Health Information Technology Advisory Committee 2018 Schedule, 9859-9860 [2018-04543]
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Federal Register / Vol. 83, No. 46 / Thursday, March 8, 2018 / Notices
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Dated: March 2, 2018.
Leslie Kux,
Associate Commissioner for Policy.
[FR Doc. 2018–04629 Filed 3–7–18; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Health Information Technology
Advisory Committee 2018 Schedule
Office of the National
Coordinator for Health Information
Technology (ONC), HHS.
ACTION: Notice of the Health Information
Technology Advisory Committee 2018
schedule.
AGENCY:
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This notice fulfills obligations
under section 3002 of the Public Health
Service Act (PHSA), as amended by the
21st Century Cures Act. Section 3002(b)
(5) of the PHSA, as amended, mandates
that the Health Information Technology
Advisory Committee shall develop a
schedule for the assessment of policy
recommendations and the Secretary
shall publish such schedule in the
Federal Register.
FOR FURTHER INFORMATION CONTACT:
Lauren Richie Designated Federal
Officer, at Lauren.Richie@hhs.gov.
SUPPLEMENTARY INFORMATION: Section
3002 of the Public Health Service Act
(PHSA), as amended by the 21st Century
Cures Act (Pub. L. 114–255), establishes
the Health Information Technology
Advisory Committee (HITAC). The
HITAC will be governed by the
provisions of the Federal Advisory
Committee Act (Pub. L. 92–463), as
amended (5 U.S.C. App.), which sets
forth standards for the formation and
use of federal advisory committees. The
HITAC, among other things, shall
identify priorities for standards
adoption and make recommendations to
the National Coordinator for Health
Information Technology (National
Coordinator) on a policy framework to
advance an interoperable health
information technology infrastructure.
SUMMARY:
Health Information Technology
Advisory Committee Schedule
Section 3002(b)(5) of the PHSA, as
amended, provides that the HITAC shall
develop a schedule for the assessment of
policy recommendations developed by
the HITAC and publish the schedule in
the Federal Register. This schedule
addresses the assessment of
recommendations outlined in the policy
framework recommended by the HITAC
to the National Coordinator.
Accordingly, the schedule for the
HITAC’s assessment of policy
recommendations is as follows:
1. Within 90 days of a charge by the
National Coordinator for
recommendations on a matter, identify
the best mechanism to organize itself to
develop recommendations, and at a
minimum, will:
a. Develop an assessment of what
policies, standards, implementation
specifications, and certification criteria
are currently available to be considered
as part of the request;
b. Consider where gaps exist and
identify potential organizations that
have the capability to address those
gaps (i.e., no policy or standard is
available or harmonization is required
because more than one standard exists)
related to the request; and
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9859
c. Create a timeline, which may also
account for the National Institute of
Standards and Technology (NIST)
testing, where appropriate, and include
dates when the HITAC is expected to
issue the recommendation to the
National Coordinator.
d. Include an opportunity for public
comment during the consideration by
the HITAC of the request by the
National Coordinator for
recommendations on a matter.
2. In responding to the National
Coordinator:
a. Approve a timeline to deliver
recommendations to the National
Coordinator; and
b. Establish a task force to conduct
analysis and solicit input, where
appropriate, and develop draft
recommendations to be considered by
the full committee in a timely manner.
3. In collaboration with NIST,
annually and through the use of public
input, review and publish priorities for
the use of health information
technology, standards, and
implementation specifications to
support those priorities.
4. Recommend to the National
Coordinator for purposes of adoption
under section 3004, standards,
implementation specifications, and
certification criteria and an order of
priority for the development,
harmonization, and recognition of such
standards, specifications, and
certification criteria. Such
recommendations shall include
recommended standards, architectures,
and software schemes for access to
electronic individually identifiable
health information across disparate
systems including user vetting,
authentication, privilege management,
and access control.
The topics in which the HITAC is
expected to address in FY2018 include,
but may not be limited to the target
areas as defined in section 3002 of the
PHSA, as amended by the 21st Century
Cures Act (Pub. L. 114–255), and they
include:
1. Achieving a health information
technology infrastructure that allows for
the electronic access, exchange, and use
of health information ;
2. The promotion and protection of
privacy and security of health
information in health information
technology;
3. The facilitation of secure access by
an individual to such individual’s
protected health information; and
4. Any other target area that the
HITAC identifies as an appropriate
target area to be considered. [42USC
§ 300jj (b)(2)(B)]
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9860
Federal Register / Vol. 83, No. 46 / Thursday, March 8, 2018 / Notices
Notice of this meeting is given under
section 3002(b)(5) of the PHSA, as
amended.
Dated: March 1, 2018.
Lauren Richie,
Branch Chief, Office of Policy, Office of the
National Coordinator for Health Information
Technology.
