Request for Nominations of Individuals and Industry Organizations for the Genetic Metabolic Diseases Advisory Committee, 86345-86346 [2023-27303]
Download as PDF
khammond on DSKJM1Z7X2PROD with NOTICES
Federal Register / Vol. 88, No. 238 / Wednesday, December 13, 2023 / Notices
in the body of your comments and you
must identify the information as
‘‘confidential.’’ Any information marked
as ‘‘confidential’’ will not be disclosed
except in accordance with 21 CFR 10.20
and other applicable disclosure law. For
more information about FDA’s posting
of comments to public dockets, see 80
FR 56469, September 18, 2015, or access
the information at: https://
www.govinfo.gov/content/pkg/FR-201509-18/pdf/2015-23389.pdf.
Docket: For access to the docket to
read background documents or the
electronic and written/paper comments
received, go to https://
www.regulations.gov and insert the
docket number, found in brackets in the
heading of this document, into the
‘‘Search’’ box and follow the prompts
and/or go to the Dockets Management
Staff, 5630 Fishers Lane, Rm. 1061,
Rockville, MD 20852, 240–402–7500.
FOR FURTHER INFORMATION CONTACT:
Moon Choi, Center for Drug Evaluation
and Research, Food and Drug
Administration, 10903 New Hampshire
Ave., Bldg. 31, Rm. 2417, Silver Spring,
MD 20993–0002, 301–796–2894,
GEMDAC@fda.hhs.gov.
SUPPLEMENTARY INFORMATION: The
Genetic Metabolic Diseases Advisory
Committee (Committee) reviews and
evaluates data on the safety and
effectiveness of marketed and
investigational human drug and biologic
products for use in the treatment of
genetic metabolic diseases and makes
appropriate recommendations to the
Commissioner.
The Committee shall consist of a core
of nine voting members including the
Chair. Members and the Chair are
selected by the Commissioner or
designee from among authorities
knowledgeable in the fields of medical
genetics, manifestations of inborn errors
of metabolism, small population trial
design, translational science, pediatrics,
epidemiology, or statistics and related
specialties. Members will be invited to
serve for overlapping terms of up to 4
years. Non-Federal members of this
committee will serve either as special
government employees or non-voting
representatives. Federal members will
serve as regular government employees.
The core of voting members may
include one technically qualified
member, selected by the Commissioner
or designee, who serves as an
individual, but who is identified with
consumer interests and is recommended
by either a consortium of consumeroriented organizations or other
interested persons.
In addition to the voting members, the
Committee may include one non-voting
VerDate Sep<11>2014
16:54 Dec 12, 2023
Jkt 262001
representative member who is identified
with industry interests. There may also
be an alternate industry representative.
Elsewhere in this issue of the Federal
Register, FDA is publishing separate
documents regarding: (1) Genetic
Metabolic Diseases Advisory
Committee: Request for Nominations for
Voting Members on a Public Advisory
Committee: Genetic Metabolic Diseases
Advisory Committee; (2) Request for
Nomination of Individuals and
Consumer Organizations for the Genetic
Metabolic Diseases Advisory
Committee; and (3) Request for
Nomination of Individuals and Industry
Organizations for the Genetic Metabolic
Diseases Advisory Committee.
FDA intends to publish in the Federal
Register a final rule adding the Genetic
Metabolic Diseases Advisory Committee
to 21 CFR 14.100.
Dated: December 7, 2023.
Lauren K. Roth,
Associate Commissioner for Policy.
[FR Doc. 2023–27304 Filed 12–12–23; 8:45 am]
BILLING CODE 4164–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2023–N–0008]
Request for Nominations of Individuals
and Industry Organizations for the
Genetic Metabolic Diseases Advisory
Committee
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Notice.
The Food and Drug
Administration (FDA or Agency) is
requesting that industry organizations
interested in participating in the
selection of a nonvoting industry
representative to serve on the Genetic
Metabolic Diseases Advisory Committee
(the Committee) in the Center for Drug
Evaluation and Research notify FDA in
writing. FDA is also requesting
nominations for a nonvoting industry
representative to serve on the
Committee. Nominees recommended to
serve as a nonvoting industry
representative may either be selfnominated or nominated by an industry
organization. Nominations will be
accepted for the current vacancy
effective with this notice.
DATES: Any industry organization
interested in participating in the
selection of an appropriate nonvoting
member to represent industry interest,
must send a letter stating that interest to
SUMMARY:
PO 00000
Frm 00031
Fmt 4703
Sfmt 4703
86345
the FDA by February 12, 2024, (see
sections I and II of this document for
details). Concurrently, nomination
materials for prospective candidates
should be sent to FDA by February 12,
2024.
