83_FR_12247 83 FR 12193 - Notice of Closed Meeting

83 FR 12193 - Notice of Closed Meeting

DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention

Federal Register Volume 83, Issue 54 (March 20, 2018)

Page Range12193-12193
FR Document2018-05577

Federal Register, Volume 83 Issue 54 (Tuesday, March 20, 2018)
[Federal Register Volume 83, Number 54 (Tuesday, March 20, 2018)]
[Notices]
[Page 12193]
From the Federal Register Online  [www.thefederalregister.org]
[FR Doc No: 2018-05577]


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DEPARTMENT OF HEALTH AND HUMAN SERVICES

Centers for Disease Control and Prevention


Notice of Closed Meeting

    Pursuant to section 10(d) of the Federal Advisory Committee Act, as 
amended, notice is hereby given of the following meeting.
    The meeting 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, and the Determination of the Director, Management 
Analysis and Services Office, CDC, pursuant to Public Law 92-463. 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.
    Name of Committee: Disease, Disability, and Injury Prevention and 
Control Special Emphasis Panel (SEP)--GH18-004, Advancing Public Health 
in Central America (Belize, Costa Rica, Dominican Republic, El 
Salvador, Guatemala, Honduras, Nicaragua, Panama).
    Date: April 17, 2018.
    Time: 9:00 a.m.-2:00 p.m., EDT.
    Place: Teleconference.
    Agenda: To review and evaluate grant applications.
    For Further Information Contact: Hylan Shoob, Ph.D., Scientific 
Review Officer, Center for Global Health, CDC, 1600 Clifton Drive, 
Atlanta, GA 30331, (404) 639-4796; [email protected].
    The Director, Management Analysis and Services Office, has been 
delegated the authority to sign Federal Register notices pertaining to 
announcements of meetings and other committee management activities, 
for both the Centers for Disease Control and Prevention and the Agency 
for Toxic Substances and Disease Registry.

Elaine L. Baker,
Director, Management Analysis and Services Office, Centers for Disease 
Control and Prevention.
[FR Doc. 2018-05577 Filed 3-19-18; 8:45 am]
BILLING CODE 4163-18-P



                                                                             Federal Register / Vol. 83, No. 54 / Tuesday, March 20, 2018 / Notices                                                  12193

