HIT Standards Committee; Schedule for the Assessment of HIT Policy Committee Recommendations, 53198-53199 [2014-21333]
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53198
Federal Register / Vol. 79, No. 173 / Monday, September 8, 2014 / Notices
Alternatives Under Consideration
As part of the EIS, GSA will study the
impacts of developing an up to 2.1
million rentable square feet
consolidated FBI HQ on three site
alternatives. These sites are:
• Greenbelt—this site is known as the
Greenbelt Metro Station located near the
intersection of Interstates 95/495 and
Greenbelt Station (exit 24) in Prince
George’s County, Maryland.
• Landover—this site is known as the
former Landover Mall located along
Brightseat Road near the intersection of
Interstates 95/495 (exit 17) and
Landover Road (MD 202) in Prince
George’s County, Maryland.
• Springfield—this site is known as
the GSA Franconia Warehouse Complex
located along Loisdale Road just south
of the Franconia-Springfield Parkway
overpass and east of Interstate 95 in
Fairfax County, Virginia.
Additionally, GSA will study
potential impacts related to the
exchange of the JEH parcel. GSA also
will evaluate a ‘‘No Action Alternative’’,
in which FBI would remain in the
current locations without consolidation
at a new permanent location.
Resource areas to be addressed in the
EIS will include, but not be limited to:
Air quality, noise, land use,
socioeconomics, traffic and
transportation, infrastructure and
community services, natural resources,
biological resources, cultural resources,
and safety and environmental hazards.
The analysis will evaluate direct,
indirect, and cumulative impacts.
Relevant and reasonable measures that
could avoid or mitigate environmental
effects will also be analyzed. In
conjunction with the NEPA process,
GSA will undertake any consultations
required by applicable laws or
regulations, including NHPA.
rmajette on DSK2TPTVN1PROD with NOTICES
Scoping Process
In accordance with NEPA, a scoping
process will be conducted to: (1) Aid in
determining the alternatives to be
considered and the scope of issues to be
addressed; and (2) identify the
significant environmental issues related
to the proposed FBI HQ consolidation
that should be addressed during the
preparation of the Draft EIS. Scoping
will be accomplished through a series of
public scoping meetings; mail and email
correspondence to potentially interested
persons, agencies, and organizations;
social media and other web-based
communications; and meetings with
agencies having an interest in the FBI
HQ consolidation. GSA is also using the
NEPA scoping process to facilitate
consultation with the public under
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Section 106 of the NHPA (36 CFR Part
800). GSA welcomes comments from the
public to ensure that the agency takes
into account the effects of the proposed
action on historic and cultural
resources.
GSA will publish announcement
notices in the Washington Post,
Washington Business Journal,
Springfield Connection, Greenbelt
Patch, and Hyattsville Patch
approximately one to two weeks prior to
the public scoping meetings. After
receiving scoping comments, GSA will
respond to them in the EIS and through
the Section 106 consultation process.
GSA will make available to the public
a comment/response matrix
summarizing the scoping and Section
106 comments in the Draft and Final
EIS.
Written Comments: Agencies and the
public are encouraged to provide
written comments on the scoping issues
related to the EIS for the proposed FBI
HQ consolidation in addition to, or in
lieu of, providing comments at the
public scoping meeting. Written
comments must be postmarked no later
than October 23, 2014, and sent to the
General Services Administration,
Attention: Nia Francis, Project Manager,
301 7th Street SW., Room 4004,
Washington, DC 20407. Email:
fbiheadquarters@gsa.gov using the
subject line: NEPA Scoping Comment.
Dated: September 3, 2014.
Mina Wright,
Director, Office of Planning and Design
Quality, National Capital Region, Public
Buildings Service.
[FR Doc. 2014–21329 Filed 9–5–14; 8:45 am]
BILLING CODE 6820–23–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
HIT Standards Committee; Schedule
for the Assessment of HIT Policy
Committee Recommendations
Office of the National
Coordinator for Health Information
Technology, HHS.