All statements of interest
from interested industry organizations
interested in participating in the
selection process of a nonvoting
industry representative should be sent
electronically to Nicholas Marsh (see
FOR FURTHER INFORMATION CONTACT). All
nominations for the nonvoting industry
representative may be submitted
electronically by accessing the FDA
Advisory Committee Membership
Nomination Portal: https://
www.accessdata.fda.gov/scripts/
FACTRSPortal/FACTRS/index.cfm or by
mail to Advisory Committee Oversight
and Management Staff, Food and Drug
Administration, 10903 New Hampshire
Ave., Bldg. 32, Rm. 5103, Silver Spring,
MD 20993–0002.
Information about becoming a
member on an FDA advisory committee
can also be obtained by visiting FDA’s
website at https://www.fda.gov/
AdvisoryCommittees/default.htm.
ADDRESSES:
FOR FURTHER INFORMATION CONTACT:
Nicolas Marsh, Center for Drug
Evaluation and Research, Food and
Drug Administration, 10903 New
Hampshire Ave., Bldg. 31, Rm. 2418,
Silver Spring, MD 20993–0002, 240–
402–5357, email: nicholas.marsh@
fda.hhs.gov.
For questions relating to the Genetic
Metabolic Diseases Advisory Committee:
Moon Choi, Center for Drug Evaluation
and Research, Food and Drug
Administration, 10903 New Hampshire
Ave., Bldg. 31, Rm. 2417, Silver Spring,
MD 20993–0002, 301–796–2894, email:
GEMDAC@fda.hhs.gov.
FDA is
requesting nominations for a nonvoting
industry representative for the Genetic
Metabolic Diseases Advisory
Committee.
Elsewhere in this issue of the Federal
Register, FDA is publishing separate
documents regarding:
SUPPLEMENTARY INFORMATION:
1. Genetic Metabolic Diseases Advisory
Committee; Notice of Establishment
2. Request for Nominations for Voting
Members for the Genetic Metabolic
Diseases Advisory Committee
3. Request for Nominations of
Individuals and Consumer
Organizations for the Genetic
Metabolic Diseases Advisory
Committee
E:\FR\FM\13DEN1.SGM
13DEN1
86346
Federal Register / Vol. 88, No. 238 / Wednesday, December 13, 2023 / Notices
I. General Description of the Genetic
Metabolic Diseases Advisory
Committee’s Duties
The Committee reviews and evaluates
data on the safety and effectiveness of
marketed and investigational human
drug and biologic products for use in
the treatment of genetic metabolic
diseases and makes appropriate
recommendations to the Commissioner
of Food and Drugs.
II. Qualifications
Persons nominated for the Committee
should be full-time employees of firms
that develop human drug and biologic
products, or consulting firms that
represent human drug and biologic
product developers or have similar
appropriate ties to industry.
khammond on DSKJM1Z7X2PROD with NOTICES
III. Selection Procedure
Any industry organization interested
in participating in the selection of an
appropriate nonvoting member to
represent industry interest must send a
letter stating that interest to the FDA
contact (see FOR FURTHER INFORMATION
CONTACT) within 30 days of publication
of this document (see DATES). Within the
subsequent 60 days, FDA will send a
letter to each organization that has
expressed an interest, attaching a
complete list of all such organizations;
and a list of all nominees along with
their current re´sume´s or curriculum
vitae. The letter will also state that it is
the responsibility of the interested
organizations to confer with one another
and to select a candidate, to represent
industry interest for the committee,
within 60 days after the receipt of the
FDA letter. The interested organizations
are not bound by the list of nominees in
selecting a candidate. However, if no
individual is selected within 60 days,
the Commissioner will select temporary
nonvoting members to represent
industry interests.
IV. Nomination Procedure
Individuals may self-nominate and/or
an organization may nominate one or
more individuals to serve as a
temporary nonvoting industry
representative. Nominations must
include a cover letter and a current,
complete re´sume´ or curriculum vitae for
each nominee, including current
business and/or home address,
telephone number, and email address if
available; and a signed copy of the
Acknowledgement and Consent form
available at the FDA Advisory
Committee Membership Nomination
Portal (see ADDRESSES). Nominations
should specify the advisory committee
for which the nominee is recommended
within 60 days of publication of this
VerDate Sep<11>2014
16:54 Dec 12, 2023
Jkt 262001
document (see DATES). Nominations
should also acknowledge that the
nominee is aware of the nomination,
unless self-nominated. FDA will
forward all nominations to the
organizations expressing interest in
participating in the selection process for
the committee. Only interested industry
organizations participate in the
selection process. Persons who
nominate themselves as nonvoting
industry representatives will not
participate in the selection process.
FDA seeks to include the views of
members of all gender groups, members
of all racial and ethnic groups, and
individuals with and without
disabilities on its advisory committees
and, therefore encourages nominations
of appropriately qualified candidates
from these groups.
