Agency Information Collection Activities: Proposed Collection; Comment Request, 32924-32926 [2019-14693]

Download as PDF 32924 Federal Register / Vol. 84, No. 132 / Wednesday, July 10, 2019 / Notices in their life would want them to do with the training information. At the end of week four, the respondent will return the actigraph. No data collection will occur during weeks five to 10 of the study. The second post-test period will be weeks 11 and 12 of the study to gather longer-term outcomes. At the beginning of week 11, the respondents will be fitted with an actigraph. The respondent will wear the actigraph and complete the sleep activity diary for the next 14 days. At the end of week 12 of the study, respondent will complete the Epworth Sleepiness Scale, Pittsburgh Sleep Quality Index, and Changes in Behaviors questionnaires. The combined response time is five minutes. The respondent will return the actigraph and study ends. The burden table lists three 10-minute meetings during the post-test period when they will return the actigraph at the end of week four, be fitted with an actigraph at the beginning of week 11 and return it at the end of week 12. The respondents will complete the sleep activity diary for 42 days, which will take two minutes each day. Study staff will use the findings from the pilot test to make improvements to the training program. The research team will reinforce or expand training content that showed less than desired results on the pilot test. Potential impacts of this project include improvements in management practices such as the design of work schedules and improvements in officers’ personal behaviors for coping with the demands of shift work and long work hours. The total estimated annualized burden hours is 334. There are no costs to respondents other than their time. ESTIMATED ANNUALIZED BURDEN HOURS Type of respondents Law Law Law Law Law Law Law Law Law enforcement enforcement enforcement enforcement enforcement enforcement enforcement enforcement enforcement officers officers officers officers officers officers officers officers officers ................................ ................................ ................................ ................................ ................................ ................................ ................................ ................................ ................................ Law enforcement officers ................................ Law enforcement officers ................................ Jeffrey M. Zirger, Lead, Information Collection Review Office, Office of Scientific Integrity, Office of Science, Centers for Disease Control and Prevention. [FR Doc. 2019–14680 Filed 7–9–19; 8:45 am] BILLING CODE 4163–18–P Centers for Medicare & Medicaid Services [Document Identifier: CMS–10328] Agency Information Collection Activities: Proposed Collection; Comment Request; Correction Centers for Medicare & Medicaid Services (CMS), HHS. ACTION: Correction of notice. AGENCY: This document corrects the information provided for [Document Identifier: CMS–10328] titled ‘‘Medicare Self-Referral Disclosure Protocol.’’ FOR FURTHER INFORMATION CONTACT: William N. Parham, III, (410) 786–4669. SUPPLEMENTARY INFORMATION: jspears on DSK30JT082PROD with NOTICES I. Background In the June 26, 2019, issue of the Federal Register (84 FR 30123), we VerDate Sep<11>2014 18:32 Jul 09, 2019 Jkt 247001 phone call for recruitment informed consent Initial meeting ................................................. Knowledge survey .......................................... Epworth Sleepiness Scale ............................. Pittsburgh Sleep Quality Index ...................... Demographics and work experience ............. Sleep Activity Diary ........................................ Online training ................................................ Feedback about Training, Barriers, and Influential People. Changes in Behaviors after Training ............. Actigraph fitting and return ............................. published a Paperwork Reduction Act notice requesting a 60-day public comment period for the information collection request identified under CMS–10328, OMB control number 0938–1106, and titled ‘‘Medicare SelfReferral Disclosure Protocol.’’ II. Explanation of Error DEPARTMENT OF HEALTH AND HUMAN SERVICES SUMMARY: Number of respondents Form name In the June 26, 2019, notice, the information provided in the second column of the notice on page 30125, was published with incorrect information in the ‘‘Number of Respondents,’’ the ‘‘Total Annual Responses,’’ and the ‘‘Total Hours’’ sections. This notice corrects the language found in the ‘‘Number of Respondents,’’ the ‘‘Total Annual Responses,’’ and the ‘‘Total Hours’’ sections under the third column in the middle of the column on page 30125 of the June 26, 2019. All of the other information contained in the June 26, 2019, notice is correct. The related public comment period remains in effect and ends August 26, 2019. III. Correction of Error In FR Doc. 2019–13608 of June 26, 2019 (84 FR 30123), page 30125, the language in the middle of the second column that begins with ‘‘[Number of PO 00000 Frm 00066 Fmt 4703 Sfmt 4703 Number of responses per respondent Average burden per response (in hours) 60 60 60 60 60 60 60 60 60 1 1 5 2 2 1 84 1 1 30/60 15/60 5/60 1/60 2/60 2/60 2/60 150/60 5/60 60 60 1 3 2/60 10/60 Respondents’’ and ends with ‘‘Total Annual Hours: 194,250.]’’ is corrected to read as follows: [Number of Respondents: 100; Total Annual Responses: 100; Total Annual Hours: 5,000.] Dated: July 3, 2019. William N. Parham, III, Director, Paperwork Reduction Staff, Office of Strategic Operations and Regulatory Affairs. [FR Doc. 2019–14650 Filed 7–9–19; 8:45 am] BILLING CODE 4120–01–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Centers for Medicare & Medicaid Services [Document Identifier: CMS–855S and CMS– 10527] Agency Information Collection Activities: Proposed Collection; Comment Request Centers for Medicare & Medicaid Services, HHS. ACTION: Notice. AGENCY: The Centers for Medicare & Medicaid Services (CMS) is announcing an opportunity for the public to SUMMARY: E:\FR\FM\10JYN1.SGM 10JYN1 jspears on DSK30JT082PROD with NOTICES Federal Register / Vol. 84, No. 132 / Wednesday, July 10, 2019 / Notices comment on CMS’ intention to collect information from the public. Under the Paperwork Reduction Act of 1995 (the PRA), federal agencies are required to publish notice in the Federal Register concerning each proposed collection of information (including each proposed extension or reinstatement of an existing collection of information) and to allow 60 days for public comment on the proposed action. Interested persons are invited to send comments regarding our burden estimates or any other aspect of this collection of information, including the necessity and utility of the proposed information collection for the proper performance of the agency’s functions, the accuracy of the estimated burden, ways to enhance the quality, utility, and clarity of the information to be collected, and the use of automated collection techniques or other forms of information technology to minimize the information collection burden. DATES: Comments must be received by September 9, 2019. ADDRESSES: When commenting, please reference the document identifier or OMB control number. To be assured consideration, comments and recommendations must be submitted in any one of the following ways: 1. Electronically. You may send your comments electronically to https:// www.regulations.gov. Follow the instructions for ‘‘Comment or Submission’’ or ‘‘More Search Options’’ to find the information collection document(s) that are accepting comments. 2. By regular mail. You may mail written comments to the following address: CMS, Office of Strategic Operations and Regulatory Affairs, Division of Regulations Development, Attention: Document Identifier/OMB Control Number llll, Room C4–26– 05, 7500 Security Boulevard, Baltimore, Maryland 21244–1850. 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. Email your request, including your address, phone number, OMB number, and CMS document identifier, to Paperwork@cms.hhs.gov. 3. Call the Reports Clearance Office at (410) 786–1326. FOR FURTHER INFORMATION CONTACT: William N. Parham at (410) 786–4669. SUPPLEMENTARY INFORMATION: VerDate Sep<11>2014 18:32 Jul 09, 2019 Jkt 247001 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–855S Medicare Enrollment Application—Durable Medical Equipment, Prosthetics, Orthotics and Supplies (DMEPOS) Suppliers CMS–10527 Annual Eligibility Redetermination, Product Discontinuation and Renewal Notices 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: Medicare Enrollment Application—Durable Medical Equipment, Prosthetics, Orthotics and Supplies (DMEPOS) Suppliers; Use: The CMS–855S is submitted by an applicant to the National Supplier Clearinghouse Medicare Administrative Contractor (NSC MAC) to initially apply for a Medicare billing number, and thereafter to add a new business location, revalidate Medicare enrollment, reactivate Medicare enrollment, to report a change to current Medicare enrollment information, changing the tax identification number, and to voluntary terminate the supplier’s Medicare enrollment, as applicable. It is used by new applicants as well as suppliers already enrolled in Medicare but need to submit the form for a reason other than initial enrollment into the Medicare program. Form Number: CMS–855S (OMB control number: 0938–1056); Frequency: Yearly; Affected Public: Private Sector, Business or other PO 00000 Frm 00067 Fmt 4703 Sfmt 4703 32925 for-profits and Not-for-profit institutions; Number of Respondents: 135,351; Total Annual Responses: 44,757; Total Annual Hours: 265,471. (For policy questions regarding this collection contact Kim McPhillips at 410–786–5374.) 2. Type of Information Collection Request: Extension of a currently approved collection; Title of information Collection: Annual Eligibility Redetermination, Product Discontinuation and Renewal Notices; Use: Section 1411(f)(1)(B) of the Affordable Care Act directs the Secretary of Health and Human Services (the Secretary) to establish procedures to redetermine the eligibility of individuals on a periodic basis in appropriate circumstances. Section 1321(a) of the Affordable Care Act provides authority for the Secretary to establish standards and regulations to implement the statutory requirements related to Exchanges, qualified health plans (QHPs) and other components of title I of the Affordable Care Act. Under section 2703 of the Public Health Service Act (PHS Act), as added by the Affordable Care Act, and former section 2712 and section 2741 of the PHS Act, enacted by the Health Insurance Portability and Accountability Act of 1996, health insurance issuers in the group and individual markets must guarantee the renewability of coverage unless an exception applies. The final rule ‘‘Patient Protection and Affordable Care Act; Annual Eligibility Redeterminations for Exchange Participation and Insurance Affordability Programs; Health Insurance Issuer Standards Under the Affordable Care Act, including Standards Related to Exchanges’’ (79 FR 52994), provides that an Exchange may choose to conduct the annual redetermination process for a plan year (1) in accordance with the existing procedures described in 45 CFR 155.335; (2) in accordance with procedures described in guidance issued by the Secretary for the coverage year; or (3) using an alternative proposed by the Exchange and approved by the Secretary. The final rule also amends the requirements for product renewal and re-enrollment (or non-renewal) notices to be sent by QHP issuers in the Exchanges and specifies content for these notices. The guidance document ‘‘Updated Federal Standard Renewal and Product Discontinuation Notices’’ (published on July 19, 2018) provides standard notices for product discontinuation and renewal to be sent by issuers of individual market QHPs and issuers in the individual market. E:\FR\FM\10JYN1.SGM 10JYN1 32926 Federal Register / Vol. 84, No. 132 / Wednesday, July 10, 2019 / Notices Issuers in the small group market may use the draft federal standard small group notices released in the June 26, 2014 bulletin ‘‘Draft