                                               containing a consent order from Nectar                  would affect compliance with the order.               Officer, Center for Global Health, CDC,
                                               Brand LLC, also d/b/a Nectar Sleep;                     Part IV requires respondent to maintain               1600 Clifton Drive, Atlanta, GA 30331,
                                               Dreamcloud, LLC; and Dreamcloud                         certain records, including records                    (404) 639–4796; HShoob@cdc.gov.
                                               Brand LLC (‘‘respondent’’).                             necessary to demonstrate compliance                     The Director, Management Analysis
                                                  The proposed consent order has been                  with the order. Part V requires                       and Services Office, has been delegated
                                               placed on the public record for thirty                  respondent to submit additional                       the authority to sign Federal Register
                                               (30) days for receipt of comments by                    compliance reports when requested by                  notices pertaining to announcements of
                                               interested persons. Comments received                   the Commission and to permit the                      meetings and other committee
                                               during this period will become part of                  Commission or its representatives to                  management activities, for both the
                                               the public record. After thirty (30) days,              interview respondent’s personnel.                     Centers for Disease Control and
                                               the Commission will again review the                       Finally, Part VI is a ‘‘sunset’’                   Prevention and the Agency for Toxic
                                               agreement and the comments received,                    provision, terminating the order after                Substances and Disease Registry.
                                               and will decide whether it should                       twenty (20) years, with certain
                                               withdraw from the agreement or make                                                                           Elaine L. Baker,
                                                                                                       exceptions.
                                               final the agreement’s proposed order.                      The purpose of this analysis is to aid             Director, Management Analysis and Services
                                                  This matter involves respondent’s                    public comment on the proposed order.                 Office, Centers for Disease Control and
                                               marketing, sale, and distribution of                                                                          Prevention.
                                                                                                       It is not intended to constitute an
                                               mattresses with claims that the products                                                                      [FR Doc. 2018–05577 Filed 3–19–18; 8:45 am]
                                                                                                       official interpretation of the proposed
                                               are assembled in the United States.                     order or to modify its terms in any way.              BILLING CODE 4163–18–P
                                                  According to the FTC’s complaint,
                                                                                                         By direction of the Commission.
                                               respondent represented that its products
                                               are ‘‘assembled in the USA.’’ In fact, the              Donald S. Clark,                                      DEPARTMENT OF HEALTH AND
                                               respondent’s mattresses are wholly                      Secretary.                                            HUMAN SERVICES
                                               imported. Therefore, this representation                [FR Doc. 2018–05613 Filed 3–19–18; 8:45 am]
                                               was false or misleading. Based on the                   BILLING CODE 6750–01–P
                                                                                                                                                             Centers for Disease Control and
                                               foregoing, the complaint alleges that                                                                         Prevention
                                               respondent engaged in deceptive acts or
                                                                                                                                                             Notice of Closed Meeting
                                               practices in violation of Section 5(a) of               DEPARTMENT OF HEALTH AND
                                               the FTC Act.                                            HUMAN SERVICES                                          Pursuant to section 10(d) of the
                                                  The proposed consent order contains                                                                        Federal Advisory Committee Act, as
                                               provisions designed to prevent                          Centers for Disease Control and                       amended, notice is hereby given of the
                                               respondent from engaging in similar                     Prevention                                            following meeting.
                                               acts and practices in the future.                                                                               The meeting will be closed to the
                                               Consistent with the FTC’s Enforcement                   Notice of Closed Meeting                              public in accordance with the
                                               Policy Statement on U.S. Origin Claims,                   Pursuant to section 10(d) of the                    provisions set forth in sections
                                               Part I prohibits respondent from making                 Federal Advisory Committee Act, as                    552b(c)(4) and 552b(c)(6), Title 5 U.S.C.,
                                               U.S.-origin claims for their products                   amended, notice is hereby given of the                as amended, and the Determination of
                                               unless either: (1) The final assembly or                following meeting.                                    the Director, Management Analysis and
                                               processing of the product occurs in the                   The meeting will be closed to the                   Services Office, CDC, pursuant to Public
                                               United States, all significant processing               public in accordance with the                         Law 92–463. The grant applications and
                                               that goes into the product occurs in the                provisions set forth in sections                      the discussions could disclose
                                               United States, and all or virtually all                 552b(c)(4) and 552b(c)(6), Title 5 U.S.C.,            confidential trade secrets or commercial
                                               ingredients or components of the                        as amended, and the Determination of                  property such as patentable material,
                                               product are made and sourced in the                     the Director, Management Analysis and                 and personal information concerning
                                               United States; (2) a clear and                          Services Office, CDC, pursuant to Public              individuals associated with the grant
                                               conspicuous qualification appears                       Law 92–463. The grant applications and                applications, the disclosure of which
                                               immediately adjacent to the                             the discussions could disclose                        would constitute a clearly unwarranted
                                               representation that accurately conveys                  confidential trade secrets or commercial              invasion of personal privacy.
                                               the extent to which the product contains                property such as patentable material,                   Name of Committee: Disease,
                                               foreign parts, ingredients or                           and personal information concerning                   Disability, and Injury Prevention and
                                               components, and/or processing; or (3)                   individuals associated with the grant                 Control Special Emphasis Panel (SEP)—
                                               for a claim that a product is assembled                 applications, the disclosure of which                 GH14–002, Addressing Emerging
                                               in the United States, the product is last               would constitute a clearly unwarranted                Infectious Diseases in Bangladesh;
                                               substantially transformed in the United                 invasion of personal privacy.                         GH16–003, Conducting Public Health
                                               States, the product’s principal assembly                  Name of Committee: Disease,                         Research in Thailand: Technical
                                               takes place in the United States, and                   Disability, and Injury Prevention and                 collaboration with the Ministry of
                                               United States assembly operations are                   Control Special Emphasis Panel (SEP)—                 Public Health in the Kingdom of
                                               substantial.                                            GH18–004, Advancing Public Health in                  Thailand (MOPH); GH16–006,
                                                  Part II prohibits respondent from                    Central America (Belize, Costa Rica,                  Conducting Public Health Research in
                                               making any country-of-origin claim                      Dominican Republic, El Salvador,                      Kenya; GH17–005, Conducting Public
                                               about a product or service unless the                   Guatemala, Honduras, Nicaragua,                       Health Research in China.
                                               claim is true, not misleading, and                      Panama).                                                Date: April 10, 2018.
daltland on DSKBBV9HB2PROD with NOTICES




                                               respondent has a reasonable basis                         Date: April 17, 2018.                                 Time: 9:00 a.m.–2:00 p.m., EDT.
                                               substantiating the representation.                        Time: 9:00 a.m.–2:00 p.m., EDT.                       Place: Teleconference.
                                                  Parts III through V are reporting and                  Place: Teleconference.                                Agenda: To review and evaluate grant
                                               compliance provisions. Part III requires                  Agenda: To review and evaluate grant                applications.
                                               the filing of compliance reports within                 applications.                                           For Further Information Contact:
                                               one year after the order becomes final                    For Further Information Contact:                    Hylan Shoob, Ph.D., Scientific Review
                                               and within 14 days of any change that                   Hylan Shoob, Ph.D., Scientific Review                 Officer, Center for Global Health, CDC,


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Document Created: 2018-03-20 01:10:44
Document Modified: 2018-03-20 01:10:44
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
DatesApril 17, 2018.
ContactHylan Shoob, Ph.D., Scientific Review Officer, Center for Global Health, CDC, 1600 Clifton Drive, Atlanta, GA 30331, (404) 639-4796; [email protected]
FR Citation83 FR 12193 

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