Request for Nominations of Individuals and Industry Organizations for the Digital Health Advisory Committee, 70675-70676 [2023-22568]
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Federal Register / Vol. 88, No. 196 / Thursday, October 12, 2023 / Notices
interoperability, personalized medicine/
genetics, decentralized clinical trials,
use of DHTs in clinical trials for medical
products, cybersecurity, DHT user
experience, and Agency policies and
regulations regarding these
technologies. The Committee provides
relevant expertise and perspective to
improve Agency understanding of the
benefits, risks, and clinical outcomes
associated with use of DHTs.
ddrumheller on DSK120RN23PROD with NOTICES1
II. Criteria for Members
Persons nominated for membership as
a consumer representative on this
committee should meet the following
criteria: (1) demonstrate an affiliation
with and/or active participation in in
consumer or community-based
organizations, (2) be able to analyze
technical data, (3) understand research
design, (4) discuss benefits and risks,
and (5) evaluate the safety and efficacy
of products under review. The
consumer representative should be able
to represent the consumer perspective
on issues and actions before the
advisory committee; serve as a liaison
between the committee and interested
consumers, associations, coalitions, and
consumer organizations; and facilitate
dialogue with the advisory committees
on scientific issues that affect
consumers.
III. Selection Procedures
Selection of members representing
consumer interests is conducted
through procedures that include the use
of organizations representing the public
interest and public advocacy groups.
These organizations recommend
nominees for the Agency’s selection.
Representatives from the consumer
health branches of Federal, State, and
local governments also may participate
in the selection process. Any consumer
organization interested in participating
in the selection of an appropriate voting
member to represent consumer interests
should send a letter stating that interest
to FDA (see ADDRESSES) within 30 days
of publication of this document.
Within the subsequent 45 days, FDA
will compile a list of consumer
organizations that will participate in the
selection process and will forward to
each such organization a ballot listing at
least two qualified nominees selected by
the Agency based on the nominations
received, together with each nominee’s
current curriculum vitae or re´sume´.
Ballots are to be filled out and returned
to FDA within 30 days. The nominee
receiving the highest number of votes
ordinarily will be selected to serve as
the member representing consumer
interests for that particular advisory
committee.
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IV. Nomination Procedures
Any interested person or organization
may nominate one or more qualified
persons to represent consumer interests
on the Digital Health Advisory
Committee with the exception of the
following: individuals who are not U.S.
citizens or nationals cannot be
appointed as Advisory Committee
Members (42 U.S.C. 217(a)) in FDA.
Self-nominations are also accepted.
Nominations must include 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; a signed copy of the
Acknowledgment and Consent form
available at the FDA Advisory
Nomination Portal (see ADDRESSES), and
a list of consumer or community-based
organizations for which the candidate
can demonstrate active participation.
Nominations should also specify the
advisory committee for which the
nominee is recommended. In addition,
nominations must also acknowledge
that the nominee is aware of the
nomination, unless self-nominated. FDA
will ask potential candidates to provide
detailed information concerning such
matters related to financial holdings,
employment, and research grants and/or
contracts to permit evaluation of
possible sources of conflicts of interest.
Members will be invited to serve for
terms up to 4 years.
FDA will review all nominations
received within the specified
timeframes and prepare a ballot
containing the names of qualified
nominees. Names not selected will
remain on a list of eligible nominees
and be reviewed periodically by FDA to
determine continued interest. After
selecting qualified nominees for the
ballot, FDA will provide those
consumer organizations that are
participating in the selection process
with the opportunity to vote on the
listed nominees. Only organizations
vote in the selection process. Persons
who nominate themselves to serve as
voting consumer representatives will
not participate in the selection process.
This notice is issued under the
Federal Advisory Committee Act (5
U.S.C. app. 2) and 21 CFR part 14,
relating to advisory committees.
Dated: October 6, 2023.
Lauren K. Roth,
Associate Commissioner for Policy.
[FR Doc. 2023–22567 Filed 10–11–23; 8:45 am]
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70675
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
Digital Health Advisory Committee
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Notice.
The Food and Drug
Administration (FDA or Agency) is
requesting nominations for temporary
nonvoting industry representatives to be
included in a pool of individuals to
serve on the Digital Health Advisory
Committee. FDA is also requesting that
industry organizations interested in
participating in the selection of a pool
of nonvoting industry representatives to
serve as temporary nonvoting members
on the Digital Health Advisory
Committee (the Committee) in the
Center for Devices and Radiological
Health notify FDA in writing. Nominees
recommended to serve as a temporary
nonvoting industry representative may
either be self-nominated or nominated
by an industry organization. This
position may be filled by representatives
of different medical device areas based
on areas of expertise relevant to the
topics being considered by the
Committee. Nominations will be
accepted for current vacancies effective
with this notice. 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.
