Agency Information Collection Activities: Proposed Collection; Comment Request, 18534-18536 [2021-07342]

Download as PDF 18534 Federal Register / Vol. 86, No. 67 / Friday, April 9, 2021 / Notices Prevention and the Agency for Toxic Substances and Disease Registry. Kalwant Smagh, Director, Strategic Business Initiatives Unit, Office of the Chief Operating Officer, Centers for Disease Control and Prevention. [FR Doc. 2021–07284 Filed 4–8–21; 8:45 am] BILLING CODE 4163–18–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Centers for Disease Control and Prevention [Docket No. CDC–2021–0039] Draft Recommendations for Prevention and Control of Infections in Neonatal Intensive Care Unit Patients: Central Line-Associated Blood Stream Infections (CLABSI) Centers for Disease Control and Prevention (CDC), Department of Health and Human Services (DHHS). ACTION: Notice with comment period. AGENCY: The Centers for Disease Control and Prevention (CDC), in the Department of Health and Human Services (DHHS), announces the opening of a docket to obtain comment on the Draft Recommendations for Prevention and Control of Infections in Neonatal Intensive Care Unit Patients: Central Line-associated Blood Stream Infections (CLABSI). (‘‘Draft Guideline’’). The Draft Guideline provides new, evidence-based recommendations specific to the prevention and control of central lineassociated blood stream infections (CLABSI) in neonatal intensive care unit (NICU) patients. DATES: Written comments must be received on or before June 8, 2021. ADDRESSES: You may submit comments, identified by Docket No. CDC–2021– 0039, by any of the following methods: • Federal eRulemaking Portal: https:// www.regulations.gov. Follow the instructions for submitting comments. • Mail: Division of Healthcare Quality Promotion, National Center for Emerging and Zoonotic Infectious Diseases, Centers for Disease Control and Prevention, Attn: Docket No. CDC– 2021–0039, HICPAC Secretariat, 1600 Clifton Rd. NE, Mailstop H16–2, Atlanta, Georgia, 30329. Instructions: All submissions received must include the agency name and Docket Number. All relevant comments received will be posted without change to https://regulations.gov, including any personal information provided. For access to the docket to read background SUMMARY: VerDate Sep<11>2014 17:45 Apr 08, 2021 Jkt 253001 documents or comments received, go to https://www.regulations.gov. FOR FURTHER INFORMATION CONTACT: Marwan Wassef, M.P.H., Division of Healthcare Quality Promotion, National Center for Emerging and Zoonotic Infectious Diseases, Centers for Disease Control and Prevention, 1600 Clifton Road NE, Mailstop H16–2, Atlanta, Georgia, 30329; Email: IPCGuidelines@ cdc.gov; Telephone: (404) 639–4000. SUPPLEMENTARY INFORMATION: Public Participation Interested persons or organizations are invited to participate by submitting written views, recommendations, and data related to the Draft Guideline. Please note that comments received, including attachments and other supporting materials, are part of the public record and are subject to public disclosure. Comments will be posted on https://www.regulations.gov. Therefore, do not include any information in your comment or supporting materials that you consider confidential or inappropriate for public disclosure. If you include your name, contact information, or other information that identifies you in the body of your comments, that information will be on public display. CDC will review all submissions and may choose to redact, or withhold, submissions containing private or proprietary information such as Social Security numbers, medical information, inappropriate language, or duplicate/near duplicate examples of a mass-mail campaign. CDC will carefully consider all comments submitted in preparation of the final Guideline for Prevention and Control of Infections in Neonatal Intensive Care Unit Patients and may revise the final document as appropriate. Background The Draft Guideline, located in the ‘‘Supporting & Related Material’’ tab of the docket, provides new, evidencebased recommendations specific to the prevention and control of CLABSI in NICU patients, including insertion and maintenance practices. The Draft Guideline is intended for use by infection prevention staff, healthcare epidemiologists, healthcare administrators, nurses, neonatologists, other healthcare providers, and persons responsible for developing, implementing, and evaluating infection prevention and control programs for NICUs. The guideline can also serve as