Advisory Committee on Heritable Disorders in Newborns and Children, 18919-18920 [2017-08220]
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18919
Federal Register / Vol. 82, No. 77 / Monday, April 24, 2017 / Notices
TOTAL ESTIMATED ANNUALIZED BURDEN HOURS
Number of
respondents
Form name
Number of
responses per
respondent
Total
responses
Average
burden per
response
(in hours)
Total burden
hours
Grantee Report ....................................................................
Client-level Report ...............................................................
54
54
1
1
54
54
6
81
324
4,374
Total ..............................................................................
* 54
........................
54
........................
4,698
* The same respondents complete the Grantee Report and the Client-level Report.
HRSA specifically requests comments
on (1) the necessity and utility of the
proposed information collection for the
proper performance of the agency’s
functions, (2) the accuracy of the
estimated burden, (3) ways to enhance
the quality, utility, and clarity of the
information to be collected, and (4) the
use of automated collection techniques
or other forms of information
technology to minimize the information
collection burden.
Jason E. Bennett,
Director, Division of the Executive Secretariat.
[FR Doc. 2017–08197 Filed 4–21–17; 8:45 am]
BILLING CODE 4165–15–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Health Resources and Services
Administration
Advisory Committee on Heritable
Disorders in Newborns and Children
Health Resources and Services
Administration (HRSA), Department of
Health and Human Services (HHS).
AGENCY:
ACTION:
Notice of meeting.
In accordance with the
Federal Advisory Committee Act, notice
is hereby given of the following meeting
for the Advisory Committee on
Heritable Disorders in Newborns and
Children (ACHDNC). The meeting will
be open to the public but advance
registration is required. The online
registration deadline is Thursday, May
4, 2017, 5:00 p.m. Eastern Time. Please
check the Web site for additional
guidance and registration information.
The registration link is https://
www.achdncmeetings.org/. Information
about the agenda for this meeting can be
obtained by accessing the following
Web site: https://www.hrsa.gov/
advisorycommittees/mchbadvisory/
heritabledisorders.
jstallworth on DSK7TPTVN1PROD with NOTICES
SUMMARY:
The meeting will be held on May
11, 2017, 9:00 a.m. to 5:00 p.m. and May
12, 2017, 9:00 a.m. to 3:00 p.m.
DATES:
VerDate Sep<11>2014
13:48 Apr 21, 2017
Jkt 241001
This meeting will be held
in-person and by webcast. The address
for the meeting is 5600 Fishers Lane, 5th
Floor Pavilion, Rockville, MD 20857.
Webcast information will be emailed to
you after you register.
FOR FURTHER INFORMATION CONTACT:
Anyone requesting information
regarding the ACHDNC should contact
Ann Ferrero, Maternal and Child Health
Bureau (MCHB), HRSA, in one of three
ways: (1) Send a request to Ann Ferrero,
MCHB, HRSA 5600 Fishers Lane, Room
18N100C, Rockville, Maryland 20857;
(2) call 301–443–3999 or (3) send an
email to: AFerrero@hrsa.gov. More
information on the Advisory Committee
is available at the Advisory Committee’s
Web site, provided above.
SUPPLEMENTARY INFORMATION: The
ACHDNC, as authorized by Public
Health Service Act, Title XI, § 1111 (42
U.S.C. 300b–10), provides advice to the
Secretary of HHS on the development of
newborn screening activities,
technologies, policies, guidelines, and
programs for effectively reducing
morbidity and mortality in newborns
and children having, or at risk for,
heritable disorders. In addition,
ACHDNC’s recommendations regarding
inclusion of additional conditions and
inherited disorders for screening which
have been adopted by the Secretary are
then included in the Recommended
Uniform Screening Panel (RUSP).
Conditions listed on the RUSP
constitute part of the comprehensive
guidelines supported by HRSA for
infants, children, and adolescents.
Pursuant to section 2713 of the Public
Health Service Act, codified at 42 U.S.C.