[FR Doc. 2018–04543 Filed 3–7–18; 8:45 am]
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DEPARTMENT OF HOMELAND
SECURITY
U.S. Citizenship and Immigration
Services
[OMB Control Number 1615–0122]
Agency Information Collection
Activities; Revision of a Currently
Approved Collection: Identity,
Credential, and Access Management
(ICAM)
U.S. Citizenship and
Immigration Services, Department of
Homeland Security.
ACTION: 60-Day notice.
AGENCY:
The Department of Homeland
Security (DHS), U.S. Citizenship and
Immigration (USCIS) invites the general
public and other Federal agencies to
comment upon this proposed revision of
a currently approved collection of
information or new collection of
information. In accordance with the
Paperwork Reduction Act (PRA) of
1995, the information collection notice
is published in the Federal Register to
obtain comments regarding the nature of
the information collection, the
categories of respondents, the estimated
burden (i.e. the time, effort, and
resources used by the respondents to
respond), the estimated cost to the
respondent, and the actual information
collection instruments.
DATES: Comments are encouraged and
will be accepted for 60 days until May
7, 2018.
ADDRESSES: All submissions received
must include the OMB Control Number
1615–0122 in the body of the letter, the
agency name and Docket ID USCIS–
2011–0015. To avoid duplicate
submissions, please use only one of the
following methods to submit comments:
(1) Online. Submit comments via the
Federal eRulemaking Portal website at
https://www.regulations.gov under
e-Docket ID number USCIS–2011–0015;
(2) Mail. Submit written comments to
DHS, USCIS, Office of Policy and
Strategy, Chief, Regulatory Coordination
Division, 20 Massachusetts Avenue NW,
Washington, DC 20529–2140.
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SUMMARY:
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FOR FURTHER INFORMATION CONTACT:
USCIS, Office of Policy and Strategy,
Regulatory Coordination Division,
Samantha Deshommes, Chief, 20
Massachusetts Avenue NW,
Washington, DC 20529–2140, telephone
number 202–272–8377 (This is not a
toll-free number. Comments are not
accepted via telephone message). Please
note contact information provided here
is solely for questions regarding this
notice. It is not for individual case
status inquiries. Applicants seeking
information about the status of their
individual cases can check Case Status
Online, available at the USCIS website
at https://www.uscis.gov, or call the
USCIS National Customer Service
Center at 800–375–5283 (TTY 800–767–
1833).
SUPPLEMENTARY INFORMATION:
Comments
You may access the information
collection instrument with instructions,
or additional information by visiting the
Federal eRulemaking Portal site at:
https://www.regulations.gov and enter
USCIS–2011–0015 in the search box.
Regardless of the method used for
submitting comments or material, all
submissions will be posted, without
change, to the Federal eRulemaking
Portal at https://www.regulations.gov,
and will include any personal
information you provide. Therefore,
submitting this information makes it
public. You may wish to consider
limiting the amount of personal
information that you provide in any
voluntary submission you make to DHS.
DHS may withhold information
provided in comments from public
viewing that it determines may impact
the privacy of an individual or is
offensive. For additional information,
please read the Privacy Act notice that
is available via the link in the footer of
https://www.regulations.gov.
Written comments and suggestions
from the public and affected agencies
should address one or more of the
following four points:
(1) 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;
(2) Evaluate the accuracy of the
agency’s estimate of the burden of the
proposed collection of information,
including the validity of the
methodology and assumptions used;
(3) Enhance the quality, utility, and
clarity of the information to be
collected; and
(4) Minimize the burden of the
collection of information on those who
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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.
Overview of This Information
Collection
(1) Type of Information Collection:
Revision of a Currently Approved
Collection.
(2) Title of the Form/Collection:
Identity, Credential, and Access
Management (ICAM).
(3) Agency form number, if any, and
the applicable component of the DHS
sponsoring the collection: ICAM; USCIS.
(4) Affected public who will be asked
or required to respond, as well as a brief
abstract: Primary: Individuals or
households. In order to interact with
USCIS electronic systems accessible
through the USCIS ICAM portal, a first
time user must establish an account.
The account creation process requires
the user to submit a valid email address;
create a password; select their
preference for receiving a one-time
password (via email address, mobile
phone, or two-factor authentication
application on a mobile device); select
five password reset questions and
responses; and indicate the account type
they want to set up (customer or legal
representative). The account creation
and the account login processes both
require the user to receive and submit
a one-time password. The one-time
password can be provided either as an
email to an email address or to a mobile
phone via text message. The customer
also has the option of receiving a onetime password readable by a two-factor
authentication application on a mobile
device. If the authentication application
option is selected, the customer can
either scan a QR code or enter a text
code.
USCIS ICAM currently grants access
to myUSCIS and the USCIS information
collections available for e-filing.
