Agency Information Collection Activities; Announcement of Office of Management and Budget Approval; Prescription Drug Marketing Act of 1987; Policies, Requirements, and Administrative Procedures, 31384-31385 [2015-13331]
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31384
Federal Register / Vol. 80, No. 105 / Tuesday, June 2, 2015 / Notices
Program Expansion for Acute
Respiratory Illness Surveillance
Financed Solely by 2015 Prevention and
Public Health Funds’’, IP–11–
00100501PPHF15.
Contact Person for More Information:
Gregory Anderson, M.S., M.P.H.,
Scientific Review Officer, CDC, 1600
Clifton Road NE., Mailstop E60, Atlanta,
Georgia 30333, Telephone: (404) 718–
8833.
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.
Elaine L. Baker,
Director, Management Analysis and Services
Office, Centers for Disease Control and
Prevention.
[FR Doc. 2015–13311 Filed 6–1–15; 8:45 am]
[FR Doc. 2015–13315 Filed 6–1–15; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
Administration for Children and
Families
Disease, Disability, and Injury
Prevention and Control Special
Emphasis Panel (SEP): Initial Review
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Secretary, HHS, summarizing the results
of completed dose reconstruction
reviews.
The agenda is subject to change as
priorities dictate.
CONTACT PERSON FOR MORE INFORMATION:
Theodore Katz, Designated Federal
Officer, NIOSH, CDC, 1600 Clifton
Road, Mailstop E–20, Atlanta GA 30333,
Telephone (513)533–6800, Toll Free
1(800) CDC–INFO, Email ocas@cdc.gov.
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.
[CFDA Number: 93.598]
In accordance with section 10(a)(2) of
the Federal Advisory Committee Act
(Pub. L. 92–463), the Centers for Disease
Control and Prevention (CDC)
announces a meeting for the initial
review of applications in response to
Funding Opportunity Announcement
(FOA), IP–11–00100501PPHF15, PPHF–
2015—Enhanced Surveillance for New
Vaccine Preventable Disease—A
Program Expansion for Acute
Respiratory Illness Surveillance
Financed Solely by 2015 Prevention and
Public Health Funds.
Time and Date: 10:00 a.m.–3:00 p.m.,
June 23, 2015 (Closed).
Place: Teleconference.
Status: The meeting will be closed to
the public in accordance with
provisions set forth in section 552b(c)(4)
and (6), Title 5 U.S.C., and the
Determination of the Director,
Management Analysis and Services
Office, CDC, pursuant to Public Law 92–
463.
Matters for Discussion: The meeting
will include the initial review,
discussion, and evaluation of
applications received in response to
‘‘PPHF–2015-Enhanced Surveillance for
New Vaccine Preventable Disease—A
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Announcement of the Award of a
Single-Source Program Expansion
Supplement Grant to the U.S.
Committee for Refugees and
Immigrants in Arlington, VA
Office of Refugee Resettlement,
ACF, HHS.
ACTION: Announcement of the award of
a single-source program expansion
supplement to the U.S. Committee for
Refugees and Immigrants (USCRI) to
support expanded services to foreign
trafficking victims, potential trafficking
victims, and certain family members.
AGENCY:
The Administration for
Children and Families (ACF), Office of
Refugee Resettlement (ORR) announces
the award of a single-source program
expansion supplement grant to U.S.
Committee for Refugees and Immigrants
in Arlington, Virginia for a total of
$1,060,805.
The supplemental funding will ensure
that clients’ essential needs, such as
housing, transportation,
communication, food, and medical care,
will be met. The supplemental funding
will also ensure that USCRI has
sufficient staff for the increased number
of cases.
SUMMARY:
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The period of support under
these supplements is June 01, 2015
through September 29, 2015.
FOR FURTHER INFORMATION CONTACT:
Maggie Wynne, Director, Division of
Anti-Trafficking in Persons, Office of
Refugee Resettlement, 901 D Street SW.,
Washington, DC 20024, Telephone (202)
401–4664. Email: maggie.wynne@
acf.hhs.gov.
SUPPLEMENTARY INFORMATION: The
National Human Trafficking Victim
Assistance Program (NHTVAP) provides
funding for comprehensive case
management services to victims of
trafficking and certain family members
on a per capita basis. The NHTVAP
grantees help clients gain access to
housing, employability services, mental
health screening and therapy, medical
care, and some legal services. During FY
2015, a grantee, U.S. Committee for
Refugees and Immigrants (USCRI),
served more clients than it had planned
for in its budget for the year. Without
the additional funding, USCRI would
have to make significant cuts in services
to current clients and limit the
enrollment of new clients. Also, without
additional funding USCRI would not
have sufficient programmatic support
for the increase in client enrollments.
