Solicitation of Written Comments on the Maternal Immunizations Working Group Phase II's Draft Report and Draft Recommendations for Overcoming Barriers and Identifying Opportunities for Developing Maternal Immunizations for Consideration by the National Vaccine Advisory Committee, 58947-58948 [2016-20525]
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Federal Register / Vol. 81, No. 166 / Friday, August 26, 2016 / Notices
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Solicitation of Written Comments on
the Maternal Immunizations Working
Group Phase II’s Draft Report and Draft
Recommendations for Overcoming
Barriers and Identifying Opportunities
for Developing Maternal Immunizations
for Consideration by the National
Vaccine Advisory Committee
National Vaccine Program
Office, Office of the Assistant Secretary
for Health, Office of the Secretary,
Department of Health and Human
Services.
ACTION: Notice.
AGENCY:
The National Vaccine
Advisory Committee (NVAC) was
established in 1987 to comply with Title
XXI of the Public Health Service Act
(Pub. L. 99–660) (§ 2105) (42 U.S. Code
Section 300aa–5). Its purpose is to
advise and make recommendations to
the Director of the National Vaccine
Program on matters related to the
program’s responsibilities. The
Assistant Secretary for Health (ASH) has
been designated by the Secretary of
Health and Human Services (HHS) as
the Director of the National Vaccine
Program. The National Vaccine Program
Office (NVPO) is located within the
Office of the Assistant Secretary for
Health (OASH), Office of the Secretary,
U.S. Department of Health and Human
Services (HHS). The NVPO provides
leadership and fosters collaboration
among the various federal agencies
involved in vaccine and immunization
activities. The NVPO also provides
management and support services for
the National Vaccine Advisory
Committee (NVAC). The NVAC advises
and makes recommendations to the
ASH in his/her capacity as the Director
of the National Vaccine Program on
matters related to the program’s
responsibilities.
Recognizing the importance and
impact of maternal immunizations on
public health, the ASH charged the
NVAC in June 2012 with reviewing the
state of maternal immunizations and
existing best practices to identify
programmatic gaps and/or barriers to
the implementation of current
recommendations regarding maternal
immunization. The NVAC established
the Maternal Immunization Working
Group (MIWG) in August 2012 to
conduct these assessments and provide
recommendations for overcoming any
identified barriers.
Through a series of teleconferences,
electronic communications, and public
discussions during the NVAC meetings,
mstockstill on DSK3G9T082PROD with NOTICES
SUMMARY:
VerDate Sep<11>2014
21:17 Aug 25, 2016
Jkt 238001
the working group identified a number
of draft recommendations for
consideration by the NVAC. These
recommendations represent
opportunities for developing and
licensing new vaccines for pregnant
women. The draft report and draft
recommendations from the working
group will inform NVAC deliberations
as the NVAC finalizes their
recommendations for transmittal to the
ASH.
On behalf of NVAC, NVPO is
soliciting public comment on the draft
report and draft recommendations from
a variety of stakeholders, including the
general public, for consideration by the
NVAC as they develop their final
recommendations to the ASH. It is
anticipated that the draft report and
draft recommendations, as revised with
consideration given to public comment
and stakeholder input, will be presented
to the NVAC for adoption in September
2016 at the quarterly NVAC meeting.
DATES: Comments for consideration by
the NVAC should be received no later
than 5:00 p.m. EDT on September 9,
2016.
(1) The draft report and
draft recommendations are available on
the web at https://www.hhs.gov/nvpo/
nvac/.
(2) Electronic responses are preferred
and may be addressed to: nvpo@
hhs.gov.
(3) Written responses should be
addressed to: National Vaccine Program
Office, U.S. Department of Health and
Human Services, 200 Independence
Avenue SW., Room 733G.5,
Washington, DC 20201, Attn: HHS
Maternal Immunizations c/o Dr. Karin
Bok.
ADDRESSES:
FOR FURTHER INFORMATION CONTACT:
Karin Bok, MS, Ph.D., National
Vaccine Program Office, Office of the
Assistant Secretary for Health,
Department of Health and Human
Services; telephone (202) 690–1191; fax
(202) 260–1165; email Karin.Bok@
hhs.gov.
