Medicare and Medicaid Program; Approval of Application From Det Norske Veritas for Continued Hospital Accreditation Program, 54510-54512 [2022-19099]

Download as PDF 54510 Federal Register / Vol. 87, No. 171 / Tuesday, September 6, 2022 / Notices DEPARTMENT OF HEALTH AND HUMAN SERVICES DEPARTMENT OF HEALTH AND HUMAN SERVICES Centers for Disease Control and Prevention Centers for Medicare & Medicaid Services Performance Review Board Members Centers for Disease Control and Prevention (CDC), Department of Health and Human Services (HHS). AGENCY: ACTION: Notice. The Centers for Disease Control and Prevention (CDC) located within the Department of Health and Human Services (HHS) is publishing the names of the Performance Review Board Members who are reviewing performance of Senior Executive Service (SES) members, title 42 (T42) executives, and Senior Level (SL) employees for Fiscal Year 2022. FOR FURTHER INFORMATION CONTACT: Henry Greene, Team Chief, Executive and Scientific Resources Office, Human Resources Office, Centers for Disease Control and Prevention, 11 Corporate Square Blvd., Mailstop US11–2, Atlanta, Georgia 30341, Telephone (770) 488– 1140. Title 5, U.S.C. 4314(c) (4) of the Civil Service Reform Act of 1978, Public Law 95–454, requires that the appointment of Performance Review Board Members be published in the Federal Register. The following persons will serve on the CDC Performance Review Board, which will oversee the evaluation of performance appraisals of Senior Executive Service members for the Fiscal Year 2022 review period: jspears on DSK121TN23PROD with NOTICES SUPPLEMENTARY INFORMATION: Bornstein, Joshua, Co-Chair Bonander, Jason Dulin, Stephanie Durst, Kelley Ethier, Kathleen, Co-Chair Kuhnert, Wendi Lindsey, Ronney L. Peeples, Amy Perry, Terrance Philip, Celeste M Tomlinson, Hank Wharton, Melinda Dated: August 29, 2022. Angela K. Oliver, Executive Secretary, Centers for Disease Control and Prevention. [FR Doc. 2022–19177 Filed 9–2–22; 8:45 am] BILLING CODE 4163–18–P 20:04 Sep 02, 2022 Medicare and Medicaid Program; Approval of Application From Det Norske Veritas for Continued Hospital Accreditation Program Centers for Medicare & Medicaid Services (CMS), HHS. ACTION: Final notice. AGENCY: SUMMARY: VerDate Sep<11>2014 [CMS–3424–FN] Jkt 256001 This final notice announces our decision to approve Det Norske Veritas for continued recognition as a national accrediting organization for hospitals that wish to participate in the Medicare or Medicaid programs. DATES: The decision announced in this final notice is effective through September 26, 2026. FOR FURTHER INFORMATION CONTACT: Joy Webb, (410) 786–1667. Lillian Williams, (410) 786–8636. SUPPLEMENTARY INFORMATION: SUMMARY: I. Background Under the Medicare program, eligible beneficiaries may receive covered services from a hospital, provided that certain requirements are met. Section 1861(e) of the Social Security Act (the Act), establishes distinct criteria for facilities seeking designation as a hospital. Regulations concerning provider agreements are at 42 CFR part 489 and those pertaining to activities relating to the survey and certification of facilities are at 42 CFR part 488. The regulations at 42 CFR part 482 specify the minimum conditions that a hospital must meet to participate in the Medicare program. Generally, to enter into an agreement, a hospital must first be certified by a State survey agency as complying with the conditions or requirements set forth in part 482 of our regulations. Thereafter, the hospital is subject to regular surveys by a State survey agency to determine whether it continues to meet these requirements. Section 1865(a)(1) of the Act provides that, if a provider entity demonstrates through accreditation by an approved national accrediting organization (AO) that all applicable Medicare conditions are met or exceeded, we may deem those provider entities as having met the requirements. Accreditation by an AO is voluntary and is not required for Medicare participation. If an AO is recognized by the Secretary of the Department of Health PO 00000 Frm 00062 Fmt 4703 Sfmt 4703 and Human Services as having standards for accreditation that meet or exceed Medicare requirements, any provider entity accredited by the national accrediting body’s approved program may be deemed to meet the Medicare conditions. A national AO applying for approval of its accreditation program under part 488, subpart A, must provide the Centers for Medicare and Medicaid Services (CMS) with reasonable assurance