Proposed Data Collection Submitted for Public Comment and Recommendations, 8527-8528 [2017-01742]
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Federal Register / Vol. 82, No. 16 / Thursday, January 26, 2017 / Notices
Leroy A. Richardson,
Chief, Information Collection Review Office,
Office of Scientific Integrity, Office of the
Associate Director for Science, Office of the
Director, Centers for Disease Control and
Prevention.
[FR Doc. 2017–01741 Filed 1–25–17; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60Day–17–0006; Docket No. CDC–2017–
0004]
Proposed Data Collection Submitted
for Public Comment and
Recommendations
Centers for Disease Control and
Prevention (CDC), Department of Health
and Human Services (HHS).
ACTION: Notice with comment period.
AGENCY:
The Centers for Disease
Control and Prevention (CDC), as part of
its continuing efforts to reduce public
burden and maximize the utility of
government information, invites the
general public and other Federal
agencies to take this opportunity to
comment on proposed and/or
continuing information collections, as
required by the Paperwork Reduction
Act of 1995. This notice invites
comment on an extension request for
the information collection titled
‘‘Statements in Support of Application
of Waiver of Inadmissibility.’’ Approved
under Office of Management and Budget
(OMB) Control Number 0920–0006, this
information collection allows CDC to
review Class A medical waiver
applications for prospective immigrants
to the United States. CDC assists DHS/
USCIS in determining whether or not a
prospective immigrant with a Class A
mental health designation may be
admitted into the United States.
DATES: Written comments must be
received on or before March 27, 2017.
ADDRESSES: You may submit comments,
identified by Docket No. CDC–2017–
0004 by any of the following methods:
• Federal eRulemaking Portal:
Regulations.gov. Follow the instructions
for submitting comments.
• Mail: Leroy A. Richardson,
Information Collection Review Office,
Centers for Disease Control and
jstallworth on DSK7TPTVN1PROD with NOTICES
SUMMARY:
VerDate Sep<11>2014
15:10 Jan 25, 2017
Jkt 241001
Prevention, 1600 Clifton Road NE., MS–
D74, Atlanta, Georgia 30329.
Instructions: All submissions received
must include the agency name and
Docket Number. All relevant comments
received will be posted without change
to Regulations.gov, including any
personal information provided. For
access to the docket to read background
documents or comments received, go to
Regulations.gov.
Please note: All public comment
should be submitted through the
Federal eRulemaking portal
(Regulations.gov) or by U.S. mail to the
address listed above.
FOR FURTHER INFORMATION CONTACT: To
request more information on the
proposed project or to obtain a copy of
the information collection plan and
instruments, contact the Information
Collection Review Office, Centers for
Disease Control and Prevention, 1600
Clifton Road NE., MS–D74, Atlanta,
Georgia 30329; phone: 404–639–7570;
Email: omb@cdc.gov.
SUPPLEMENTARY INFORMATION:
Under the Paperwork Reduction Act
of 1995 (PRA) (44 U.S.C. 3501–3520),
Federal agencies must obtain approval
from the Office of Management and
Budget (OMB) for each collection of
information they conduct or sponsor. In
addition, the PRA also requires Federal
agencies to provide a 60-day notice in
the Federal Register concerning each
proposed collection of information,
including each new proposed
collection, each proposed extension of
existing collection of information, and
each reinstatement of previously
approved information collection before
submitting the collection to OMB for
approval. To comply with this
requirement, we are publishing this
notice of a proposed data collection as
described below.