SUPPLEMENTARY INFORMATION:
I. Background
Maternal immunizations have been an
effective strategy to protect both the
mother and the young infant against
vaccine-preventable diseases. However,
significant barriers remain that prevent
the development and licensing of
additional vaccines for use in maternal
immunization strategies. Some of those
barriers include ethics and policy
considerations about including pregnant
women in clinical research, the need for
continued support of pre-clinical and
PO 00000
Frm 00046
Fmt 4703
Sfmt 4703
58947
clinical research on immunity, the
impact and safety of immunizations
during pregnancy, and educating
obstetrical providers about the benefits
of immunizations during pregnancy and
the importance of including pregnant
women in clinical research in order to
provide the highest quality of
healthcare.
HHS recognized the need to address
these barriers and subsequently charged
the NVAC with making
recommendations that would address
the problem. The NVAC separated the
task into two sections as it was first
necessary to address and understand the
demand for maternal immunizations in
order to then address the challenges in
developing maternal immunizations.
The MIWG Phase I focused on
understanding the demand for maternal
immunization programs by identifying
existing patient and provider barriers to
maternal immunization, which
addressed the first part of the charge.
Then, the MIWG Phase II focused on the
second part of the charge, which was to
identify barriers to and opportunities for
developing vaccines for pregnant
women and to make recommendations
to overcome these barriers. Through a
series of teleconferences, electronic
communications, and public
discussions during the NVAC meetings,
the working group identified a number
of draft recommendations. These
recommendations were categorized into
four priority areas that represent
opportunities for developing and
licensing new vaccines for pregnant
women. These four categories include:
Focus Area 1: Ethical Issues
Focus Area 2: Policy Issues
Focus Area 3: Pre-Clinical and Clinical
Research Issues
Focus Area 4: Provider Education and
Support Issues
Within each focus area the NVAC report
details key recommendations to
overcoming challenges in these areas.
The NVAC report also provides the
rationale for these recommendations
and input on how the ASH might
support HHS activities in these areas.
II. Request for Comment
NVPO, on behalf of the NVAC MIWG
Phase II, requests input on the draft
report and draft recommendations. In
addition to general comments on the
draft report and draft recommendations,
NVPO is seeking input on efforts and/
or barriers to maternal immunizations
not presented in the report where HHS
efforts could advance maternal
immunization efforts. Please limit your
comments to six (6) pages.
E:\FR\FM\26AUN1.SGM
26AUN1
58948
Federal Register / Vol. 81, No. 166 / Friday, August 26, 2016 / Notices
III. Potential Responders
HHS invites input from a broad range
of stakeholders including individuals
and organizations that have interests in
maternal immunization efforts and the
role of HHS in advancing those efforts.
Examples of potential responders
include, but are not limited to, the
following:
—General public;
—advocacy groups, non-profit
organizations, and public interest
organizations;
—academics, professional societies, and
healthcare organizations;
—public health officials and
immunization program managers;
—obstetrical care provider groups
including all physician and nonphysician providers that administer
healthcare services to pregnant
women, including pharmacists; and
—representatives from the private
sector.
When responding, please self-identify
with any of the above or other categories
(include all that apply) and your name.
Anonymous submissions will not be
considered. Written submissions should
not exceed six (6) pages. Please do not
send proprietary, commercial, financial,
business, confidential, trade secret, or
personal information.
Dated: August 16, 2016.
Bruce Gellin,
Executive Secretary, National Vaccine
Advisory Committee, Deputy Assistant
Secretary for Health, Director, National
Vaccine Program Office.
[FR Doc. 2016–20525 Filed 8–25–16; 8:45 am]
BILLING CODE 4150–44–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
mstockstill on DSK3G9T082PROD with NOTICES
National Institute of Diabetes and
Digestive and Kidney Diseases; Notice
of Closed Meetings
Pursuant to section 10(d) of the
Federal Advisory Committee Act, as
amended (5 U.S.C. App.), notice is
hereby given of the following meetings.
The meetings will be closed to the
public in accordance with the
provisions set forth in sections
552b(c)(4) and 552b(c)(6), title 5 U.S.C.,
as amended. The grant applications and
the discussions could disclose
confidential trade secrets or commercial
property such as patentable material,
and personal information concerning
individuals associated with the grant
applications, the disclosure of which
would constitute a clearly unwarranted
invasion of personal privacy.
