Record of Decision for the Final Supplemental Environmental Impact Statement for the Roybal Campus 2025 Master Plan; Correction, 77843-77844 [2022-27584]
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77843
Federal Register / Vol. 87, No. 243 / Tuesday, December 20, 2022 / Notices
information collection request (ICR)
titled ‘‘Awardee Lead Profile
Assessment (ALPA)’’ (OMB Control No.
0920–1215; Exp. Date 03/31/2024). The
goal of this ICR is to build on the CDC’s
existing childhood lead poisoning
prevention program. CDC requires that
ongoing and new CDC Childhood Lead
Poisoning Prevention Programs
(CLPPPs), including the FY21
‘‘Childhood Lead Poisoning Prevention
and Surveillance of Blood Lead Levels
in Children’’ (CDC–RFA–EH21–2102),
complete the ALPA annually. This
annual information collection will be
used to identify jurisdictional legal
frameworks governing CDC-funded
childhood lead poisoning programs
(CLPPPs) in the United States and
strategies for implementing childhood
will be eliminated. This program
management survey has been revised in
several ways, including the addition of
new answer options and questions to
understand usage of the updated blood
lead reference value (BLRV). The time
per response is the same from the 2021
estimate (47 minutes per response)
despite revisions to the survey. This
updated estimate is based on recent
pilot tests of the revised survey among
nine respondents, and includes the time
needed to review the ALPA Training
Manual.
CDC is requesting OMB approval for
a total time burden of 59 hours and a
total number of 75 respondents per year.
These estimates remain unchanged from
the previous PRA clearance.
lead poisoning prevention activities.
CDC will use this information to inform
guidance, resource development, and
technical assistance activities in support
of the ultimate goal, which is
eliminating lead exposure in children.
The dissemination of these ALPA
results will ensure that both funded and
non-funded jurisdictions are able to: (1)
identify policies and other factors that
support or hinder childhood lead
poisoning prevention efforts; (2)
understand what strategies are being
used by funded public health agencies
to implement childhood lead poisoning
prevention activities; and (3) use this
knowledge to develop and apply similar
strategies to support the national agenda
to eliminate childhood lead poisoning.
CDC will now use one data collection
mode, a web survey. Reporting via email
ESTIMATED ANNUALIZED BURDEN HOURS
Number of
responses per
respondent
Average
burden per
response
(in hours)
Total burden
hours
Form name
State or Local Governments (or their
bona fide fiscal agents).
ALPA Web Survey ...........................
75
1
47/60
59
Total ...........................................
..........................................................
........................
........................
........................
59
Jeffrey M. Zirger,
Lead, Information Collection Review Office,
Office of Scientific Integrity, Office of Science,
Centers for Disease Control and Prevention.
[FR Doc. 2022–27508 Filed 12–19–22; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
Centers for Disease Control and
Prevention (CDC)/Health Resources
and Services Administration (HRSA)
Advisory Committee on HIV, Viral
Hepatitis and STD Prevention and
Treatment (CHAC); Notice of Charter
Renewal
Centers for Disease Control and
Prevention (CDC), Department of Health
and Human Services (HHS).
ACTION: Notice of charter renewal.
AGENCY:
This gives notice under the
Federal Advisory Committee Act of
October 6, 1972, that the Centers for
Disease Control and Prevention (CDC)/
Health Resources and Services
Administration (HRSA) Advisory
Committee on HIV, Viral Hepatitis and
STD Prevention and Treatment (CHAC),
Centers for Disease Control and
SUMMARY:
lotter on DSK11XQN23PROD with NOTICES1
Number of
respondents
Type of respondent
VerDate Sep<11>2014
18:41 Dec 19, 2022
Jkt 259001
Prevention, Department of Health and
Human Services, has been renewed for
a 2-year period through November 25,
2024.
FOR FURTHER INFORMATION CONTACT:
CAPT Deron Burton, MD, JD, MPH,
Acting Designed Federal Officer,
Centers for Disease Control and
Prevention (CDC)/Health Resources and
Services Administration (HRSA)
Advisory Committee on HIV, Viral
Hepatitis and STD Prevention and
Treatment (CHAC), CDC, HHS, 1600
Clifton Road, NE, Mailstop US8–6,
Atlanta, Georgia 30329–4027;
Telephone (404) 639–1506; Email:
DBurton@cdc.gov.
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announcements of meetings and other
committee management activities, for
both the Centers for Disease Control and
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. 2022–27481 Filed 12–19–22; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[Docket No. CDC–2022–0014]
Record of Decision for the Final
Supplemental Environmental Impact
Statement for the Roybal Campus 2025
Master Plan; Correction
Centers for Disease Control and
Prevention (CDC), Department of Health
and Human Services (HHS).
ACTION: General notice.
