tribes and territories are exempted from the 
monthly caseworker visits reporting requirement of the APSR. There are 
approximately 180 Tribal entities that are eligible for IV-B funding. 
There are 52 States (including Puerto Rico and the District of 
Columbia) that must complete the CFSP, APSR, and CFS-101. There are a 
total of 232 possible respondents.

[[Page 73197]]



                                             Annual Burden Estimates
----------------------------------------------------------------------------------------------------------------
                                                                     Number of        Average
                   Instrument                        Number of     responses per   burden hours    Total burden
                                                    respondents     respondent     per response        hours
----------------------------------------------------------------------------------------------------------------
APSR............................................             232               1           76.58       17,766.56
CFSP............................................             232               1          120.25       27,898
CFS-101, Parts I, II, and III...................             232               1            4.38        1,016.16
Caseworker Visits...............................              52               1           99.33        5,165.16
                                                 ---------------------------------------------------------------
    Estimated Total Annual Burden Hours:........  ..............  ..............  ..............       51,845.88
----------------------------------------------------------------------------------------------------------------

    In compliance with the requirements of Section 506(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, 370 L'Enfant Promenade SW., 
Washington, DC 20447, 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.

Robert Sargis,
Reports Clearance Officer.
[FR Doc. 2013-29083 Filed 12-4-13; 8:45 am]
BILLING CODE 4184-01-P