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 November 13, 2023, (see
sections I and II of this document for
details). Concurrently, nomination
materials for prospective candidates
should be sent to FDA by November 13,
2023.
ADDRESSES: All statements of interest
from interested industry organizations
interested in participating in the
selection process of a pool of nonvoting
industry representatives should be sent
electronically to Margaret Ames (see FOR
FURTHER INFORMATION CONTACT). All
nominations for nonvoting industry
representatives may be submitted
electronically by accessing the FDA
SUMMARY:
E:\FR\FM\12OCN1.SGM
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70676
Federal Register / Vol. 88, No. 196 / Thursday, October 12, 2023 / Notices
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:
Margaret Ames, Center for Devices and
Radiological Health, Food and Drug
Administration, 10903 New Hampshire
Ave., Bldg. 66, Rm. 5213, Silver Spring,
MD 20993–0002, 301–796–5960, email:
margaret.ames@fda.hhs.gov.
For questions relating to the Digital
Health Advisory Committee, contact
James Swink, Center for Devices and
Radiological Health, Food and Drug
Administration, 10903 New Hampshire
Ave., Bldg. 66, Room 5211, Silver
Spring, MD 20993–0002, 301–796–6313,
James.swink@fda.hhs.gov.
SUPPLEMENTARY INFORMATION: FDA is
requesting nominations for a pool of
nonvoting industry representatives for
the Digital Health Advisory Committee
(this position may be filled by
representatives of different medical
device areas based on areas of expertise
relevant to the topics being considered
by the Advisory Committee).
Elsewhere in this Federal Register,
FDA is publishing separate documents
regarding:
1. Digital Health Advisory Committee;
Notice of Establishment
2. Request for Nominations for Voting
Members for the Digital Health
Advisory Committee
3. Request for Nominations of
Individuals and Consumer
Organizations for the Digital Health
Advisory Committee
ddrumheller on DSK120RN23PROD with NOTICES1
I. General Description of the
Committee’s Duties
The Committee provides advice on
complex scientific and technical issues
related to Digital Health Technologies
(DHTs). This also may include advice
on the regulation of DHTs, and/or their
use, including use of DHTs in clinical
trials or postmarket studies subject to
FDA regulation. Topics relating to
DHTs, such as artificial intelligence/
machine learning, augmented reality,
virtual reality, digital therapeutics,
wearables, remote patient monitoring,
and software, may be considered by the
Committee. The Committee advises the
Commissioner on issues related to
VerDate Sep<11>2014
17:34 Oct 11, 2023
Jkt 262001
DHTs, including, for example, realworld data, real-world evidence,
patient-generated health data,
interoperability, personalized medicine/
genetics, decentralized clinical trials,
use of DHTs in clinical trials for medical
products, cybersecurity, DHT user
experience, and Agency policies and
regulations regarding these
technologies. The Committee provides
relevant expertise and perspective to
improve Agency understanding of the
benefits, risks, and clinical outcomes
associated with use of DHTs. The
Committee performs its duties by
providing advice and recommendations
on new approaches to develop and
evaluate DHTs and to promote
innovation of DHTs, as well as
identifying risks, barriers, or unintended
consequences that could result from
proposed or established Agency policy
or regulation for topics related to DHTs.
II. Qualifications
Persons nominated for the Digital
Health Advisory Committee should be
full-time employees of firms that
manufacture medical device products,
or consulting firms that represent
manufacturers 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 45 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 resumes 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 or candidates
(to serve in a pool of individuals, with
varying areas of expertise), 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 or candidates.
However, if no individual is selected
within 60 days, the Commissioner will
select temporary nonvoting members (or
pool of individuals) 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
PO 00000
Frm 00039
Fmt 4703
Sfmt 4703
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 30 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.
This notice is issued under the
Federal Advisory Committee Act (5
U.S.C. app. 2) and 21 CFR part 14,
relating to advisory committees.
Dated: October 6, 2023.
Lauren K. Roth,
Associate Commissioner for Policy.
[FR Doc. 2023–22568 Filed 10–11–23; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2023–N–4181]
Agency Information Collection
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Prohibited From Use in Animal Food or
Feed
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Notice.
The Food and Drug
Administration (FDA, Agency, or we) is
announcing an opportunity for public
comment on the proposed collection of
certain information by the Agency.
