Agency Forms Undergoing Paperwork Reduction Act Review, 25290-25291 [2017-11263]
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25290
Federal Register / Vol. 82, No. 104 / Thursday, June 1, 2017 / Notices
Control and Prevention (CDC),
Department of Health and Human
Services (HHS).
ACTION: Notice and extension of
comment period.
On September 15, 2016 the
National Institute for Occupational
Safety and Health (NIOSH) of the
Centers for Disease Control and
Prevention (CDC), published a notice in
the Federal Register announcing a
public meeting and request for public
comment on a draft testing protocol.
Written comments were to be received
by December 7, 2016. NIOSH initially
extended the public comment period to
June 7, 2017 [81 FR 88687]. NIOSH is
extending the public comment period
for a second time to August 30, 2017.
The longer timeframe will allow
companies to test the protocol with the
proposed challenge agents.
FOR FURTHER INFORMATION CONTACT:
Deborah V. Hirst, NIOSH, Alice
Hamilton Laboratories, 1090 Tusculum
Avenue, MS–R–5, Cincinnati, Ohio
45226, telephone (513) 841–4141 (not a
toll free number), Email: DHirst@
cdc.gov.
SUMMARY:
You may submit comments,
identified by CDC–2016–0090 and
Docket Number NIOSH 288–A, by either
of the following two methods:
• Federal eRulemaking Portal: https://
www.regulations.gov. Follow the
instructions for submitting comments.
• Mail: National Institute for
Occupational Safety and Health, NIOSH
Docket Office, 1090 Tusculum Avenue,
MS C–34, Cincinnati, Ohio 45226–1998.
ADDRESSES:
John Howard,
Director, National Institute for Occupational
Safety and Health, Centers for Disease Control
and Prevention.
[FR Doc. 2017–11292 Filed 5–31–17; 8:45 am]
BILLING CODE 4163–19–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[30Day–17–0263]
mstockstill on DSK30JT082PROD with NOTICES
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
VerDate Sep<11>2014
18:32 May 31, 2017
Jkt 241001
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 (OMB Control No. 0920–0263;
Expiration Date 09/30/2017)—
Revision—National Center for Emerging
and Zoonotic Infectious Diseases,
Centers for Disease Control and
Prevention (CDC).
Background and Brief Description
Under the 42 CFR 71.53, CDC collects
information pertaining to importers and
imported nonhuman primates. This
information collection enables CDC to
evaluate compliance with pre-arrival of
shipment notification requirements, to
investigate the number and species of
imported nonhuman primates, and to
determine if adequate measures being
taken for the prevention of exposure to
persons and animals during
importation.
Since May 1990, CDC has monitored
the arrival and/or uncrating of certain
shipments of non-human primates
PO 00000
Frm 00067
Fmt 4703
Sfmt 4703
imported in to the United States. In
February 2013, CDC promulgated two
regulations pertaining to the
importation of nonhuman primates. The
first rule, Establishment of User Fees for
Filovirus Testing of Nonhuman Primate
Liver Samples, outlines a process by
which importers can send liver tissues
to CDC from primates that die during
importation from reasons other than
trauma (78 FR 9828, February 12, 2013).
CDC performs these tests due to the
absence of a private sector option. The
second rule, Requirements for Importers
of Nonhuman Primates, consolidates
into 42 CFR 71.53 the requirements
previously found in 42 CFR 71.53 with
those found in the Special Permit to
Import Cynomolgus, African Green, or
Rhesus Monkeys into the United States
(78 FR 11522, February 15, 2013). It also
rescinded the six-month special-permit
requirements for cynomolgus, African
green, and rhesus monkeys and
extended the time period for
registration/permit renewal from 180
days to 2 years, reducing much of the
respondent burden. CDC feels these
regulatory changes and reporting
requirements balance the public health
risks posed by the importation of
nonhuman primates with the burden
imposed on regulating their
importation.
Based on the number of registered
importers and the number of filovirus
samples processed by CDC, CDC is
adjusting downward the number of
burden hours for the following
collections:
• Recordkeeping and reporting
requirements for importing NHPs:
Notification of shipment arrival 71.53(n)
(no form): Reduction of two hours.
• Quarantine release 71.53(l) (No
form): Reduction of two hours.
• 71.53(v): Form: Filovirus Diagnostic
Specimen Submission Form for Nonhuman Primate Materials: Reduction of
17 hours.