a resource for societies or organizations to develop more detailed implementation guidance for the prevention of infection in NICU patients. PO 00000 Frm 00041 Fmt 4703 Sfmt 4703 The Healthcare Infection Control Practices Advisory Committee (HICPAC), a federal advisory committee chartered to provide advice and guidance to the CDC, worked with national partners, academicians, public health professionals, healthcare providers, and other partners to develop this Draft Guideline. HICPAC includes representatives from public health, infectious diseases, regulatory and other federal agencies, professional societies, and other stakeholders. The draft recommendations in this Draft Guideline are informed by a systematic review of the best available literature through February 2017 and of relevant references published since February 2017 suggested by subject matter experts. This Draft Guideline will not be a federal rule or regulation. Dated: April 6, 2021. Sandra Cashman, Executive Secretary, Centers for Disease Control and Prevention. [FR Doc. 2021–07337 Filed 4–8–21; 8:45 am] BILLING CODE 4163–18–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Centers for Medicare & Medicaid Services [Document Identifier: CMS–10209, CMS– 10701, CMS–10516, CMS–855O and CMS– 216–94] Agency Information Collection Activities: Proposed Collection; Comment Request Centers for Medicare & Medicaid Services, Health and Human 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 (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 SUMMARY: E:\FR\FM\09APN1.SGM 09APN1 Federal Register / Vol. 86, No. 67 / Friday, April 9, 2021 / Notices 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 June 8, 2021. 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: CMS–P–0015A, 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 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–10209 Medicare Advantage Chronic Care Improvement Program (CCIP) Attestations CMS–10701 Medicare Beneficiary Experiences with Care Survey (MBECS) System CMS–10516 Program Integrity II CMS–855O Medicare Registration Application CMS–216–94 Organ Procurement Organization/Histocompatibility Laboratory Cost Report Under the PRA (44 U.S.C. 3501– 3520), federal agencies must obtain approval from the Office of Management VerDate Sep<11>2014 17:45 Apr 08, 2021 Jkt 253001 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 Advantage Chronic Care Improvement Program (CCIP) Attestations; Use: Section 1852(e) of the Social Security Act (the Act) requires that Medicare Advantage (MA) organizations (MAOs) have an ongoing Quality Improvement (QI) Program. CMS regulations at 42 CFR 422.152(a) outline the QI Program requirements for MAOs, which include the development and implementation of a Chronic Care Improvement Program (CCIP) that meets the requirements of 422.152(c) for each contract. MAOs must use the Health Plan Management System (HPMS) to report the status of their CCIP to CMS by December 31 annually. Submissions include an attestation by the MAO regarding its compliance with the ongoing CCIP requirement (42 CFR 422.152(c)(2)). MAOs are only required to attest electronically that they are complying with the ongoing CCIP requirement. In addition, MAOs should assess and internally document activities related to the CCIP on an ongoing basis, as well as modify interventions and/or processes as necessary. A less frequent collection would not allow CMS to ensure that annual requirements are being met. This collection allows CMS to ensure that annual requirements are still being met, while also reducing plan burden. Form Number: CMS–10209 (OMB Control number: 0938–1023); Frequency: Annually; Affected Public: Private Sector—Business or other for-profits; Number of Respondents: 645; Total Annual Responses: 645; Total Annual Hours: 161 (For policy questions regarding this collection contact Lynn Pereira at 410–786–2274) PO 00000 Frm 00042 Fmt 4703 Sfmt 4703 18535 2. Type of Information Collection Request: New collection (Request for a new OMB control number); Title of Information Collection: Medicare Beneficiary Experiences with Care Survey (MBECS) System; Use: The MBECS system is designed to conduct population specific surveys that will be administered to the group of interest, fielded one time. This means that over the three-year period, two individual surveys will be administered. This will allow CMS OMH to respond quickly to the data needs of stakeholders with interests in these underrepresented groups. Data collected through the MBECS