82_FR_34823 82 FR 34681 - Patient Engagement Advisory Committee; Notice of Meeting

82 FR 34681 - Patient Engagement Advisory Committee; Notice of Meeting

DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration

Federal Register Volume 82, Issue 142 (July 26, 2017)

Page Range34681-34682
FR Document2017-15657

The Food and Drug Administration (FDA) announces a forthcoming public advisory committee meeting of the Patient Engagement Advisory Committee (PEAC). The general function of the committee is to provide advice and recommendations to the Agency on complex issues relating to medical devices, the regulation of devices, and their use by patients. The meeting will be open to the public. This meeting will be the inaugural meeting of a new advisory committee.

Federal Register, Volume 82 Issue 142 (Wednesday, July 26, 2017)
[Federal Register Volume 82, Number 142 (Wednesday, July 26, 2017)]
[Notices]
[Pages 34681-34682]
From the Federal Register Online  [www.thefederalregister.org]
[FR Doc No: 2017-15657]


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DEPARTMENT OF HEALTH AND HUMAN SERVICES

Food and Drug Administration

[Docket No. FDA-2017-N-0001]


Patient Engagement Advisory Committee; Notice of Meeting

AGENCY: Food and Drug Administration, HHS.

ACTION: Notice.

-----------------------------------------------------------------------

SUMMARY: The Food and Drug Administration (FDA) announces a forthcoming 
public advisory committee meeting of the Patient Engagement Advisory 
Committee (PEAC). The general function of the committee is to provide 
advice and recommendations to the Agency on complex issues relating to 
medical devices, the regulation of devices, and their use by patients. 
The meeting will be open to the public. This meeting will be the 
inaugural meeting of a new advisory committee.

DATES: The meeting will be held on October 11, 2017, from 1 p.m. to 5 
p.m. and October 12, 2017, from 8 a.m. to 5 p.m.

ADDRESSES: Hilton Washington DC North/Gaithersburg, Grand Ballroom, 620 
Perry Pkwy., Gaithersburg, MD 20877. The hotel's telephone number is 
301-977-8900. Answers to commonly asked questions including information 
regarding special accommodations due to a disability, visitor parking, 
and transportation may be accessed at: http://www.fda.gov/AdvisoryCommittees/AboutAdvisoryCommittees/ucm408555.htm.

FOR FURTHER INFORMATION CONTACT: Letise Williams, Center for Devices 
and Radiological Health, Food and Drug Administration, 10903 New 
Hampshire Ave., Bldg. 66, Rm. 5441, Silver Spring, MD 20993-0002, 301-
796-8398, or FDA Advisory Committee Information Line, 1-800-741-8138 
(301-443-0572 in the Washington, DC area). A notice in the Federal 
Register about last minute modifications that impact a previously 
announced advisory committee meeting cannot always be published quickly 
enough to provide timely notice. Therefore, you should always check the 
Agency's Web site at http://www.fda.gov/AdvisoryCommittees/default.htm 
and scroll down to the appropriate advisory committee meeting link, or 
call the advisory committee information line to learn about possible 
modifications before coming to the meeting.

SUPPLEMENTARY INFORMATION:
    Agenda: On October 11 and 12, 2017, the committee will discuss and 
make recommendations on the topic of patient input into medical device 
clinical trials. This meeting will provide the opportunity to bring 
patients, patient organization, FDA, industry, and other medical and 
scientific experts together for a broader discussion on this important 
patient-related issue.
    This meeting is a key part of FDA's goal to help assure the needs 
and experiences of patients are included as part of FDA's deliberations 
involving the regulation of medical devices and their use by patients. 
For this meeting, FDA is seeking input from the PEAC and the public on 
topics such as to: (1) Better understand challenges for patients in 
medical device clinical trials, (2) better understand how patient input 
and engagement is being used to overcome these challenges (potential 
solutions), and (3) receive