• 71.53(g)(1)(iii) and (h)
Documentation and Standard Operating
Procedures (no form) (Registered
Importer): Reduction of one hour.
Estimated Annualized Burden Hours
All registered importers of nonhuman primates are required by 42 CFR
71.53 to maintain certain disease control
procedures and keep certain records.
Standard business practices likely
dictate that importers already keep
records on the origin, transportation,
and disposition of the nonhuman
primates. Thus, CDC asks for
information which should already be
maintained by the importers and need
only be assembled and reported. The
estimate of burden hours totals 922,
E:\FR\FM\01JNN1.SGM
01JNN1
25291
Federal Register / Vol. 82, No. 104 / Thursday, June 1, 2017 / Notices
which reflects assembling and reporting
only.
Form name/CFR reference
Nonhuman Primate
Importer.
Nonhuman Primate
Importer.
Nonhuman Primate
Importer.
Nonhuman Primate
Importer.
Nonhuman Primate
Importer.
Nonhuman Primate
Importer.
Nonhuman Primate
Importer.
Importer/Filer ..............
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) ...............................................
Importer/Filer ..............
Importer/Filer ..............
Number of
responses
per
respondent
Number of
respondents
Type of respondent
Average
burden per
response
(in hours)
1
10/60
12
1
10/60
1
1
10
12
1
30/60
24
6
15/60
24
6
15/60
10
10
20/60
150
1
15/60
2280
1
15/60
2280
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) ..................................
1
1
5/60
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.
comments were to be received by June
5, 2017. In response to a request from
an interested party, NIOSH is extending
the comment period until October 1,
2017.
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
[FR Doc. 2017–11263 Filed 5–31–17; 8:45 am]
DATES:
NIOSH is extending the
comment period on the request for
information published March 7, 2017
[82 FR 12819]. Electronic or written
comments must be received by October
1, 2017.
Submission for OMB Review;
Comment Request
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[CDC–2017–0015; Docket Number NIOSH
295]
Health Risks to Workers Associated
With Occupational Exposures to
Peracetic Acid; Extension of Comment
Period
National Institute for
Occupational Safety and Health
(NIOSH) of the Centers for Disease
Control and Prevention (CDC),
Department of Health and Human
Services (HHS).
ACTION: Notice and extension of
comment period.
AGENCY:
On March 7, 2017 the
National Institute for Occupational
Safety and Health (NIOSH) of the
Centers for Disease Control and
Prevention (CDC), published a notice in
the Federal Register announcing a
request for information to evaluate the
scientific and technical data on
occupational exposure to peracetic acid
(CAS #79–21–0, also known as
peroxyacetic acid and PAA). Written
mstockstill on DSK30JT082PROD with NOTICES
SUMMARY:
VerDate Sep<11>2014
18:32 May 31, 2017
Jkt 241001
G.
Scott Dotson, NIOSH, Education and
Information Division, Robert A. Taft
Laboratories, 1090 Tusculum Avenue,
Cincinnati, Ohio 45226, telephone (513)
533–8540 (not a toll free number).
FOR FURTHER INFORMATION CONTACT:
You may submit comments,
identified by CDC–2017–0015 and
Docket Number NIOSH 295, by either of
the following two methods:
• Federal eRulemaking Portal: https://
www.regulations.gov. Follow the
instructions for submitting comments.
• Mail: National Institute for
Occupational Safety and Health, NIOSH
Docket Office, 1090 Tusculum Avenue,
MS C–34, Cincinnati, Ohio 45226–1998.
ADDRESSES:
John Howard,
Director, National Institute for Occupational
Safety and Health, Centers for Disease Control
and Prevention.
[FR Doc. 2017–11288 Filed 5–31–17; 8:45 am]
BILLING CODE 4163–19–P
PO 00000
Frm 00068
Fmt 4703
Sfmt 4703
Administration for Children and
Families
Proposed Projects
Title: Income Withholding Order/
Notice for Support (IWO).
OMB No.: 0970–0154.
Description: The Income Withholding
Order/Notice for Support (IWO) is the
standard form that must be used to
order and notify employers and income
providers to withhold child support
payments from an obligor’s income. It
also indicates where employers and
other income providers must remit the
payments and other information they
need to withhold correctly.
