Agency Forms Undergoing Paperwork Reduction Act Review, 33925-33926 [2014-13824]
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33925
Federal Register / Vol. 79, No. 114 / Friday, June 13, 2014 / Notices
from 60–90 minutes, depending on
whether the respondent is a districtlevel administrator, a school-level
administrator, or another school staff
member. The burden estimates
presented here are based on the
assumption of a 1-hour response time
per district-level and school-level
administrator response and a 1.5-hour
response time per school staff member
response. The estimated annualized
burden of this data collection is 58
hours for respondents.
There are no costs to respondents
other than their time.
The two information collections
combine for a total estimated
annualized burden of 367 hours for
respondents.
based instrument or participate in the
interviews with no penalty and no
impact on their job or relationship with
the LEA. Participation is completely
voluntary.
For the Web-based instrument, the
estimated burden per response ranges
from 20–25 minutes. This variation in
burden is due to the slight variability in
skip patterns that may occur with
certain responses and variations in the
reading speed of respondents. The
burden estimates presented here are
based on the assumption of a 25-minute
response time per response. The
estimated annualized burden of this
data collection is 306 hours for
respondents.
For the Web-based instrument, the
estimated burden per response ranges
Both the Web-based instrument and
in-person interviews will be
administered in 2014 and 2016. These
data collection points coincide with the
initiation of project activities and the
mid-way points of the PS13–1308
cooperative agreement. Although some
staff may participate in the data
collection in multiple years, this is not
a longitudinal design and individual
staff member responses will not be
tracked across the years. No personally
identifiable information will be
collected.
All school staff members will receive
informed consent forms prior to
participation in the information
collection. The consent form explains
the study and also explains participants
may choose not to complete the Web-
ESTIMATED ANNUALIZE BURDEN HOURS
Form name
School staff ....................
Web-based instrument for Broward County Public Schools.
Web-based instrument for Los Angeles Unified
School District.
Web-based instrument for San Francisco Unified School District.
School Climate Index Interview Guide for District-level Administrators.
School Climate Index Interview Guide for
School-level Administrators.
School Climate Index Interview Guide for School
Staff.
School staff ....................
School staff ....................
District-level Administrators.
School-level Administrators.
School Staff ...................
Total ........................
..............................................................................
Leroy 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. 2014–13825 Filed 6–12–14; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
mstockstill on DSK4VPTVN1PROD with NOTICES
[30-Day–14–0263]
Agency Forms Undergoing Paperwork
Reduction Act Review
The Centers for Disease Control and
Prevention (CDC) has submitted the
following information collection request
to the Office of Management and Budget
(OMB) for review and approval in
accordance with the Paperwork
Reduction Act of 1995. The notice for
VerDate Mar<15>2010
18:01 Jun 12, 2014
Jkt 232001
Number of
responses per
respondent
Number of
respondents
Respondents
Frm 00034
Fmt 4703
Total burden
(in hours)
245
1
25/60
102
245
1
25/60
102
245
1
25/60
102
2
1
1
2
14
1
1
14
28
1
1.5
42
........................
........................
........................
364
the proposed information collection is
published to obtain comments from the
public and affected agencies.
Written comments and suggestions
from the public and affected agencies
concerning the proposed collection of
information are encouraged. Your
comments should address any of the
following: (a) Evaluate whether the
proposed collection of information is
necessary for the proper performance of
the functions of the agency, including
whether the information will have
practical utility; (b) Evaluate the
accuracy of the agencies estimate of the
burden of the proposed collection of
information, including the validity of
the methodology and assumptions used;
(c) Enhance the quality, utility, and
clarity of the information to be
collected; (d) Minimize the burden of
the collection of information on those
who are to respond, including through
the use of appropriate automated,
electronic, mechanical, or other
technological collection techniques or
PO 00000
Average
burden per
response
(in hours)
Sfmt 4703
other forms of information technology,
e.g., permitting electronic submission of
responses; and (e) Assess information
collection costs.