(5) An estimate of the total number of
respondents and the amount of time
estimated for an average respondent to
respond: The estimated total number of
respondents for the information
collection ICAM is 1,772,600 and the
estimated hour burden per response is
0.167 hours.
(6) An estimate of the total public
burden (in hours) associated with the
collection: The total estimated annual
hour burden associated with this
collection is 296,024 hours.
(7) An estimate of the total public
burden (in cost) associated with the
collection: The estimated total annual
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Agencies
[Federal Register Volume 83, Number 46 (Thursday, March 8, 2018)]
[Notices]
[Pages 9859-9860]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2018-04543]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Health Information Technology Advisory Committee 2018 Schedule
AGENCY: Office of the National Coordinator for Health Information
Technology (ONC), HHS.
ACTION: Notice of the Health Information Technology Advisory Committee
2018 schedule.
-----------------------------------------------------------------------
SUMMARY: This notice fulfills obligations under section 3002 of the
Public Health Service Act (PHSA), as amended by the 21st Century Cures
Act. Section 3002(b) (5) of the PHSA, as amended, mandates that the
Health Information Technology Advisory Committee shall develop a
schedule for the assessment of policy recommendations and the Secretary
shall publish such schedule in the Federal Register.
FOR FURTHER INFORMATION CONTACT: Lauren Richie Designated Federal
Officer, at [email protected].
SUPPLEMENTARY INFORMATION: Section 3002 of the Public Health Service
Act (PHSA), as amended by the 21st Century Cures Act (Pub. L. 114-255),
establishes the Health Information Technology Advisory Committee
(HITAC). The HITAC will be governed by the provisions of the Federal
Advisory Committee Act (Pub. L. 92-463), as amended (5 U.S.C. App.),
which sets forth standards for the formation and use of federal
advisory committees. The HITAC, among other things, shall identify
priorities for standards adoption and make recommendations to the
National Coordinator for Health Information Technology (National
Coordinator) on a policy framework to advance an interoperable health
information technology infrastructure.
Health Information Technology Advisory Committee Schedule
Section 3002(b)(5) of the PHSA, as amended, provides that the HITAC
shall develop a schedule for the assessment of policy recommendations
developed by the HITAC and publish the schedule in the Federal
Register. This schedule addresses the assessment of recommendations
outlined in the policy framework recommended by the HITAC to the
National Coordinator.
Accordingly, the schedule for the HITAC's assessment of policy
recommendations is as follows:
1. Within 90 days of a charge by the National Coordinator for
recommendations on a matter, identify the best mechanism to organize
itself to develop recommendations, and at a minimum, will:
a. Develop an assessment of what policies, standards,
implementation specifications, and certification criteria are currently
available to be considered as part of the request;
b. Consider where gaps exist and identify potential organizations
that have the capability to address those gaps (i.e., no policy or
standard is available or harmonization is required because more than
one standard exists) related to the request; and
c. Create a timeline, which may also account for the National
Institute of Standards and Technology (NIST) testing, where
appropriate, and include dates when the HITAC is expected to issue the
recommendation to the National Coordinator.
d. Include an opportunity for public comment during the
consideration by the HITAC of the request by the National Coordinator
for recommendations on a matter.
2. In responding to the National Coordinator:
a. Approve a timeline to deliver recommendations to the National
Coordinator; and
b. Establish a task force to conduct analysis and solicit input,
where appropriate, and develop draft recommendations to be considered
by the full committee in a timely manner.
3. In collaboration with NIST, annually and through the use of
public input, review and publish priorities for the use of health
information technology, standards, and implementation specifications to
support those priorities.
4. Recommend to the National Coordinator for purposes of adoption
under section 3004, standards, implementation specifications, and
certification criteria and an order of priority for the development,
harmonization, and recognition of such standards, specifications, and
certification criteria. Such recommendations shall include recommended
standards, architectures, and software schemes for access to electronic
individually identifiable health information across disparate systems
including user vetting, authentication, privilege management, and
access control.
The topics in which the HITAC is expected to address in FY2018
include, but may not be limited to the target areas as defined in
section 3002 of the PHSA, as amended by the 21st Century Cures Act
(Pub. L. 114-255), and they include:
1. Achieving a health information technology infrastructure that
allows for the electronic access, exchange, and use of health
information ;
2. The promotion and protection of privacy and security of health
information in health information technology;
3. The facilitation of secure access by an individual to such
individual's protected health information; and
4. Any other target area that the HITAC identifies as an
appropriate target area to be considered. [42USC Sec. 300jj (b)(2)(B)]
[[Page 9860]]
Notice of this meeting is given under section 3002(b)(5) of the
PHSA, as amended.
Dated: March 1, 2018.
Lauren Richie,
Branch Chief, Office of Policy, Office of the National Coordinator for
Health Information Technology.
[FR Doc. 2018-04543 Filed 3-7-18; 8:45 am]
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