Submission for OMB Review; National Medical Support Notice-Part A, 33266-33267 [2019-14834]

Download as PDF 33266 Federal Register / Vol. 84, No. 134 / Friday, July 12, 2019 / Notices which is generally viewed as a faster payment alternative offered by those depository institutions. In addition, the FR 3066b attempts to collect comprehensive fraud data from P2P and money transfer processors, including those processors offering faster payment methods. The Board will retain the questions as written. Board of Governors of the Federal Reserve System, July 9, 2019. Michele Taylor Fennell, Assistant Secretary of the Board. [FR Doc. 2019–14874 Filed 7–11–19; 8:45 am] All employees of the Department of Energy, its predecessor agencies, and their contractors and subcontractors who worked at the Idaho National Laboratory (INL) in Scoville, Idaho, and who were monitored for external radiation at the Idaho Chemical Processing Plant (CPP) (e.g., at least one film badge or TLD dosimeter from CPP) between January 1, 1963, and February 28, 1970, for a number of work days aggregating at least 250 work days, occurring either solely under this employment, or in combination with work days within the parameters established for one or more other classes of employees in the Special Exposure Cohort. This designation will become effective on July 21, 2019, unless Congress provides otherwise prior to the effective date. After this effective date, HHS will publish a notice in the Federal Register reporting the addition of this class to the SEC or the result of any provision by Congress regarding the decision by HHS to add the class to the SEC. BILLING CODE 6210–01–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Centers for Disease Control and Prevention Designation of a Class of Employees for Addition to the Special Exposure Cohort Authority: 42 U.S.C. 7384q(b). 42 U.S.C. 7384l(14)(C). National Institute for Occupational Safety and Health (NIOSH), Centers for Disease Control and Prevention, Department of Health and Human Services (HHS). ACTION: Notice. [FR Doc. 2019–14816 Filed 7–11–19; 8:45 am] AGENCY: HHS gives notice of a decision to designate a class of employees from the Idaho National Laboratory in Scoville, Idaho, as an addition to the Special Exposure Cohort (SEC) under the Energy Employees Occupational Illness Compensation Program Act of 2000. FOR FURTHER INFORMATION CONTACT: Grady Calhoun, Director, Division of Compensation Analysis and Support, NIOSH, 1090 Tusculum Avenue, MS C– 46, Cincinnati, OH 45226–1938, Telephone 1–877–222–7570. Information requests can also be submitted by email to DCAS@CDC.GOV. SUPPLEMENTARY INFORMATION: On June 21, 2019, as provided for under 42 U.S.C. 7384l(14)(C), the Secretary of HHS designated the following class of employees as an addition to the SEC: SUMMARY: John J. Howard, Director, National Institute for Occupational Safety and Health. BILLING CODE 4163–19–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Administration for Children and Families Submission for OMB Review; National Medical Support Notice—Part A Office of Child Support Enforcement; Administration for Children and Families; HHS. ACTION: Request for public comment. AGENCY: The Administration for Children and Families (ACF) is requesting a three year extension of the form National Medical Support Notice (NMSN) Part A (OMB #0970–0222 expiration 8/31/2019). Changes were made to the form based on comments received during the 60 day Notice. SUMMARY: Comments due within 30 days of publication. 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. DATES: 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. 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. SUPPLEMENTARY INFORMATION: Description: The National Medical Support Notice (NMSN) is a two-part document completed by state child support enforcement agencies, employers, and health plan administrators to enforce health care coverage provisions in a child support order. The Department of Health and Human Services (DHHS) 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. The Administration for Children and Families is requesting that the NMSN Part A expiration dates continue to be synchronize with the expiration date of NMSN Part B submitted by DOL. Respondents: State child support enforcement agencies, employers, and health plan administrators. ADDRESSES: jbell on DSK3GLQ082PROD with NOTICES ANNUAL BURDEN ESTIMATES Instrument Respondents National Medical Support Notice—Part A—Notice to Withhold for Health Care Coverage. State .............. Employers ...... Estimated Total Annual Burden Hours: 1,644,725. VerDate Sep<11>2014 16:55 Jul 11, 2019 Jkt 247001 Annual number of respondents 54 1,275,624 Comments: The Department specifically requests comments on (a) whether the proposed collection of PO 00000 Frm 00049 Fmt 4703 Sfmt 4703 Number of responses per respondent 89,634 3.79 Average burden hours per response .17 .17 Annual burden hours 822,840 821,885 information is necessary for the proper performance of the functions of the agency, including whether the E:\FR\FM\12JYN1.SGM 12JYN1 Federal Register / Vol. 84, No. 134 / Friday, July 12, 2019 / Notices 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. Authorities: Section 466(a)(19) of the Social Security Act (42 U.S.C. 666(a)(19)), section 609(a)(5)(C) of the Employee Retirement Income Security Act of 1974 (ERISA) (29 U.S.C. 1169(a)(5)(C)), and for State and local government and church plans sections 401(e) and (f) of the Child Support Performance and Incentive Act of 1998 (29 CFR 2590.609–2). Mary B. Jones, ACF/OPRE Certifying Officer. [FR Doc. 2019–14834 Filed 7–11–19; 8:45 am] BILLING CODE 4184–14–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Food and Drug Administration [Docket No. FDA–2019–N–1346] Development of Antiviral Drugs for the Treatment of Adenoviral Infection in Immunocompromised Patients; Public Workshop; Cancellation AGENCY: Food and Drug Administration, HHS. ACTION: Notice. The Food and Drug Administration is announcing the cancellation of a public workshop entitled ‘‘Development of Antiviral Drugs for the Treatment of Adenoviral Infection in Immunocompromised Patients’’ that was previously scheduled for August 8, 2019, from 8:30 a.m. to 4:30 p.m. This public workshop was announced in the Federal Register of May 2, 2019. The meeting has been cancelled due to unforeseen changes in the adenovirus drug development landscape. SUMMARY: Lori Benner and/or Jessica Barnes, Center for Drug Evaluation and Research, Food and Drug Administration, 10903 New Hampshire Ave., Bldg. 22, Rm. 6221, Silver Spring, MD 20993–0002, 301– 796–1300, about this public workshop, which was announced in the Federal Register of May 2, 2019 (84 FR 18848). jbell on DSK3GLQ082PROD with NOTICES FOR FURTHER INFORMATION CONTACT: VerDate Sep<11>2014 16:55 Jul 11, 2019 Jkt 247001 Dated: July 8, 2019. Lowell J. Schiller, Principal Associate Commissioner for Policy. [FR Doc. 2019–14887 Filed 7–11–19; 8:45 am] BILLING CODE 4164–01–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Food and Drug Administration [Docket No. FDA–2019–D–2398] Population Pharmacokinetics; Revised Draft Guidance for Industry; Availability AGENCY: Food and Drug Administration, HHS. ACTION: Notice of availability. The Food and Drug Administration (FDA or Agency) is announcing the availability of a revised draft guidance for industry entitled ‘‘Population Pharmacokinetics.’’ This revised draft guidance assists sponsors in the application of population pharmacokinetics (population PK) during the drug development process to inform drug use and includes FDA’s current thinking on the data and model requirements for population PK analyses submitted as part of new drug applications (NDAs) and biologic license applications (BLAs). The revised draft guidance also provides expectations regarding the format and content of the population PK report as well as any labeling recommendations resulting from such analyses. DATES: Although you can comment on any guidance at any time (see 21 CFR 10.115(g)(5)), to ensure that the Agency considers your comment on this draft guidance before it begins work on the final version of the guidance, submit either electronic or written comments on the draft guidance by September 10, 2019. ADDRESSES: You may submit comments as follows: SUMMARY: Electronic Submissions Submit electronic comments in the following way: • Federal eRulemaking Portal: https://www.regulations.gov. Follow the instructions for submitting comments. Comments submitted electronically, including attachments, to https:// www.regulations.gov will be posted to 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 PO 00000 Frm 00050 Fmt 4703 Sfmt 4703 33267 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 https://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’’). Written/Paper Submissions Submit written/paper submissions as follows: • Mail/Hand Delivery/Courier (for written/paper submissions): Dockets Management Staff (HFA–305), Food and Drug Administration, 5630 Fishers Lane, Rm. 1061, Rockville, MD 20852. • For written/paper comments submitted to the Dockets Management Staff, 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 2019– D–2398 for ‘‘Population Pharmacokinetics.’’ Received comments will be placed in the docket and, except for those submitted as ‘‘Confidential Submissions,’’ publicly viewable at https://www.regulations.gov or at the Dockets Management Staff 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 https://www.regulations.gov. Submit both copies to the Dockets Management Staff. 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 E:\FR\FM\12JYN1.SGM 12JYN1