Standard Notices When Discontinuing or Renewing a Product in the Small Group or Individual Market’’, or any forms of the notice otherwise permitted by applicable laws and regulations. States that are enforcing the guaranteed renewability provisions of the Affordable Care Act may develop their own standard notices for product discontinuances, renewals, or both, provided the state-developed notices are at least as protective as the federal standard notices. Form Number: CMS– 10527 (OMB control number 0938– 1254); Frequency: Annually; Affected Public: Private Sector, State Governments; Number of Respondents: 1,805; Total Annual Responses: 7,420; Total Annual Hours: 90,331. For policy questions regarding this collection contact Usree Bandyopadhyay at 410– 786–6650. Dated: July 5, 2019. William N. Parham, III, Director, Paperwork Reduction Staff, Office of Strategic Operations and Regulatory Affairs. [FR Doc. 2019–14693 Filed 7–9–19; 8:45 am] BILLING CODE 4120–01–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Centers for Medicare & Medicaid Services [Document Identifier: CMS–10003] Agency Information Collection Activities: Submission for OMB Review; Comment Request Centers for Medicare & Medicaid Services, HHS. ACTION: Notice. AGENCY: The Centers for Medicare & Medicaid Services (CMS) is announcing an opportunity for the public to comment on CMS’ intention to collect information from the public. Under the Paperwork Reduction Act of 1995 (PRA), federal agencies are required to publish notice in the Federal Register concerning each proposed collection of information, including each proposed extension or reinstatement of an existing collection of information, and to allow a second opportunity for public comment on the notice. Interested persons are invited to send comments regarding the burden estimate or any other aspect of this collection of information, including the necessity and utility of the proposed information jspears on DSK30JT082PROD with NOTICES SUMMARY: VerDate Sep<11>2014 18:32 Jul 09, 2019 Jkt 247001 collection for the proper performance of the agency’s functions, the accuracy of the estimated burden, ways to enhance the quality, utility, and clarity of the information to be collected, and the use of automated collection techniques or other forms of information technology to minimize the information collection burden. DATES: Comments on the collection(s) of information must be received by the OMB desk officer by August 9, 2019. ADDRESSES: When commenting on the proposed information collections, please reference the document identifier or OMB control number. To be assured consideration, comments and recommendations must be received by the OMB desk officer via one of the following transmissions: OMB, Office of Information and Regulatory Affairs, Attention: CMS Desk Officer, Fax Number: (202) 395–5806 OR, Email: OIRA_submission@omb.eop.gov 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 https://www.cms.gov/Regulations-andGuidance/Legislation/ PaperworkReductionActof1995/PRAListing.html. 2. Email your request, including your address, phone number, OMB number, and CMS document identifier, to Paperwork@cms.hhs.gov. 3. Call the Reports Clearance Office at (410) 786–1326. FOR FURTHER INFORMATION CONTACT: William Parham at (410) 786–4669. SUPPLEMENTARY INFORMATION: Under the Paperwork Reduction Act of 1995 (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 (44 U.S.C. 3506(c)(2)(A)) requires federal agencies to publish a 30-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 that summarizes the following proposed collection(s) of information for public comment: PO 00000 Frm 00068 Fmt 4703 Sfmt 4703 1. Type of Information Collection: Revision with change of a currently approved collection; Title of Information Collection: Notice of Denial of Medical Coverage (or Payment) (NDMCP); Use: Section 1852(g)(1)(B) of the Social Security Act (the Act) requires Medicare health plans to provide enrollees with a written notice in understandable language of the reasons for the denial and a description of the applicable appeals processes. Medicare health plans, including Medicare Advantage plans, cost plans, and Health Care Prepayment Plans (HCPPs), are required to issue the Notice of Denial of Medical Coverage (or Payment) (NDMCP) when a request for either a medical service or payment is denied, in whole or in part. Additionally, the notices inform Medicare enrollees of their right to file an appeal, outlining the steps and timeframes for filing. All Medicare health plans are required to use these standardized notices. In 2013, Medicaid appeal rights were integrated into form CMS–10003 for beneficiaries who are eligible for Medicare and full Medicaid benefits under a State Medicaid plan. These appeal rights are provided in instances where a Medicare health plan enrollee receives full benefits under a State Medical Assistance (Medicaid) program being managed by the plan and the plan denies a service or item that is also subject to Medicaid appeal rights. Changes to the collection from the 60day package to the 30-day package include: • Removal of language related to State Fair Hearings to comply with the change in Medicaid managed care rules at 42 CFR 438.402(c)(1)(i), effective 2017, that all Medicaid managed care denials must now first have a plan-level review before a State Fair Hearing can be requested. • Updates to comply with the Medicare Advantage final rule, published May 23, 2019, Federal Register, 84 FR 23832, effective January 1, 2020, regarding the change in timeframes for Medicare Advantage appeals related to Part B drugs. • Removing the option to delete sections related to expedited payment requests (if applicable); plans are to leave all language regarding fast appeals. Text has been added to the notice informing enrollees they do not have a right to request an expedited appeal if they are asking to be paid back for an item or service already received (42 CFR 422.570(a)). • The addition of language in the instructions that ‘‘applicable integrated plans’’ should follow notification requirements under final rule published E:\FR\FM\10JYN1.SGM 10JYN1