ACTION: Notice.
AGENCY:
Section 3003(b)(3) of the
American Recovery and Reinvestment
Act of 2009 mandates that the HIT
Standards Committee develop a
schedule for the assessment of policy
recommendations developed by the HIT
Policy Committee and publish it in the
Federal Register. This notice fulfills the
requirements of Section 3003(b)(3) and
updates the schedule posted in the
Federal Register on May 8, 2013. In
anticipation of receiving
SUMMARY:
PO 00000
Frm 00037
Fmt 4703
Sfmt 4703
recommendations originally developed
by the HIT Policy Committee, the HIT
Standards Committee has created six (6)
workgroups to analyze the following
areas: (1) Content standards; (2)
semantic standards; (3) transport and
security; (4) implementation,
certification, and testing; (5)
architecture, services and application
program interfaces (APIs); (6) a steering
committee to provide continuity across
all other groups. Other groups are
convened to address specific issues as
needed.
HIT Standards Committee’s Schedule
for the Assessment of HIT Policy
Committee Recommendations is as
follows:
The National Coordinator will
establish priority areas based in part on
recommendations received from the HIT
Policy Committee regarding health
information technology standards,
implementation specifications, and/or
certification criteria. Once the HIT
Standards Committee is informed of
those priority areas, it will:
(A) Direct the appropriate workgroup
or other special group to develop a
report for the HIT Standards Committee,
to the extent possible, within 90 days,
which will include, among other items,
the following:
(1) An assessment of what standards,
implementation specifications, and
certification criteria are currently
available to meet the priority area;
(2) An assessment of where gaps exist
(i.e., no standard is available or
harmonization is required because more
than one standard exists) and identify
potential organizations that have the
capability to address those gaps; and
(3) a timeline, which may also
account for NIST testing, where
appropriate, and include dates when the
HIT Standards Committee is expected to
issue recommendation(s) to the National
Coordinator.
(B) Upon receipt of a report from a
workgroup or other special group, the
HIT Standards Committee will:
(1) Accept the timeline provided by
the subcommittee, and, if necessary,
revise it; and
(2) assign subcommittee(s) to conduct
research and solicit testimony, where
appropriate, and issue
recommendations to the full committee
in a timely manner.
(C) Advise the National Coordinator,
consistent with the accepted timeline in
(B)(1) and after NIST testing, where
appropriate, on standards,
implementation specifications, and/or
certification criteria, for the National
Coordinator’s review and determination
whether or not to endorse the
recommendations, and possible
E:\FR\FM\08SEN1.SGM
08SEN1
53199
Federal Register / Vol. 79, No. 173 / Monday, September 8, 2014 / Notices
adoption of the proposed
recommendations by the Secretary of
the Department of Health and Human
Services.
The standards and related topics
which the HIT Standards Committee is
expected to address over the coming
year include, but may not be limited to:
Quality measurement; the extended
portfolio of standards for the nationwide
health information network; distributed
queries and results; radiology;
consumer-mediated information
exchange; public health; data
portability; and a process for the
maintenance of standards.
For a listing of upcoming HIT
Standards Committee meetings, please
visit the ONC Web site at https://
www.healthit.gov/facas/calendar.
Notice of this schedule is given under
the American Recovery and
Reinvestment Act of 2009 (Pub. L. 111–
5), section 3003.
Dated: August 18, 2014.
Michelle Consolazio,
FACA Lead, Office of Policy, Office of the
National Coordinator for Health Information
Technology.
[FR Doc. 2014–21333 Filed 9–5–14; 8:45 am]
BILLING CODE 4150–45–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[30Day–14–0666]
Agency Forms Undergoing Paperwork
Reduction Act Review
The Centers for Disease Control and
Prevention (CDC) has submitted the
following information collection request
to the Office of Management and Budget
(OMB) for review and approval in
accordance with the Paperwork
Reduction Act of 1995. The notice for
the proposed information collection is
published to obtain comments from the
public and affected agencies.
