Submission for OMB Review; Comment Request, 37600-37601 [2016-13682]

Download as PDF 37600 Federal Register / Vol. 81, No. 112 / Friday, June 10, 2016 / Notices submitter can resubmit the request with appropriate supporting documentation. • Scenario 4: When the HHA provides the treatment to the beneficiary and submits the claim to the MAC for payment without submitting a pre-claim review request, the home health claim will be stopped for prepayment review and documentation will be requested. If the claim is determined to be not medically necessary or not sufficiently documented, the claim will be denied and all current policies and procedures regarding liability for payment will apply. The HHA, the beneficiary, or both can appeal the claim denial if they believe the claim was payable. If the claim is determined to be payable on appeal, it will be paid. After the first 3 months of the demonstration, we will reduce payment by 25 percent for claims that after such prepayment review are deemed payable but did not first receive a pre-claim review decision. This payment reduction is not subject to appeal. After a claim is submitted, processed, and denied, appeal rights for the claim denial would become available in accordance with 42 CFR part 405, subpart I. The 25-percent payment reduction cannot be charged to the beneficiary. The beneficiary would not be liable for more than he or she would otherwise be if the demonstration were not in place. Additional information is available on the CMS’ Web site at https:// www.cms.gov/Research-Statistics-Dataand-Systems/Monitoring-Programs/ Medicare-FFS-Compliance-Programs/ Overview.html. III. Collection of Information Requirements asabaliauskas on DSK3SPTVN1PROD with NOTICES We announced and solicited comments for the information collection requirements associated with the Medicare Prior Authorization of Home Health Services Demonstration in a 60day Federal Register notice that published on February 5, 2016 (81 FR 6275). The information collection requirements do not take effect until they are approved by OMB and issued a valid OMB control number. Dated: May 26, 2016. Andrew M. Slavitt, Acting Administrator, Centers for Medicare & Medicaid Services. [FR Doc. 2016–13755 Filed 6–8–16; 4:15 pm] BILLING CODE 4120–01–P VerDate Sep<11>2014 19:02 Jun 09, 2016 Jkt 238001 DEPARTMENT OF HEALTH AND HUMAN SERVICES Administration for Children and Families [CFDA Number: 93.092] Announcing the Intent To Award Single-Source Expansion Supplement Grants to Two Personal Responsibility Education Program Innovative Strategies (PREIS) Grantees Family and Youth Services Bureau, ACYF, ACF. ACTION: This notice announces the intent to award single-source expansion supplement grants under the Personal Responsibility Education Program Innovative Strategies (PREIS) program to Children’s Hospital of Los Angeles in Los Angeles, CA and Education Development Center, Inc. in Newton, MA. AGENCY: The Administration for Children and Families (ACF), Administration on Children, Youth and Families (ACYF), Family and Youth Services Bureau (FYSB), Adolescent Pregnancy Prevention Program, announces its intent to award a singlesource expansion supplement grant of up to $151,265 to Children’s Hospital of Los Angeles and up to $55, 917.20 to Education Development Center, Inc. DATES: The period of support for the single-source expansion supplements is September 30, 2015, through September 29, 2016. FOR FURTHER INFORMATION CONTACT: LeBretia White, Program Manager, Adolescent Pregnancy Prevention Program, Division of Adolescent Development and Support, Family and Youth Services Bureau, 330 C Street SW., Washington, DC 20201. Telephone: 202–205–9605; Email: LeBretia.White@ acf.hhs.gov. SUPPLEMENTARY INFORMATION: Children’s Hospital of Los Angeles is funded under the Personal Responsibility Education Program Innovative Strategies (PREIS) program to adapt an existing evidencebased pregnancy prevention program for pregnant and parenting teens and rigorously evaluate the program for its impact on reducing repeat pregnancy. The supplemental award will be used to review, code, and analyze digital recordings, employ intensive tracking and follow up efforts with participants to administer the 36-month follow-up survey, conduct additional advanced analyses, develop manuscripts and briefs based on additional analyses, and disseminate study findings. Education Development Center, Inc. is funded under the Personal SUMMARY: PO 00000 Frm 00035 Fmt 4703 Sfmt 4703 Responsibility Education Program Innovative Strategies (PREIS) program to implement a parent education program for Latino youth (Salud y Exito/Health and Success) and to rigorously evaluate the intervention to determine impact on reducing sexual risk-taking behavior. The supplement award will be used to augment dissemination efforts for the intervention by developing a social media campaign to promote the intervention Web site and to analyze social media data to determine the campaign’s reach. Statutory Authority: The statutory authority for the award is Sec. 513 of the Social Security Act (42 U.S.C. 713). Sec. 2953 of the Patient Protection and Affordable Care Act of 2010 (Pub. L. 111–148) established PREP and funded it for FY 2010 through 2014. Sec. 206 of the Protecting Access to Medicare Act of 2014 (Pub. L. 113–93) extended that funding through FY 2015. Sec. 215 of the Medicare Access and CHIP Reauthorization Act of 2015 (Pub. L. 114–10) extended funding through FY 2017. Christopher Beach, Senior Grants Policy Specialist, Division of Grants Policy, Office of Administration, Administration for Children and Families. [FR Doc. 2016–13698 Filed 6–9–16; 8:45 am] BILLING CODE 8414–37–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Administration for Children and Families Submission for OMB Review; Comment Request Title: National Survey of Child and Adolescent Well-Being-Third Cohort (NSCAW III): Agency Recruitment. OMB No.: 0970–0202. Description: The Administration for Children and Families (ACF) within the U.S. Department of Health and Human Services (HHS) intends to collect data on a third cohort of children and families for the National Survey of Child and Adolescent Well-Being (NSCAW). NSCAW is the only source of nationally representative, longitudinal, firsthand information about the functioning