[[Page 34682]]

recommendations from the PEAC on top areas for FDA to consider for 
action.
    FDA intends to make background material available to the public no 
later than 2 business days before the meeting. If FDA is unable to post 
the background material on its Web site prior to the meeting, the 
background material will be made publicly available at the location of 
the advisory committee meeting, and the background material will be 
posted on FDA's Web site after the meeting. Background material is 
available at http://www.fda.gov/AdvisoryCommittees/Calendar/default.htm. Scroll down to the appropriate advisory committee meeting 
link.
    Procedure: Interested persons may present data, information, or 
views, orally or in writing, on issues pending before the committee. 
Written submissions may be made to the contact person on or before 
September 20, 2017. Oral presentations from the public will be 
scheduled between approximately 3:40 p.m. to 4:10 p.m. on October 11, 
2017, and approximately 9 a.m. to 9:30 a.m. and 2:30 p.m. to 3 p.m. on 
October 12, 2017. Those individuals interested in making formal oral 
presentations should notify the contact person and submit a brief 
statement of the general nature of the evidence or arguments they wish 
to present, the names and addresses of proposed participants, and an 
indication of the approximate time requested to make their presentation 
on or before September 12, 2017. Time allotted for each presentation 
may be limited. If the number of registrants requesting to speak is 
greater than can be reasonably accommodated during the scheduled open 
public hearing session, FDA may conduct a lottery to determine the 
speakers for the scheduled open public hearing session. The contact 
person will notify interested persons regarding their request to speak 
by September 13, 2017.
    Persons attending FDA's advisory committee meetings are advised 
that the Agency is not responsible for providing access to electrical 
outlets.
    FDA welcomes the attendance of the public at its advisory committee 
meetings and will make every effort to accommodate persons with 
disabilities. If you require accommodations due to a disability, please 
contact AnnMarie Williams at [email protected], or 301-796-
5966 at least 7 days in advance of the meeting.
    FDA is committed to the orderly conduct of its advisory committee 
meetings. Please visit our Web site at http://www.fda.gov/AdvisoryCommittees/AboutAdvisoryCommittees/ucm111462.htm for procedures 
on public conduct during advisory committee meetings. Please be advised 
that, for the round table portion of the meeting, FDA will prepare a 
summary of discussion instead of detailed transcripts.
    Notice of this meeting is given under the Federal Advisory 
Committee Act (5 U.S.C. app. 2).

    Dated: July 20, 2017.
Anna K. Abram,
Deputy Commiissioner for Policy, Planning, Legislation, and Analysis.
[FR Doc. 2017-15657 Filed 7-25-17; 8:45 am]
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                                                                                 Federal Register / Vol. 82, No. 142 / Wednesday, July 26, 2017 / Notices                                            34681