system will be used to better understand—and thus serve the needs of—Medicare beneficiaries in minority populations. The core questionnaire will collect information on communication with medical professionals, coordination of health care, experiences getting needed health care, experiences with personal doctors and specialists, and key demographics. Data will be compared to benchmarks from the FFS CAHPS, MA CAHPS, and NAM CAHPS surveys. The populationspecific questionnaire module described and submitted via a specific collection request will collect information about issues most relevant for that particular group of interest. The goal of this umbrella data collection effort is to gather data via separate surveys on a variety of minority Medicare beneficiaries’ experiences. Topics and questions of interest may ask about beneficiaries’ communication with medical professionals, coordination of health care, experiences getting needed health care, and experiences with personal doctors and specialists. CMS OMH will compare survey data to benchmarks from the general population of Medicare beneficiaries while controlling for population characteristics, as appropriate. Survey respondents will have the opportunity to respond to an MBECS survey via a self-administered webbased survey (also called computerassisted web interview or CAWI). CAWI technology minimizes respondent burden by (1) Automatically providing text fills within questions and handling skip patterns based on responses to each question; (2) allowing respondents to complete the survey at a convenient time; (3) allowing respondents to stop and re-enter the survey if needed; and (4) capturing data in real-time, thereby eliminating the need for manual data entry. Form Number: CMS–10701 (OMB Control number: 0938–New); Frequency: Annually; Affected Public: Individuals and Households; Number of E:\FR\FM\09APN1.SGM 09APN1 18536 Federal Register / Vol. 86, No. 67 / Friday, April 9, 2021 / Notices Respondents: 13,000; Total Annual Responses: 13,000; Total Annual Hours: 4,290 (For policy questions regarding this collection contact Luis Pons Perez at 410–786–8557) 3. Type of Information Collection: Extension of a currently approved collection; Title of Information Collection: Program Integrity II; Use: On June 19, 2013, HHS published proposed rule CMS–9957–P: Program Integrity: Exchanges, SHOP, Premium Stabilization Programs, and Market Standards (78 FR 37302) (Program Integrity Proposed Rule) which, among other things, contained third party disclosure requirements and data collections that supported the oversight of premium stabilization programs, State Exchanges, and qualified health plan (QHP) issuers in Federallyfacilitated Exchanges (FFEs). Parts of the proposed rule were finalized as Patient Protection and Affordable Care Act; Program Integrity: Exchange, Premium Stabilization Programs, and Market Standards; Amendments to the HHS Notice of Benefit and Payment Parameters for 2014; Final Rule (Program Integrity Final Rule II), 78 FR 25326 (October 24, 2013). This ICR relates to a portion of the information collection request (ICR) requirements set forth in the final rule. Form Number: CMS–10516 (OMB control number: 0938–1277); Frequency: Annually; Affected Public: Private Sector, State, Business, and Not-for Profits; Number of Respondents: 428; Number of Responses: 428; Total Annual Hours: 40,420. (For questions regarding this collection, contact Joshua Van Drei at (410–786–1659). 4. Type of Information Collection Request: Revision of a currently approved information collection; Title of Information Collection: Medicare Registration Application; Use: Physicians and practitioners complete the Medicare Enrollment Application— Enrollment for Eligible Ordering, Certifying Physicians and Other Eligible Professionals if they are enrolling in Medicare not to obtain Medicare billing privileges but strictly to order, refer, or certify certain Medicare items and services. It is used by Medicare contractors to collect data that helps ensure the applicant has the necessary credentials to order and certify certain Medicare items and services. The MAC establishes Medicare Identification Numbers. The MACs store these numbers and information in CMS’ Provider Enrollment, Chain and Ownership System (PECOS). The application is used by the CMS’ contractors to collect data ensures that the applicant has the necessary VerDate Sep<11>2014 17:45 Apr 08, 2021 Jkt 253001 information for unique identification. The license numbers are validated