To request additional information on
the proposed project or to obtain a copy
of the information collection plan and
instruments, call (404) 639–7570 or
send an email to omb@cdc.gov. Written
comments and/or suggestions regarding
the items contained in this notice
should be directed to the Attention:
CDC Desk Officer, Office of Management
and Budget, Washington, DC 20503 or
by fax to (202) 395–5806. Written
comments should be received within 30
days of this notice.
Proposed Project
Requirements for the Importation of
Nonhuman Primates into the United
States—Revision—(expiration date:
4/30/2016)—National Center for
Emerging and Zoonotic Infectious
Diseases (NCEZID), Division of Global
Migration and Quarantine (DGMQ),
E:\FR\FM\13JNN1.SGM
13JNN1
33926
Federal Register / Vol. 79, No. 114 / Friday, June 13, 2014 / Notices
Centers for Disease Control and
Prevention (CDC).
Background and Brief Description
CDC is submitting this revision to
obtain authority to collect electronic
information from importers/filers on
nonhuman primate and nonhuman
primate products over which CDC has
authority, notably those found in 42
CFR part 71. This request is consistent
with requirements of the Security and
Accountability for Every (SAFE) Port
Act that states that all agencies that
require documentation for clearing or
licensing the importation and
exportation of cargo participate in the
International Trade Data System (ITDS),
and is also consistent with CDC
authorities under Section 361 of the
Public Health Service Act (PHSA) (42
U.S.C. 264).
This electronic data is specified by
CDC using Partner Government Agency
(PGA) Message Sets and is collected by
Customs and Border Protection (CBP)
from importers/filers when they submit
the information needed through
International Trade Data System (ITDS)
and the Automated Commercial
Environment (ITDS/ACE) to clear an
import. CDC has developed a PGA
message set for each regulated import
specified in 42 CFR part 71, and each
PGA Message Set includes only those
data requirements necessary in order to
determine whether or not a CDCregulated import poses a risk to public
health and that the importer has met
CDC’s regulatory requirements for entry.
CDC including the PGA Message Sets
for review because there is no set form
or format for the electronic submission
of import related data to CBP and CDC.
CDC is permitted access to the
Automated Commercial Environment
(ACE) data pursuant to 6 CFR 29.8(b)
and 49 CFR 1520.11(b), which permit
federal employees with a need to know
to have access to this data.
CDC is maintaining its authority to
collect hard copies of required
documentation, as currently authorized
by the Office of Management and
Budget, because the use of ITDS/ACE
will not be required for imports entering
the United States until a later date. CDC
will accept both hard copy and
electronic filing of import-related
documentation until the use of ACE is
required for cargo entering the United
States.
Through this revision, CDC is
requesting a net increase in the
estimated number of burden hours in
the amount of 798 hours. Of these
additional hours, 608 hours pertain to
requests for CDC Message Set data via
ITDS/ACE, and 190 hours pertain to
required statements/documentation of
products being rendered non-infectious.
Because the use of ITDS/ACE will not
be required for imports entering the
United States until a later date, CDC is
maintaining its authority to collect hard
copies of required documentation, as
currently authorized by the Office of
Management and Budget. CDC will
accept both hard copy and electronic
filing of import-related documentation
until the use of ACE is required for
cargo entering the United States.
Respondents to this data collection
have not changed and remain new and
registered importers of live nonhuman
primates and importers of nonhuman
primate products. The number of
additional hours requested for this
information collection total 798 hours.
The total burden for this information
collection request is 944 hours. There
are no costs to respondents except for
their time to complete the forms, and
complete and submit data and
documentation.
ESTIMATED ANNUALIZED BURDEN HOURS
Type of
respondent
Form name/CFR
reference
Nonhuman Primate Importer ..
CDC 75.10A Application for Registration as an Importer of
Nonhuman Primates (New Importer).
CDC 75.10A Application for Registration as an Importer of
Nonhuman Primates (Re-Registration).
71.53(g)(1)(iii) and (h) Documentation and Standard Operating Procedures (no form) (New Importer).
