Agency Information Collection Activities; Proposed Collection; Public Comment Request, 13007-13008 [2015-05619]
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Federal Register / Vol. 80, No. 48 / Thursday, March 12, 2015 / Notices
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
Center for Scientific Review; Notice of
Closed Meetings
Pursuant to section 10(d) of the
Federal Advisory Committee Act, as
amended (5 U.S.C. App.), notice is
hereby given of the following meetings.
The meetings 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. 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: Center for Scientific
Review Special Emphasis Panel; Member
Conflict: Neuroblastomas, Glioblastomas, and
Multiple Sclerosis and Viruses.
Date: April 2, 2015.
Time: 10:00 a.m. to 11:30 a.m.
Agenda: To review and evaluate grant
applications.
Place: National Institutes of Health, 6701
Rockledge Drive, Bethesda, MD 20892,
(Telephone Conference Call).
Contact Person: Samuel C Edwards, Ph.D.,
IRG CHIEF, Center for Scientific Review,
National Institutes of Health, 6701 Rockledge
Drive, Room 5210, MSC 7846, Bethesda, MD
20892, (301) 435–1246, edwardss@
csr.nih.gov.
Name of Committee: Center for Scientific
Review Special Emphasis Panel; RFA–14–
011: 4D Nucleome Network Data
Coordination and Integration Center (U01).
Date: April 9, 2015.
Time: 11:00 a.m. to 6:00 p.m.
Agenda: To review and evaluate grant
applications.
Place: National Institutes of Health, 6701
Rockledge Drive, Bethesda, MD 20892,
(Virtual Meeting).
Contact Person: Mark Caprara, Ph.D.,
Scientific Review Officer, Center for
Scientific Review, National Institutes of
Health, 6701 Rockledge Drive, Room 5156,
MSC 7844, Bethesda, MD 20892, 301–435–
1042, capraramg@mail.nih.gov.
Name of Committee: Center for Scientific
Review Special Emphasis Panel; Member
Conflict: Reproductive Biology.
Date: April 10, 2015.
Time: 12:00 p.m. to 3:00 p.m.
Agenda: To review and evaluate grant
applications.
Place: National Institutes of Health, 6701
Rockledge Drive, Bethesda, MD 20892,
(Virtual Meeting).
Contact Person: Michael Knecht, Ph.D.,
Scientific Review Officer, Center for
Scientific Review, National Institutes of
Health, 6701 Rockledge Drive, Room 6176,
MSC 7892, Bethesda, MD 20892, (301) 435–
1046, knechtm@csr.nih.gov.
(Catalogue of Federal Domestic Assistance
Program Nos. 93.306, Comparative Medicine;
93.333, Clinical Research, 93.306, 93.333,
93.337, 93.393–93.396, 93.837–93.844,
93.846–93.878, 93.892, 93.893, National
Institutes of Health, HHS)
Dated: March 6, 2015.
Anna Snouffer,
Deputy Director, Office of Federal Advisory
Committee Policy.
[FR Doc. 2015–05566 Filed 3–11–15; 8:45 am]
BILLING CODE 4140–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Office of the Secretary
[Document Identifier: HHS–OS–0990—New–
60D]
Agency Information Collection
Activities; Proposed Collection; Public
Comment Request
Office of the Secretary, HHS.
Notice.
AGENCY:
ACTION:
In compliance with section
3506(c)(2)(A) of the Paperwork
Reduction Act of 1995, the Office of the
Secretary (OS), Department of Health
and Human Services, announces plans
to submit a new Information Collection
Request (ICR), described below, to the
Office of Management and Budget
(OMB). Prior to submitting the ICR to
OMB, OS seeks comments from the
SUMMARY:
public regarding the burden estimate,
below, or any other aspect of the ICR.
Comments on the ICR must be
received on or before May 11, 2015.
DATES:
Submit your comments to
Information.CollectionClearance
@hhs.gov or by calling (202) 690–6162.
ADDRESSES:
FOR FURTHER INFORMATION CONTACT:
Information Collection Clearance staff,
Information.CollectionClearance
@hhs.gov or (202) 690–6162.
When
submitting comments or requesting
information, please include the
document identifier HHS–OS–0990—
New–60D for reference.
Information Collection Request Title:
Privacy and Security Capacity
Assessment of the Title X Network.