Agencies

[Federal Register Volume 84, Number 134 (Friday, July 12, 2019)]
[Notices]
[Pages 33266-33267]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2019-14834]


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DEPARTMENT OF HEALTH AND HUMAN SERVICES

Administration for Children and Families


Submission for OMB Review; National Medical Support Notice--Part 
A

AGENCY: Office of Child Support Enforcement; Administration for 
Children and Families; HHS.

ACTION: Request for public comment.

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

SUMMARY: The Administration for Children and Families (ACF) is 
requesting a three year extension of the form National Medical Support 
Notice (NMSN) Part A (OMB #0970-0222 expiration 8/31/2019). Changes 
were made to the form based on comments received during the 60 day 
Notice.

DATES: Comments due within 30 days of publication. 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.

ADDRESSES: 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: 
[email protected]. Attn: Desk Officer for the Administration 
for Children and Families.
    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: 
[email protected].

SUPPLEMENTARY INFORMATION:
    Description: The National Medical Support Notice (NMSN) is a two-
part document completed by state child support enforcement agencies, 
employers, and health plan administrators to enforce health care 
coverage provisions in a child support order. The Department of Health 
and Human Services (DHHS) 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.
    The Administration for Children and Families is requesting that the 
NMSN Part A expiration dates continue to be synchronize with the 
expiration date of NMSN Part B submitted by DOL.
    Respondents: State child support enforcement agencies, employers, 
and health plan administrators.

                                             Annual Burden Estimates
----------------------------------------------------------------------------------------------------------------
                                                  Annual  number     Number of        Average
         Instrument               Respondents           of         responses per   burden hours   Annual  burden
                                                    respondents     respondent     per response        hours
----------------------------------------------------------------------------------------------------------------
National Medical Support      State.............              54          89,634             .17         822,840
 Notice--Part A--Notice to
 Withhold for Health Care
 Coverage.
                              Employers.........       1,275,624            3.79             .17         821,885
----------------------------------------------------------------------------------------------------------------

    Estimated Total Annual Burden Hours: 1,644,725.
    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

[[Page 33267]]

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.
    Authorities: Section 466(a)(19) of the Social Security Act (42 
U.S.C. 666(a)(19)), section 609(a)(5)(C) of the Employee Retirement 
Income Security Act of 1974 (ERISA) (29 U.S.C. 1169(a)(5)(C)), and for 
State and local government and church plans sections 401(e) and (f) of 
the Child Support Performance and Incentive Act of 1998 (29 CFR 
2590.609-2).

Mary B. Jones,
ACF/OPRE Certifying Officer.
[FR Doc. 2019-14834 Filed 7-11-19; 8:45 am]
BILLING CODE 4184-14-P