VerDate Sep<11>2014
21:17 Aug 25, 2016
Jkt 238001
Name of Committee: National Institute of
Diabetes and Digestive and Kidney Diseases
Special Emphasis Panel; R18 and R34.
Date: September 15, 2016.
Time: 9:00 a.m. to 5:00 p.m.
Agenda: To review and evaluate grant
applications.
Place: Bethesda Marriott Suites, 6711
Democracy Boulevard, Bethesda, MD 20817.
Contact Person: Michele L. Barnard, Ph.D.,
Scientific Review Officer, Review Branch,
DEA, NIDDK, National Institutes of Health,
Room 7353, 6707 Democracy Boulevard,
Bethesda, MD 20892–2542, (301) 594–8898,
barnardm@extra.niddk.nih.gov.
Name of Committee: National Institute of
Diabetes and Digestive and Kidney Diseases
Special Emphasis Panel; NIDDK Ancillary
Studies (R01).
Date: September 15, 2016.
Time: 11:00 a.m. to 12:30 p.m.
Agenda: To review and evaluate grant
applications.
Place: National Institutes of Health, Two
Democracy Plaza, 6707 Democracy Blvd.,
Bethesda, MD 20892 (Telephone Conference
Call).
Contact Person: Jian Yang, Ph.D., Scientific
Review Officer, Review Branch, DEA,
NIDDK, National Institutes of Health, Room
7111, 6707 Democracy Boulevard, Bethesda,
MD 20892–5452, (301) 594–7799, yangj@
extra.niddk.nih.gov.
Name of Committee: National Institute of
Diabetes and Digestive and Kidney Diseases
Special Emphasis Panel; Time-Sensitive
Obesity.
Date: September 19, 2016.
Time: 2:00 p.m. to 4:00 p.m.
Agenda: To review and evaluate grant
applications.
Place: National Institutes of Health, Two
Democracy Plaza, 6707 Democracy
Boulevard, Bethesda, MD 20892 (Telephone
Conference Call).
Contact Person: Michele L. Barnard, Ph.D.,
Scientific Review Officer, Review Branch,
DEA, NIDDK, National Institutes of Health,
Room 7353, 6707 Democracy Boulevard,
Bethesda, MD 20892–2542, (301) 594–8898,
barnardm@extra.niddk.nih.gov.
Name of Committee: National Institute of
Diabetes and Digestive and Kidney Diseases
Special Emphasis Panel; PAR–13–228:
Biomarkers for Diabetes, Digestive, Kidney
and Urologic Diseases using NIDDK
Biorepository Samples (R01).
Date: September 21, 2016.
Time: 12:00 p.m. to 3:00 p.m.
Agenda: To review and evaluate grant
applications.
Place: National Institutes of Health, Two
Democracy Plaza, 6707 Democracy
Boulevard, Bethesda, MD 20892 (Telephone
Conference Call).
Contact Person: Najma Begum, Ph.D.,
Scientific Review Officer, Review Branch,
DEA, NIDDK, National Institutes of Health,
Room 7349, 6707 Democracy Boulevard,
Bethesda, MD 20892–5452, (301) 594–8894,
begumn@niddk.nih.gov.
Name of Committee: National Institute of
Diabetes and Digestive and Kidney Diseases
Special Emphasis Panel; PAR–16–126: High
Impact, Interdisciplinary Science in DDK
Research Areas (RC2)–CKD.
PO 00000
Frm 00047
Fmt 4703
Sfmt 4703
Date: September 26, 2016.
Time: 12:00 p.m. to 2:00 p.m.
Agenda: To review and evaluate grant
applications.
Place: National Institutes of Health, Two
Democracy Plaza, 6707 Democracy
Boulevard, Bethesda, MD 20892 (Telephone
Conference Call).
Contact Person: Najma Begum, Ph.D.,
Scientific Review Officer, Review Branch,
DEA, NIDDK, National Institutes of Health,
Room 7349, 6707 Democracy Boulevard,
Bethesda, MD 20892–5452, (301) 594–8894,
begumn@niddk.nih.gov.
Name of Committee: National Institute of
Diabetes and Digestive and Kidney Diseases
Special Emphasis Panel; PAR–15–067:
NIDDK Multi-Center Clinical Study
Cooperative Agreement (U01): CKD and
Mineral Bone Disorders in Children.
Date: September 27, 2016.
Time: 12:00 p.m. to 2:00 p.m.
