Proposed Data Collection Submitted for Public Comment and Recommendations, 60905-60906 [2015-25647]
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Federal Register / Vol. 80, No. 195 / Thursday, October 8, 2015 / Notices
Proposed Merger is consummated. If the
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not an acceptable acquirer, or that the
manner of the divestitures is not
acceptable, the proposed Order requires
the parties to unwind the sale of rights
to Integra and then divest the products
to a Commission-approved acquirer
within six months of the date the Order
becomes final. The proposed Order
further allows the Commission to
appoint a trustee in the event the parties
fail to divest the products as required.
The Order also requires the parties to
appoint Quantic Regulatory Services,
LLC as interim monitor to ensure the
parties comply with the obligations
pursuant to the Consent Agreement and
to keep the Commission informed about
the status of the transfer of the assets
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The purpose of this analysis is to
facilitate public comment on the
Consent Agreement, and it is not
intended to constitute an official
interpretation of the proposed Order or
to modify its terms in any way.
By direction of the Commission.
Donald S. Clark,
Secretary.
[FR Doc. 2015–25604 Filed 10–7–15; 8:45 am]
BILLING CODE 6750–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60Day–16–15BHD; Docket No. CDC–2016–
0088]
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 Congenital Heart
Surveillance to Recognize Outcomes,
Needs and well-being (CHSTRONG).
CDC seeks to collect data for the
purpose of providing insight into the
public health questions that remain for
mstockstill on DSK4VPTVN1PROD with NOTICES
SUMMARY:
VerDate Sep<11>2014
16:41 Oct 07, 2015
Jkt 238001
the population and to develop services
and allocate resources to improve longterm health and wellbeing.
DATES: Written comments must be
received on or before December 7, 2015.
ADDRESSES: You may submit comments,
identified by Docket No. CDC–2016–
0088 by any of the following methods:
• Federal eRulemaking Portal:
Regulation.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.
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
PO 00000
Frm 00034
Fmt 4703
Sfmt 4703
60905
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
Congenital Heart Surveillance To
Recognize Outcomes, Needs, and Wellbeing (CHSTRONG)—New—National
Center on Birth Defects and
Developmental Disabilities (NCBDDD),
Centers for Disease Control and
Prevention (CDC).
Background and Brief Description
Congenital heart defects (CHDs) are
the most common type of structural
birth defects, affecting approximately 1
in 110 live-born children. In prior
decades, many CHDs were considered
fatal during infancy or childhood, but
with tremendous advances in pediatric
cardiology and cardiac surgery, at least
85% of patients now survive to
adulthood and there are approximately
1.5 million adults with CHD living in
the United States. With vast declines in
mortality from pediatric heart disease
over the past 30 years, it is vital to
evaluate long term outcomes and quality
of life issues for adults with CHD.
However, U.S. data on long term
outcomes, quality of life issues, and
comorbidities of adults born with CHD
are lacking. U.S. data is needed to
provide insight into the public health
questions that remain for this
population and to develop services and
allocate resources to improve long-term
health and wellbeing.
For this one-year project, we will use
data from U.S. state birth defect
surveillance systems to identify a
population-based sample of individuals
18 to 45 years of age born with CHD. We
will then use state databases and online
search engines to find current addresses
for those individuals and mail surveys
to them inquiring about their barriers to
E:\FR\FM\08OCN1.SGM
08OCN1
60906
Federal Register / Vol. 80, No. 195 / Thursday, October 8, 2015 / Notices
health care, quality of life, social and
educational outcomes, and transition of
care from childhood to adulthood. The
information collected from this
population-based survey will be used to
inform current knowledge, allocate
resources, develop services, and,
ultimately, improve long-term health of
adults born with CHD.
We estimate identifying 7,500
individuals with CHD in the birth
defects surveillance systems, obtaining
current addresses and sending surveys
to 5,625 individuals with CHD (75%),
and receiving completed surveys from
4,500 individuals (80%). The survey
takes approximately 25 minutes to
complete, which includes 5 minutes to
read the informed consent and 20
minutes to answer survey questions.
Therefore, we estimate the total burden
hours are 1,875.
There are no costs to participants
other than their time.
ESTIMATED ANNUALIZED BURDEN HOURS
Number of
respondents
Number of
responses per
respondent
Average
burden per
response
(in hours)
Total burden
hours
Type of respondent
Form name
Individuals with CHD .........................