against state licensing websites. All the license numbers are captured and stored in the MAC database. Social Security Numbers (SSNs) are validated against the Social Security Administration database (SSA) and only the valid entries are allowed to proceed in the process of getting a Medicare billing number. Correspondence address and contact information is captured to contact the provider/supplier. The collection and verification of this information defends and protects our beneficiaries from illegitimate providers/suppliers. These procedures also protect the Medicare Trust Fund against fraud. It gathers information that allow Medicare contractors to ensure that the physician or eligible professional is not sanctioned from the Medicare and/or Medicaid program(s), or debarred, or excluded from any other Federal agency or program. The data collected also ensures that the applicant has the necessary credentials to order and certify health care services. This is sole instrument implemented for this purpose. Form Number: CMS–855O (OMB Control Number: 0938–1135); Frequency: Occasionally; Affected Public: Private Sector (Business or other for-profits), State, Local, or Tribal Governments; Number of Respondents: 448,000; Number of Responses: 24,000; Total Annual Hours: 243,600. (For questions regarding this collection contact Kimberly McPhillips (410–786– 8438.) 5. Type of Information Collection Request: Reinstatement without change of a previously approved collection; Title of Information Collection: Organ Procurement Organization Histocompatibility Laboratory Cost Report; Use: The Form CMS–216–94 cost report is needed to determine Organ Procurement Organization (OPO)/ Histocompatibility Lab (HL) reasonable costs incurred in procuring and transporting organs for transplant into Medicare beneficiaries and reimbursement due to or from the provider. The reasonable costs of procuring and transporting organs cannot be determined for the fiscal year until the OPO/HL files its cost report and costs are verified by the Medicare contractor. During the fiscal year, an interim rate is established based on cost report data from the previous year. The OPO/HL bills the transplant hospital for services rendered. The transplant hospital pays interim payments, approximating reasonable cost, to the OPO/HL. The Form CMS–216–94 cost report is filed by each OPO/HL at the end of its fiscal year and there is a cost PO 00000 Frm 00043 Fmt 4703 Sfmt 4703 report settlement to take into account increases or decreases in costs. The cost report reconciliation and settlement take into consideration the difference between the total reasonable costs minus the total interim payments received or receivable from the transplant centers. Form Number: CMS– 216–94 (OMB Control number: 0938– 0102); Frequency: Annually; Affected Public: Private Sector—Business or other for-profits; Number of Respondents: 95; Total Annual Responses: 95; Total Annual Hours: 4,275 (For policy questions regarding this collection contact Luann Piccione at 410–786–5423) Dated: April 6, 2021. William N. Parham, III, Director, Paperwork Reduction Staff, Office of Strategic Operations and Regulatory Affairs. [FR Doc. 2021–07342 Filed 4–8–21; 8:45 am] BILLING CODE 4120–01–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Administration for Community Living Availability of Program Application Instructions for the Title VII, Part C of the Act, Centers for Independent Living (CILs) To Expand COVID–19 Vaccine Access for People With Disabilities Title: Expanding Disabilities Network’s (CILs) Access to COVID–19 Vaccines. Announcement Type: Initial. Statutory Authority: The statutory authority for grants under this program announcement is contained in Section 711 and Section 712 of the Rehabilitation Act of 1973 [Pub. L. 93– 112] [As Amended Through Pub. L. 114–95, Enacted December 10, 2015]. Catalog of Federal Domestic Assistance (CFDA) Number: 93.432. DATES: The deadline date for the submission of the Expanding Disabilities Network’s (CILs) Access to COVID–19 Vaccines is 11:59 p.m. Eastern Time April 23, 2021. I. Funding Opportunity Description The Administration for Community Living (ACL) announced a new funding opportunity to increase vaccine access for people with disabilities. With funding and partnership support from the Centers for Disease Control (CDC), ACL is providing grants to disability networks to provide critical services to help communities combat COVID–19. A leading priority of this joint effort is to E:\FR\FM\09APN1.SGM 09APN1

