Submission for OMB Review; Information Comparison With Insurance Data (OMB #0970-0342), 68885-68886 [2020-24141]

Download as PDF 68885 Federal Register / Vol. 85, No. 211 / Friday, October 30, 2020 / Notices To obtain copies of a supporting statement and any related forms for the proposed collection(s) summarized in this notice, you may make your request using one of following: 1. Access CMS’ website address at website address at https://www.cms.gov/ Regulations-and-Guidance/Legislation/ PaperworkReductionActof1995/PRAListing.html. 2. Call the Reports Clearance Office at (410) 786–1326. FOR FURTHER INFORMATION CONTACT: William N. Parham at (410) 786–4669. SUPPLEMENTARY INFORMATION: Contents This notice sets out a summary of the use and burden associated with the following information collections. More detailed information can be found in each collection’s supporting statement and associated materials (see ADDRESSES). CMS–381 Identification of Extension Units of Medicare Approved Outpatient Physical Therapy/ Outpatient Speech Pathology (OPT/ OSP) Providers and Supporting Regulations Under the PRA (44 U.S.C. 3501– 3520), federal agencies must obtain approval from the Office of Management and Budget (OMB) for each collection of information they conduct or sponsor. The term ‘‘collection of information’’ is defined in 44 U.S.C. 3502(3) and 5 CFR 1320.3(c) and includes agency requests or requirements that members of the public submit reports, keep records, or provide information to a third party. Section 3506(c)(2)(A) of the PRA requires federal agencies to publish a 60-day notice in the Federal Register concerning each proposed collection of information, including each proposed extension or reinstatement of an existing collection of information, before submitting the collection to OMB for approval. To comply with this requirement, CMS is publishing this notice. Information Collection 1. Type of Information Collection Request: Revision of a currently approved collection; Title of Information Collection: Identification of Extension Units of Medicare Approved Outpatient Physical Therapy/Outpatient Speech Pathology (OPT/OSP) Providers and Supporting Regulations; Use: Form CMS–381 was developed to ensure that each OPT/OSP extension location at which OPT/OSP providers furnish services, must be reported by the providers to the State Survey Agencies (SAs). Form CMS–381 is completed when: (1) New OPT/OSP providers enter the Medicare program; (2) when existing OPT/OPS providers delete or add a service, or close or add an extension location; or, (3) when existing OPT/OSP providers are recertified by the State Survey Agency every 6 years. Form Number: CMS–381 (OMB control number: 0938–0273); Frequency: Occasionally; Affected Public: Private Sector; Business or other for-profit and not-for-profit institutions; Number of Respondents: 2,083; Total Annual Responses: 443; Total Annual Hours: 111. (For policy questions regarding this collection contact Caroline Gallaher at 410–786–8705.) Dated: October 27, 2020. William N. Parham, III, Director, Paperwork Reduction Staff, Office of Strategic Operations and Regulatory Affairs. [FR Doc. 2020–24132 Filed 10–29–20; 8:45 am] BILLING CODE 4120–01–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Administration for Children and Families Submission for OMB Review; Information Comparison With Insurance Data (OMB #0970–0342) Office of Child Support Enforcement, Administration for Children and Families, HHS. ACTION: Request for Public Comment. AGENCY: The Administration for Children and Families’ (ACF) Office of Child Support Enforcement (OCSE) is requesting a 3-year extension of the currently approved Information Comparison with Insurance Data (OMB #0970–0342; Expires 1/31/2021). DATES: Comments due within 30 days of publication. OMB is required to make a SUMMARY: 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 within 30 days of publication of this notice to www.reginfo.gov/public/do/ PRAMain. Find this particular information collection by selecting ‘‘Currently under 30-day Review—Open for Public Comments’’ or by using the search function. ADDRESSES: SUPPLEMENTARY INFORMATION: Description: The Deficit Reduction Act of 2005 amended Section 452 of the Social Security Act to authorize the Secretary, through the Federal Parent Locator Service (FPLS), to conduct comparisons of information concerning individuals owing past-due child support with information maintained by insurers (or their agents) concerning insurance claims, settlements, awards, and payments. The two options to participate in the Information Comparison with Insurance Data program are (1) insurers submit information concerning claims, settlements, awards, and payments to the federal OCSE. OCSE compares it to information pertaining to parents who owe past-due support. (2) OCSE will send a file containing information about parents who owe past-due support to the insurer, or their agent, to compare with their claims, settlements, awards, and