Abstract: The Office of the Assistant
Secretary for Health Office of
Population Affairs, (OPA) is requesting
an approval by Office of Management
and Budget (OMB) for a new
information collection (Privacy and
Security Capacity Assessment) which
seeks to collect feedback from the Title
X network regarding Title X grantees’
and service sites’ current privacy and
security capabilities for health
information exchange. This voluntary
form will be administered at most
annually and enable the Title X network
to share important information to
critically inform OPA’s development of
Family Planning Annual Report (FPAR
2.0), as well as identify any training
assistance and inform guidance that
OPA may offer in the future. OPA will
solicit feedback from Title X agencies to
advise our work on privacy and
security, and proposes to make this data
collection form available for up to 3
years so that OPA can accept feedback
from the network regarding any changes
or trends that might alter our approach
to privacy and security as we proceed
through the design and build process for
the planned FPAR 2.0 data repository.
Likely Respondents: Title X Grantees,
Sub recipients, and Service Sites.
SUPPLEMENTARY INFORMATION:
TOTAL ESTIMATED ANNUALIZED BURDEN—HOURS
Number of
respondents
asabaliauskas on DSK5VPTVN1PROD with NOTICES
Form name
Number of
responses per
respondent
Average
burden per
response
(in hours)
Total burden
hours
Data Element Survey .......................................................................................
818
1
20/60
273
Total ..........................................................................................................
818
1
20/60
273
OPA specifically requests comments
on (1) the necessity and utility of the
proposed information collection for the
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proper performance of the agency’s
functions, (2) the accuracy of the
estimated burden, (3) ways to enhance
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the quality, utility, and clarity of the
information to be collected, and (4) the
use of automated collection techniques
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Federal Register / Vol. 80, No. 48 / Thursday, March 12, 2015 / Notices
other committee management activities, for
both the Centers for Disease Control and
Prevention and the Agency for Toxic
Substances and Disease Registry.
or other forms of information
technology to minimize the information
collection burden.
Terry S. Clark,
Deputy Information Collection Clearance
Officer.
Elaine L. Baker,
Director, Management Analysis and Services
Office, Centers for Disease Control and
Prevention.
[FR Doc. 2015–05619 Filed 3–11–15; 8:45 am]
BILLING CODE 4150–28–P
[FR Doc. 2015–05577 Filed 3–11–15; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
Food and Drug Administration
Disease, Disability, and Injury
Prevention and Control Special
Emphasis Panel (SEP): Initial Review
[Docket No. FDA–2015–N–0001]
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
[(FOA) GH15–001, Conducting Public
Health Research in Kenya, Funding
Opportunity Announcement.
Time and Date: 12:00 p.m.—5:00 p.m.,
April 1, 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 ‘‘Conducting Public Health
Research in Kenya, FOA GH15–001’’.
Contact Person for More Information:
Hylan Shoob, Scientific Review Officer,
Center for Global Health (CGH) Science
Office, CGH, CDC, 1600 Clifton Road, NE.,
Mailstop D–69, Atlanta, Georgia 30033,
Telephone: (404) 639–4796.
The Director, Management Analysis and
Services Office, has been delegated the
authority to sign Federal Register notices
pertaining to announcements of meetings and
2015 Parenteral Drug Association/Food
and Drug Administration Joint
Conference
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Notice of public conference.
The Food and Drug Administration
(FDA), is announcing a public
conference, to be held in co-sponsorship
with the Parenteral Drug Association
(PDA), entitled ‘‘Mission Possible:
Patient-Focused Manufacturing,
Quality, and Regulatory Solutions.’’ The
conference will cover current issues
affecting the industry as well as explore
strategies to facilitate the development
and continuous improvement of safe
and effective medical products. The
conference establishes a unique forum
to discuss the foundations, emerging
technologies, and innovations in
regulatory science, as well as the current
quality and compliance areas of
concerns. Meeting participants will hear
from FDA and industry speakers about
the requirements and best practices to
consider while implementing robust
quality systems in order to deliver the
best quality product.
Date and Time: The public conference
will be held on September 28, 2015,
from 7 a.m. to 7:30 p.m.; September 29,
2015, from 7 a.m. to 9:30 p.m.; and
September 30, 2015, from 7 a.m. to
12:30 p.m.
Location: The public conference will
be held at the Renaissance Washington
Hotel, 999 Ninth Street NW.,
Washington, DC 20001, 202–898–9000,
FAX: 202–289–0947.
Contact: Wanda Neal, Parenteral Drug
Association, PDA Global Headquarters,
Bethesda Towers, 4350 East West Hwy.,
Suite 150, Bethesda, MD 20814, 301–
656–5900, ext. 111, FAX: 301–986–
1093, email: info@pda.org; or Ken
Nolan, Office of Communications, Food
and Drug Administration, 10903 New
Hampshire Ave., Silver Spring, MD
20993, 301–796–8629, email:
kenneth.nolan@fda.hhs.gov.
Accommodations: Attendees are
responsible for their own
accommodations. To make reservations,
contact the Renaissance Washington
Hotel (see Location) and reference ‘‘the
2015 PDA/FDA Joint Regulatory
Conference’’ to receive the PDA group
rate. Room rates are: Single: $305 plus
14.5 percent State and local taxes.