Agenda: To review and evaluate
cooperative agreement applications.
Place: National Institutes of Health, Two
Democracy Plaza, 6707 Democracy
Boulevard, Bethesda, MD 20892 (Telephone
Conference Call).
Contact Person: Najma Begum, Ph.D.,
Scientific Review Officer, Review Branch,
DEA, NIDDK, National Institutes of Health,
Room 7349, 6707 Democracy Boulevard,
Bethesda, MD 20892–5452, (301) 594–8894,
begumn@niddk.nih.gov.
(Catalogue of Federal Domestic Assistance
Program Nos. 93.847, Diabetes,
Endocrinology and Metabolic Research;
93.848, Digestive Diseases and Nutrition
Research; 93.849, Kidney Diseases, Urology
and Hematology Research, National Institutes
of Health, HHS)
Dated: August 22, 2016.
David Clary,
Program Analyst, Office of Federal Advisory
Committee Policy.
[FR Doc. 2016–20446 Filed 8–25–16; 8:45 am]
BILLING CODE 4140–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
National Institute of Diabetes and
Digestive and Kidney Diseases; Notice
of Closed Meetings
Pursuant to section 10(d) of the
Federal Advisory Committee Act, as
amended (5 U.S.C. App.), notice is
hereby given of the following meetings.
The meetings will be closed to the
public in accordance with the
provisions set forth in sections
552b(c)(4) and 552b(c)(6), title 5 U.S.C.,
as amended. The grant applications and
the discussions could disclose
confidential trade secrets or commercial
property such as patentable material,
and personal information concerning
individuals associated with the grant
E:\FR\FM\26AUN1.SGM
26AUN1
Agencies
[Federal Register Volume 81, Number 166 (Friday, August 26, 2016)]
[Notices]
[Pages 58947-58948]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2016-20525]
[[Page 58947]]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Solicitation of Written Comments on the Maternal Immunizations
Working Group Phase II's Draft Report and Draft Recommendations for
Overcoming Barriers and Identifying Opportunities for Developing
Maternal Immunizations for Consideration by the National Vaccine
Advisory Committee
AGENCY: National Vaccine Program Office, Office of the Assistant
Secretary for Health, Office of the Secretary, Department of Health and
Human Services.
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: The National Vaccine Advisory Committee (NVAC) was established
in 1987 to comply with Title XXI of the Public Health Service Act (Pub.
L. 99-660) (Sec. 2105) (42 U.S. Code Section 300aa-5). Its purpose is
to advise and make recommendations to the Director of the National
Vaccine Program on matters related to the program's responsibilities.
The Assistant Secretary for Health (ASH) has been designated by the
Secretary of Health and Human Services (HHS) as the Director of the
National Vaccine Program. The National Vaccine Program Office (NVPO) is
located within the Office of the Assistant Secretary for Health (OASH),
Office of the Secretary, U.S. Department of Health and Human Services
(HHS). The NVPO provides leadership and fosters collaboration among the
various federal agencies involved in vaccine and immunization
activities. The NVPO also provides management and support services for
the National Vaccine Advisory Committee (NVAC). The NVAC advises and
makes recommendations to the ASH in his/her capacity as the Director of
the National Vaccine Program on matters related to the program's
responsibilities.
Recognizing the importance and impact of maternal immunizations on
public health, the ASH charged the NVAC in June 2012 with reviewing the
state of maternal immunizations and existing best practices to identify
programmatic gaps and/or barriers to the implementation of current
recommendations regarding maternal immunization. The NVAC established
the Maternal Immunization Working Group (MIWG) in August 2012 to
conduct these assessments and provide recommendations for overcoming
any identified barriers.
Through a series of teleconferences, electronic communications, and
public discussions during the NVAC meetings, the working group
identified a number of draft recommendations for consideration by the
NVAC. These recommendations represent opportunities for developing and
licensing new vaccines for pregnant women. The draft report and draft
recommendations from the working group will inform NVAC deliberations
as the NVAC finalizes their recommendations for transmittal to the ASH.
On behalf of NVAC, NVPO is soliciting public comment on the draft
report and draft recommendations from a variety of stakeholders,
including the general public, for consideration by the NVAC as they
develop their final recommendations to the ASH. It is anticipated that
the draft report and draft recommendations, as revised with
consideration given to public comment and stakeholder input, will be
presented to the NVAC for adoption in September 2016 at the quarterly
NVAC meeting.
