Proposed Data Collection Submitted for Public Comment and Recommendations, 52875-52876 [2016-18934]
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Federal Register / Vol. 81, No. 154 / Wednesday, August 10, 2016 / Notices
Jeffrey M. Zirger,
Health Scientist, Acting 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. 2016–18935 Filed 8–9–16; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60Day–16–16AWE: Docket No. CDC–2016–
0078]
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 Information Collection
for Tuberculosis Data from Referring
Entities to CureTB. CureTB is intended
to provide continuity of care for
individuals affected by TB who enter
US jurisdictions from foreign nations
who or who leave US jurisdictions
bound for foreign nations.
DATES: Written comments must be
received on or before October 11, 2016.
ADDRESSES: You may submit comments,
identified by Docket No. CDC–2016–
0078 by any of the following methods:
• Federal eRulemaking Portal:
Regulations.gov. Follow the instructions
for submitting comments.
• Mail: Jeffrey M. Zirger, 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
mstockstill on DSK3G9T082PROD with NOTICES
SUMMARY:
VerDate Sep<11>2014
17:34 Aug 09, 2016
Jkt 238001
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
PO 00000
Frm 00066
Fmt 4703
Sfmt 4703
52875
transmit or otherwise disclose the
information.
Proposed Project
Information Collection for Tuberculosis
Data From Referring Entities to
CureTB—New—National Center for
Emerging Zoonotic and Infectious
Diseases (NCEZID), Centers for Disease
Control and Prevention (CDC)
Background and Brief Description
CDC is assuming the administration of
the CureTB program from the San Diego
Public Health Department. CureTB
works with domestic and international
programs to protect the U.S. public by
preventing the global development of
drug resistance and reducing disease
transmission and importation of
infectious TB. These goals are
accomplished through CureTB referral
and continuity of care services for
mobile TB patients.
CDC is seeking OMB clearance for
three years of information collection.
Lack of treatment adherence and
inappropriate selection of medications
are prime reasons for the continued
emergence and spread of resistant
strains. To combat this, CureTB assures
patients understand how to remain
adherent despite moving between
nations and provides information to the
health care team that will be continuing
care about each patient’s TB strain and
tailored medication regimen. CureTB
gathers demographic and clinical
information for each patient, and
connects that individual to care through
provision of accurate information about
how to locate the correct downstream
provider and assurance that real-time
information is given directly to medical
providers and public health authorities
in receiving nations.
The respondents are entities within
the United States and other countries
who provide diagnostic and treatment
services to individuals affected by TB.
The entities are primarily state and local
health departments, but include
immigration centers, correctional
facilities, and national TB programs. All
50 US states and territories may refer TB
patients to the CureTB program. To
date, CureTB has also received referrals
from Mexico and Guatemala.
Respondents are generally public
health field nurses and will submit
CureTB referral forms as they request
referral services. The number of referrals
varies widely between respondents. The
average time to complete and send a
CureTB referral form is estimated at 30
minutes. CureTB currently receives
approximately 600 referrals per year. An
estimated 100 respondents send
referrals, with a range from 1–20 per
E:\FR\FM\10AUN1.SGM
10AUN1
52876
Federal Register / Vol. 81, No. 154 / Wednesday, August 10, 2016 / Notices
respondent, and an average of 5 per
respondent annually.
There are no costs to respondents
other than the time required to submit
the referral documents. Authorizing
legislation comes from Section 361 of
the Public Health Service Act
regulations found in 42 Code of Federal
Regulations part 70 and 71. The
estimated annualized burden hours for
this data collection are 300 hours.
ESTIMATED ANNUALIZED BURDEN HOURS
Type of respondents
Health departments
health authorities.
Health departments
health authorities.
Number of
responses per
respondent
Number of
respondents
Form name
Average
burden per
response
(in hrs.)
Total burden
(in hrs.)
and
partner
CureTB Transnational Notification ...
100
5
30/60
250
and
partner
CureTB Contact/Source Investigation (CI/SI) Notification.
20
5
30/60
50
Total ...........................................
...........................................................
........................
........................
........................
300
Jeffrey M. Zirger,
Health Scientist, Acting 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. 2016–18934 Filed 8–9–16; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60Day–16–16AWK: Docket No. CDC–2016–
0079]
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 Survey of Surveillance
Records of Aedes aegypti and Aedes
albopictus from 1960 to Present. This
project consists of the collection of
county and sub-county-level records for
Aedes aegypti and Ae. albopictus, the
vectors of Zika virus.