300gg–13, non-grandfathered health
plans and health insurance issuers are
required to cover screenings included in
the HRSA-supported comprehensive
guidelines without charging a copayment, co-insurance, or deductible for
plan years (i.e., policy years) beginning
on or after the date that is one year from
the Secretary’s adoption of the
condition for screening. the meeting
will include: (1) Presentations and
discussion on the process of identifying
and following up on out of range
ADDRESSES:
PO 00000
Frm 00031
Fmt 4703
Sfmt 4703
newborn screening results; (2) a
presentation on newborn screening
quality assurance programs; (3)
presentations on the clinical and public
health impact of Critical Congenital
Heart Defects screening; (4) discussion
and possible vote on a report on
Medical Foods for Inborn Errors of
Metabolism; (5) a presentation,
discussion, and possible vote on
whether to move a nomination forward
to evidence review for spinal muscular
atrophy (SMA); and (6) updates from the
Laboratory Standards and Procedures
workgroup, Follow-up and Treatment
workgroup, and Education and Training
workgroup.
The Committee will not be voting on
a proposed addition of a condition to
the RUSP. The final meeting agenda will
be available two (2) days prior to the
meeting on the Committee’s Web site:
https://www.hrsa.gov/
advisorycommittees/mchbadvisory/
heritabledisorders.
Members of the public may submit
written and/or present oral comments at
the meeting. All comments are part of
the official Committee record. Advance
registration is required to submit written
comments and/or present oral
comments. Written comments must be
submitted by April 28, 2017, 12:00 p.m.
Eastern Time to be included in the May
meeting briefing book. Written
comments should identify the
individual’s name, address, email,
telephone number, professional or
organization affiliation, background or
area of expertise (i.e., parent, family
member, researcher, clinician, public
health, etc.) and the topic/subject
matter.
Individuals who wish to provide oral
comments must register by Thursday,
May 4, 2017, 5:00 p.m. Eastern Time. To
ensure that all individuals who have
registered to make oral comments can be
accommodated, the allocated time may
be limited. Individuals who are
associated with groups or have similar
interests may be requested to combine
their comments and present them
through a single representative. No
audiovisual presentations are permitted.
E:\FR\FM\24APN1.SGM
24APN1
18920
Federal Register / Vol. 82, No. 77 / Monday, April 24, 2017 / Notices
For additional information or questions
on public comments, please contact
Ann Ferrero, MCHB, HRSA; email:
AFerrero@hrsa.gov.
The 5600 Fishers Lane building
requires a security screening on entry.
To facilitate your access to the building,
please contact Ann Ferrero at 301–443–
3999. Individuals who plan to attend
and need special assistance, such as
sign language interpretation or other
reasonable accommodations, should
notify Ann Ferrero, MCHB, HRSA;
email: AFerrero@hrsa.gov, at least 10
days prior to the meeting.
Jason E. Bennett,
Director, Division of the Executive Secretariat.
[FR Doc. 2017–08220 Filed 4–21–17; 8:45 am]
BILLING CODE 4165–15–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Office of the Secretary
[Document Identifier: 0955–New–30D]
Agency Information Collection
Activities; Submission to OMB for
Review and Approval; Public Comment
Request
Office of the Secretary, HHS.
Notice.
AGENCY:
ACTION:
In compliance with section
3507(a)(1)(D) of the Paperwork
Reduction Act of 1995, the Office of the
Secretary (OS), Department of Health
and Human Services, has submitted an
Information Collection Request (ICR),
described below, to the Office of
Management and Budget (OMB) for
SUMMARY:
review and approval. The ICR is for a
new collection. Comments submitted
during the first public review of this ICR
will be provided to OMB. OMB will
accept further comments from the
public on this ICR during the review
and approval period.
DATES: Comments on the ICR must be
received on or before May 24, 2017.
ADDRESSES: Submit your comments to
OIRA_submission@omb.eop.gov or via
facsimile to (202) 395–5806.
FOR FURTHER INFORMATION CONTACT:
Information Collection Clearance staff,
Information.CollectionClearance@
hhs.gov or (202) 795–7714.
SUPPLEMENTARY INFORMATION: When
submitting comments or requesting
information, please include the
Information Collection Request Title
and document identifier 0955–New–
30D for reference.
Information Collection Request Title:
National Council for Behavioral Health’s
Information Technology Survey.