payments. The insurer or their agent sends any resulting insurance data matches to OCSE. On a daily basis, OCSE sends the results of the insurance data match in an ‘‘Insurance Match Response Record’’ to child support agencies responsible for collecting pastdue support. The child support agencies use the insurance data matches to collect past-due support from the insurance proceeds. Respondents: Insurers or their agents, including the U.S. Department of Labor and state agencies administering workers’ compensation programs, and the Insurance Services Office. jbell on DSKJLSW7X2PROD with NOTICES ANNUAL BURDEN ESTIMATES Total number of respondents annually Instrument Insurance Match File: Monthly, Reporting Electronically ................................ Insurance Match File: Weekly, Reporting Electronically ................................. VerDate Sep<11>2014 21:10 Oct 29, 2020 Jkt 253001 PO 00000 Frm 00053 Fmt 4703 Sfmt 4703 Total number of annual responses per respondent Average annual burden hours per response 12 52 0.083 0.083 26 9 E:\FR\FM\30OCN1.SGM 30OCN1 Total/annual burden hours 25.90 38.84 68886 Federal Register / Vol. 85, No. 211 / Friday, October 30, 2020 / Notices ANNUAL BURDEN ESTIMATES—Continued Total number of respondents annually Instrument Insurance Match File: Daily, Reporting Electronically ..................................... Match File: Daily, Reporting Manually ............................................................. Estimated Total Annual Burden Hours: 2,817.21. Authority: 42 U.S.C. 652(a)(9), which requires OCSE to operate the FPLS established by 42 U.S.C. 653(a)(1) and 42 U.S.C. 652(m), which authorizes OCSE, through the FPLS, to compare information concerning individuals owing past-due support with information maintained by insurers (or their agents) concerning insurance claims, settlements, awards, and payments, and to furnish information resulting from the data matches to the state child support agencies responsible for collecting child support from the individuals. Mary B. Jones, ACF/OPRE Certifying Officer. [FR Doc. 2020–24141 Filed 10–29–20; 8:45 am] BILLING CODE 4184–41–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Food and Drug Administration [Docket No. FDA–2015–N–3326] Reauthorization of the Biosimilar User Fee Act; Public Meeting; Request for Comments AGENCY: Food and Drug Administration, HHS. Notice of public meeting; request for comments. ACTION: The Food and Drug Administration (FDA or Agency) is hosting a virtual public meeting on the reauthorization of the Biosimilar User Fee Act (BsUFA) for fiscal years (FYs) 2023 through 2027. BsUFA authorizes FDA to collect user fees to support the process for the review of biosimilar biological products. The current legislative authority for BsUFA expires in September 2022. At that time, new legislation will be required for FDA to continue collecting user fees in future fiscal years. FDA begins the BsUFA reauthorization process by publishing a notice in the Federal Register requesting public input and holding a public meeting where the public may present its views on the reauthorization. FDA invites public comment as the Agency begins the process to reauthorize the program for FYs 2023 through 2027. These comments will be jbell on DSKJLSW7X2PROD with NOTICES SUMMARY: VerDate Sep<11>2014 21:10 Oct 29, 2020 Jkt 253001 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 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 Frm 00054 Fmt 4703 Sfmt 4703 Average annual burden hours per response 251 251 0.083 0.1 2 108 published and available on FDA’s website. DATES: The public meeting will be held on November 19, 2020, from 9 a.m. to 12:30 p.m., and will be held by webcast only. Registration to attend the meeting and other information can be found at https://bsufaiiipublicmeeting.eventbrite.com. Submit either electronic or written comments on this public meeting by December 19, 2020. See the SUPPLEMENTARY INFORMATION section for registration date and information. ADDRESSES: You may submit comments as follows. Please note that late, untimely filed comments will not be considered. Electronic comments must be submitted on or before December 19, 2020. The https://www.regulations.gov electronic filing system will accept comments until 11:59 p.m. Eastern Time at the end of December 19, 2020. Comments received by mail/hand delivery/courier (for written/paper submissions) will be considered timely if they are postmarked or the delivery service acceptance receipt is on or before that date. PO 00000 Total number of annual responses per respondent Total/annual burden hours 41.67 2,710.80 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, 240–402–7500. • 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– 2015–N–3326 for ‘‘Reauthorization of the Biosimilar User Fee Act; Public Meeting; Request for Comments.’’ Received comments, those filed in a timely manner (see ADDRESSES), 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 E:\FR\FM\30OCN1.SGM 30OCN1