DATES: Written comments must be
received on or before October 11, 2016.
ADDRESSES: You may submit comments,
identified by Docket No. CDC–2016–
0079 by any of the following methods:
mstockstill on DSK3G9T082PROD with NOTICES
SUMMARY:
VerDate Sep<11>2014
17:34 Aug 09, 2016
Jkt 238001
• Federal eRulemaking Portal:
Regulations.gov. Follow the instructions
for submitting comments.
• Mail: Jeffrey M. Zirger, 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
PO 00000
Frm 00067
Fmt 4703
Sfmt 4703
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
Survey of Surveillance Records of
Aedes aegypti and Aedes albopictus
from 1960 to Present—New—National
Center for Emerging and Zoonotic
Infectious Diseases (NCEZID), Centers
for Disease Control and Prevention
(CDC).
E:\FR\FM\10AUN1.SGM
10AUN1
Agencies
[Federal Register Volume 81, Number 154 (Wednesday, August 10, 2016)]
[Notices]
[Pages 52875-52876]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2016-18934]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[60Day-16-16AWE: Docket No. CDC-2016-0078]
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 the Information
Collection for Tuberculosis Data from Referring Entities to CureTB.
CureTB is intended to provide continuity of care for individuals
affected by TB who enter US jurisdictions from foreign nations who or
who leave US jurisdictions bound for foreign nations.
DATES: Written comments must be received on or before October 11, 2016.
ADDRESSES: You may submit comments, identified by Docket No. CDC-2016-
0078 by any of the following methods:
Federal eRulemaking Portal: Regulations.gov. Follow the
instructions for submitting comments.
Mail: Jeffrey M. Zirger, 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
Information Collection for Tuberculosis Data From Referring Entities to
CureTB--New--National Center for Emerging Zoonotic and Infectious
Diseases (NCEZID), Centers for Disease Control and Prevention (CDC)
Background and Brief Description
CDC is assuming the administration of the CureTB program from the
San Diego Public Health Department. CureTB works with domestic and
international programs to protect the U.S. public by preventing the
global development of drug resistance and reducing disease transmission
and importation of infectious TB. These goals are accomplished through
CureTB referral and continuity of care services for mobile TB patients.
CDC is seeking OMB clearance for three years of information
collection.
Lack of treatment adherence and inappropriate selection of
medications are prime reasons for the continued emergence and spread of
resistant strains. To combat this, CureTB assures patients understand
how to remain adherent despite moving between nations and provides
information to the health care team that will be continuing care about
each patient's TB strain and tailored medication regimen. CureTB
gathers demographic and clinical information for each patient, and
connects that individual to care through provision of accurate
information about how to locate the correct downstream provider and
assurance that real-time information is given directly to medical
providers and public health authorities in receiving nations.
The respondents are entities within the United States and other
countries who provide diagnostic and treatment services to individuals
affected by TB. The entities are primarily state and local health
departments, but include immigration centers, correctional facilities,
and national TB programs. All 50 US states and territories may refer TB
patients to the CureTB program. To date, CureTB has also received
referrals from Mexico and Guatemala.
Respondents are generally public health field nurses and will
submit CureTB referral forms as they request referral services. The
number of referrals varies widely between respondents. The average time
to complete and send a CureTB referral form is estimated at 30 minutes.
CureTB currently receives approximately 600 referrals per year. An
estimated 100 respondents send referrals, with a range from 1-20 per
[[Page 52876]]
respondent, and an average of 5 per respondent annually.
There are no costs to respondents other than the time required to
submit the referral documents. Authorizing legislation comes from
Section 361 of the Public Health Service Act regulations found in 42
Code of Federal Regulations part 70 and 71. The estimated annualized
burden hours for this data collection are 300 hours.
Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
Number of Average burden
Type of respondents Form name Number of responses per per response Total burden
respondents respondent (in hrs.) (in hrs.)
----------------------------------------------------------------------------------------------------------------
Health departments and partner CureTB 100 5 30/60 250
health authorities. Transnational
Notification.
Health departments and partner CureTB Contact/ 20 5 30/60 50
health authorities. Source
Investigation
(CI/SI)
Notification.
---------------------------------------------------------------
Total..................... ................ .............. .............. .............. 300
----------------------------------------------------------------------------------------------------------------
Jeffrey M. Zirger,
Health Scientist, Acting 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. 2016-18934 Filed 8-9-16; 8:45 am]
BILLING CODE 4163-18-P