                                                  https://www.regulations.gov. Submit                        GRASE. This guidance explains the                     meeting will be open to the public. This
                                                  both copies to the Dockets Management                      scope of the final rule and identifies                meeting will be the inaugural meeting of
                                                  Staff. If you do not wish your name and                    which active ingredients were found not               a new advisory committee.
                                                  contact information to be made publicly                    to be GRASE for use in consumer                       DATES: The meeting will be held on
                                                  available, you can provide this                            antiseptic wash products. This guidance               October 11, 2017, from 1 p.m. to 5 p.m.
                                                  information on the cover sheet and not                     explains when and how manufacturers                   and October 12, 2017, from 8 a.m. to 5
                                                  in the body of your comments and you                       must comply with the final rule. This                 p.m.
                                                  must identify this information as                          guidance also explains the significance
                                                                                                                                                                   ADDRESSES: Hilton Washington DC
                                                  ‘‘confidential.’’ Any information marked                   of triclosan and triclocarban under this
                                                                                                                                                                   North/Gaithersburg, Grand Ballroom,
                                                  as ‘‘confidential’’ will not be disclosed                  final rule. In addition, this guidance
                                                                                                                                                                   620 Perry Pkwy., Gaithersburg, MD
                                                  except in accordance with 21 CFR 10.20                     identifies which consumer antiseptic
                                                                                                                                                                   20877. The hotel’s telephone number is
                                                  and other applicable disclosure law. For                   wash active ingredients were deferred
                                                                                                                                                                   301–977–8900. Answers to commonly
                                                  more information about FDA’s posting                       from the final rule and explains what
                                                                                                                                                                   asked questions including information
                                                  of comments to public dockets, see 80                      the effectiveness and safety criteria are
                                                                                                                                                                   regarding special accommodations due
                                                  FR 56469, September 18, 2015, or access                    for these deferred consumer antiseptic
                                                                                                                                                                   to a disability, visitor parking, and
                                                  the information at: https://www.gpo.gov/                   wash active ingredients.
                                                                                                                This guidance is being issued                      transportation may be accessed at:
                                                  fdsys/pkg/FR-2015-09-18/pdf/2015-                                                                                http://www.fda.gov/Advisory
                                                  23389.pdf.                                                 consistent with FDA’s good guidance
                                                                                                             practices regulation (21 CFR 10.115).                 Committees/AboutAdvisoryCommittees/
                                                     Docket: For access to the docket to                                                                           ucm408555.htm.
                                                  read background documents or the                           The guidance represents the current
                                                  electronic and written/paper comments                      thinking of FDA on how small                          FOR FURTHER INFORMATION CONTACT:
                                                  received, go to https://                                   businesses can better understand and                  Letise Williams, Center for Devices and
                                                  www.regulations.gov and insert the                         comply with the consumer antiseptic                   Radiological Health, Food and Drug
                                                  docket number, found in brackets in the                    wash final rule. It does not establish any            Administration, 10903 New Hampshire
                                                  heading of this document, into the                         rights for any person and is not binding              Ave., Bldg. 66, Rm. 5441, Silver Spring,
                                                  ‘‘Search’’ box and follow the prompts                      on FDA or the public. You can use an                  MD 20993–0002, 301–796–8398, or FDA
                                                  and/or go to the Dockets Management                        alternative approach if it satisfies the              Advisory Committee Information Line,
                                                  Staff, 5630 Fishers Lane, Rm. 1061,                        requirements of the applicable statutes               1–800–741–8138 (301–443–0572 in the
