Proposed Data Collection Submitted for Public Comment and Recommendations, 96456-96457 [2016-31739]
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96456
Federal Register / Vol. 81, No. 251 / Friday, December 30, 2016 / Notices
Respondents will also be interviewed.
They will be asked about demographic
and lifestyle factors, hobbies, health
conditions that may affect fish
consumption and fishing habits, and
types of jobs which can contribute to
chemical exposure. Some dietary
questions will be asked with a focus on
consumption of Great Lakes fish.
clinic visits for body measurements and
biological specimen collection (blood,
urine, and hair). Their blood will be
tested for polychlorinated biphenyls,
metals, perfluorinated compounds,
persistent pesticides, and lipids. Urine
will be tested for polycyclic aromatic
hydrocarbons and creatinine. The hair
samples (optional) will be saved for a
later analysis.
Participation in the study is voluntary
and there is no cost to respondents other
than their time. The estimated
annualized burden for the program
averaged over the three-year study
period is 231 hours among 166
respondents. There is no cost to
respondents other than their time spent
in the study.
ESTIMATED ANNUALIZED BURDEN HOURS
Number of
respondents
Number of
responses per
respondent
Average
burden per
response
(in hours)
Total burden
(in hours)
Type of respondents
Form name
Licensed Anglers ...........
Eligibility Screening Survey (paper) ....................
Eligibility Screening Survey (online) ....................
Study Questionnaire (paper) ...............................
Study Questionnaire (online) ...............................
Clinic Visit Checklist and Body Measurements ...
Follow-up Survey .................................................
Eligibility Screening Survey .................................
Contact Information Form ....................................
Study Questionnaire ............................................
Clinic Visit Checklist and Body Measurements ...
Network Size Questions ......................................
Follow-up Survey .................................................
156
28
58
87
133
133
42
33
33
33
33
33
1
1
1
1
1
1
1
1
1
1
1
1
5/60
5/60
30/60
30/60
35/60
5/60
5/60
5/60
40/60
35/60
5/60
5/60
13
2
29
44
78
11
4
3
22
19
3
3
..............................................................................
........................
........................
........................
231
Burmese Refugees ........
Total ........................
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. 2016–31738 Filed 12–29–16; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60Day–17–0576; Docket No. CDC–2016–
0125]
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 effort 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
srobinson on DSK5SPTVN1PROD with NOTICES
SUMMARY:
VerDate Sep<11>2014
19:18 Dec 29, 2016
Jkt 241001
Act of 1995. This notice invites
comment on a proposed revision of the
CDC information collection project
entitled ‘‘Possession, Use, and Transfer
of Select Agents and Toxins.’’
DATES: Written comments must be
received on or before February 28, 2017.
ADDRESSES: You may submit comments,
identified by Docket No. CDC–2016–
0125 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 comments
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
PO 00000
Frm 00024
Fmt 4703
Sfmt 4703
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
E:\FR\FM\30DEN1.SGM
30DEN1
96457
Federal Register / Vol. 81, No. 251 / Friday, December 30, 2016 / Notices
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 is 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 to respond to a collection of
information, search data sources, and
complete and review the collection of
information; and to transmit or
otherwise disclose the information.
Proposed Project
Possession, Use, and Transfer of
Select Agents and Toxins (42 CFR 73)
(OMB Control No. 0920–0576, exp. 12/
31/2018)—Revision—Office of Public
Health Preparedness and Response
(OPHPR), Centers for Disease Control
and Prevention (CDC).
Background and Brief Description
Subtitle A of the Public Health
Security and Bioterrorism Preparedness
and Response Act of 2002, (42 U.S.C.
262a), requires the United States
Department of Health and Human
Services (HHS) to regulate the
possession, use, and transfer of
biological agents or toxins that have the
potential to pose a severe threat to
public health and safety (select agents
and toxins). Subtitle B of the Public
Health Security and Bioterrorism
Preparedness and Response Act of 2002
(which may be cited as the Agricultural
Bioterrorism Protection Act of 2002), (7
U.S.C. 8401), requires the United States
Department of Agriculture (USDA) to
regulate the possession, use, and
transfer of biological agents or toxins
that have the potential to pose a severe
threat to animal or plant health, or
animal or plant products (select agents
and toxins). The HHS Secretary
delegated the responsibility for
promulgating and implementing select
agent regulations found at 42 CFR part
73 to CDC Division of Select Agents and
Toxins (DSAT). The Animal and Plant
Health Inspection Service (APHIS)/
Agriculture Select Agent Services
(AgSAS) was delegated responsibility by
USDA for select agent regulations (7
CFR part 331, and 9 CFR part 121). The
Federal Select Agent Program (FSAP) is
the collaboration of the DSAT and
AgSAS to administer the select agent
regulations in a manner to minimize the
administrative burden on persons
subject to the select agent regulations.
Accordingly, CDC and APHIS have
adopted an identical system to collect
information for the possession, use, and
transfer of select agents and toxins.
CDC is requesting OMB approval to
revise the collected information under
the select agent regulations through the
use of the APHIS/CDC Form 3 (Report
of Theft, Loss, or Release of Select
Agents and Toxins). The Report of
Theft, Loss, or Release of Select Agent
and Toxin form (42 CFR 73.19(a),(b))
must be completed by an individual or
an entity whenever the individual or
entity experiences a theft, loss, or
release of a select agent or toxin.
CDC is proposing to revise the form to
further clarify what needs to be reported
as a ‘‘release’’ and ‘‘loss’’ and additional
fields to assist with categorizing the
type of release (e.g., spill within
secondary containment, occupational
exposure, possible breach of facility
containment, etc.), type of exposure,
and the understanding of safety and
security risk levels relative to human
illness. Estimated average time to
complete this form is one hour.
