60 day FRN

12962

Federal Register / Vol. 82, No. 44 / Wednesday, March 8, 2017 / Notices

Simerl at (404) 679–1888 if you do not
receive an acknowledgement.
ADDRESSES:
Email: [email protected].
Mail: ATTN: HITC Appointments,
U.S. GAO, 441 G Street NW.,
Washington, DC 20548.
FOR FURTHER INFORMATION CONTACT:
GAO Office of Public Affairs, (202) 512–
4800.
Authority: Pub. L. 114–255, § 3002(d)
(2016).
Gene L. Dodaro,
Comptroller General of the United States.
[FR Doc. 2017–04456 Filed 3–7–17; 8:45 am]
BILLING CODE 1610–02–M

DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60Day–17–0263; Docket No. CDC–2017–
0021]

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 a revision request for the
information collection titled
‘‘Requirements for the Importation of
Nonhuman Primates into the United
States.’’ This information collection
contains the reporting and
documentation requirements for
registered importers of nonhuman
primates.
DATES: Written comments must be
received on or before May 8, 2017.
ADDRESSES: You may submit comments,
identified by Docket No. CDC–2017–
0021 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.

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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: [email protected].
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

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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
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 and
to investigate the number and species of
imported nonhuman primates. Also, it
enables CDC to determine if adequate
measures are 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 into 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 (2/12/2013, Vol.78, No. 29, p.
9828). 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 part 71.53 with those found in the
Special Permit to Import Cynomolgus,
African Green, or Rhesus Monkeys into
the United States (2/15/2013, Vol. 78,
No. 32/p. 11522). 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

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Federal Register / Vol. 82, No. 44 / Wednesday, March 8, 2017 / Notices
requirements balance the public health
risks posed by the importation of
nonhuman primates with the burden
imposed on regulating their
importation.
All registered importers of nonhuman primates are required by 42 CFR

part 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 and costs
reflects assembling and reporting only.

ESTIMATED ANNUALIZED BURDEN HOURS
Form name

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 .....................................
Importer/Filer .....................................
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. 2017–04507 Filed 3–7–17; 8:45 am]

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6

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24

6

15/60

36

10

10

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150

1

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2,280

1

15/60

570

2,280

1

5/60

190

........................

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922

DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60 Day–17–0729; Docket No. CDC–2017–
0023]

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.

mstockstill on DSK3G9T082PROD with NOTICES

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

SUMMARY:

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hours

1

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response
(in hours)

Number of
responses per
respondent

Number of
respondents

Type of respondent

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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 Customer Surveys
Generic Clearance for the National
Center for Health Statistics. The surveys
are used to assess National Center for
Health Statistics (NCHS) customer
satisfaction with the content, quality
and relevance of the information NCHS
produces.
Written comments must be
received on or before May 8, 2017.

DATES:

You may submit comments,
identified by Docket No. CDC–2017–
0023 by any of the following methods:

ADDRESSES:

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