                                                  Rockville, MD 20852.                                       and regulations. This guidance is not                 Washington, DC area). A notice in the
                                                     Submit written requests for single                      subject to Executive Order 12866.                     Federal Register about last minute
                                                  copies of this guidance to the Division                                                                          modifications that impact a previously
                                                                                                             II. Electronic Access
                                                  of Drug Information, Center for Drug                                                                             announced advisory committee meeting
                                                  Evaluation and Research, Food and                             Persons with access to the Internet                cannot always be published quickly
                                                  Drug Administration, 10001 New                             may obtain the guidance at either                     enough to provide timely notice.
                                                  Hampshire Ave., Hillandale Building,                       https://www.fda.gov/Drugs/Guidance                    Therefore, you should always check the
                                                  4th Floor, Silver Spring, MD 20993–                        ComplianceRegulatoryInformation/                      Agency’s Web site at http://
                                                  0002. Send one self-addressed adhesive                     Guidances/default.htm or https://                     www.fda.gov/AdvisoryCommittees/
                                                  label to assist that office in processing                  www.regulations.gov.                                  default.htm and scroll down to the
                                                  your requests. See the SUPPLEMENTARY                         Dated: July 20, 2017.                               appropriate advisory committee meeting
                                                  INFORMATION section for electronic                         Anna K. Abram,                                        link, or call the advisory committee
                                                  access to the guidance document.                           Deputy Commissioner for Policy, Planning,             information line to learn about possible
                                                  FOR FURTHER INFORMATION CONTACT:                           Legislation, and Analysis.                            modifications before coming to the
                                                  Pranvera Ikonomi, Center for Drug                          [FR Doc. 2017–15653 Filed 7–25–17; 8:45 am]           meeting.
                                                  Evaluation and Research, Food and                          BILLING CODE 4164–01–P                                SUPPLEMENTARY INFORMATION:
                                                  Drug Administration, 10903 New                                                                                      Agenda: On October 11 and 12, 2017,
                                                  Hampshire Ave., Bldg. 22, Rm. 5418,                                                                              the committee will discuss and make
                                                  Silver Spring, MD 20993–0002, 240–                         DEPARTMENT OF HEALTH AND                              recommendations on the topic of patient
                                                  402–0272.                                                  HUMAN SERVICES                                        input into medical device clinical trials.
                                                  SUPPLEMENTARY INFORMATION:                                                                                       This meeting will provide the
                                                                                                             Food and Drug Administration
                                                                                                                                                                   opportunity to bring patients, patient
                                                  I. Background                                              [Docket No. FDA–2017–N–0001]                          organization, FDA, industry, and other
                                                     FDA is announcing the availability of                                                                         medical and scientific experts together
                                                  a guidance for industry entitled                           Patient Engagement Advisory                           for a broader discussion on this
                                                  ‘‘Consumer Antiseptic Wash Final Rule                      Committee; Notice of Meeting                          important patient-related issue.
                                                  Questions and Answers.’’ We are                            AGENCY:    Food and Drug Administration,                 This meeting is a key part of FDA’s
                                                  issuing this guidance in accordance                        HHS.                                                  goal to help assure the needs and
                                                  with section 212 of the Small Business                     ACTION:   Notice.                                     experiences of patients are included as
                                                  Regulatory Enforcement Fairness Act                                                                              part of FDA’s deliberations involving
                                                  (Pub. L. 104–121, as amended by Pub.                       SUMMARY:  The Food and Drug                           the regulation of medical devices and
                                                  L. 110–28) 1 to assist small businesses in                 Administration (FDA) announces a                      their use by patients. For this meeting,
                                                  better understanding and complying                         forthcoming public advisory committee                 FDA is seeking input from the PEAC
mstockstill on DSK30JT082PROD with NOTICES