With the supplemental funding, USCRI
will be able to ensure that all of the
clients’ essential needs will be met.
DATES:
Statutory Authority: Trafficking Victims
Protection Act of 2000 (TVPA), as amended,
Section 107(b)(1)(B), 22 U.S.C. 7105(b)(1)(B),
authorizes funding for benefits and services
to foreign victims of severe forms of
trafficking in persons in the United States,
potential victims of trafficking seeking HHS
Certification, and certain family members.
Christopher Beach,
Senior Grants Policy Specialist, Office of
Administration.
[FR Doc. 2015–13177 Filed 6–1–15; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2011–N–0279]
Agency Information Collection
Activities; Announcement of Office of
Management and Budget Approval;
Prescription Drug Marketing Act of
1987; Policies, Requirements, and
Administrative Procedures
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Notice.
The Food and Drug
Administration (FDA) is announcing
SUMMARY:
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Federal Register / Vol. 80, No. 105 / Tuesday, June 2, 2015 / Notices
Dated: May 28, 2015.
Leslie Kux,
Associate Commissioner for Policy.
perform outreach to schoolchildren
using FDA-approved food safety and
nutrition messages. This proposed
cooperative agreement requires the
supporting organization to provide
teachers for one school year to extend
CFSAN’s outreach into schools.
DATES: The application due date is July
1, 2015, by 11:59 p.m. Eastern Time.
ADDRESSES: Submit electronic
applications to: https://www.grants.gov.
For more information, see section III of
the SUPPLEMENTARY INFORMATION section
of this notice.
FOR FURTHER INFORMATION CONTACT:
Louise Dickerson, Center for Food
Safety and Applied Nutrition, CPK1,
Rm. 2C–006 (HFS–008), Food and Drug
Administration, 5100 Paint Branch
Pkwy., College Park, MD 20740, 240–
402–2129, email:
Louise.Dickerson@fda.hhs.gov; or
Kimberly Pendleton Chew, Office of
Acquisition and Grant Services, FHSL,
Rm. 2031, Food and Drug
Administration, 5630 Fishers Lane,
Rockville, MD 20857, 240–402–7610,
email: Kimberly.Pendleton@fda.hhs.gov.
For more information on this funding
opportunity announcement (FOA) and
to obtain detailed requirements, please
refer to the full FOA located at https://
www.grants.gov. Search by Funding
Opportunity Number: RFA–FD–15–011.
SUPPLEMENTARY INFORMATION:
[FR Doc. 2015–13331 Filed 6–1–15; 8:45 am]
I. Funding Opportunity Description
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RFA–FD–15–011
93.103
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
A. Background
that a collection of information entitled
‘‘Prescription Drug Marketing Act of
1987; Policies, Requirements, and
Administrative Procedures’’ has been
approved by the Office of Management
and Budget (OMB) under the Paperwork
Reduction Act of 1995.
FOR FURTHER INFORMATION CONTACT: FDA
PRA Staff, Office of Operations, Food
and Drug Administration, 8455
Colesville Rd., COLE–14526, Silver
Spring, MD 20993–0002, PRAStaff@
fda.hhs.gov.
SUPPLEMENTARY INFORMATION: On March
06, 2015, the Agency submitted a
proposed collection of information
entitled ‘‘Prescription Drug Marketing
Act of 1987; Policies, Requirements, and
Administrative Procedures’’ to OMB for
review and clearance under 44 U.S.C.
3507. An Agency may not conduct or
sponsor, and a person is not required to
respond to, a collection of information
unless it displays a currently valid OMB
control number. OMB has now
approved the information collection and
has assigned OMB control number
0910–0435. The approval expires on
May 31, 2018. A copy of the supporting
statement for this information collection
is available on the Internet at https://
www.reginfo.gov/public/do/PRAMain.
Food and Drug Administration
[Docket No. FDA–2015–N–0012]
The Food and Drug Administration’s
Education and Outreach Program
Targeting School-Aged Children
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Notice; U48.
The Food and Drug
Administration (FDA) is announcing the
availability of grant funds for the
support of the Center for Food Safety
and Applied Nutrition’s (CFSAN)
Education and Outreach Program
Targeting School-Aged Children (U48).