Agencies

[Federal Register Volume 84, Number 132 (Wednesday, July 10, 2019)]
[Notices]
[Pages 32924-32926]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2019-14693]


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DEPARTMENT OF HEALTH AND HUMAN SERVICES

Centers for Medicare & Medicaid Services

[Document Identifier: CMS-855S and CMS-10527]


Agency Information Collection Activities: Proposed Collection; 
Comment Request

AGENCY: Centers for Medicare & Medicaid Services, HHS.

ACTION: Notice.

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

SUMMARY: The Centers for Medicare & Medicaid Services (CMS) is 
announcing an opportunity for the public to

[[Page 32925]]

comment on CMS' intention to collect information from the public. Under 
the Paperwork Reduction Act of 1995 (the PRA), federal agencies are 
required to publish notice in the Federal Register concerning each 
proposed collection of information (including each proposed extension 
or reinstatement of an existing collection of information) and to allow 
60 days for public comment on the proposed action. Interested persons 
are invited to send comments regarding our burden estimates or any 
other aspect of this collection of information, including the necessity 
and utility of the proposed information collection for the proper 
performance of the agency's functions, the accuracy of the estimated 
burden, ways to enhance the quality, utility, and clarity of the 
information to be collected, and the use of automated collection 
techniques or other forms of information technology to minimize the 
information collection burden.

DATES: Comments must be received by September 9, 2019.

ADDRESSES: When commenting, please reference the document identifier or 
OMB control number. To be assured consideration, comments and 
recommendations must be submitted in any one of the following ways:
    1. Electronically. You may send your comments electronically to 
https://www.regulations.gov. Follow the instructions for ``Comment or 
Submission'' or ``More Search Options'' to find the information 
collection document(s) that are accepting comments.
    2. By regular mail. You may mail written comments to the following 
address: CMS, Office of Strategic Operations and Regulatory Affairs, 
Division of Regulations Development, Attention: Document Identifier/OMB 
Control Number ____, Room C4-26-05, 7500 Security Boulevard, Baltimore, 
Maryland 21244-1850.
    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/PRA-Listing.html.
    2. Email your request, including your address, phone number, OMB 
number, and CMS document identifier, to [email protected].
    3. 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-855S Medicare Enrollment Application--Durable Medical Equipment, 
Prosthetics, Orthotics and Supplies (DMEPOS) Suppliers
CMS-10527 Annual Eligibility Redetermination, Product Discontinuation 
and Renewal Notices