                                                  with the consumer antiseptic wash final                    meeting of the Patient Engagement                     and the public on topics such as to: (1)
                                                  rule (September 6, 2016, 81 FR 61106),                     Advisory Committee (PEAC). The                        Better understand challenges for
                                                  which established that certain active                      general function of the committee is to               patients in medical device clinical
                                                  ingredients used in OTC consumer                           provide advice and recommendations to                 trials, (2) better understand how patient
                                                  antiseptic wash products are not                           the Agency on complex issues relating                 input and engagement is being used to
                                                                                                             to medical devices, the regulation of                 overcome these challenges (potential
                                                    15   U.S.C. 601 (note).                                  devices, and their use by patients. The               solutions), and (3) receive


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                                                  34682                        Federal Register / Vol. 82, No. 142 / Wednesday, July 26, 2017 / Notices

                                                  recommendations from the PEAC on top                     public conduct during advisory                        HHS (Secretary) on policy, program
                                                  areas for FDA to consider for action.                    committee meetings. Please be advised                 development, and other matters of
                                                     FDA intends to make background                        that, for the round table portion of the              significance concerning the activities
                                                  material available to the public no later                meeting, FDA will prepare a summary                   under section 747 of Title VII of the
                                                  than 2 business days before the meeting.                 of discussion instead of detailed                     Public Health Service (PHS) Act,
                                                  If FDA is unable to post the background                  transcripts.                                          including dentistry activities.
                                                  material on its Web site prior to the                       Notice of this meeting is given under              ACTPCMD prepares an annual report
                                                  meeting, the background material will                    the Federal Advisory Committee Act (5                 describing the activities of the
                                                  be made publicly available at the                        U.S.C. app. 2).                                       Committee, including findings and
                                                  location of the advisory committee                         Dated: July 20, 2017.                               recommendations made by the
                                                  meeting, and the background material                                                                           Committee concerning the activities
                                                                                                           Anna K. Abram,
                                                  will be posted on FDA’s Web site after                                                                         under section 747, including dentistry
                                                  the meeting. Background material is                      Deputy Commiissioner for Policy, Planning,
                                                                                                           Legislation, and Analysis.                            activities. The annual report is
                                                  available at http://www.fda.gov/                                                                               submitted to the Secretary and ranking
                                                  AdvisoryCommittees/Calendar/                             [FR Doc. 2017–15657 Filed 7–25–17; 8:45 am]
                                                                                                                                                                 members of the Senate Committee on
                                                  default.htm. Scroll down to the                          BILLING CODE 4164–01–P
                                                                                                                                                                 Health, Education, Labor and Pensions,
                                                  appropriate advisory committee meeting                                                                         and the House of Representatives
                                                  link.                                                                                                          Committee on Energy and Commerce.
                                                     Procedure: Interested persons may                     DEPARTMENT OF HEALTH AND
                                                                                                           HUMAN SERVICES                                        The Committee also develops,
                                                  present data, information, or views,                                                                           publishes, and implements performance
                                                  orally or in writing, on issues pending                                                                        measures and guidelines for
                                                                                                           Health Resources and Services
                                                  before the committee. Written                                                                                  longitudinal evaluations of programs
                                                  submissions may be made to the contact                   Administration
                                                                                                                                                                 authorized under Title VII, Part C, of the
                                                  person on or before September 20, 2017.                  Advisory Committee on Training in                     PHS Act, and recommends
                                                  Oral presentations from the public will                  Primary Care Medicine and Dentistry                   appropriation levels for programs under
                                                  be scheduled between approximately                                                                             this Part.
                                                  3:40 p.m. to 4:10 p.m. on October 11,                    AGENCY: Health Resources and Services
                                                                                                                                                                   During the August 16, 2017, meeting,
                                                  2017, and approximately 9 a.m. to 9:30                   Administration (HRSA), Department of
                                                                                                                                                                 ACTPCMD will discuss issues related to
                                                  a.m. and 2:30 p.m. to 3 p.m. on October                  Health and Human Services (HHS).
                                                                                                                                                                 the Committee reports under
                                                  12, 2017. Those individuals interested                   ACTION: Notice of meeting.                            development. Agenda items are subject
                                                  in making formal oral presentations
                                                                                                           SUMMARY:   The Advisory Committee on                  to change as priorities dictate.
                                                  should notify the contact person and
                                                  submit a brief statement of the general                  Training in Primary Care Medicine and                   Members of the public will have the
                                                  nature of the evidence or arguments                      Dentistry (ACTPCMD) has scheduled a                   opportunity to provide comments.
                                                  they wish to present, the names and                      meeting. This meeting will be open to                 Public participants may submit written
                                                  addresses of proposed participants, and                  the public. Information about                         statements in advance of the scheduled
                                                  an indication of the approximate time                    ACTPCMD and the agenda for this                       meeting. Oral comments will be
                                                  requested to make their presentation on                  meeting can be found on the ACTPCMD                   honored in the order they are requested
                                                  or before September 12, 2017. Time                       Web site at http://www.hrsa.gov/                      and may be limited as time allows.
                                                  allotted for each presentation may be                    advisorycommittees/bhpradvisory/                      Requests to submit a written statement
                                                  limited. If the number of registrants                    ACTPCMD.                                              or make oral comments to ACTPCMD
                                                  requesting to speak is greater than can                                                                        should be sent to Kennita R. Carter, MD,
                                                                                                           DATES:   August 16, 2017, 10:00 a.m.–2:30             DFO, using the contact information
                                                  be reasonably accommodated during the                    p.m. ET.
                                                  scheduled open public hearing session,                                                                         above at least 3 business days prior to
                                                                                                           ADDRESSES: This meeting will be held                  the meeting.
                                                  FDA may conduct a lottery to determine
                                                                                                           by webinar and teleconference. The                      Individuals who need special
                                                  the speakers for the scheduled open
                                                                                                           address for the meeting is 5600 Fishers               assistance or another reasonable
                                                  public hearing session. The contact
                                                                                                           Lane, Rockville, Maryland 20857.                      accommodation should notify Dr.
                                                  person will notify interested persons
                                                                                                             • The webinar link: https://                        Kennita R. Carter at the address and
                                                  regarding their request to speak by
                                                                                                           hrsa.connectsolutions.com/actpcmd.                    phone number listed above at least 10
                                                  September 13, 2017.                                        • The conference call-in number:
                                                     Persons attending FDA’s advisory                                                                            days prior to the meeting.
                                                                                                           1–888–946–3804. Passcode: 3214611.
                                                  committee meetings are advised that the                                                                        Amy McNulty,
                                                  Agency is not responsible for providing                  FOR FURTHER INFORMATION CONTACT:
                                                                                                           Anyone requesting information                         Acting Director, Division of the Executive
                                                  access to electrical outlets.                                                                                  Secretariat.
                                                     FDA welcomes the attendance of the                    regarding ACTPCMD should contact
                                                                                                           Kennita R. Carter, MD, Designated                     [FR Doc. 2017–15665 Filed 7–25–17; 8:45 am]
                                                  public at its advisory committee
                                                  meetings and will make every effort to                   Federal Officer (DFO), Division of                    BILLING CODE 4165–15–P