Under the Paperwork Reduction Act of
1995 (PRA), Federal Agencies are
required to publish notice in the
Federal Register concerning each
proposed collection of information,
including each proposed extension of an
existing collection of information, and
to allow 60 days for public comment in
SUMMARY:
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Agencies
[Federal Register Volume 88, Number 196 (Thursday, October 12, 2023)]
[Notices]
[Pages 70675-70676]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2023-22568]
-----------------------------------------------------------------------
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 Digital Health Advisory Committee
AGENCY: Food and Drug Administration, HHS.
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: The Food and Drug Administration (FDA or Agency) is requesting
nominations for temporary nonvoting industry representatives to be
included in a pool of individuals to serve on the Digital Health
Advisory Committee. FDA is also requesting that industry organizations
interested in participating in the selection of a pool of nonvoting
industry representatives to serve as temporary nonvoting members on the
Digital Health Advisory Committee (the Committee) in the Center for
Devices and Radiological Health notify FDA in writing. Nominees
recommended to serve as a temporary nonvoting industry representative
may either be self-nominated or nominated by an industry organization.
This position may be filled by representatives of different medical
device areas based on areas of expertise relevant to the topics being
considered by the Committee. Nominations will be accepted for current
vacancies effective with this notice. 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.
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
November 13, 2023, (see sections I and II of this document for
details). Concurrently, nomination materials for prospective candidates
should be sent to FDA by November 13, 2023.
ADDRESSES: All statements of interest from interested industry
organizations interested in participating in the selection process of a
pool of nonvoting industry representatives should be sent
electronically to Margaret Ames (see FOR FURTHER INFORMATION CONTACT).
All nominations for nonvoting industry representatives may be submitted
electronically by accessing the FDA
[[Page 70676]]
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: Margaret Ames, Center for Devices and
Radiological Health, Food and Drug Administration, 10903 New Hampshire
Ave., Bldg. 66, Rm. 5213, Silver Spring, MD 20993-0002, 301-796-5960,
email: [email protected].
For questions relating to the Digital Health Advisory Committee,
contact James Swink, Center for Devices and Radiological Health, Food
and Drug Administration, 10903 New Hampshire Ave., Bldg. 66, Room 5211,
Silver Spring, MD 20993-0002, 301-796-6313, [email protected].
SUPPLEMENTARY INFORMATION: FDA is requesting nominations for a pool of
nonvoting industry representatives for the Digital Health Advisory
Committee (this position may be filled by representatives of different
medical device areas based on areas of expertise relevant to the topics
being considered by the Advisory Committee).
Elsewhere in this Federal Register, FDA is publishing separate
documents regarding:
1. Digital Health Advisory Committee; Notice of Establishment
2. Request for Nominations for Voting Members for the Digital Health
Advisory Committee
3. Request for Nominations of Individuals and Consumer Organizations
for the Digital Health Advisory Committee
I. General Description of the Committee's Duties
The Committee provides advice on complex scientific and technical
issues related to Digital Health Technologies (DHTs). This also may
include advice on the regulation of DHTs, and/or their use, including
use of DHTs in clinical trials or postmarket studies subject to FDA
regulation. Topics relating to DHTs, such as artificial intelligence/
machine learning, augmented reality, virtual reality, digital
therapeutics, wearables, remote patient monitoring, and software, may
be considered by the Committee. The Committee advises the Commissioner
on issues related to DHTs, including, for example, real-world data,
real-world evidence, patient-generated health data, interoperability,
personalized medicine/genetics, decentralized clinical trials, use of
DHTs in clinical trials for medical products, cybersecurity, DHT user
experience, and Agency policies and regulations regarding these
technologies. The Committee provides relevant expertise and perspective
to improve Agency understanding of the benefits, risks, and clinical
outcomes associated with use of DHTs. The Committee performs its duties
by providing advice and recommendations on new approaches to develop
and evaluate DHTs and to promote innovation of DHTs, as well as
identifying risks, barriers, or unintended consequences that could
result from proposed or established Agency policy or regulation for
topics related to DHTs.
II. Qualifications
Persons nominated for the Digital Health Advisory Committee should
be full-time employees of firms that manufacture medical device
products, or consulting firms that represent manufacturers 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 45 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 resumes 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 or
candidates (to serve in a pool of individuals, with varying areas of
expertise), 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 or
candidates. However, if no individual is selected within 60 days, the
Commissioner will select temporary nonvoting members (or pool of
individuals) 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 30 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.
This notice is issued under the Federal Advisory Committee Act (5
U.S.C. app. 2) and 21 CFR part 14, relating to advisory committees.
Dated: October 6, 2023.
Lauren K. Roth,
Associate Commissioner for Policy.
[FR Doc. 2023-22568 Filed 10-11-23; 8:45 am]
BILLING CODE 4164-01-P