that the AO requires the accredited provider entities to meet requirements that are at least as stringent as the Medicare conditions. Our regulations concerning the approval of accrediting organizations are set forth at § 488.5. The regulations at § 488.5(e)(2)(i) require AOs to reapply for continued approval of its accreditation program every 6 years or sooner as determined by CMS. Det Norske Veritas’s (DNV’s) current term of approval for their hospital accreditation program expires September 26, 2022. II. Application Approval Process Section 1865(a)(3)(A) of the Act provides a statutory timetable to ensure that our review of applications for CMS approval of an accreditation program is conducted in a timely manner. The Act provides us 210 days after the date of receipt of a complete application, with any documentation necessary to make the determination, to complete our survey activities and application process. Within 60 days after receiving a complete application, we must publish a notice in the Federal Register that identifies the national accrediting body making the request, describes the request, and provides no less than a 30day public comment period. At the end of the 210-day period, we must publish a notice in the Federal Register approving or denying the application. III. Provisions of the Proposed Notice On April 18, 2022, we published a proposed notice in the Federal Register (87 FR 22894), announcing DNV’s request for continued approval of its Medicare hospital accreditation program. In the proposed notice, we detailed our evaluation criteria. Under section 1865(a)(2) of the Act and in our regulations at § 488.5, we conducted a review of DNV’s Medicare hospital accreditation renewal application in accordance with the criteria specified by our regulations, which include, but are not limited to, the following: • An administrative review of DNV’s—(1) corporate policies; (2) financial and human resources available to accomplish the proposed surveys; (3) procedures for training, monitoring, and evaluation of its hospital surveyors; (4) E:\FR\FM\06SEN1.SGM 06SEN1 Federal Register / Vol. 87, No. 171 / Tuesday, September 6, 2022 / Notices jspears on DSK121TN23PROD with NOTICES ability to investigate and respond appropriately to complaints against accredited hospitals; and (5) survey review and decision-making process for accreditation. • The comparison of DNV’s Medicare hospital accreditation program standards to our current Medicare hospitals Conditions of Participation (CoPs). • A documentation review of DNV’s survey process to do the following: ++ Determine the composition of the survey team, surveyor qualifications, and DNV’s ability to provide continuing surveyor training. ++ Compare DNV’s processes to those we require of state survey agencies, including periodic resurvey and the ability to investigate and respond appropriately to complaints against accredited hospitals. ++ Evaluate DNV’s procedures for monitoring accredited hospitals it has found to be out of compliance with DNV’s program requirements. (This pertains only to monitoring procedures when DNV identifies non-compliance. If noncompliance is identified by a state survey agency through a validation survey, the state survey agency monitors corrections as specified at § 488.9(c)). ++ Assess DNV’s ability to report deficiencies to the surveyed hospital and respond to the hospital’s plan of correction in a timely manner. ++ Establish DNV’s ability to provide CMS with electronic data and reports necessary for effective validation and assessment of the organization’s survey process. ++ Determine the adequacy of DNV’s staff and other resources. ++ Confirm DNV’s ability to provide adequate funding for performing required surveys. ++ Confirm DNV’s policies with respect to surveys being unannounced. ++ Confirm DNV’s policies and procedures to avoid conflicts of interest, including the appearance of conflicts of interest, involving individuals who conduct surveys or participate in accreditation decisions. ++ Obtain DNV’s agreement to provide CMS with a copy of the most current accreditation survey together with any other information related to the survey as we may require, including corrective action plans. IV. Analysis of and Response to Public Comments on the Proposed Notice In accordance with section 1865(a)(3)(A) of the Act, the April 18, 2022 proposed notice also solicited public comments regarding whether DNV’s requirements met or exceeded the Medicare CoPs for hospitals. We VerDate Sep<11>2014 20:04 Sep 