Agencies

[Federal Register Volume 86, Number 67 (Friday, April 9, 2021)]
[Notices]
[Pages 18534-18536]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2021-07342]


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

DEPARTMENT OF HEALTH AND HUMAN SERVICES

Centers for Medicare & Medicaid Services

[Document Identifier: CMS-10209, CMS-10701, CMS-10516, CMS-855O and 
CMS-216-94]


Agency Information Collection Activities: Proposed Collection; 
Comment Request

AGENCY: Centers for Medicare & Medicaid Services, Health and Human 
Services (HHS).

ACTION: Notice.

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

SUMMARY: 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 (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

[[Page 18535]]

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 June 8, 2021.

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: CMS-P-0015A, 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

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-10209 Medicare Advantage Chronic Care Improvement Program (CCIP) 
Attestations
CMS-10701 Medicare Beneficiary Experiences with Care Survey (MBECS) 
System
CMS-10516 Program Integrity II
CMS-855O Medicare Registration Application
CMS-216-94 Organ Procurement Organization/Histocompatibility Laboratory 
Cost Report

    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 
Advantage Chronic Care Improvement Program (CCIP) Attestations; Use: 
Section 1852(e) of the Social Security Act (the Act) requires that 
Medicare Advantage (MA) organizations (MAOs) have an ongoing Quality 
Improvement (QI) Program. CMS regulations at 42 CFR 422.152(a) outline 
the QI Program requirements for MAOs, which include the development and 
implementation of a Chronic Care Improvement Program (CCIP) that meets 
the requirements of 422.152(c) for each contract.
    MAOs must use the Health Plan Management System (HPMS) to report 
the status of their CCIP to CMS by December 31 annually. Submissions 
include an attestation by the MAO regarding its compliance with the 
ongoing CCIP requirement (42 CFR 422.152(c)(2)). MAOs are only required 
to attest electronically that they are complying with the ongoing CCIP 
requirement. In addition, MAOs should assess and internally document 
activities related to the CCIP on an ongoing basis, as well as modify 
interventions and/or processes as necessary. A less frequent collection 
would not allow CMS to ensure that annual requirements are being met. 
This collection allows CMS to ensure that annual requirements are still 
being met, while also reducing plan burden. Form Number: CMS-10209 (OMB 
Control number: 0938-1023); Frequency: Annually; Affected Public: 
Private Sector--Business or other for-profits; Number of Respondents: 
645; Total Annual Responses: 645; Total Annual Hours: 161 (For policy 
questions regarding this collection contact Lynn Pereira at 410-786-
2274)
    2. Type of Information Collection Request: New collection (Request 
for a new OMB control number); Title of Information Collection: 
Medicare Beneficiary Experiences with Care Survey (MBECS) System; Use: 
The MBECS system is designed to conduct population specific surveys 
that will be administered to the group of interest, fielded one time. 
This means that over the three-year period, two individual surveys will 
be administered. This will allow CMS OMH to respond quickly to the data 
needs of stakeholders with interests in these underrepresented groups. 
Data collected through the MBECS system will be used to better 
understand--and thus serve the needs of--Medicare beneficiaries in 
minority populations. The core questionnaire will collect information 
on communication with medical professionals, coordination of health 
care, experiences getting needed health care, experiences with personal 
doctors and specialists, and key demographics. Data will be compared to 
benchmarks from the FFS CAHPS, MA CAHPS, and NAM CAHPS surveys. The 
population-specific questionnaire module described and submitted via a 
specific collection request will collect information about issues most 
relevant for that particular group of interest.
    The goal of this umbrella data collection effort is to gather data 
via separate surveys on a variety of minority Medicare beneficiaries' 
experiences. Topics and questions of interest may ask about 
beneficiaries' communication with medical professionals, coordination 
of health care, experiences getting needed health care, and experiences 
with personal doctors and specialists. CMS OMH will compare survey data 
to benchmarks from the general population of Medicare beneficiaries 
while controlling for population characteristics, as appropriate.
    Survey respondents will have the opportunity to respond to an MBECS 
survey via a self-administered web-based survey (also called computer-
assisted web interview or CAWI). CAWI technology minimizes respondent 
burden by (1) Automatically providing text fills within questions and 
handling skip patterns based on responses to each question; (2) 
allowing respondents to complete the survey at a convenient time; (3) 
allowing respondents to stop and re-enter the survey if needed; and (4) 
capturing data in real-time, thereby eliminating the need for manual 
data entry. Form Number: CMS-10701 (OMB Control number: 0938-New); 
Frequency: Annually; Affected Public: Individuals and Households; 
Number of

[[Page 18536]]

