Submission for OMB Review; Comment Request, 41543-41544 [2016-15046]

Download as PDF 41543 Federal Register / Vol. 81, No. 123 / Monday, June 27, 2016 / Notices 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. 2016–15116 Filed 6–24–16; 8:45 am] BILLING CODE 4163–18–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Administration for Children and Families Submission for OMB Review; Comment Request Title: ACF–OGM–PPR-Form B— Program Indicators. OMB No.: 0970–0406. Description: The Office of Grants Management (OGM), in the Administration for Children and families (ACF) is proposing the collection of program performance data for ACF’s discretionary grantees. To collect this data OGM has developed a form from the basic template of the OMB-approved reporting format of the Program Performance Report. OGM will use this data to determine if grantees are proceeding in a satisfactory manner in meeting the approved goals and objectives of the project, and if funding should be continued for another budget period. The requirement for grantees to report on performance is OMB grants policy. Specific citations are contained in: (1) 2 CFR 215 Uniform Administrative Requirements, cost Principles, and Audit Requirements for Federal Awards and (2) 45 CFR 75, Uniform Administrative Requirements, Cost Principles, and Audit Requirements for Department of Health and Human Services Awards. Respondents: All ACF Discretionary Grantees. State governments, Native American Tribal governments, Native American Tribal Organizations, Local Governments, and Nonprofits with or without 501 (c)(3) status with the IRS. ANNUAL BURDEN ESTIMATES Instrument Number of respondents Number of responses per respondent Average burden hours per response Total burden hours ACF–OGM–PPR–B ......................................................................................... 6000 1 1 6000 Estimated Total Annual Burden Hours: 6000. 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, 370 L’Enfant Promenade, SW., Washington, DC 20447, Attn: ACF Reports Clearance Officer. All requests should be identified by the title of the information collection. Email address: infocollection@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, Reports Clearance Officer. [FR Doc. 2016–15094 Filed 6–24–16; 8:45 am] BILLING CODE 4184–01–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Administration for Children and Families Submission for OMB Review; Comment Request Title: National Medical Support Notice OMB No.: 0970–0222 Description: The National Medical Support Notice (NMSN) is a two-part document that requires information from State child support enforcement agencies, employers, and health plan administrators to assist in enforcing health care coverage provisions in a child support order. The Department of Health and Human Services (DHHS), Administration for Children and Families (ACF) developed and maintains part A of the NMSN, which is sent to an obligor’s employer for completion; the Department of Labor (DOL) developed and maintains part B of the NMSN, which is provided to health care administrators following completion of part A. DOL revised part B to conform with changes to the currently approved part A and is seeking a three-year approval from OMB. To avoid burdening the State child support enforcement agencies with potential reprogramming at varying times due to future changes in part A or B, ACF is resubmitting an unchanged information collection package and requesting an extension to the current OMB approval of NMSN part A to synchronize the expiration date with NMSN part B. Respondents: State child support enforcement agencies, employers, and health plan administrators. ANNUAL BURDEN ESTIMATES mstockstill on DSK3G9T082PROD with NOTICES Instrument Number of respondents Number of responses per respondent Average burden hours per response Total burden hours National Medical Support Notice–Part A ......................................................... 54 76,499 .17 hours 702,261 Estimated Total Annual Burden Hours: 702,261. VerDate Sep<11>2014 18:52 Jun 24, 2016 Jkt 238001 Additional Information: Copies of the proposed collection may be obtained by PO 00000 Frm 00036 Fmt 4703 Sfmt 4703 writing to the Administration for Children and Families, Office of E:\FR\FM\27JNN1.SGM 27JNN1 41544 Federal Register / Vol. 81, No. 123 / Monday, June 27, 2016 / Notices Planning, Research and Evaluation, 330 C Street SW., Washington, DC 20201. Attention Reports Clearance Officer. All requests should be identified by the title of the information collection. Email address: infocollection@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. the docket unchanged. Because your comment will be made public, you are solely responsible for ensuring that your comment does not include any confidential information that you or a third party may not wish to be posted, such as medical information, your or anyone else’s Social Security number, or confidential business information, such as a manufacturing process. Please note that if you include your name, contact information, or other information that identifies you in the body of your comments, that information will be posted on http://www.regulations.gov. • If you want to submit a comment with confidential information that you do not wish to be made available to the public, submit the comment as a written/paper submission and in the manner detailed (see ‘‘Written/Paper Submissions’’ and ‘‘Instructions’’). Robert Sargis, Reports Clearance Officer. Written/Paper Submissions Submit written/paper submissions as follows: • Mail/Hand delivery/Courier (for written/paper submissions): Division of Dockets Management (HFA–305), Food and Drug Administration, 5630 Fishers Lane, Rm. 1061, Rockville, MD 20852. • For written/paper comments submitted to the Division of Dockets Management, FDA will post your comment, as well as any attachments, except for information submitted, marked and identified, as confidential, if submitted as detailed in ‘‘Instructions.’’ Instructions: All submissions received must include the Docket No. FDA– 2016–D–1174 for ‘‘Special Protocol Assessment; Draft Guidance for Industry.’’ Received comments will be placed in the docket and, except for those submitted as ‘‘Confidential Submissions,’’ publicly viewable at http://www.regulations.gov or at the Division of Dockets Management between 9 a.m. and 4 p.m., Monday through Friday. • Confidential Submissions—To submit a comment with confidential information that you do not wish to be made publicly available, submit your comments only as a written/paper submission. You should submit two copies total. One copy will include the information you claim to be confidential with a heading or cover note that states ‘‘THIS DOCUMENT CONTAINS CONFIDENTIAL INFORMATION.’’ The Agency will review this copy, including the claimed confidential information, in its consideration of comments. The second copy, which will have the claimed confidential information redacted/blacked out, will be available for public viewing and posted on http:// [FR Doc. 2016–15046 Filed 6–24–16; 8:45 am] BILLING CODE 4184–01–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Food and Drug Administration [Docket No. FDA–2016–D–1174] Special Protocol Assessment; Draft Guidance for Industry; Extension of the Comment Period AGENCY: Food and Drug Administration, HHS. Notice; extension of the comment period. ACTION: The Food and Drug Administration (FDA or we) is extending the comment period for the notice of availability, published in the Federal Register of May 4, 2016 (81 FR 26799), announcing the draft guidance for industry entitled ‘‘Special Protocol Assessment.’’ We are taking this action due to maintenance on the Federal eRulemaking portal from July 1 through July 5, 2016. DATES: Submit either electronic or written comments by July 19, 2016. ADDRESSES: You may submit comments as follows: SUMMARY: mstockstill on DSK3G9T082PROD with NOTICES Electronic Submissions Submit electronic comments in the following way: • Federal eRulemaking Portal: http:// www.regulations.gov. Follow the instructions for submitting comments. Comments submitted electronically, including attachments, to http:// www.regulations.gov will be posted to VerDate Sep<11>2014 18:52 Jun 24, 2016 Jkt 238001 PO 00000 Frm 00037 Fmt 4703 Sfmt 9990 www.regulations.gov. Submit both copies to the Division of Dockets Management. If you do not wish your name and contact information to be made publicly available, you can provide this information on the cover sheet and not in the body of your comments and you must identify this information as ‘‘confidential.’’ Any information marked as ‘‘confidential’’ will not be disclosed except in accordance with 21 CFR 10.20 and other applicable disclosure law. For more information about FDA’s posting of comments to public dockets, see 80 FR 56469, September 18, 2015, or access the information at: http://www.fda.gov/ regulatoryinformation/dockets/ default.htm. Docket: For access to the docket to read background documents or the electronic and written/paper comments received, go to http:// www.regulations.gov and insert the docket number, found in brackets in the heading of this document, into the ‘‘Search’’ box and follow the prompts and/or go to the Division of Dockets Management, 5630 Fishers Lane, Rm. 1061, Rockville, MD 20852. FOR FURTHER INFORMATION CONTACT: Amalia Himaya, Center for Drug Evaluation and Research, Food and Drug Administration, 10903 New Hampshire Ave., Bldg. 22, Rm. 6439, Silver Spring, MD 20993–0002, 301– 796–0700; or Stephen Ripley, Center for Biologics Evaluation and Research, Food and Drug Administration, 10903 New Hampshire Ave., Bldg. 71, Rm. 3128, Silver Spring, MD 20993–0002, 240–402–7911. In the Federal Register of May 4, 2016 (81 FR 26799), FDA published a notice of availability. Interested persons were originally given until July 5, 2016, to comment on the draft guidance for industry entitled ‘‘Special Protocol Assessment.’’ From July 1 through July 5, 2016, the Federal eRulemaking Portal, http:// www.regulations.gov, is undergoing maintenance. We are, therefore, extending the comment period for the draft guidance for industry entitled ‘‘Special Protocol Assessment.’’ The extended comment period will close on July 19, 2016. SUPPLEMENTARY INFORMATION: Dated: June 21, 2016. Leslie Kux, Associate Commissioner for Policy. [FR Doc. 2016–15106 Filed 6–24–16; 8:45 am] BILLING CODE 4164–01–P E:\FR\FM\27JNN1.SGM 27JNN1