02, 2022 Jkt 256001 received one comment in response to our proposed notice. The comment received expressed support for DNV’s hospital accreditation program. The proposed notice described CMS’ process and oversight activities in Section III., Evaluation of Deeming Authority Request, which highlighted the evaluation CMS conducts before granting deeming authority to an AO. In Section V. of this final notice, CMS is highlighting areas, which were identified to have discrepancies or lack of clarity within DNV’s standards and survey processes. We note that DNV corrected these discrepancies prior to renewal of their deeming authority for their CMS-approved hospital accreditation program. CMS continues to strive for increased oversight of AOs. V. Provisions of the Final Notice A. Differences Between DNV’s Standards and Requirements for Accreditation and Medicare Conditions and Survey Requirements We compared DNV’s hospital accreditation program requirements and survey process with the Medicare CoPs at 42 CFR part 482, and the survey and certification process requirements of parts 488 and 489. Our review and evaluation of DNV’s hospital application, which were conducted as described in Section III. of this final notice, yielded the following areas where, as of the date of this notice, DNV has revised its standards and certification processes in order to meet our requirements at: • Section 482.13(e)(8)(i)(A) through (C). DNV clarified the specific age-based limits with respect to applicable to the amount of time a patient could spend in restraint and seclusion in hospitals; these limits would supersede any conflicting state law. • Section 482.15(a)(1). DNV changed its standard to include communitybased risk assessment in its requirements and all-hazards definition in interpretive guidelines. • Section 482.15(b)(7). DNV addressed the requirement that states make arrangements with others hospitals and other providers to receive patients in the event of limitation or cessation of operations, in order to maintain the continuity of services to hospital patients. • Section 482.23(b)(4). DNV addressed our concerns pertaining to nursing assessment and care plan, to ensure that the requirements are comparable with CMS’ requirement. • Sections 482.24(c)(4)(i)(A) through 482.24(c)(4)(i)(C). DNV revised its PO 00000 Frm 00063 Fmt 4703 Sfmt 4703 54511 standards to fully meet CMS requirements. • Section 482.28(b)(2). DNV revised its language from a restrictive requirement to include an all patient diet. • Section 482.41(c). DNV revised language regarding the applicability of National Fire Protection Association (NFPA) to correspond to 2012 NFPA 99, Section 1.3 Application. • Section 482.52(c)(2). DNV clarified the requirement regarding deferral to state anesthesia practice standards; its prior language was unclear. • Section 482.53(d). DNV clarified its standard regarding nuclear medicine documentation requirements to include signed and dated language, showing authorship. • Section 482.57. DNV revised its respiratory care standards to include language reflecting ‘‘the needs of the patients’’ in order to fully reflect CMS’ requirement. • Section 482.58. DNV clarified its standards to include the governing body of the hospital bears the responsibility of assuring medical staff has written policies. • Section 482.58(b)(1). DNV revised the standard to be more specific and to fully meet the regulatory requirement. DNV’s standard had not made it clear that the patients have the right to be informed of total health status in the language they can understand, but rather focused on rules, regulations, and facility responsibilities during facility stay. B. Term of Approval Based on our review and observations described in Sections III. and V. of this final notice, we approve DNV as a national accreditation organization for hospitals that request participation in the Medicare program. The decision announced in this final notice is effective September 26, 2022 through September 26, 2026 (4 years). In accordance with § 488.5(e)(2)(i), the term of the approval will not exceed 6 years. Due to travel restrictions and the reprioritization of survey activities brought on by the 2019 Novel Coronavirus Disease (COVID–19) Public Health Emergency (PHE), CMS was unable to observe a hospital survey completed by DNV surveyors as part of the application review process, which is typically one component of the comparability evaluation. Therefore, we are providing DNV with a shorter period of approval. Based on our discussions