DATES: Comments for consideration by the NVAC should be received no
later than 5:00 p.m. EDT on September 9, 2016.
ADDRESSES: (1) The draft report and draft recommendations are available
on the web at https://www.hhs.gov/nvpo/nvac/.
(2) Electronic responses are preferred and may be addressed to:
nvpo@hhs.gov.
(3) Written responses should be addressed to: National Vaccine
Program Office, U.S. Department of Health and Human Services, 200
Independence Avenue SW., Room 733G.5, Washington, DC 20201, Attn: HHS
Maternal Immunizations c/o Dr. Karin Bok.
FOR FURTHER INFORMATION CONTACT:
Karin Bok, MS, Ph.D., National Vaccine Program Office, Office of
the Assistant Secretary for Health, Department of Health and Human
Services; telephone (202) 690-1191; fax (202) 260-1165; email
Karin.Bok@hhs.gov.
SUPPLEMENTARY INFORMATION:
I. Background
Maternal immunizations have been an effective strategy to protect
both the mother and the young infant against vaccine-preventable
diseases. However, significant barriers remain that prevent the
development and licensing of additional vaccines for use in maternal
immunization strategies. Some of those barriers include ethics and
policy considerations about including pregnant women in clinical
research, the need for continued support of pre-clinical and clinical
research on immunity, the impact and safety of immunizations during
pregnancy, and educating obstetrical providers about the benefits of
immunizations during pregnancy and the importance of including pregnant
women in clinical research in order to provide the highest quality of
healthcare.
HHS recognized the need to address these barriers and subsequently
charged the NVAC with making recommendations that would address the
problem. The NVAC separated the task into two sections as it was first
necessary to address and understand the demand for maternal
immunizations in order to then address the challenges in developing
maternal immunizations. The MIWG Phase I focused on understanding the
demand for maternal immunization programs by identifying existing
patient and provider barriers to maternal immunization, which addressed
the first part of the charge. Then, the MIWG Phase II focused on the
second part of the charge, which was to identify barriers to and
opportunities for developing vaccines for pregnant women and to make
recommendations to overcome these barriers. Through a series of
teleconferences, electronic communications, and public discussions
during the NVAC meetings, the working group identified a number of
draft recommendations. These recommendations were categorized into four
priority areas that represent opportunities for developing and
licensing new vaccines for pregnant women. These four categories
include:
Focus Area 1: Ethical Issues
Focus Area 2: Policy Issues
Focus Area 3: Pre-Clinical and Clinical Research Issues
Focus Area 4: Provider Education and Support Issues
Within each focus area the NVAC report details key recommendations to
overcoming challenges in these areas. The NVAC report also provides the
rationale for these recommendations and input on how the ASH might
support HHS activities in these areas.
II. Request for Comment
NVPO, on behalf of the NVAC MIWG Phase II, requests input on the
draft report and draft recommendations. In addition to general comments
on the draft report and draft recommendations, NVPO is seeking input on
efforts and/or barriers to maternal immunizations not presented in the
report where HHS efforts could advance maternal immunization efforts.
Please limit your comments to six (6) pages.
[[Page 58948]]
III. Potential Responders
HHS invites input from a broad range of stakeholders including
individuals and organizations that have interests in maternal
immunization efforts and the role of HHS in advancing those efforts.
Examples of potential responders include, but are not limited to,
the following:
--General public;
--advocacy groups, non-profit organizations, and public interest
organizations;
--academics, professional societies, and healthcare organizations;
--public health officials and immunization program managers;
--obstetrical care provider groups including all physician and non-
physician providers that administer healthcare services to pregnant
women, including pharmacists; and
--representatives from the private sector.
When responding, please self-identify with any of the above or other
categories (include all that apply) and your name. Anonymous
submissions will not be considered. Written submissions should not
exceed six (6) pages. Please do not send proprietary, commercial,
financial, business, confidential, trade secret, or personal
information.
Dated: August 16, 2016.
Bruce Gellin,
Executive Secretary, National Vaccine Advisory Committee, Deputy
Assistant Secretary for Health, Director, National Vaccine Program
Office.
[FR Doc. 2016-20525 Filed 8-25-16; 8:45 am]
BILLING CODE 4150-44-P