Abstract: The Office of the National
Coordinator for Health IT (ONC) in
coordination with Substance Abuse and
Mental Health Services Administration
(SAMHSA) seeks to conduct a survey in
2017 of SAMSHA to examine the
adoption and use of health IT as well as
interoperability across community
behavioral health care settings. Data
from the survey will help ONC and
SAMSHA monitor progress and enhance
programs and policy to improve the use
of health IT and expand interoperability
across these settings. In 2015, ONC
outlined a strategy by which both
private and public stakeholders would
work together to improve
interoperability. This strategy called for
measuring and reporting on the state of
interoperability across the care
continuum, including for behavioral
health care providers; however, there
are no recent national data available for
this care setting. Addressing this gap is
critical in order to also determine these
providers’ readiness to serve as partners
in delivery system reform efforts that are
underway and that will be expanded
with the implementation of Medicare
Access and CHIP Reauthorization Act of
2015 (MACRA). Although behavioral
health care providers won’t be
participating in the MACRA initiative at
the outset, the Secretary of Health and
Human Services may include behavioral
health providers, such as psychologists
and social workers to participate in
value-based payment initiatives such as
the Merit-Based Incentive Payment
System (MIPs) in the future.
Need and Proposed Use of the
Information: This data collection effort
will allow for us to assess health IT
adoption and interoperability progress
since 2015, enable comparisons to
physician and hospital settings and
contribute to strategic efforts to improve
behavioral healthcare providers’
adoption and use of health IT.
Likely Respondents: The respondents
will include mid-level and executive
level staff (IT Directors, CIO, and CEOs)
of behavioral healthcare organizations
that are involved in the management
and maintenance of their organization’s
health IT infrastructure.
The total annual burden hours
estimated for this ICR are summarized
in the table below.
TOTAL ESTIMATED ANNUALIZED BURDEN—HOURS
Number of
respondents
Form name
Number of
responses
per
respondent
Average
burden per
response
(in hours)
Total burden
hours
National Council for Behavioral Health’s Information Technology Survey ......
533
1
20/60
178
Total ..........................................................................................................
533
1
20/60
178
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
[FR Doc. 2017–08188 Filed 4–21–17; 8:45 am]
Office of the Secretary
BILLING CODE 4150–45–P
jstallworth on DSK7TPTVN1PROD with NOTICES
Terry S. Clark,
Asst Information Collection Clearance
Officer.
[Document Identifier: 0990–0452–30D]
Agency Information Collection
Activities; Submission to OMB for
Review and Approval; Public Comment
Request
Office of the Secretary, HHS.
Notice.
AGENCY:
ACTION:
VerDate Sep<11>2014
13:48 Apr 21, 2017
Jkt 241001
PO 00000
Frm 00032
Fmt 4703
Sfmt 4703
In compliance with section
3507(a)(1)(D) of the Paperwork
Reduction Act of 1995, the Office of the
Secretary (OS), Department of Health
and Human Services, has submitted an
Information Collection Request (ICR),
described below, to the Office of
Management and Budget (OMB) for
review and approval. The ICR is for
revision of the approved information
collection assigned OMB control
number 0990–0452, scheduled to expire
on January 31, 2020. Comments
SUMMARY:
E:\FR\FM\24APN1.SGM
24APN1
Agencies
[Federal Register Volume 82, Number 77 (Monday, April 24, 2017)]
[Notices]
[Pages 18919-18920]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2017-08220]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Health Resources and Services Administration
Advisory Committee on Heritable Disorders in Newborns and
Children
AGENCY: Health Resources and Services Administration (HRSA), Department
of Health and Human Services (HHS).
ACTION: Notice of meeting.
-----------------------------------------------------------------------
SUMMARY: In accordance with the Federal Advisory Committee Act, notice
is hereby given of the following meeting for the Advisory Committee on
Heritable Disorders in Newborns and Children (ACHDNC). The meeting will
be open to the public but advance registration is required. The online
registration deadline is Thursday, May 4, 2017, 5:00 p.m. Eastern Time.
Please check the Web site for additional guidance and registration
information. The registration link is https://www.achdncmeetings.org/.
Information about the agenda for this meeting can be obtained by
accessing the following Web site: https://www.hrsa.gov/advisorycommittees/mchbadvisory/heritabledisorders.
DATES: The meeting will be held on May 11, 2017, 9:00 a.m. to 5:00 p.m.
and May 12, 2017, 9:00 a.m. to 3:00 p.m.