with DNV and the information provided in its application, we are confident that DNV will continue to ensure that its deemed hospitals continue to meet or E:\FR\FM\06SEN1.SGM 06SEN1 54512 Federal Register / Vol. 87, No. 171 / Tuesday, September 6, 2022 / Notices exceed our required standards. While DNV has taken actions based on the findings noted in section V.A. of this final notice (Differences Between TJC’s Standards and Requirements for Accreditation and Medicare Conditions and Survey Requirements), as authorized under § 488.8, we will continue ongoing review of DNV’s hospital surveys. In keeping with CMS’s initiative to broadly increase AO oversight, and to ensure that our requested revisions by DNV are completed, CMS expects to perform more frequent review of DNV’s activities in the future. VI. Collection of Information Requirements This document does not impose information collection requirements, that is, reporting, recordkeeping, or third-party disclosure requirements. Consequently, there is no need for review by the Office of Management and Budget under the authority of the Paperwork Reduction Act of 1995 (44 U.S.C. 3501 et seq.). The Administrator of the Centers for Medicare & Medicaid Services (CMS), Chiquita Brooks-LaSure, having reviewed and approved this document, authorizes Trenesha Fultz-Mimms, who is the Federal Register Liaison, to electronically sign this document for purposes of publication in the Federal Register. Trenesha Fultz-Mimms, Federal Register Liaison, Center for Medicare & Medicaid Services. [FR Doc. 2022–19099 Filed 9–2–22; 8:45 am] BILLING CODE 4120–01–P DEPARTMENT OF HEALTH AND HUMAN SERVICES [Docket No. FDA–2022–N–1946] Pulmonary-Allergy Drugs Advisory Committee; Notice of Meeting; Establishment of a Public Docket; Request for Comments Food and Drug Administration, HHS. Notice; establishment of a public docket; request for comments. ACTION: The Food and Drug Administration (FDA) announces a forthcoming public advisory committee meeting of the Pulmonary-Allergy Drugs Advisory Committee. The general function of the committee is to provide advice and recommendations to FDA on regulatory issues. The meeting will be open to the public. FDA is establishing jspears on DSK121TN23PROD with NOTICES SUMMARY: VerDate Sep<11>2014 20:04 Sep 02, 2022 Jkt 256001 The meeting will take place virtually on November 8, 2022, from 10 a.m. to 4 p.m. eastern time. ADDRESSES: Please note that due to the impact of this COVID–19 pandemic, all meeting participants will be joining this advisory committee meeting via an online teleconferencing platform. Answers to commonly asked questions about FDA advisory committee meetings may be accessed at: https:// www.fda.gov/AdvisoryCommittees/ AboutAdvisoryCommittees/ ucm408555.htm. FDA is establishing a docket for public comment on this meeting. The docket number is FDA–2022–N–1946. The docket will close on November 7, 2022. Either electronic or written comments on this public meeting must be submitted by November 7, 2022. Please note that late, untimely filed comments will not be considered. The https://www.regulations.gov electronic filing system will accept comments until 11:59 p.m. eastern time at the end of November 7, 2022. Comments received by mail/hand delivery/courier (for written/paper submissions) will be considered timely if they are received on or before that date. Comments received on or before October 25, 2022, will be provided to the committee. Comments received after that date will be taken into consideration by FDA. In the event that the meeting is cancelled, FDA will continue to evaluate any relevant applications or information, and consider any comments submitted to the docket, as appropriate. You may submit comments as follows: DATES: Electronic Submissions Food and Drug Administration AGENCY: a docket for public comment on this document. 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 PO 00000 Frm 00064 Fmt 4703 Sfmt 4703 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– 2022–N–1946 for ‘‘Pulmonary-Allergy Drugs Advisory Committee; Notice of Meeting; Establishment of a Public Docket; 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, 240–402–7500. • 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.’’ FDA 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 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 the information as ‘‘confidential.’’ Any information marked as ‘‘confidential’’ will not be disclosed except in accordance with 21 CFR 10.20 E:\FR\FM\06SEN1.SGM 06SEN1