Agencies

[Federal Register Volume 81, Number 123 (Monday, June 27, 2016)]
[Notices]
[Pages 41543-41544]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2016-15046]


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DEPARTMENT OF HEALTH AND HUMAN SERVICES

Administration for Children and Families


Submission for OMB Review; Comment Request

    Title: National Medical Support Notice
    OMB No.: 0970-0222
    Description: The National Medical Support Notice (NMSN) is a two-
part document that requires information from State child support 
enforcement agencies, employers, and health plan administrators to 
assist in enforcing health care coverage provisions in a child support 
order. The Department of Health and Human Services (DHHS), 
Administration for Children and Families (ACF) developed and maintains 
part A of the NMSN, which is sent to an obligor's employer for 
completion; the Department of Labor (DOL) developed and maintains part 
B of the NMSN, which is provided to health care administrators 
following completion of part A.
    DOL revised part B to conform with changes to the currently 
approved part A and is seeking a three-year approval from OMB. To avoid 
burdening the State child support enforcement agencies with potential 
reprogramming at varying times due to future changes in part A or B, 
ACF is resubmitting an unchanged information collection package and 
requesting an extension to the current OMB approval of NMSN part A to 
synchronize the expiration date with NMSN part B.
    Respondents: State child support enforcement agencies, employers, 
and health plan administrators.

                                             Annual Burden Estimates
----------------------------------------------------------------------------------------------------------------
                                                                  Number of     Average  burden
                 Instrument                      Number of      responses per      hours  per     Total  burden
                                                respondents       respondent        response          hours
----------------------------------------------------------------------------------------------------------------
National Medical Support Notice-Part A......              54           76,499        .17 hours          702,261
----------------------------------------------------------------------------------------------------------------

    Estimated Total Annual Burden Hours: 702,261.
    Additional Information: Copies of the proposed collection may be 
obtained by writing to the Administration for Children and Families, 
Office of

[[Page 41544]]

Planning, Research and Evaluation, 330 C Street SW., Washington, DC 
20201. Attention Reports Clearance Officer. All requests should be 
identified by the title of the information collection. Email address: 
infocollection@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,
Reports Clearance Officer.
[FR Doc. 2016-15046 Filed 6-24-16; 8:45 am]
 BILLING CODE 4184-01-P