The total estimated annualized
burden for this collection was
calculated using data obtained from the
FSAP database and is estimated as 430
hours. Information will be collected via
fax, email and hard copy mail from
respondents. Upon OMB approval, CDC
will continue use of the revised form
through November 2018. There is no
cost to the respondents.
ESTIMATED ANNUALIZED BURDEN HOURS
Number of
respondents
Number of
responses per
respondent
Average
burden per
response
(in hours)
Total burden
hours
Type of respondents
Form name
73.19 Section .................
Report of Theft, Loss, or Release of Select
Agents and Toxins.
215
1
2
430
Total ........................
..............................................................................
........................
........................
........................
430
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.
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
[FR Doc. 2016–31739 Filed 12–29–16; 8:45 am]
[60Day–17–1074; Docket No. CDC–2016–
0123]
srobinson on DSK5SPTVN1PROD with NOTICES
BILLING CODE 4163–18–P
Centers for Disease Control and
Prevention
Proposed Data Collection Submitted
for Public Comment and
Recommendations
Centers for Disease Control and
Prevention (CDC), Department of Health
and Human Services (HHS).
AGENCY:
ACTION:
VerDate Sep<11>2014
19:18 Dec 29, 2016
Jkt 241001
PO 00000
Notice with comment period.
Frm 00025
Fmt 4703
Sfmt 4703
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 revision of the
information collection entitled
‘‘Colorectal Cancer Control Program
(CRCCP) Monitoring Activities.’’ The
change to the collection will include a
SUMMARY:
E:\FR\FM\30DEN1.SGM
30DEN1
Agencies
[Federal Register Volume 81, Number 251 (Friday, December 30, 2016)]
[Notices]
[Pages 96456-96457]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2016-31739]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[60Day-17-0576; Docket No. CDC-2016-0125]
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 effort 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 a proposed
revision of the CDC information collection project entitled
``Possession, Use, and Transfer of Select Agents and Toxins.''
DATES: Written comments must be received on or before February 28,
2017.
ADDRESSES: You may submit comments, identified by Docket No. CDC-2016-
0125 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 comments 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
[[Page 96457]]
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 is
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 to respond to a collection of information, search
data sources, and complete and review the collection of information;
and to transmit or otherwise disclose the information.
Proposed Project
Possession, Use, and Transfer of Select Agents and Toxins (42 CFR
73) (OMB Control No. 0920-0576, exp. 12/31/2018)--Revision--Office of
Public Health Preparedness and Response (OPHPR), Centers for Disease
Control and Prevention (CDC).
Background and Brief Description
Subtitle A of the Public Health Security and Bioterrorism
Preparedness and Response Act of 2002, (42 U.S.C. 262a), requires the
United States Department of Health and Human Services (HHS) to regulate
the possession, use, and transfer of biological agents or toxins that
have the potential to pose a severe threat to public health and safety
(select agents and toxins). Subtitle B of the Public Health Security
and Bioterrorism Preparedness and Response Act of 2002 (which may be
cited as the Agricultural Bioterrorism Protection Act of 2002), (7
U.S.C. 8401), requires the United States Department of Agriculture
(USDA) to regulate the possession, use, and transfer of biological
agents or toxins that have the potential to pose a severe threat to
animal or plant health, or animal or plant products (select agents and
toxins). The HHS Secretary delegated the responsibility for
promulgating and implementing select agent regulations found at 42 CFR
part 73 to CDC Division of Select Agents and Toxins (DSAT). The Animal
and Plant Health Inspection Service (APHIS)/Agriculture Select Agent
Services (AgSAS) was delegated responsibility by USDA for select agent
regulations (7 CFR part 331, and 9 CFR part 121). The Federal Select
Agent Program (FSAP) is the collaboration of the DSAT and AgSAS to
administer the select agent regulations in a manner to minimize the
administrative burden on persons subject to the select agent
regulations. Accordingly, CDC and APHIS have adopted an identical
system to collect information for the possession, use, and transfer of
select agents and toxins.
CDC is requesting OMB approval to revise the collected information
under the select agent regulations through the use of the APHIS/CDC
Form 3 (Report of Theft, Loss, or Release of Select Agents and Toxins).
The Report of Theft, Loss, or Release of Select Agent and Toxin form
(42 CFR 73.19(a),(b)) must be completed by an individual or an entity
whenever the individual or entity experiences a theft, loss, or release
of a select agent or toxin.
CDC is proposing to revise the form to further clarify what needs
to be reported as a ``release'' and ``loss'' and additional fields to
assist with categorizing the type of release (e.g., spill within
secondary containment, occupational exposure, possible breach of
facility containment, etc.), type of exposure, and the understanding of
safety and security risk levels relative to human illness. Estimated
average time to complete this form is one hour.
The total estimated annualized burden for this collection was
calculated using data obtained from the FSAP database and is estimated
as 430 hours. Information will be collected via fax, email and hard
copy mail from respondents. Upon OMB approval, CDC will continue use of
the revised form through November 2018. There is no cost to the
respondents.
Estimated Annualized Burden Hours
--------------------------------------------------------------------------------------------------------------------------------------------------------
Number of Average burden
Type of respondents Form name Number of responses per per response Total burden
respondents respondent (in hours) hours
--------------------------------------------------------------------------------------------------------------------------------------------------------
73.19 Section.................................. Report of Theft, Loss, or Release of 215 1 2 430
Select Agents and Toxins.
---------------------------------------------------------------
Total...................................... ....................................... .............. .............. .............. 430
--------------------------------------------------------------------------------------------------------------------------------------------------------
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. 2016-31739 Filed 12-29-16; 8:45 am]
BILLING CODE 4163-18-P