Agencies

[Federal Register Volume 87, Number 171 (Tuesday, September 6, 2022)]
[Notices]
[Pages 54510-54512]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2022-19099]


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

DEPARTMENT OF HEALTH AND HUMAN SERVICES

Centers for Medicare & Medicaid Services

[CMS-3424-FN]


Medicare and Medicaid Program; Approval of Application From Det 
Norske Veritas for Continued Hospital Accreditation Program

AGENCY: Centers for Medicare & Medicaid Services (CMS), HHS.

ACTION: Final notice.

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

SUMMARY: This final notice announces our decision to approve Det Norske 
Veritas for continued recognition as a national accrediting 
organization for hospitals that wish to participate in the Medicare or 
Medicaid programs.

DATES: The decision announced in this final notice is effective through 
September 26, 2026.

FOR FURTHER INFORMATION CONTACT: 
    Joy Webb, (410) 786-1667.
    Lillian Williams, (410) 786-8636.

SUPPLEMENTARY INFORMATION: 

I. Background

    Under the Medicare program, eligible beneficiaries may receive 
covered services from a hospital, provided that certain requirements 
are met. Section 1861(e) of the Social Security Act (the Act), 
establishes distinct criteria for facilities seeking designation as a 
hospital. Regulations concerning provider agreements are at 42 CFR part 
489 and those pertaining to activities relating to the survey and 
certification of facilities are at 42 CFR part 488. The regulations at 
42 CFR part 482 specify the minimum conditions that a hospital must 
meet to participate in the Medicare program.
    Generally, to enter into an agreement, a hospital must first be 
certified by a State survey agency as complying with the conditions or 
requirements set forth in part 482 of our regulations. Thereafter, the 
hospital is subject to regular surveys by a State survey agency to 
determine whether it continues to meet these requirements.
    Section 1865(a)(1) of the Act provides that, if a provider entity 
demonstrates through accreditation by an approved national accrediting 
organization (AO) that all applicable Medicare conditions are met or 
exceeded, we may deem those provider entities as having met the 
requirements. Accreditation by an AO is voluntary and is not required 
for Medicare participation.
    If an AO is recognized by the Secretary of the Department of Health 
and Human Services as having standards for accreditation that meet or 
exceed Medicare requirements, any provider entity accredited by the 
national accrediting body's approved program may be deemed to meet the 
Medicare conditions. A national AO applying for approval of its 
accreditation program under part 488, subpart A, must provide the 
Centers for Medicare and Medicaid Services (CMS) with reasonable 
assurance that the AO requires the accredited provider entities to meet 
requirements that are at least as stringent as the Medicare conditions. 
Our regulations concerning the approval of accrediting organizations 
are set forth at Sec.  488.5. The regulations at Sec.  488.5(e)(2)(i) 
require AOs to reapply for continued approval of its accreditation 
program every 6 years or sooner as determined by CMS. Det Norske 
Veritas's (DNV's) current term of approval for their hospital 
accreditation program expires September 26, 2022.

II. Application Approval Process

    Section 1865(a)(3)(A) of the Act provides a statutory timetable to 
ensure that our review of applications for CMS approval of an 
accreditation program is conducted in a timely manner. The Act provides 
us 210 days after the date of receipt of a complete application, with 
any documentation necessary to make the determination, to complete our 
survey activities and application process. Within 60 days after 
receiving a complete application, we must publish a notice in the 
Federal Register that identifies the national accrediting body making 
the request, describes the request, and provides no less than a 30-day 
public comment period. At the end of the 210-day period, we must 
publish a notice in the Federal Register approving or denying the 
application.