and well-being, service needs, and service utilization of children and families who come to the attention of the child welfare system. The first two cohorts of NSCAW were collected beginning in 1999 and 2008 and studied children who had been the subject of investigation by Child Protective Services. Children were sampled from child welfare agencies nationwide. The proposed data collection plan for the third cohort of NSCAW includes two phases: Phase 1 includes child E:\FR\FM\10JNN1.SGM 10JNN1 37601 Federal Register / Vol. 81, No. 112 / Friday, June 10, 2016 / Notices welfare agency recruitment and collection of files for sampling children, and Phase 2 includes baseline data collection and an 18-month follow-up data collection. The current data collection plan calls for selecting a new cohort of 4,565 children and families and repeating similar data collection procedures as the previous two cohorts. This Notice is specific to Phase 1. The overall goal is to recruit child welfare agencies in 83 primary sampling units nationwide. Child welfare agencies will be selected with probability proportional to size, based on the current distributions in the child welfare system. Child welfare agency recruitment will include: mail, email, phone calls, and site visits with child welfare agency administrators. Respondents: Child welfare agency administrators and other personnel. Data collection will take place over a 2year period. ANNUAL BURDEN ESTIMATES Total number of respondents Instrument Information package for agency administrators .................. Initial call with agency staff .................................................. In-person visit with agency staff .......................................... Visit or call with agency staff explaining the sample file process ............................................................................. Agency staff monthly sample file generation and transmission ............................................................................. Estimated Total Annual Burden Hours: 795. Additional Information: Copies of the proposed collection may be obtained by writing to the Administration for Children and Families, Office of Planning, Research and Evaluation, 330 C Street, SW., Washington, DC 20201, Attn: OPRE Reports Clearance Officer. All requests should be identified by the title of the information collection. Email address: OPREinfocollection@ acf.hhs.gov. OMB Comment: OMB is required to make a decision concerning the collection of information between 30 and 60 days after publication of this document in the Federal Register. Therefore, a comment is best assured of having its full effect if OMB receives it within 30 days of publication. Written comments and recommendations for the proposed information collection should be sent directly to the following: Office of Management and Budget, Paperwork Reduction Project, Email: OIRA_ SUBMISSION@OMB.EOP.GOV, Attn: Desk Officer for the Administration for Children and Families. Robert Sargis, ACF Certifying Officer. [FR Doc. 2016–13682 Filed 6–9–16; 8:45 am] asabaliauskas on DSK3SPTVN1PROD with NOTICES BILLING CODE 4184–01–P Annual number of respondents 1 1 1 0.25 1 1 14 57 10 83 42 1 2 84 83 42 15 1 630 [Docket No. FDA–2016–N–0001] Arthritis Advisory Committee; Notice of Meeting Food and Drug Administration, HHS. Notice. The Food and Drug Administration (FDA) announces a forthcoming public advisory committee meeting of the Arthritis Advisory Committee. The general function of the committee is to provide advice and recommendations to the Agency on FDA’s regulatory issues. The meeting will be open to the public. DATES: The meeting will be held on July 13, 2016, from 7:30 a.m. to 5 p.m. ADDRESSES: FDA White Oak Campus, 10903 New Hampshire Ave., Bldg. 31, Conference Center, the Great Room (Rm. 1503), Silver Spring, MD 20993–0002. Answers to commonly asked questions including information regarding special accommodations due to a disability, visitor parking, and transportation may be accessed at: http://www.fda.gov/ AdvisoryCommittees/ AboutAdvisoryCommittees/ ucm408555.htm. SUMMARY: FOR FURTHER INFORMATION CONTACT: Moon Hee Choi, Center for Drug Evaluation and Research, Food and Drug Administration, 10903 New Hampshire Ave., Bldg. 31, Rm. 2417, Silver Spring, MD 20993–0002, 301– 796–9001, FAX: 301–847–8533, AAC@ fda.hhs.gov, or FDA Advisory Committee Information Line, 1–800– VerDate Sep<11>2014 19:02 Jun 09, 2016 Jkt 238001 PO 00000 Annual burden hours 57 57 10 Food and Drug Administration ACTION: Average burden hours per response 114 114 20 DEPARTMENT OF HEALTH AND HUMAN SERVICES AGENCY: Number of responses per respondent Frm 00036 Fmt 4703 Sfmt 4703 741–8138 (301–443–0572 in the Washington, DC area). A notice in the Federal Register about last minute modifications that impact a previously announced advisory committee meeting cannot always be published quickly enough to provide timely notice. Therefore, you should always check the Agency’s Web site at http:// www.fda.gov/AdvisoryCommittees/ default.htm and scroll down to the appropriate advisory committee meeting link, or call the advisory committee information line to learn about possible modifications before coming to the meeting. SUPPLEMENTARY INFORMATION: Agenda: The committee will discuss biologics license application 761042, for GP2015, a proposed biosimilar to Amgen Inc.’s ENBREL (etanercept) submitted by Sandoz, Inc. The proposed indications (uses) for this product are: (1) Reducing signs and symptoms, inducing major clinical response, inhibiting the progression of structural damage, and improving physical function in patients with moderately to severely active rheumatoid arthritis (in combination with methotrexate (MTX) or used alone); (2) reducing signs and symptoms of moderately to severely active polyarticular juvenile idiopathic arthritis in patients ages 2 and older; (3) reducing signs and symptoms, inhibiting the progression of structural damage of active arthritis, and improving physical function in patients with psoriatic arthritis (in combination with MTX in patients who do not respond adequately to MTX alone); (4) reducing signs and symptoms in patients with active ankylosing spondylitis; and (5) treatment of adult patients (18 years or older) with chronic E:\FR\FM\10JNN1.SGM 10JNN1