Agencies

[Federal Register Volume 85, Number 211 (Friday, October 30, 2020)]
[Notices]
[Pages 68885-68886]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2020-24141]


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DEPARTMENT OF HEALTH AND HUMAN SERVICES

Administration for Children and Families


Submission for OMB Review; Information Comparison With Insurance 
Data (OMB #0970-0342)

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) Office of 
Child Support Enforcement (OCSE) is requesting a 3-year extension of 
the currently approved Information Comparison with Insurance Data (OMB 
#0970-0342; Expires 1/31/2021).

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 within 30 days of publication of 
this notice to www.reginfo.gov/public/do/PRAMain. Find this particular 
information collection by selecting ``Currently under 30-day Review--
Open for Public Comments'' or by using the search function.

SUPPLEMENTARY INFORMATION:
    Description: The Deficit Reduction Act of 2005 amended Section 452 
of the Social Security Act to authorize the Secretary, through the 
Federal Parent Locator Service (FPLS), to conduct comparisons of 
information concerning individuals owing past-due child support with 
information maintained by insurers (or their agents) concerning 
insurance claims, settlements, awards, and payments. The two options to 
participate in the Information Comparison with Insurance Data program 
are (1) insurers submit information concerning claims, settlements, 
awards, and payments to the federal OCSE. OCSE compares it to 
information pertaining to parents who owe past-due support. (2) OCSE 
will send a file containing information about parents who owe past-due 
support to the insurer, or their agent, to compare with their claims, 
settlements, awards, and payments. The insurer or their agent sends any 
resulting insurance data matches to OCSE. On a daily basis, OCSE sends 
the results of the insurance data match in an ``Insurance Match 
Response Record'' to child support agencies responsible for collecting 
past-due support. The child support agencies use the insurance data 
matches to collect past-due support from the insurance proceeds.
    Respondents: Insurers or their agents, including the U.S. 
Department of Labor and state agencies administering workers' 
compensation programs, and the Insurance Services Office.

                                             Annual Burden Estimates
----------------------------------------------------------------------------------------------------------------
                                                   Total  number   Total number       Average
                                                        of           of annual     annual burden   Total/annual
                   Instrument                       respondents    responses per     hours per     burden hours
                                                     annually       respondent       response
----------------------------------------------------------------------------------------------------------------
Insurance Match File: Monthly, Reporting                      26              12           0.083           25.90
 Electronically.................................
Insurance Match File: Weekly, Reporting                        9              52           0.083           38.84
 Electronically.................................

[[Page 68886]]

 
Insurance Match File: Daily, Reporting                         2             251           0.083           41.67
 Electronically.................................
Match File: Daily, Reporting Manually...........             108             251             0.1        2,710.80
----------------------------------------------------------------------------------------------------------------

    Estimated Total Annual Burden Hours: 2,817.21.

    Authority: 42 U.S.C. 652(a)(9), which requires OCSE to operate 
the FPLS established by 42 U.S.C. 653(a)(1) and 42 U.S.C. 652(m), 
which authorizes OCSE, through the FPLS, to compare information 
concerning individuals owing past-due support with information 
maintained by insurers (or their agents) concerning insurance 
claims, settlements, awards, and payments, and to furnish 
information resulting from the data matches to the state child 
support agencies responsible for collecting child support from the 
individuals.

Mary B. Jones,
ACF/OPRE Certifying Officer.
[FR Doc. 2020-24141 Filed 10-29-20; 8:45 am]
BILLING CODE 4184-41-P