Written comments and suggestions
from the public and affected agencies
concerning the proposed collection of
information are encouraged. Your
comments should address any of the
following: (a) Evaluate whether the
proposed collection of information is
necessary for the proper performance of
the functions of the agency, including
whether the information will have
practical utility; (b) Evaluate the
accuracy of the agencies estimate of the
burden of the proposed collection of
information, including the validity of
the methodology and assumptions used;
(c) Enhance the quality, utility, and
clarity of the information to be
collected; (d) Minimize the burden of
the collection of information on those
who are to respond, including through
the use of appropriate automated,
electronic, mechanical, or other
technological collection techniques or
other forms of information technology,
e.g., permitting electronic submission of
responses; and (e) Assess information
collection costs.
To request additional information on
the proposed project or to obtain a copy
of the information collection plan and
instruments, call (404) 639–7570 or
send an email to omb@cdc.gov. Written
comments and/or suggestions regarding
the items contained in this notice
should be directed to the Attention:
CDC Desk Officer, Office of Management
and Budget, Washington, DC 20503 or
by fax to (202) 395–5806. Written
comments should be received within 30
days of this notice.
Proposed Project
National Healthcare Safety Network
(NHSN) (OMB No. 0920–0666), exp. 12/
31/2015—Revision—National Center for
Emerging and Zoonotic Infectious
Diseases (NCEZID), Centers for Disease
Control and Prevention (CDC).
Background and Brief Description
The National Healthcare Safety
Network (NHSN) is a system designed to
accumulate, exchange, and integrate
relevant information and resources
among private and public stakeholders
to support local and national efforts to
protect patients and promote healthcare
safety. Specifically, the data is used to
determine the magnitude of various
healthcare-associated adverse events
and trends in the rates of these events
among patients and healthcare workers
with similar risks. The data will be used
to detect changes in the epidemiology of
adverse events resulting from new and
current medical therapies and changing
risks. The NHSN currently consists of
five components: Patient Safety,
Healthcare Personnel Safety,
Biovigilance, Long-Term Care Facility
(LTCF), and Dialysis. Two new
components will be added within the
next one to two years: Outpatient
Procedure and Antimicrobial Use &
Resistance.
The Antimicrobial Use and Resistance
(AUR) component will be launched
within NHSN that will specifically
examine antimicrobial use (AU) and
antimicrobial resistance (AR) within
healthcare facilities. The goal of the
AUR component is to provide a
mechanism for facilities to report and
analyze antimicrobial use and/or
resistance as part of local or regional
efforts to reduce antimicrobial resistant
infections through antimicrobial
stewardship efforts or interruption of
transmission of resistant pathogens at
their facility. This revision submission
includes one new form specific to the
NHSN AUR component.
Significant additions were made to
three NHSN facility surveys. Questions
about infection control practices were
added to gain a better understanding of
current practices and identify areas to
target prevention efforts among facilities
that have reported a multidrug-resistant
organism. Questions about antibiotic
stewardship were added to gain a better
understanding of current efforts to
improve antibiotic use in hospitals and
to assess the quality of hospital
antibiotic stewardship programs.
Additionally, minor revisions have
been made to 31 other forms within the
package to clarify and/or update
surveillance definitions. Three forms are
being removed as patient vaccination
monitoring will be removed from
NHSN.
The previously approved NSHN
package included 56 individual
collection forms; the current revision
request adds one new form and removes
three forms for a total of 54 forms. The
reporting burden will increase by
172,943 hours, for a total of 4,277,716
hours.
rmajette on DSK2TPTVN1PROD with NOTICES
ESTIMATED ANNUALIZED BURDEN HOURS
Number of
respondents
Type of respondents
Form name
Registered Nurse (Infection Preventionist) .....
Registered Nurse (Infection Preventionist) .....
Registered Nurse (Infection Preventionist) .....