                                                  accommodate persons with disabilities.                   Medicine and Dentistry, Bureau of
                                                  If you require accommodations due to a                   Health Workforce, HRSA, in one of
                                                                                                           three ways: (1) Send a request to the                 DEPARTMENT OF HEALTH AND
                                                  disability, please contact AnnMarie
                                                                                                           following address: Kennita R. Carter,                 HUMAN SERVICES
                                                  Williams at Annmarie.Williams@
                                                  fda.hhs.gov, or 301–796–5966 at least 7                  MD, DFO, Division of Medicine and
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                                                                                                                                                                 Agency Information Collection
                                                  days in advance of the meeting.                          Dentistry, HRSA, 5600 Fishers Lane,
                                                                                                                                                                 Activities: Proposed Collection;
                                                     FDA is committed to the orderly                       15N–116, Rockville, Maryland 20857;
                                                                                                                                                                 Comment Request; Generic Clearance
                                                  conduct of its advisory committee                        (2) call 301–945–3505; or (3) send an
                                                                                                                                                                 for the Collection of Qualitative
                                                  meetings. Please visit our Web site at                   email to KCarter@hrsa.gov.
                                                                                                                                                                 Feedback on Agency Service Delivery
                                                  http://www.fda.gov/Advisory                              SUPPLEMENTARY INFORMATION:
                                                  Committees/AboutAdvisoryCommittees/                      ACTPCMD provides advice and                           AGENCY:Department of Health and
                                                  ucm111462.htm for procedures on                          recommendations to the Secretary of                   Human Services (HHS).


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Document Created: 2017-07-26 01:29:40
Document Modified: 2017-07-26 01:29:40
CategoryRegulatory Information
CollectionFederal Register
sudoc ClassAE 2.7:
GS 4.107:
AE 2.106:
PublisherOffice of the Federal Register, National Archives and Records Administration
SectionNotices
ActionNotice.
DatesThe meeting will be held on October 11, 2017, from 1 p.m. to 5 p.m. and October 12, 2017, from 8 a.m. to 5 p.m.
ContactLetise Williams, Center for Devices and Radiological Health, Food and Drug Administration, 10903 New Hampshire Ave., Bldg. 66, Rm. 5441, Silver Spring, MD 20993-0002, 301- 796-8398, or FDA Advisory Committee Information Line, 1-800-741-8138 (301-443-0572 in the Washington, DC area). A notice in the Federal Register about last minute modifications that impact a previously announced advisory committee meeting cannot always be published quickly enough to provide timely notice. Therefore, you should always check the Agency's Web site at http://www.fda.gov/AdvisoryCommittees/default.htm and scroll down to the appropriate advisory committee meeting link, or call the advisory committee information line to learn about possible modifications before coming to the meeting.
FR Citation82 FR 34681 

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