Respondents: 13,000; Total Annual Responses: 13,000; Total Annual 
Hours: 4,290 (For policy questions regarding this collection contact 
Luis Pons Perez at 410-786-8557)
    3. Type of Information Collection: Extension of a currently 
approved collection; Title of Information Collection: Program Integrity 
II; Use: On June 19, 2013, HHS published proposed rule CMS-9957-P: 
Program Integrity: Exchanges, SHOP, Premium Stabilization Programs, and 
Market Standards (78 FR 37302) (Program Integrity Proposed Rule) which, 
among other things, contained third party disclosure requirements and 
data collections that supported the oversight of premium stabilization 
programs, State Exchanges, and qualified health plan (QHP) issuers in 
Federally-facilitated Exchanges (FFEs). Parts of the proposed rule were 
finalized as Patient Protection and Affordable Care Act; Program 
Integrity: Exchange, Premium Stabilization Programs, and Market 
Standards; Amendments to the HHS Notice of Benefit and Payment 
Parameters for 2014; Final Rule (Program Integrity Final Rule II), 78 
FR 25326 (October 24, 2013). This ICR relates to a portion of the 
information collection request (ICR) requirements set forth in the 
final rule. Form Number: CMS-10516 (OMB control number: 0938-1277); 
Frequency: Annually; Affected Public: Private Sector, State, Business, 
and Not-for Profits; Number of Respondents: 428; Number of Responses: 
428; Total Annual Hours: 40,420. (For questions regarding this 
collection, contact Joshua Van Drei at (410-786-1659).
    4. Type of Information Collection Request: Revision of a currently 
approved information collection; Title of Information Collection: 
Medicare Registration Application; Use: Physicians and practitioners 
complete the Medicare Enrollment Application--Enrollment for Eligible 
Ordering, Certifying Physicians and Other Eligible Professionals if 
they are enrolling in Medicare not to obtain Medicare billing 
privileges but strictly to order, refer, or certify certain Medicare 
items and services. It is used by Medicare contractors to collect data 
that helps ensure the applicant has the necessary credentials to order 
and certify certain Medicare items and services.
    The MAC establishes Medicare Identification Numbers. The MACs store 
these numbers and information in CMS' Provider Enrollment, Chain and 
Ownership System (PECOS). The application is used by the CMS' 
contractors to collect data ensures that the applicant has the 
necessary information for unique identification. The license numbers 
are validated against state licensing websites. All the license numbers 
are captured and stored in the MAC database. Social Security Numbers 
(SSNs) are validated against the Social Security Administration 
database (SSA) and only the valid entries are allowed to proceed in the 
process of getting a Medicare billing number. Correspondence address 
and contact information is captured to contact the provider/supplier.
    The collection and verification of this information defends and 
protects our beneficiaries from illegitimate providers/suppliers. These 
procedures also protect the Medicare Trust Fund against fraud. It 
gathers information that allow Medicare contractors to ensure that the 
physician or eligible professional is not sanctioned from the Medicare 
and/or Medicaid program(s), or debarred, or excluded from any other 
Federal agency or program. The data collected also ensures that the 
applicant has the necessary credentials to order and certify health 
care services. This is sole instrument implemented for this purpose. 
Form Number: CMS-855O (OMB Control Number: 0938-1135); Frequency: 
Occasionally; Affected Public: Private Sector (Business or other for-
profits), State, Local, or Tribal Governments; Number of Respondents: 
448,000; Number of Responses: 24,000; Total Annual Hours: 243,600. (For 
questions regarding this collection contact Kimberly McPhillips (410-
786-8438.)
    5. Type of Information Collection Request: Reinstatement without 
change of a previously approved collection; Title of Information 
Collection: Organ Procurement Organization Histocompatibility 
Laboratory Cost Report; Use: The Form CMS-216-94 cost report is needed 
to determine Organ Procurement Organization (OPO)/Histocompatibility 
Lab (HL) reasonable costs incurred in procuring and transporting organs 
for transplant into Medicare beneficiaries and reimbursement due to or 
from the provider. The reasonable costs of procuring and transporting 
organs cannot be determined for the fiscal year until the OPO/HL files 
its cost report and costs are verified by the Medicare contractor. 
During the fiscal year, an interim rate is established based on cost 
report data from the previous year. The OPO/HL bills the transplant 
hospital for services rendered. The transplant hospital pays interim 
payments, approximating reasonable cost, to the OPO/HL. The Form CMS-
216-94 cost report is filed by each OPO/HL at the end of its fiscal 
year and there is a cost report settlement to take into account 
increases or decreases in costs. The cost report reconciliation and 
settlement take into consideration the difference between the total 
reasonable costs minus the total interim payments received or 
receivable from the transplant centers. Form Number: CMS-216-94 (OMB 
Control number: 0938-0102); Frequency: Annually; Affected Public: 
Private Sector--Business or other for-profits; Number of Respondents: 
95; Total Annual Responses: 95; Total Annual Hours: 4,275 (For policy 
questions regarding this collection contact Luann Piccione at 410-786-
5423)

    Dated: April 6, 2021.
William N. Parham, III,
Director, Paperwork Reduction Staff, Office of Strategic Operations and 
Regulatory Affairs.
[FR Doc. 2021-07342 Filed 4-8-21; 8:45 am]
BILLING CODE 4120-01-P
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