Agencies

[Federal Register Volume 81, Number 112 (Friday, June 10, 2016)]
[Notices]
[Pages 37600-37601]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2016-13682]


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

DEPARTMENT OF HEALTH AND HUMAN SERVICES

Administration for Children and Families


Submission for OMB Review; Comment Request

    Title: National Survey of Child and Adolescent Well-Being-Third 
Cohort (NSCAW III): Agency Recruitment.
    OMB No.: 0970-0202.
    Description: The Administration for Children and Families (ACF) 
within the U.S. Department of Health and Human Services (HHS) intends 
to collect data on a third cohort of children and families for the 
National Survey of Child and Adolescent Well-Being (NSCAW). NSCAW is 
the only source of nationally representative, longitudinal, firsthand 
information about the functioning and well-being, service needs, and 
service utilization of children and families who come to the attention 
of the child welfare system. The first two cohorts of NSCAW were 
collected beginning in 1999 and 2008 and studied children who had been 
the subject of investigation by Child Protective Services. Children 
were sampled from child welfare agencies nationwide.
    The proposed data collection plan for the third cohort of NSCAW 
includes two phases: Phase 1 includes child

[[Page 37601]]

welfare agency recruitment and collection of files for sampling 
children, and Phase 2 includes baseline data collection and an 18-month 
follow-up data collection. The current data collection plan calls for 
selecting a new cohort of 4,565 children and families and repeating 
similar data collection procedures as the previous two cohorts. This 
Notice is specific to Phase 1. The overall goal is to recruit child 
welfare agencies in 83 primary sampling units nationwide. Child welfare 
agencies will be selected with probability proportional to size, based 
on the current distributions in the child welfare system. Child welfare 
agency recruitment will include: mail, email, phone calls, and site 
visits with child welfare agency administrators.
    Respondents: Child welfare agency administrators and other 
personnel. Data collection will take place over a 2-year period.

                                             Annual Burden Estimates
----------------------------------------------------------------------------------------------------------------
                                                  Annual  number     Number of        Average
           Instrument              Total number         of         responses per   burden hours    Annual burden
                                  of respondents    respondents     respondent     per response        hours
----------------------------------------------------------------------------------------------------------------
Information package for agency               114              57               1            0.25              14
 administrators.................
Initial call with agency staff..             114              57               1               1              57
In-person visit with agency                   20              10               1               1              10
 staff..........................
Visit or call with agency staff               83              42               1               2              84
 explaining the sample file
 process........................
Agency staff monthly sample file              83              42              15               1             630
 generation and transmission....
----------------------------------------------------------------------------------------------------------------

    Estimated Total Annual Burden Hours: 795.
    Additional Information: Copies of the proposed collection may be 
obtained by writing to the Administration for Children and Families, 
Office of Planning, Research and Evaluation, 330 C Street, SW., 
Washington, DC 20201, Attn: OPRE Reports Clearance Officer. All 
requests should be identified by the title of the information 
collection. Email address: OPREinfocollection@acf.hhs.gov.
    OMB Comment: OMB is required to make a decision concerning the 
collection of information between 30 and 60 days after publication of 
this document in the Federal Register. Therefore, a comment is best 
assured of having its full effect if OMB receives it within 30 days of 
publication. Written comments and recommendations for the proposed 
information collection should be sent directly to the following: Office 
of Management and Budget, Paperwork Reduction Project, Email: 
OIRA_SUBMISSION@OMB.EOP.GOV, Attn: Desk Officer for the Administration 
for Children and Families.

Robert Sargis,
ACF Certifying Officer.
[FR Doc. 2016-13682 Filed 6-9-16; 8:45 am]
 BILLING CODE 4184-01-P