NHSN Registration Form ...............................
Facility Contact Information ...........................
Patient Safety Component—Annual Hospital
Survey.
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Fmt 4703
Sfmt 4703
E:\FR\FM\08SEN1.SGM
2,000
2,000
6,000
08SEN1
Number of
responses
per
respondent
Average
burden per
response
(in hrs.)
1
1
1
5/60
10/60
50/60
Agencies
[Federal Register Volume 79, Number 173 (Monday, September 8, 2014)]
[Notices]
[Pages 53198-53199]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2014-21333]
=======================================================================
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
HIT Standards Committee; Schedule for the Assessment of HIT
Policy Committee Recommendations
AGENCY: Office of the National Coordinator for Health Information
Technology, HHS.
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: Section 3003(b)(3) of the American Recovery and Reinvestment
Act of 2009 mandates that the HIT Standards Committee develop a
schedule for the assessment of policy recommendations developed by the
HIT Policy Committee and publish it in the Federal Register. This
notice fulfills the requirements of Section 3003(b)(3) and updates the
schedule posted in the Federal Register on May 8, 2013. In anticipation
of receiving recommendations originally developed by the HIT Policy
Committee, the HIT Standards Committee has created six (6) workgroups
to analyze the following areas: (1) Content standards; (2) semantic
standards; (3) transport and security; (4) implementation,
certification, and testing; (5) architecture, services and application
program interfaces (APIs); (6) a steering committee to provide
continuity across all other groups. Other groups are convened to
address specific issues as needed.
HIT Standards Committee's Schedule for the Assessment of HIT Policy
Committee Recommendations is as follows:
The National Coordinator will establish priority areas based in
part on recommendations received from the HIT Policy Committee
regarding health information technology standards, implementation
specifications, and/or certification criteria. Once the HIT Standards
Committee is informed of those priority areas, it will:
(A) Direct the appropriate workgroup or other special group to
develop a report for the HIT Standards Committee, to the extent
possible, within 90 days, which will include, among other items, the
following:
(1) An assessment of what standards, implementation specifications,
and certification criteria are currently available to meet the priority
area;
(2) An assessment of where gaps exist (i.e., no standard is
available or harmonization is required because more than one standard
exists) and identify potential organizations that have the capability
to address those gaps; and
(3) a timeline, which may also account for NIST testing, where
appropriate, and include dates when the HIT Standards Committee is
expected to issue recommendation(s) to the National Coordinator.
(B) Upon receipt of a report from a workgroup or other special
group, the HIT Standards Committee will:
(1) Accept the timeline provided by the subcommittee, and, if
necessary, revise it; and
(2) assign subcommittee(s) to conduct research and solicit
testimony, where appropriate, and issue recommendations to the full
committee in a timely manner.
(C) Advise the National Coordinator, consistent with the accepted
timeline in (B)(1) and after NIST testing, where appropriate, on
standards, implementation specifications, and/or certification
criteria, for the National Coordinator's review and determination
whether or not to endorse the recommendations, and possible
[[Page 53199]]
adoption of the proposed recommendations by the Secretary of the
Department of Health and Human Services.
The standards and related topics which the HIT Standards Committee
is expected to address over the coming year include, but may not be
limited to: Quality measurement; the extended portfolio of standards
for the nationwide health information network; distributed queries and
results; radiology; consumer-mediated information exchange; public
health; data portability; and a process for the maintenance of
standards.
For a listing of upcoming HIT Standards Committee meetings, please
visit the ONC Web site at https://www.healthit.gov/facas/calendar.
Notice of this schedule is given under the American Recovery and
Reinvestment Act of 2009 (Pub. L. 111-5), section 3003.
Dated: August 18, 2014.
Michelle Consolazio,
FACA Lead, Office of Policy, Office of the National Coordinator for
Health Information Technology.
[FR Doc. 2014-21333 Filed 9-5-14; 8:45 am]
BILLING CODE 4150-45-P