Comments are invited on: (a) Whether
the proposed collection of information
is necessary for the proper performance
of the functions of the agency, including
whether the information shall have
practical utility; (b) the accuracy of the
agency’s estimate of the burden of the
proposed collection of information; (c)
ways to enhance the quality, utility, and
clarity of the information to be
collected; (d) ways to minimize the
burden of the collection of information
on respondents, including through the
use of automated collection techniques
or other forms of information
PO 00000
Frm 00025
Fmt 4703
Sfmt 4703
8527
technology; and (e) estimates of capital
or start-up costs and costs of operation,
maintenance, and purchase of services
to provide information. Burden means
the total time, effort, or financial
resources expended by persons to
generate, maintain, retain, disclose or
provide information to or for a Federal
agency. This includes the time needed
to review instructions; to develop,
acquire, install and utilize technology
and systems for the purpose of
collecting, validating and verifying
information, processing and
maintaining information, and disclosing
and providing information; to train
personnel and to be able to respond to
a collection of information, to search
data sources, to complete and review
the collection of information; and to
transmit or otherwise disclose the
information.
Proposed Project
Statements in Support of Application
of Waiver of Inadmissibility (OMB
Control No. 0920–0006; Expires 8/31/
2017)—Extension—National Center for
Emerging and Zoonotic Infectious
Diseases (NCEZID), Centers for Disease
Control and Prevention (CDC).
Background and Brief Description
Section 212(a)(1) of the Immigration
and Nationality Act states that aliens
with specific health related conditions
are ineligible for admission into the
United States. The Attorney General
may waive application of this
inadmissibility on health-related
grounds if an application for waiver is
filed and approved by the consular
office considering the application for
visa. CDC uses this application
primarily to collect information to
establish and maintain records of waiver
applicants in order to notify the U.S.
Citizenship and Immigration Services
when terms, conditions and controls
imposed by waiver are not met.
CDC is requesting approval from OMB
to collect this data for another three
years. Based on a review of the number
of waivers processed by CDC over the
last three years, CDC does not request a
change in the amount of burden.
Respondents must mail these
documents to CDC, and this entails an
additional cost. CDC estimates that
respondents will spend approximately
$15 per year on postal fees, for a total
of $3,000 annually.
E:\FR\FM\26JAN1.SGM
26JAN1
8528
Federal Register / Vol. 82, No. 16 / Thursday, January 26, 2017 / Notices
ESTIMATE OF ANNUALIZED BURDEN HOURS
Number of
respondents
Number of
responses per
respondent
Average
burden per
response
(in hours)
Total
burden
hours
Type of respondent
Form
Physician ...........................................
Physician ...........................................
CDC 4.422–1 ...................................
CDC 4.422–1a or letter ....................
200
200
1
1
10/60
20/60
33
67
Total ...........................................
...........................................................
........................
........................
........................
100
Leroy A. Richardson,
Chief, Information Collection Review Office,
Office of Scientific Integrity, Office of the
Associate Director for Science, Office of the
Director, Centers for Disease Control and
Prevention.
[FR Doc. 2017–01742 Filed 1–25–17; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Office of the Secretary
[Document Identifier: 0990–0419–60D]
Agency Information Collection
Activities; Proposed Collection; Public
Comment Request
Office of the Secretary, HHS.
60-Day 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 an Information Collection
Request (ICR), described below, to the
Office of Management and Budget
(OMB). The ICR is for extending the use
of the approved information collection
assigned OMB control number 0990–
SUMMARY:
0419, which expires on June 30, 2017.
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 March 27, 2017.
ADDRESSES: Submit your comments to
Information.CollectionClearance@
hhs.gov or by calling (202) 690–5683.
SUPPLEMENTARY INFORMATION: When
submitting comments or requesting
information, please include the
document identifier 0990–0419–60D for
reference.
Information Collection Request Title:
Acquisition Regulation Clause Patent
Rights and Rights and Data.
OMB No.: 0990–0419.