This notice is issued under the
Federal Advisory Committee Act (5
U.S.C. 1001 et seq.) and 21 CFR part 14,
relating to advisory committees.
Dated: December 7, 2023.
Lauren K. Roth,
Associate Commissioner for Policy.
[FR Doc. 2023–27303 Filed 12–12–23; 8:45 am]
BILLING CODE 4164–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Health Resources and Services
Administration
Agency Information Collection
Activities: Proposed Collection: Public
Comment Request; Information
Collection Request Title: Applications
for Deemed Public Health Service
Employment With Liability Protections
Under the Federal Tort Claims Act for
Health Centers, Deemed Health Center
Volunteers, and Free Clinic Sponsored
Individuals, OMB No. 0906–XXXX–New
Health Resources and Services
Administration (HRSA), Department of
Health and Human Services.
ACTION: Notice.
AGENCY:
In compliance with the
requirement for opportunity for public
comment on proposed data collection
projects of the Paperwork Reduction Act
of 1995, HRSA announces plans to
submit an Information Collection
Request (ICR), described below, to the
Office of Management and Budget
(OMB). Prior to submitting the ICR to
OMB, HRSA seeks comments from the
public regarding the burden estimate,
below, or any other aspect of the ICR.
DATES: Comments on this ICR should be
received no later than February 12,
2024.
SUMMARY:
PO 00000
Frm 00032
Fmt 4703
Sfmt 4703
Submit your comments to
paperwork@hrsa.gov or mail the HRSA
Information Collection Clearance
Officer, Room 14N39, 5600 Fishers
Lane, Rockville, Maryland 20857.
FOR FURTHER INFORMATION CONTACT: To
request more information on the
proposed project or to obtain a copy of
the data collection plans and draft
instruments, email paperwork@hrsa.gov
or call Joella Roland, the HRSA
Information Collection Clearance
Officer, at (301) 443–3983.
SUPPLEMENTARY INFORMATION: When
submitting comments or requesting
information, please include the ICR title
for reference.
Information Collection Request Title:
Applications for Deemed Public Health
Service (PHS) Employment with
Liability Protections Under the Federal
Tort Claims Act (FTCA) for Health
Centers, Deemed Health Center
Volunteers, and Free Clinic Sponsored
Individuals, OMB No. 0906–XXXX–
New.
Abstract: Section 224(g)–(n) of the
PHS Act (42 U.S.C. 233(g)–(n)) states
that entities receiving funds under
section 330 of the PHS Act and
specified individuals of that entity may
be deemed to be PHS employees for the
purpose of eligibility for liability
protections, including FTCA coverage,
for the performance of medical, surgical,
dental, and related functions within the
scope of deemed employment upon
approval of an application for deemed
employment. The Health Center
Program and Health Center FTCA
Program are administered by HRSA.
Health centers submit deeming
applications annually to HRSA in the
prescribed form and manner in order to
obtain deemed PHS employee status,
with the associated eligibility for FTCA
coverage. Such applications must be
approved by HRSA in a Notice of
Deeming Action. Deemed health centers
must resubmit applications annually
meeting all deeming requirements in
order to maintain deemed status.
ADDRESSES:
Volunteer Health Professionals (VHPs)
Section 224(q) of the PHS Act (42
U.S.C. 233(q)) extends eligibility for
deemed PHS employee status to VHPs
sponsored by deemed health centers
upon approval of an individual
sponsorship application for deemed
PHS employment. The Health Center
VHP FTCA Program is administered by
HRSA. In order to maintain deemed
status for VHPs, deemed health centers
must submit to HRSA an annual
deeming sponsorship application on
behalf of individually named VHPs. For
liability protections to apply, such
E:\FR\FM\13DEN1.SGM
13DEN1
Agencies
[Federal Register Volume 88, Number 238 (Wednesday, December 13, 2023)]
[Notices]
[Pages 86345-86346]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2023-27303]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA-2023-N-0008]
Request for Nominations of Individuals and Industry Organizations
for the Genetic Metabolic Diseases Advisory Committee
AGENCY: Food and Drug Administration, HHS.
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: The Food and Drug Administration (FDA or Agency) is requesting
that industry organizations interested in participating in the
selection of a nonvoting industry representative to serve on the
Genetic Metabolic Diseases Advisory Committee (the Committee) in the
Center for Drug Evaluation and Research notify FDA in writing. FDA is
also requesting nominations for a nonvoting industry representative to
serve on the Committee. Nominees recommended to serve as a nonvoting
industry representative may either be self-nominated or nominated by an
industry organization. Nominations will be accepted for the current
vacancy effective with this notice.
DATES: Any industry organization interested in participating in the
selection of an appropriate nonvoting member to represent industry
interest, must send a letter stating that interest to the FDA by
February 12, 2024, (see sections I and II of this document for
details). Concurrently, nomination materials for prospective candidates
should be sent to FDA by February 12, 2024.