Requests will be processed on a firstcome, first-served basis.
Registration: Attendees are
encouraged to register at their earliest
convenience. The PDA registration fees
cover the cost of facilities, materials,
and refreshments. Seats are limited;
please submit your registration as soon
as possible. Conference space will be
filled in order of receipt of registration.
Those accepted for the conference will
receive confirmation. Registration will
close after the conference is filled.
Onsite registration will be available on
a space available basis beginning at 1
p.m. on September 27, 2015, and at 7
a.m. from September 28 through 30,
2015. The cost of registration is as
follows:
COST OF REGISTRATION
Before July
19, 2015
Affiliation
July 19–
August 18,
2015
After August
18, 2015
asabaliauskas on DSK5VPTVN1PROD with NOTICES
Premier Package (Includes Conference and Workshop Registration)
Member ....................................................................................................................................................
Nonmember .............................................................................................................................................
$3,240
3,599
$3,490
3,849
$3,740
4,099
1,895
2,154
700
800
700
800
2,095
2,354
700
800
700
800
2,295
2,554
700
800
700
800
Conference Only
Member ....................................................................................................................................................
Nonmember .............................................................................................................................................
Government/Health Authority Member ....................................................................................................
Government/Health Authority Nonmember * ...........................................................................................
Academic Member ...................................................................................................................................
Academic Nonmember * ..........................................................................................................................
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Agencies
[Federal Register Volume 80, Number 48 (Thursday, March 12, 2015)]
[Notices]
[Pages 13007-13008]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2015-05619]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Office of the Secretary
[Document Identifier: HHS-OS-0990--New-60D]
Agency Information Collection Activities; Proposed Collection;
Public Comment Request
AGENCY: Office of the Secretary, HHS.
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: In compliance with section 3506(c)(2)(A) of the Paperwork
Reduction Act of 1995, the Office of the Secretary (OS), Department of
Health and Human Services, announces plans to submit a new Information
Collection Request (ICR), described below, to the Office of Management
and Budget (OMB). Prior to submitting the ICR to OMB, OS seeks comments
from the public regarding the burden estimate, below, or any other
aspect of the ICR.
DATES: Comments on the ICR must be received on or before May 11, 2015.
ADDRESSES: Submit your comments to
Information.CollectionClearance@hhs.gov or by calling (202) 690-6162.
FOR FURTHER INFORMATION CONTACT: Information Collection Clearance
staff, Information.CollectionClearance@hhs.gov or (202) 690-6162.
SUPPLEMENTARY INFORMATION: When submitting comments or requesting
information, please include the document identifier HHS-OS-0990--New-
60D for reference.
Information Collection Request Title: Privacy and Security Capacity
Assessment of the Title X Network.
Abstract: The Office of the Assistant Secretary for Health Office
of Population Affairs, (OPA) is requesting an approval by Office of
Management and Budget (OMB) for a new information collection (Privacy
and Security Capacity Assessment) which seeks to collect feedback from
the Title X network regarding Title X grantees' and service sites'
current privacy and security capabilities for health information
exchange. This voluntary form will be administered at most annually and
enable the Title X network to share important information to critically
inform OPA's development of Family Planning Annual Report (FPAR 2.0),
as well as identify any training assistance and inform guidance that
OPA may offer in the future. OPA will solicit feedback from Title X
agencies to advise our work on privacy and security, and proposes to
make this data collection form available for up to 3 years so that OPA
can accept feedback from the network regarding any changes or trends
that might alter our approach to privacy and security as we proceed
through the design and build process for the planned FPAR 2.0 data
repository.
Likely Respondents: Title X Grantees, Sub recipients, and Service
Sites.
Total Estimated Annualized Burden--Hours
----------------------------------------------------------------------------------------------------------------
Average
Number of Number of burden per Total burden
Form name respondents responses per response (in hours
respondent hours)
----------------------------------------------------------------------------------------------------------------
Data Element Survey............................. 818 1 20/60 273
---------------------------------------------------------------
Total....................................... 818 1 20/60 273
----------------------------------------------------------------------------------------------------------------
OPA specifically requests comments on (1) the necessity and utility
of the proposed information collection for the proper performance of
the agency's functions, (2) the accuracy of the estimated burden, (3)
ways to enhance the quality, utility, and clarity of the information to
be collected, and (4) the use of automated collection techniques
[[Page 13008]]
or other forms of information technology to minimize the information
collection burden.
Terry S. Clark,
Deputy Information Collection Clearance Officer.
[FR Doc. 2015-05619 Filed 3-11-15; 8:45 am]
BILLING CODE 4150-28-P