Abstract: The Department of Health
and Human Services; Office of the
Assistant Secretary for Financial
Resources and Office of Grants and
Acquisition Policy and Accountability,
Division of Acquisition, is requesting an
approval by OMB for an extension of a
previously approved information
collection request, 0990–0419—
Acquisition Regulation Clause Patent
rights and Rights in Data. HHS found
that systematically, over a period of
several years, when Determination of
Exceptional Circumstances (DEC) were
executed, additional legal protection for
the patent and data rights of third
parties beyond those covered by FAR
27.306 were necessary. A DEC is
executed consistent with the policy and
objectives of the Bayh-Dole Act, 35
U.S.C. 200, et seq., to ensure that subject
inventions made under contracts and
subcontracts (at all tiers) are used in a
manner to promote free competition and
enterprise without unduly encumbering
future research and discovery; to
encourage maximum participation of
small business firms in federally
supported research and development
efforts; to promote collaboration
between commercial concerns and
nonprofit organizations including
universities; to ensure that the
Government obtains sufficient rights in
federally supported inventions to meet
its needs; to protect the public against
nonuse or unreasonable use of
inventions; and in the case of fulfilling
the mission of the U.S. Department of
Health and Human Services, to
ultimately to benefit the public health.
Likely Respondents: Administrative,
technical, legal and management
personnel.
The total annual burden hours
estimated for this ICR are summarized
in the table below.
TOTAL ESTIMATED ANNUALIZED BURDEN—HOURS
Information
collection
Type of respondent and hours for each
(a) ...............
Technical (4) ............................................................................
Legal (2) ..................................................................................
Management (2) ......................................................................
Technical (8) ............................................................................
Legal (2) ..................................................................................
Management (2) ......................................................................
Technical (8) ............................................................................
Legal (3) ..................................................................................
Management (1) ......................................................................
Technical (8) ............................................................................
Legal (4) ..................................................................................
Management (2) ......................................................................
Technical (6) ............................................................................
Legal (2) ..................................................................................
Management (2) ......................................................................
(b) ...............
jstallworth on DSK7TPTVN1PROD with NOTICES
(c) ...............
(d) ...............
(e) ...............
VerDate Sep<11>2014
15:10 Jan 25, 2017
Jkt 241001
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Frm 00026
Fmt 4703
Number of
respondents
Sfmt 4703
Number of
responses per
respondent
Average
burden per
response
(hours)
Total burden
hours
63
1
8
504
63
1
12
756
63
3
12 (36)
2268
63
3
14 (42)
2646
63
1
10
630
E:\FR\FM\26JAN1.SGM
26JAN1
]]>Agencies
[Federal Register Volume 82, Number 16 (Thursday, January 26, 2017)]
[Notices]
[Pages 8527-8528]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2017-01742]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[60Day-17-0006; Docket No. CDC-2017-0004]
Proposed Data Collection Submitted for Public Comment and
Recommendations
AGENCY: Centers for Disease Control and Prevention (CDC), Department of
Health and Human Services (HHS).
ACTION: Notice with comment period.
-----------------------------------------------------------------------
SUMMARY: The Centers for Disease Control and Prevention (CDC), as part
of its continuing efforts to reduce public burden and maximize the
utility of government information, invites the general public and other
Federal agencies to take this opportunity to comment on proposed and/or
continuing information collections, as required by the Paperwork
Reduction Act of 1995. This notice invites comment on an extension
request for the information collection titled ``Statements in Support
of Application of Waiver of Inadmissibility.'' Approved under Office of
Management and Budget (OMB) Control Number 0920-0006, this information
collection allows CDC to review Class A medical waiver applications for
prospective immigrants to the United States. CDC assists DHS/USCIS in
determining whether or not a prospective immigrant with a Class A
mental health designation may be admitted into the United States.
DATES: Written comments must be received on or before March 27, 2017.
ADDRESSES: You may submit comments, identified by Docket No. CDC-2017-
0004 by any of the following methods:
Federal eRulemaking Portal: Regulations.gov. Follow the
instructions for submitting comments.
Mail: Leroy A. Richardson, Information Collection Review
Office, Centers for Disease Control and Prevention, 1600 Clifton Road
NE., MS-D74, Atlanta, Georgia 30329.
Instructions: All submissions received must include the agency name
and Docket Number. All relevant comments received will be posted
without change to Regulations.gov, including any personal information
provided. For access to the docket to read background documents or
comments received, go to Regulations.gov.