    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: Medicare 
Enrollment Application--Durable Medical Equipment, Prosthetics, 
Orthotics and Supplies (DMEPOS) Suppliers; Use: The CMS-855S is 
submitted by an applicant to the National Supplier Clearinghouse 
Medicare Administrative Contractor (NSC MAC) to initially apply for a 
Medicare billing number, and thereafter to add a new business location, 
revalidate Medicare enrollment, reactivate Medicare enrollment, to 
report a change to current Medicare enrollment information, changing 
the tax identification number, and to voluntary terminate the 
supplier's Medicare enrollment, as applicable. It is used by new 
applicants as well as suppliers already enrolled in Medicare but need 
to submit the form for a reason other than initial enrollment into the 
Medicare program. Form Number: CMS-855S (OMB control number: 0938-
1056); Frequency: Yearly; Affected Public: Private Sector, Business or 
other for-profits and Not-for-profit institutions; Number of 
Respondents: 135,351; Total Annual Responses: 44,757; Total Annual 
Hours: 265,471. (For policy questions regarding this collection contact 
Kim McPhillips at 410-786-5374.)
    2. Type of Information Collection Request: Extension of a currently 
approved collection; Title of information Collection: Annual 
Eligibility Redetermination, Product Discontinuation and Renewal 
Notices; Use: Section 1411(f)(1)(B) of the Affordable Care Act directs 
the Secretary of Health and Human Services (the Secretary) to establish 
procedures to redetermine the eligibility of individuals on a periodic 
basis in appropriate circumstances. Section 1321(a) of the Affordable 
Care Act provides authority for the Secretary to establish standards 
and regulations to implement the statutory requirements related to 
Exchanges, qualified health plans (QHPs) and other components of title 
I of the Affordable Care Act. Under section 2703 of the Public Health 
Service Act (PHS Act), as added by the Affordable Care Act, and former 
section 2712 and section 2741 of the PHS Act, enacted by the Health 
Insurance Portability and Accountability Act of 1996, health insurance 
issuers in the group and individual markets must guarantee the 
renewability of coverage unless an exception applies.
    The final rule ``Patient Protection and Affordable Care Act; Annual 
Eligibility Redeterminations for Exchange Participation and Insurance 
Affordability Programs; Health Insurance Issuer Standards Under the 
Affordable Care Act, including Standards Related to Exchanges'' (79 FR 
52994), provides that an Exchange may choose to conduct the annual 
redetermination process for a plan year (1) in accordance with the 
existing procedures described in 45 CFR 155.335; (2) in accordance with 
procedures described in guidance issued by the Secretary for the 
coverage year; or (3) using an alternative proposed by the Exchange and 
approved by the Secretary.
    The final rule also amends the requirements for product renewal and 
re-enrollment (or non-renewal) notices to be sent by QHP issuers in the 
Exchanges and specifies content for these notices. The guidance 
document ``Updated Federal Standard Renewal and Product Discontinuation 
Notices'' (published on July 19, 2018) provides standard notices for 
product discontinuation and renewal to be sent by issuers of individual 
market QHPs and issuers in the individual market.

[[Page 32926]]

Issuers in the small group market may use the draft federal standard 
small group notices released in the June 26, 2014 bulletin ``Draft 
Standard Notices When Discontinuing or Renewing a Product in the Small 
Group or Individual Market'', or any forms of the notice otherwise 
permitted by applicable laws and regulations. States that are enforcing 
the guaranteed renewability provisions of the Affordable Care Act may 
develop their own standard notices for product discontinuances, 
renewals, or both, provided the state-developed notices are at least as 
protective as the federal standard notices. Form Number: CMS-10527 (OMB 
control number 0938-1254); Frequency: Annually; Affected Public: 
Private Sector, State Governments; Number of Respondents: 1,805; Total 
Annual Responses: 7,420; Total Annual Hours: 90,331. For policy 
questions regarding this collection contact Usree Bandyopadhyay at 410-
786-6650.

    Dated: July 5, 2019.
William N. Parham, III,
Director, Paperwork Reduction Staff, Office of Strategic Operations and 
Regulatory Affairs.
[FR Doc. 2019-14693 Filed 7-9-19; 8:45 am]
BILLING CODE 4120-01-P


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