71.53(g)(1)(iii) and (h) Documentation and Standard Operating Procedures (no form) (Registered Importer).
Recordkeeping and reporting requirements for importing
NHPs: Notification of shipment arrival 71.53(n) (no form).
Quarantine release 71.53(l) (No form) ...................................
71.53(v) Form: Filovirus Diagnostic Specimen Submission
Form for Non-human Primate Materials.
CDC Partner Government Agency Message Set for Importing Live Nonhuman Primates.
CDC Partner Government Agency Message Set for Importing Nonhuman Primate Products.
Documentation of Non-infectiousness 71.53(t) ......................
Nonhuman Primate Importer ..
Nonhuman Primate Importer ..
Nonhuman Primate Importer ..
Nonhuman Primate Importer ..
Nonhuman Primate Importer ..
Nonhuman Primate Importer ..
Importer/Filer ...........................
Importer/Filer ...........................
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Importer/Filer ...........................
Number of
responses
per
respondent
Number of
respondents
1
1
10/60
12
1
10/60
1
1
10
12
1
30/60
25
6
15/60
25
10
6
15
15/60
20/60
150
1
15/60
2280
1
15/60
2280
1
5/60
Leroy 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. 2014–13824 Filed 6–12–14; 8:45 am]
BILLING CODE 4163–18–P
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18:01 Jun 12, 2014
Jkt 232001
PO 00000
Frm 00035
Fmt 4703
Sfmt 9990
E:\FR\FM\13JNN1.SGM
Average
burden per
response
(in hours)
13JNN1
Agencies
[Federal Register Volume 79, Number 114 (Friday, June 13, 2014)]
[Notices]
[Pages 33925-33926]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2014-13824]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[30-Day-14-0263]
Agency Forms Undergoing Paperwork Reduction Act Review
The Centers for Disease Control and Prevention (CDC) has submitted
the following information collection request to the Office of
Management and Budget (OMB) for review and approval in accordance with
the Paperwork Reduction Act of 1995. The notice for the proposed
information collection is published to obtain comments from the public
and affected agencies.
Written comments and suggestions from the public and affected
agencies concerning the proposed collection of information are
encouraged. Your comments should address any of the following: (a)
Evaluate whether the proposed collection of information is necessary
for the proper performance of the functions of the agency, including
whether the information will have practical utility; (b) Evaluate the
accuracy of the agencies estimate of the burden of the proposed
collection of information, including the validity of the methodology
and assumptions used; (c) Enhance the quality, utility, and clarity of
the information to be collected; (d) Minimize the burden of the
collection of information on those who are to respond, including
through the use of appropriate automated, electronic, mechanical, or
other technological collection techniques or other forms of information
technology, e.g., permitting electronic submission of responses; and
(e) Assess information collection costs.
To request additional information on the proposed project or to
obtain a copy of the information collection plan and instruments, call
(404) 639-7570 or send an email to omb@cdc.gov. Written comments and/or
suggestions regarding the items contained in this notice should be
directed to the Attention: CDC Desk Officer, Office of Management and
Budget, Washington, DC 20503 or by fax to (202) 395-5806. Written
comments should be received within 30 days of this notice.
Proposed Project
Requirements for the Importation of Nonhuman Primates into the
United States--Revision--(expiration date: 4/30/2016)--National Center
for Emerging and Zoonotic Infectious Diseases (NCEZID), Division of
Global Migration and Quarantine (DGMQ),
[[Page 33926]]
Centers for Disease Control and Prevention (CDC).
Background and Brief Description
CDC is submitting this revision to obtain authority to collect
electronic information from importers/filers on nonhuman primate and
nonhuman primate products over which CDC has authority, notably those
found in 42 CFR part 71. This request is consistent with requirements
of the Security and Accountability for Every (SAFE) Port Act that
states that all agencies that require documentation for clearing or
licensing the importation and exportation of cargo participate in the
International Trade Data System (ITDS), and is also consistent with CDC
authorities under Section 361 of the Public Health Service Act (PHSA)
(42 U.S.C. 264).