Please note: All public comment should be submitted through the
Federal eRulemaking portal (Regulations.gov) or by U.S. mail to the
address listed above.
FOR FURTHER INFORMATION CONTACT: To request more information on the
proposed project or to obtain a copy of the information collection plan
and instruments, contact the Information Collection Review Office,
Centers for Disease Control and Prevention, 1600 Clifton Road NE., MS-
D74, Atlanta, Georgia 30329; phone: 404-639-7570; Email: omb@cdc.gov.
SUPPLEMENTARY INFORMATION:
Under the Paperwork Reduction Act of 1995 (PRA) (44 U.S.C. 3501-
3520), Federal agencies must obtain approval from the Office of
Management and Budget (OMB) for each collection of information they
conduct or sponsor. In addition, the PRA also requires Federal agencies
to provide a 60-day notice in the Federal Register concerning each
proposed collection of information, including each new proposed
collection, each proposed extension of existing collection of
information, and each reinstatement of previously approved information
collection before submitting the collection to OMB for approval. To
comply with this requirement, we are publishing this notice of a
proposed data collection as described below.
Comments are invited on: (a) Whether the proposed collection of
information is necessary for the proper performance of the functions of
the agency, including whether the information shall have practical
utility; (b) the accuracy of the agency's estimate of the burden of the
proposed collection of information; (c) ways to enhance the quality,
utility, and clarity of the information to be collected; (d) ways to
minimize the burden of the collection of information on respondents,
including through the use of automated collection techniques or other
forms of information technology; and (e) estimates of capital or start-
up costs and costs of operation, maintenance, and purchase of services
to provide information. Burden means the total time, effort, or
financial resources expended by persons to generate, maintain, retain,
disclose or provide information to or for a Federal agency. This
includes the time needed to review instructions; to develop, acquire,
install and utilize technology and systems for the purpose of
collecting, validating and verifying information, processing and
maintaining information, and disclosing and providing information; to
train personnel and to be able to respond to a collection of
information, to search data sources, to complete and review the
collection of information; and to transmit or otherwise disclose the
information.
Proposed Project
Statements in Support of Application of Waiver of Inadmissibility
(OMB Control No. 0920-0006; Expires 8/31/2017)--Extension--National
Center for Emerging and Zoonotic Infectious Diseases (NCEZID), Centers
for Disease Control and Prevention (CDC).
Background and Brief Description
Section 212(a)(1) of the Immigration and Nationality Act states
that aliens with specific health related conditions are ineligible for
admission into the United States. The Attorney General may waive
application of this inadmissibility on health-related grounds if an
application for waiver is filed and approved by the consular office
considering the application for visa. CDC uses this application
primarily to collect information to establish and maintain records of
waiver applicants in order to notify the U.S. Citizenship and
Immigration Services when terms, conditions and controls imposed by
waiver are not met.
CDC is requesting approval from OMB to collect this data for
another three years. Based on a review of the number of waivers
processed by CDC over the last three years, CDC does not request a
change in the amount of burden.
Respondents must mail these documents to CDC, and this entails an
additional cost. CDC estimates that respondents will spend
approximately $15 per year on postal fees, for a total of $3,000
annually.
[[Page 8528]]
Estimate of Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
Number of Average burden
Type of respondent Form Number of responses per per response Total burden
respondents respondent (in hours) hours
----------------------------------------------------------------------------------------------------------------
Physician..................... CDC 4.422-1..... 200 1 10/60 33
Physician..................... CDC 4.422-1a or 200 1 20/60 67
letter.
---------------------------------------------------------------
Total..................... ................ .............. .............. .............. 100
----------------------------------------------------------------------------------------------------------------
Leroy A. Richardson,
Chief, Information Collection Review Office, Office of Scientific
Integrity, Office of the Associate Director for Science, Office of the
Director, Centers for Disease Control and Prevention.
[FR Doc. 2017-01742 Filed 1-25-17; 8:45 am]
BILLING CODE 4163-18-P