Child support agencies, courts,
private attorneys, custodial parties, and
others must use the IWO form to initiate
and amend an income withholding
order for support and give notice of
income withholding. Child support
agencies are required to have automated
systems containing current order and
case information. Child support
agencies providing services to custodial
and/or noncustodial parties enter the
terms of a child support order
established by a tribunal into the state’s
automated system, which automatically
populates the IWO form.
Employers and income providers also
use the form to respond to the order/
notice with termination or income
status information. Employers and other
E:\FR\FM\01JNN1.SGM
01JNN1
]]>Agencies
[Federal Register Volume 82, Number 104 (Thursday, June 1, 2017)]
[Notices]
[Pages 25290-25291]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2017-11263]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[30Day-17-0263]
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 (OMB Control No. 0920-0263; Expiration Date 09/30/2017)--
Revision--National Center for Emerging and Zoonotic Infectious
Diseases, Centers for Disease Control and Prevention (CDC).
Background and Brief Description
Under the 42 CFR 71.53, CDC collects information pertaining to
importers and imported nonhuman primates. This information collection
enables CDC to evaluate compliance with pre-arrival of shipment
notification requirements, to investigate the number and species of
imported nonhuman primates, and to determine if adequate measures being
taken for the prevention of exposure to persons and animals during
importation.
Since May 1990, CDC has monitored the arrival and/or uncrating of
certain shipments of non-human primates imported in to the United
States. In February 2013, CDC promulgated two regulations pertaining to
the importation of nonhuman primates. The first rule, Establishment of
User Fees for Filovirus Testing of Nonhuman Primate Liver Samples,
outlines a process by which importers can send liver tissues to CDC
from primates that die during importation from reasons other than
trauma (78 FR 9828, February 12, 2013). CDC performs these tests due to
the absence of a private sector option. The second rule, Requirements
for Importers of Nonhuman Primates, consolidates into 42 CFR 71.53 the
requirements previously found in 42 CFR 71.53 with those found in the
Special Permit to Import Cynomolgus, African Green, or Rhesus Monkeys
into the United States (78 FR 11522, February 15, 2013). It also
rescinded the six-month special-permit requirements for cynomolgus,
African green, and rhesus monkeys and extended the time period for
registration/permit renewal from 180 days to 2 years, reducing much of
the respondent burden. CDC feels these regulatory changes and reporting
requirements balance the public health risks posed by the importation
of nonhuman primates with the burden imposed on regulating their
importation.
Based on the number of registered importers and the number of
filovirus samples processed by CDC, CDC is adjusting downward the
number of burden hours for the following collections:
Recordkeeping and reporting requirements for importing
NHPs: Notification of shipment arrival 71.53(n) (no form): Reduction of
two hours.
Quarantine release 71.53(l) (No form): Reduction of two
hours.
71.53(v): Form: Filovirus Diagnostic Specimen Submission
Form for Non-human Primate Materials: Reduction of 17 hours.
71.53(g)(1)(iii) and (h) Documentation and Standard
Operating Procedures (no form) (Registered Importer): Reduction of one
hour.
Estimated Annualized Burden Hours
All registered importers of non-human primates are required by 42
CFR 71.53 to maintain certain disease control procedures and keep
certain records. Standard business practices likely dictate that
importers already keep records on the origin, transportation, and
disposition of the nonhuman primates. Thus, CDC asks for information
which should already be maintained by the importers and need only be
assembled and reported. The estimate of burden hours totals 922,
[[Page 25291]]
which reflects assembling and reporting only.
----------------------------------------------------------------------------------------------------------------
Number of Average burden
Type of respondent Form name/CFR reference Number of responses per per response
respondents respondent (in hours)
----------------------------------------------------------------------------------------------------------------
Nonhuman Primate Importer............. CDC 75.10A Application 1 1 10/60
for Registration as an
Importer of Nonhuman
Primates (New Importer).
Nonhuman Primate Importer............. CDC 75.10A Application 12 1 10/60
for 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 24 6 15/60
reporting requirements
for importing NHPs:
Notification of
shipment arrival
71.53(n) (no form).
Nonhuman Primate Importer............. Quarantine release 24 6 15/60
71.53(l) (No form).
Nonhuman Primate Importer............. 71.53(v) Form: Filovirus 10 10 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 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. 2017-11263 Filed 5-31-17; 8:45 am]
BILLING CODE 4163-18-P