ADDRESSES: All statements of interest from interested industry
organizations interested in participating in the selection process of a
nonvoting industry representative should be sent electronically to
Nicholas Marsh (see FOR FURTHER INFORMATION CONTACT). All nominations
for the nonvoting industry representative may be submitted
electronically by accessing the FDA Advisory Committee Membership
Nomination Portal: https://www.accessdata.fda.gov/scripts/FACTRSPortal/FACTRS/index.cfm or by mail to Advisory Committee Oversight and
Management Staff, Food and Drug Administration, 10903 New Hampshire
Ave., Bldg. 32, Rm. 5103, Silver Spring, MD 20993-0002.
Information about becoming a member on an FDA advisory committee
can also be obtained by visiting FDA's website at https://www.fda.gov/AdvisoryCommittees/default.htm.
FOR FURTHER INFORMATION CONTACT: Nicolas Marsh, Center for Drug
Evaluation and Research, Food and Drug Administration, 10903 New
Hampshire Ave., Bldg. 31, Rm. 2418, Silver Spring, MD 20993-0002, 240-
402-5357, email: [email protected].
For questions relating to the Genetic Metabolic Diseases Advisory
Committee: Moon Choi, Center for Drug Evaluation and Research, Food and
Drug Administration, 10903 New Hampshire Ave., Bldg. 31, Rm. 2417,
Silver Spring, MD 20993-0002, 301-796-2894, email: [email protected].
SUPPLEMENTARY INFORMATION: FDA is requesting nominations for a
nonvoting industry representative for the Genetic Metabolic Diseases
Advisory Committee.
Elsewhere in this issue of the Federal Register, FDA is publishing
separate documents regarding:
1. Genetic Metabolic Diseases Advisory Committee; Notice of
Establishment
2. Request for Nominations for Voting Members for the Genetic Metabolic
Diseases Advisory Committee
3. Request for Nominations of Individuals and Consumer Organizations
for the Genetic Metabolic Diseases Advisory Committee
[[Page 86346]]
I. General Description of the Genetic Metabolic Diseases Advisory
Committee's Duties
The Committee reviews and evaluates data on the safety and
effectiveness of marketed and investigational human drug and biologic
products for use in the treatment of genetic metabolic diseases and
makes appropriate recommendations to the Commissioner of Food and
Drugs.
II. Qualifications
Persons nominated for the Committee should be full-time employees
of firms that develop human drug and biologic products, or consulting
firms that represent human drug and biologic product developers or have
similar appropriate ties to industry.
III. Selection Procedure
Any industry organization interested in participating in the
selection of an appropriate nonvoting member to represent industry
interest must send a letter stating that interest to the FDA contact
(see FOR FURTHER INFORMATION CONTACT) within 30 days of publication of
this document (see DATES). Within the subsequent 60 days, FDA will send
a letter to each organization that has expressed an interest, attaching
a complete list of all such organizations; and a list of all nominees
along with their current r[eacute]sum[eacute]s or curriculum vitae. The
letter will also state that it is the responsibility of the interested
organizations to confer with one another and to select a candidate, to
represent industry interest for the committee, within 60 days after the
receipt of the FDA letter. The interested organizations are not bound
by the list of nominees in selecting a candidate. However, if no
individual is selected within 60 days, the Commissioner will select
temporary nonvoting members to represent industry interests.
IV. Nomination Procedure
Individuals may self-nominate and/or an organization may nominate
one or more individuals to serve as a temporary nonvoting industry
representative. Nominations must include a cover letter and a current,
complete r[eacute]sum[eacute] or curriculum vitae for each nominee,
including current business and/or home address, telephone number, and
email address if available; and a signed copy of the Acknowledgement
and Consent form available at the FDA Advisory Committee Membership
Nomination Portal (see ADDRESSES). Nominations should specify the
advisory committee for which the nominee is recommended within 60 days
of publication of this document (see DATES). Nominations should also
acknowledge that the nominee is aware of the nomination, unless self-
nominated. FDA will forward all nominations to the organizations
expressing interest in participating in the selection process for the
committee. Only interested industry organizations participate in the
selection process. Persons who nominate themselves as nonvoting
industry representatives will not participate in the selection process.
FDA seeks to include the views of members of all gender groups,
members of all racial and ethnic groups, and individuals with and
without disabilities on its advisory committees and, therefore
encourages nominations of appropriately qualified candidates from these
groups.
This notice is issued under the Federal Advisory Committee Act (5
U.S.C. 1001 et seq.) and 21 CFR part 14, relating to advisory
committees.
Dated: December 7, 2023.
Lauren K. Roth,
Associate Commissioner for Policy.
[FR Doc. 2023-27303 Filed 12-12-23; 8:45 am]
BILLING CODE 4164-01-P