III. Provisions of the Proposed Notice

    On April 18, 2022, we published a proposed notice in the Federal 
Register (87 FR 22894), announcing DNV's request for continued approval 
of its Medicare hospital accreditation program. In the proposed notice, 
we detailed our evaluation criteria. Under section 1865(a)(2) of the 
Act and in our regulations at Sec.  488.5, we conducted a review of 
DNV's Medicare hospital accreditation renewal application in accordance 
with the criteria specified by our regulations, which include, but are 
not limited to, the following:
     An administrative review of DNV's--(1) corporate policies; 
(2) financial and human resources available to accomplish the proposed 
surveys; (3) procedures for training, monitoring, and evaluation of its 
hospital surveyors; (4)

[[Page 54511]]

ability to investigate and respond appropriately to complaints against 
accredited hospitals; and (5) survey review and decision-making process 
for accreditation.
     The comparison of DNV's Medicare hospital accreditation 
program standards to our current Medicare hospitals Conditions of 
Participation (CoPs).
     A documentation review of DNV's survey process to do the 
following:
    ++ Determine the composition of the survey team, surveyor 
qualifications, and DNV's ability to provide continuing surveyor 
training.
    ++ Compare DNV's processes to those we require of state survey 
agencies, including periodic resurvey and the ability to investigate 
and respond appropriately to complaints against accredited hospitals.
    ++ Evaluate DNV's procedures for monitoring accredited hospitals it 
has found to be out of compliance with DNV's program requirements. 
(This pertains only to monitoring procedures when DNV identifies non-
compliance. If noncompliance is identified by a state survey agency 
through a validation survey, the state survey agency monitors 
corrections as specified at Sec.  488.9(c)).
    ++ Assess DNV's ability to report deficiencies to the surveyed 
hospital and respond to the hospital's plan of correction in a timely 
manner.
    ++ Establish DNV's ability to provide CMS with electronic data and 
reports necessary for effective validation and assessment of the 
organization's survey process.
    ++ Determine the adequacy of DNV's staff and other resources.
    ++ Confirm DNV's ability to provide adequate funding for performing 
required surveys.
    ++ Confirm DNV's policies with respect to surveys being 
unannounced.
    ++ Confirm DNV's policies and procedures to avoid conflicts of 
interest, including the appearance of conflicts of interest, involving 
individuals who conduct surveys or participate in accreditation 
decisions.
    ++ Obtain DNV's agreement to provide CMS with a copy of the most 
current accreditation survey together with any other information 
related to the survey as we may require, including corrective action 
plans.

IV. Analysis of and Response to Public Comments on the Proposed Notice

    In accordance with section 1865(a)(3)(A) of the Act, the April 18, 
2022 proposed notice also solicited public comments regarding whether 
DNV's requirements met or exceeded the Medicare CoPs for hospitals. We 
received one comment in response to our proposed notice. The comment 
received expressed support for DNV's hospital accreditation program.
    The proposed notice described CMS' process and oversight activities 
in Section III., Evaluation of Deeming Authority Request, which 
highlighted the evaluation CMS conducts before granting deeming 
authority to an AO. In Section V. of this final notice, CMS is 
highlighting areas, which were identified to have discrepancies or lack 
of clarity within DNV's standards and survey processes. We note that 
DNV corrected these discrepancies prior to renewal of their deeming 
authority for their CMS-approved hospital accreditation program. CMS 
continues to strive for increased oversight of AOs.

V. Provisions of the Final Notice

A. Differences Between DNV's Standards and Requirements for 
Accreditation and Medicare Conditions and Survey Requirements