Individuals with CHD .........................
Informed consent ...........................
Survey ............................................
4,500
4,500
1
1
5/60
20/60
375
1,500
Total ...........................................
.........................................................
........................
..........................
........................
1,875
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. 2015–25647 Filed 10–7–15; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60 Day–16–15BHH; Docket No. CDC–2016–
0087]
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 the Personal Protective
Equipment Information (PPE-Info)
Database which is a compendium of
personal protective equipment (PPE)
Federal regulations and consensus
standards.
mstockstill on DSK4VPTVN1PROD with NOTICES
SUMMARY:
Written comments must be
received on December 7, 2015.
DATES:
VerDate Sep<11>2014
16:41 Oct 07, 2015
Jkt 238001
You may submit comments,
identified by Docket No. CDC–2016–
0087 by any of the following methods:
Federal eRulemaking Portal:
Regulation.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.
ADDRESSES:
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.
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
FOR FURTHER INFORMATION CONTACT:
PO 00000
Frm 00035
Fmt 4703
Sfmt 4703
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.
E:\FR\FM\08OCN1.SGM
08OCN1
]]>Agencies
[Federal Register Volume 80, Number 195 (Thursday, October 8, 2015)]
[Notices]
[Pages 60905-60906]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2015-25647]
=======================================================================
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[60Day-16-15BHD; Docket No. CDC-2016-0088]
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 Congenital Heart
Surveillance to Recognize Outcomes, Needs and well-being (CHSTRONG).
CDC seeks to collect data for the purpose of providing insight into the
public health questions that remain for the population and to develop
services and allocate resources to improve long-term health and
wellbeing.
DATES: Written comments must be received on or before December 7, 2015.
ADDRESSES: You may submit comments, identified by Docket No. CDC-2016-
0088 by any of the following methods:
Federal eRulemaking Portal: Regulation.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.
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
Congenital Heart Surveillance To Recognize Outcomes, Needs, and
Well-being (CHSTRONG)--New--National Center on Birth Defects and
Developmental Disabilities (NCBDDD), Centers for Disease Control and
Prevention (CDC).
Background and Brief Description
Congenital heart defects (CHDs) are the most common type of
structural birth defects, affecting approximately 1 in 110 live-born
children. In prior decades, many CHDs were considered fatal during
infancy or childhood, but with tremendous advances in pediatric
cardiology and cardiac surgery, at least 85% of patients now survive to
adulthood and there are approximately 1.5 million adults with CHD
living in the United States. With vast declines in mortality from
pediatric heart disease over the past 30 years, it is vital to evaluate
long term outcomes and quality of life issues for adults with CHD.
However, U.S. data on long term outcomes, quality of life issues, and
comorbidities of adults born with CHD are lacking. U.S. data is needed
to provide insight into the public health questions that remain for
this population and to develop services and allocate resources to
improve long-term health and wellbeing.
For this one-year project, we will use data from U.S. state birth
defect surveillance systems to identify a population-based sample of
individuals 18 to 45 years of age born with CHD. We will then use state
databases and online search engines to find current addresses for those
individuals and mail surveys to them inquiring about their barriers to
[[Page 60906]]
health care, quality of life, social and educational outcomes, and
transition of care from childhood to adulthood. The information
collected from this population-based survey will be used to inform
current knowledge, allocate resources, develop services, and,
ultimately, improve long-term health of adults born with CHD.
We estimate identifying 7,500 individuals with CHD in the birth
defects surveillance systems, obtaining current addresses and sending
surveys to 5,625 individuals with CHD (75%), and receiving completed
surveys from 4,500 individuals (80%). The survey takes approximately 25
minutes to complete, which includes 5 minutes to read the informed
consent and 20 minutes to answer survey questions. Therefore, we
estimate the total burden hours are 1,875.
There are no costs to participants other than their time.
Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
Average
Number of Number of burden per Total burden
Type of respondent Form name respondents responses per response (in hours
respondent hours)
----------------------------------------------------------------------------------------------------------------
Individuals with CHD......... Informed consent 4,500 1 5/60 375
Individuals with CHD......... Survey.......... 4,500 1 20/60 1,500
----------------------------------------------------------------
Total.................... ................ .............. ............... .............. 1,875
----------------------------------------------------------------------------------------------------------------
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. 2015-25647 Filed 10-7-15; 8:45 am]
BILLING CODE 4163-18-P