This electronic data is specified by CDC using Partner Government
Agency (PGA) Message Sets and is collected by Customs and Border
Protection (CBP) from importers/filers when they submit the information
needed through International Trade Data System (ITDS) and the Automated
Commercial Environment (ITDS/ACE) to clear an import. CDC has developed
a PGA message set for each regulated import specified in 42 CFR part
71, and each PGA Message Set includes only those data requirements
necessary in order to determine whether or not a CDC-regulated import
poses a risk to public health and that the importer has met CDC's
regulatory requirements for entry. CDC including the PGA Message Sets
for review because there is no set form or format for the electronic
submission of import related data to CBP and CDC. CDC is permitted
access to the Automated Commercial Environment (ACE) data pursuant to 6
CFR 29.8(b) and 49 CFR 1520.11(b), which permit federal employees with
a need to know to have access to this data.
CDC is maintaining its authority to collect hard copies of required
documentation, as currently authorized by the Office of Management and
Budget, because the use of ITDS/ACE will not be required for imports
entering the United States until a later date. CDC will accept both
hard copy and electronic filing of import-related documentation until
the use of ACE is required for cargo entering the United States.
Through this revision, CDC is requesting a net increase in the
estimated number of burden hours in the amount of 798 hours. Of these
additional hours, 608 hours pertain to requests for CDC Message Set
data via ITDS/ACE, and 190 hours pertain to required statements/
documentation of products being rendered non-infectious.
Because the use of ITDS/ACE will not be required for imports
entering the United States until a later date, CDC is maintaining its
authority to collect hard copies of required documentation, as
currently authorized by the Office of Management and Budget. CDC will
accept both hard copy and electronic filing of import-related
documentation until the use of ACE is required for cargo entering the
United States.
Respondents to this data collection have not changed and remain new
and registered importers of live nonhuman primates and importers of
nonhuman primate products. The number of additional hours requested for
this information collection total 798 hours. The total burden for this
information collection request is 944 hours. There are no costs to
respondents except for their time to complete the forms, and complete
and submit data and documentation.
Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
Average
Number of Number of burden per
Type of respondent Form name/CFR reference respondents responses per response (in
respondent hours)
----------------------------------------------------------------------------------------------------------------
Nonhuman Primate Importer.......... CDC 75.10A Application for 1 1 10/60
Registration as an
Importer of Nonhuman
Primates (New Importer).
Nonhuman Primate Importer.......... CDC 75.10A Application for 12 1 10/60
Registration as an
Importer of Nonhuman
Primates (Re-Registration).
Nonhuman Primate Importer.......... 71.53(g)(1)(iii) and (h) 1 1 10
Documentation and Standard
Operating Procedures (no
form) (New Importer).
Nonhuman Primate Importer.......... 71.53(g)(1)(iii) and (h) 12 1 30/60
Documentation and Standard
Operating Procedures (no
form) (Registered
Importer).
Nonhuman Primate Importer.......... Recordkeeping and reporting 25 6 15/60
requirements for importing
NHPs: Notification of
shipment arrival 71.53(n)
(no form).
Nonhuman Primate Importer.......... Quarantine release 71.53(l) 25 6 15/60
(No form).
Nonhuman Primate Importer.......... 71.53(v) Form: Filovirus 10 15 20/60
Diagnostic Specimen
Submission Form for Non-
human Primate Materials.
Importer/Filer..................... CDC Partner Government 150 1 15/60
Agency Message Set for
Importing Live Nonhuman
Primates.
Importer/Filer..................... CDC Partner Government 2280 1 15/60
Agency Message Set for
Importing Nonhuman Primate
Products.
Importer/Filer..................... Documentation of Non- 2280 1 5/60
infectiousness 71.53(t).
----------------------------------------------------------------------------------------------------------------
Leroy 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. 2014-13824 Filed 6-12-14; 8:45 am]
BILLING CODE 4163-18-P