    We compared DNV's hospital accreditation program requirements and 
survey process with the Medicare CoPs at 42 CFR part 482, and the 
survey and certification process requirements of parts 488 and 489. Our 
review and evaluation of DNV's hospital application, which were 
conducted as described in Section III. of this final notice, yielded 
the following areas where, as of the date of this notice, DNV has 
revised its standards and certification processes in order to meet our 
requirements at:
     Section 482.13(e)(8)(i)(A) through (C). DNV clarified the 
specific age-based limits with respect to applicable to the amount of 
time a patient could spend in restraint and seclusion in hospitals; 
these limits would supersede any conflicting state law.
     Section 482.15(a)(1). DNV changed its standard to include 
community-based risk assessment in its requirements and all-hazards 
definition in interpretive guidelines.
     Section 482.15(b)(7). DNV addressed the requirement that 
states make arrangements with others hospitals and other providers to 
receive patients in the event of limitation or cessation of operations, 
in order to maintain the continuity of services to hospital patients.
     Section 482.23(b)(4). DNV addressed our concerns 
pertaining to nursing assessment and care plan, to ensure that the 
requirements are comparable with CMS' requirement.
     Sections 482.24(c)(4)(i)(A) through 482.24(c)(4)(i)(C). 
DNV revised its standards to fully meet CMS requirements.
     Section 482.28(b)(2). DNV revised its language from a 
restrictive requirement to include an all patient diet.
     Section 482.41(c). DNV revised language regarding the 
applicability of National Fire Protection Association (NFPA) to 
correspond to 2012 NFPA 99, Section 1.3 Application.
     Section 482.52(c)(2). DNV clarified the requirement 
regarding deferral to state anesthesia practice standards; its prior 
language was unclear.
     Section 482.53(d). DNV clarified its standard regarding 
nuclear medicine documentation requirements to include signed and dated 
language, showing authorship.
     Section 482.57. DNV revised its respiratory care standards 
to include language reflecting ``the needs of the patients'' in order 
to fully reflect CMS' requirement.
     Section 482.58. DNV clarified its standards to include the 
governing body of the hospital bears the responsibility of assuring 
medical staff has written policies.
     Section 482.58(b)(1). DNV revised the standard to be more 
specific and to fully meet the regulatory requirement. DNV's standard 
had not made it clear that the patients have the right to be informed 
of total health status in the language they can understand, but rather 
focused on rules, regulations, and facility responsibilities during 
facility stay.

B. Term of Approval

    Based on our review and observations described in Sections III. and 
V. of this final notice, we approve DNV as a national accreditation 
organization for hospitals that request participation in the Medicare 
program. The decision announced in this final notice is effective 
September 26, 2022 through September 26, 2026 (4 years). In accordance 
with Sec.  488.5(e)(2)(i), the term of the approval will not exceed 6 
years. Due to travel restrictions and the reprioritization of survey 
activities brought on by the 2019 Novel Coronavirus Disease (COVID-19) 
Public Health Emergency (PHE), CMS was unable to observe a hospital 
survey completed by DNV surveyors as part of the application review 
process, which is typically one component of the comparability 
evaluation. Therefore, we are providing DNV with a shorter period of 
approval. Based on our discussions with DNV and the information 
provided in its application, we are confident that DNV will continue to 
ensure that its deemed hospitals continue to meet or

[[Page 54512]]

exceed our required standards. While DNV has taken actions based on the 
findings noted in section V.A. of this final notice (Differences 
Between TJC's Standards and Requirements for Accreditation and Medicare 
Conditions and Survey Requirements), as authorized under Sec.  488.8, 
we will continue ongoing review of DNV's hospital surveys. In keeping 
with CMS's initiative to broadly increase AO oversight, and to ensure 
that our requested revisions by DNV are completed, CMS expects to 
perform more frequent review of DNV's activities in the future.

VI. Collection of Information Requirements

    This document does not impose information collection requirements, 
that is, reporting, recordkeeping, or third-party disclosure 
requirements. Consequently, there is no need for review by the Office 
of Management and Budget under the authority of the Paperwork Reduction 
Act of 1995 (44 U.S.C. 3501 et seq.).
    The Administrator of the Centers for Medicare & Medicaid Services 
(CMS), Chiquita Brooks-LaSure, having reviewed and approved this 
document, authorizes Trenesha Fultz-Mimms, who is the Federal Register 
Liaison, to electronically sign this document for purposes of 
publication in the Federal Register.

Trenesha Fultz-Mimms,
Federal Register Liaison, Center for Medicare & Medicaid Services.
[FR Doc. 2022-19099 Filed 9-2-22; 8:45 am]
BILLING CODE 4120-01-P
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