ADDRESSES: This meeting will be held in-person and by webcast. The
address for the meeting is 5600 Fishers Lane, 5th Floor Pavilion,
Rockville, MD 20857. Webcast information will be emailed to you after
you register.
FOR FURTHER INFORMATION CONTACT: Anyone requesting information
regarding the ACHDNC should contact Ann Ferrero, Maternal and Child
Health Bureau (MCHB), HRSA, in one of three ways: (1) Send a request to
Ann Ferrero, MCHB, HRSA 5600 Fishers Lane, Room 18N100C, Rockville,
Maryland 20857; (2) call 301-443-3999 or (3) send an email to:
AFerrero@hrsa.gov. More information on the Advisory Committee is
available at the Advisory Committee's Web site, provided above.
SUPPLEMENTARY INFORMATION: The ACHDNC, as authorized by Public Health
Service Act, Title XI, Sec. 1111 (42 U.S.C. 300b-10), provides advice
to the Secretary of HHS on the development of newborn screening
activities, technologies, policies, guidelines, and programs for
effectively reducing morbidity and mortality in newborns and children
having, or at risk for, heritable disorders. In addition, ACHDNC's
recommendations regarding inclusion of additional conditions and
inherited disorders for screening which have been adopted by the
Secretary are then included in the Recommended Uniform Screening Panel
(RUSP). Conditions listed on the RUSP constitute part of the
comprehensive guidelines supported by HRSA for infants, children, and
adolescents. Pursuant to section 2713 of the Public Health Service Act,
codified at 42 U.S.C. 300gg-13, non-grandfathered health plans and
health insurance issuers are required to cover screenings included in
the HRSA-supported comprehensive guidelines without charging a co-
payment, co-insurance, or deductible for plan years (i.e., policy
years) beginning on or after the date that is one year from the
Secretary's adoption of the condition for screening. the meeting will
include: (1) Presentations and discussion on the process of identifying
and following up on out of range newborn screening results; (2) a
presentation on newborn screening quality assurance programs; (3)
presentations on the clinical and public health impact of Critical
Congenital Heart Defects screening; (4) discussion and possible vote on
a report on Medical Foods for Inborn Errors of Metabolism; (5) a
presentation, discussion, and possible vote on whether to move a
nomination forward to evidence review for spinal muscular atrophy
(SMA); and (6) updates from the Laboratory Standards and Procedures
workgroup, Follow-up and Treatment workgroup, and Education and
Training workgroup.
The Committee will not be voting on a proposed addition of a
condition to the RUSP. The final meeting agenda will be available two
(2) days prior to the meeting on the Committee's Web site: https://www.hrsa.gov/advisorycommittees/mchbadvisory/heritabledisorders.
Members of the public may submit written and/or present oral
comments at the meeting. All comments are part of the official
Committee record. Advance registration is required to submit written
comments and/or present oral comments. Written comments must be
submitted by April 28, 2017, 12:00 p.m. Eastern Time to be included in
the May meeting briefing book. Written comments should identify the
individual's name, address, email, telephone number, professional or
organization affiliation, background or area of expertise (i.e.,
parent, family member, researcher, clinician, public health, etc.) and
the topic/subject matter.
Individuals who wish to provide oral comments must register by
Thursday, May 4, 2017, 5:00 p.m. Eastern Time. To ensure that all
individuals who have registered to make oral comments can be
accommodated, the allocated time may be limited. Individuals who are
associated with groups or have similar interests may be requested to
combine their comments and present them through a single
representative. No audiovisual presentations are permitted.
[[Page 18920]]
For additional information or questions on public comments, please
contact Ann Ferrero, MCHB, HRSA; email: AFerrero@hrsa.gov.
The 5600 Fishers Lane building requires a security screening on
entry. To facilitate your access to the building, please contact Ann
Ferrero at 301-443-3999. Individuals who plan to attend and need
special assistance, such as sign language interpretation or other
reasonable accommodations, should notify Ann Ferrero, MCHB, HRSA;
email: AFerrero@hrsa.gov, at least 10 days prior to the meeting.
Jason E. Bennett,
Director, Division of the Executive Secretariat.
[FR Doc. 2017-08220 Filed 4-21-17; 8:45 am]
BILLING CODE 4165-15-P