Agency Forms Undergoing Paperwork Reduction Act Review, 33925-33926 [2014-13824]

Download as PDF 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 ........................... mstockstill on DSK4VPTVN1PROD with NOTICES 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 VerDate Mar<15>2010 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
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