AGENCY:
On November 17, 2022, the
Centers for Disease Control and
Prevention (CDC), within the
Department of Health and Human
Services (HHS), published a notice in
the Federal Register announcing the
Record of Decision (ROD) for the Final
Supplemental Environmental Impact
Statement (SEIS) for CDC’s Roybal
Campus in Atlanta, Georgia. In the
Decision section of the notice, the
description of the incinerator was
incorrect.
FOR FURTHER INFORMATION CONTACT:
Thayra Riley, NEPA Coordinator, Office
of Safety, Security, and Asset
Management, Centers for Disease
Control and Prevention, 1600 Clifton
SUMMARY:
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77844
Federal Register / Vol. 87, No. 243 / Tuesday, December 20, 2022 / Notices
Road NE, Mailstop H20–4, Atlanta,
Georgia 30329. Email: cdc-roybalgaseis@cdc.gov. Telephone: 770–488–
8170.
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
SUPPLEMENTARY INFORMATION:
[CMS–1774–FN]
Correction
In the Decision section of the Federal
Register notice of November 17, 2022
(87 FR 69023), center column, the
description of the incinerator was
labeled as a Hazardous/Medical/
Infectious Waste Incinerator. The
correct description is a Hospital/
Medical/Infectious Waste Incinerator.
The correct Decision section to read:
Decision
Dated: December 15, 2022.
Angela K. Oliver,
Executive Secretary, Centers for Disease
Control and Prevention.
lotter on DSK11XQN23PROD with NOTICES1
Centers for Medicare &
Medicaid Services (CMS), HHS.
ACTION: Notice.
AGENCY:
This notice announces our
decision to approve the request from
Doctors Hospital at Renaissance, Ltd.’s
for an exception to the prohibition on
expansion of facility capacity.
DATES: The decision announced in this
notice is applicable on December 16,
2022.
SUMMARY:
Based on the Final SEIS, CDC has
decided to implement Alternative 1
(Preferred Alternative) as the selected
alternative. This Alternative includes
the construction and operation of a new
Hospital/Medical/Infectious Waste
Incinerator in a new laboratory building,
the operation of two proposed
emergency standby power diesel
generators to support that laboratory,
and annual testing of the generators.
According to the analysis, no potential
significant impacts were identified for
the selected alternative.
CDC’s decision is based on an
analysis of the potential impacts of the
alternatives considered in the SEIS
weighed against CDC’s continuing need
to fulfill its unique and critical public
health mission and its ability to mitigate
in whole or in part the adverse impacts.
CDC also considered the input from the
public and agencies, such as the U.S.
Fish and Wildlife Service, Georgia
Department of Natural Resources,
Georgia Environmental Protection
Division, and Georgia Historic
Preservation Division.
Availability of the ROD: The ROD is
available in the Supplemental Materials
tab of the docket found on the Federal
eRulemaking Portal at https://
www.regulations.gov, identified by
Docket No. CDC–2022–0014.
[FR Doc. 2022–27584 Filed 12–19–22; 8:45 am]
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VerDate Sep<11>2014
Medicare Program; Approval of
Request for an Exception to the
Prohibition on Expansion of Facility
Capacity Under the Hospital
Ownership and Rural Provider
Exceptions to the Physician SelfReferral Prohibition
18:41 Dec 19, 2022
Jkt 259001
POH-ExceptionRequests@
cms.hhs.gov.
ADDRESSES:
I. Background
Section 1877 of the Social Security
Act (the Act), also known as the
physician self-referral law: (1) prohibits
a physician from making referrals for
certain designated health services
payable by Medicare to an entity with
which he or she (or an immediate family
member) has a financial relationship
unless the requirements of an applicable
exception are satisfied; and (2) prohibits
the entity from filing claims with
Medicare (or billing another individual,
entity, or third party payer) for any
improperly referred designated health
services. A financial relationship may
be an ownership or investment interest
in the entity or a compensation
arrangement with the entity. The statute
establishes a number of specific
exceptions and grants the Secretary of
the Department of Health and Human
Services (the Secretary) the authority to
create regulatory exceptions for
financial relationships that do not pose
a risk of program or patient abuse.
Section 1877(d) of the Act sets forth
exceptions related to ownership or
investment interests held by a physician
(or an immediate family member of a
physician) in an entity that furnishes
designated health services. Section
1877(d)(2) of the Act provides an
exception for ownership or investment
interests in rural providers (the ‘‘rural
provider exception’’). In order to qualify
for the rural provider exception, the
designated health services must be
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furnished in a rural area (as defined in
section 1886(d)(2) of the Act) and
substantially all the designated health
services furnished by the entity must be
furnished to individuals residing in a
rural area. In addition, in the case where
the entity is a hospital, the hospital
must meet the requirements of section
1877(i)(1) of the Act no later than
September 23, 2011. Section 1877(d)(3)
of the Act provides an exception for
ownership or investment interests in a
hospital located outside of Puerto Rico
(the ‘‘whole hospital exception’’). In
order to qualify for the whole hospital
exception, the referring physician must
be authorized to perform services at the
hospital, the ownership or investment
interest must be in the hospital itself
(and not merely in a subdivision of the
hospital), and the hospital must meet
the requirements of section 1877(i)(1) of
the Act no later than September 23,
2011.