The goal of the Education and Outreach
Program Targeting School-Aged
Children (U48) is to support educational
outreach programs targeting school-aged
children which promotes FDA’s
mission. As part of FDA’s mission to
promote and protect public health, the
educational program’s mission is to
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SUMMARY:
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This FOA is soliciting an application
from the Graduate School USA to
support and extend the education
programs of the Education Team in the
Office of Analytics and Outreach. As
part of its mission to promote and
protect public health, the Education
Team is tasked to implement targeted
education programs that reach schoolaged children using FDA-approved food
safety and nutrition messages. This
cooperative agreement requires the
grantee to provide 37 teachers for one
school year to extend CFSAN’s reach
into additional U.S. schools. The
selected grantee must train and ensure
that these 37 teachers will use the FDA
curriculum Science and Our Food
Supply (SOFS), which has been
approved by FDA scientists. The grantee
shall also guarantee that these teachers
will use CFSAN’s educational materials
and, in turn, support and promote food
safety and nutrition on a national scale.
This cooperative agreement will
support the commitment of 37 middle
and high school teachers to implement
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the FDA-National Science Teachers
Association (NSTA) supplementary food
science curriculum SOFS, and includes
one week of targeted training with this
curriculum as the basis of instruction. It
also includes a 1-day Enhancement
Training session at the December NSTA
Regional Conference. SOFS content is
linked to specific national science
education standards to help teachers
integrate this content into their existing
classroom materials. The course covers
the latest research on food safety, food
microbiology, epidemiology, and
nutrition from FDA experts and
scientists. These 37 teachers must
conduct a train-the-teacher session for
other science teachers in their area of
the country on how to successfully use
SOFS in their classrooms. To date, 620
teachers have completed the week-long
program, reaching approximately 13,000
teachers and more than 7 million
students across the country. Teachers in
this program have represented all 50
states, the District of Columbia, the U.S.
Virgin Islands, Guam, and Puerto Rico.
In recent years, CFSAN has added
other training and online resources
through the NSTA Learning Center, as
well as FDA and Graduate School Web
sites. The grantee shall assume the
responsibilities of arranging print and
electronic program advertisements to
science teachers through science teacher
journals, Web-based formats, and
listservs (where appropriate). The
grantee shall act as a National Training
Coordinator for the year-round SOFS
content delivery by teachers. In
addition, the grantee shall oversee and
coordinate exhibiting at one regional
NSTA conference in the fall of 2015 and
one national NSTA conference in spring
2016. The goal of this cooperative
agreement is to provide continued
support for this program, which requires
around-the-calendar attention to cover
the various stages of teacher primary
training, in-school SOFS curriculum
implementation, secondary training,
and train-the-teacher programs, as well
as to distribute food science education
materials to teachers to promote student
education in food safety and nutrition.
B. Research Objectives
Specific objectives of this support are
to:
• Provide 37 teachers from diverse
U.S. schools a weeklong course in food
science in the Washington, DC
metropolitan area;
• distribute approved food science
curricula and other materials for the
train-the-teacher session and exhibit at
the national NSTA and regional NSTA
conferences; and
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Agencies
[Federal Register Volume 80, Number 105 (Tuesday, June 2, 2015)]
[Notices]
[Pages 31384-31385]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2015-13331]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA-2011-N-0279]
Agency Information Collection Activities; Announcement of Office
of Management and Budget Approval; Prescription Drug Marketing Act of
1987; Policies, Requirements, and Administrative Procedures
AGENCY: Food and Drug Administration, HHS.
ACTION: Notice.
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SUMMARY: The Food and Drug Administration (FDA) is announcing
[[Page 31385]]
that a collection of information entitled ``Prescription Drug Marketing
Act of 1987; Policies, Requirements, and Administrative Procedures''
has been approved by the Office of Management and Budget (OMB) under
the Paperwork Reduction Act of 1995.
FOR FURTHER INFORMATION CONTACT: FDA PRA Staff, Office of Operations,
Food and Drug Administration, 8455 Colesville Rd., COLE-14526, Silver
Spring, MD 20993-0002, PRAStaff@fda.hhs.gov.
SUPPLEMENTARY INFORMATION: On March 06, 2015, the Agency submitted a
proposed collection of information entitled ``Prescription Drug
Marketing Act of 1987; Policies, Requirements, and Administrative
Procedures'' to OMB for review and clearance under 44 U.S.C. 3507. An
Agency may not conduct or sponsor, and a person is not required to
respond to, a collection of information unless it displays a currently
valid OMB control number. OMB has now approved the information
collection and has assigned OMB control number 0910-0435. The approval
expires on May 31, 2018. A copy of the supporting statement for this
information collection is available on the Internet at https://www.reginfo.gov/public/do/PRAMain.
Dated: May 28, 2015.
Leslie Kux,
Associate Commissioner for Policy.
[FR Doc. 2015-13331 Filed 6-1-15; 8:45 am]
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