II. Prohibition on Facility Expansion
Section 6001(a)(3) of the Patient
Protection and Affordable Care Act
(Affordable Care Act) (Pub. L. 111–148)
amended the rural provider and whole
hospital exceptions to provide that a
hospital may not increase the number of
operating rooms, procedure rooms, and
beds beyond that for which the hospital
was licensed on March 23, 2010 (or, in
the case of a hospital that did not have
a provider agreement in effect as of this
date, but did have a provider agreement
in effect on December 31, 2010, the
effective date of such provider
agreement) (the hospital’s ‘‘baseline
number of operating rooms, procedure
rooms, and beds’’). Thus, since March
23, 2010, a physician-owned hospital
that seeks to avail itself of either
exception is prohibited from expanding
the number of operating rooms,
procedure rooms, and beds (‘‘facility
capacity’’) unless it has been granted an
exception to the prohibition by the
Secretary.
Section 6001(a)(3) of the Affordable
Care Act added new section
1877(i)(3)(A)(i) of the Act, which
required the Secretary to establish and
implement a process for granting
exceptions to the prohibition on
expansion of facility capacity for
hospitals that qualify as an ‘‘applicable
hospital.’’ Section 1106 of the Health
Care and Education Reconciliation Act
of 2010 (Pub. L. 111–152) amended
section 1877(i)(3)(A)(i) of the Act to
require the Secretary to establish and
implement a process for granting
exceptions to the prohibition on
expansion of facility capacity for
hospitals that qualify as either an
‘‘applicable hospital’’ or a ‘‘high
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Agencies
[Federal Register Volume 87, Number 243 (Tuesday, December 20, 2022)]
[Notices]
[Pages 77843-77844]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2022-27584]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[Docket No. CDC-2022-0014]
Record of Decision for the Final Supplemental Environmental
Impact Statement for the Roybal Campus 2025 Master Plan; Correction
AGENCY: Centers for Disease Control and Prevention (CDC), Department of
Health and Human Services (HHS).
ACTION: General notice.
-----------------------------------------------------------------------
SUMMARY: On November 17, 2022, the Centers for Disease Control and
Prevention (CDC), within the Department of Health and Human Services
(HHS), published a notice in the Federal Register announcing the Record
of Decision (ROD) for the Final Supplemental Environmental Impact
Statement (SEIS) for CDC's Roybal Campus in Atlanta, Georgia. In the
Decision section of the notice, the description of the incinerator was
incorrect.
FOR FURTHER INFORMATION CONTACT: Thayra Riley, NEPA Coordinator, Office
of Safety, Security, and Asset Management, Centers for Disease Control
and Prevention, 1600 Clifton
[[Page 77844]]
Road NE, Mailstop H20-4, Atlanta, Georgia 30329. Email: [email protected]. Telephone: 770-488-8170.
SUPPLEMENTARY INFORMATION:
Correction
In the Decision section of the Federal Register notice of November
17, 2022 (87 FR 69023), center column, the description of the
incinerator was labeled as a Hazardous/Medical/Infectious Waste
Incinerator. The correct description is a Hospital/Medical/Infectious
Waste Incinerator. The correct Decision section to read:
Decision
Based on the Final SEIS, CDC has decided to implement Alternative 1
(Preferred Alternative) as the selected alternative. This Alternative
includes the construction and operation of a new Hospital/Medical/
Infectious Waste Incinerator in a new laboratory building, the
operation of two proposed emergency standby power diesel generators to
support that laboratory, and annual testing of the generators.
According to the analysis, no potential significant impacts were
identified for the selected alternative.
CDC's decision is based on an analysis of the potential impacts of
the alternatives considered in the SEIS weighed against CDC's
continuing need to fulfill its unique and critical public health
mission and its ability to mitigate in whole or in part the adverse
impacts. CDC also considered the input from the public and agencies,
such as the U.S. Fish and Wildlife Service, Georgia Department of
Natural Resources, Georgia Environmental Protection Division, and
Georgia Historic Preservation Division.
Availability of the ROD: The ROD is available in the Supplemental
Materials tab of the docket found on the Federal eRulemaking Portal at
https://www.regulations.gov, identified by Docket No. CDC-2022-0014.
Dated: December 15, 2022.
Angela K. Oliver,
Executive Secretary, Centers for Disease Control and Prevention.
[FR Doc. 2022-27584 Filed 12-19-22; 8:45 am]
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