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typically consists of one moderator and
4 to 10 participants, depending on the
research question. In-depth or
ethnographic interviews are one-on-one
interviews designed to elicit the
understandings or terminology that are
necessary for question design, as well as
to gather detailed information that can
contribute to the analysis of both
qualitative and quantitative data.
Usability tests are typically one-on-one
interviews that are used to determine
how a given survey or information
collection tool functions in the field,
and how the mode and layout of the
instrument itself may contribute to

Additionally, field or pilot tests may be
conducted on both representative and
non-representative samples, including
those obtained from commercial survey
and web panel vendors. Beyond looking
at traditional measures of survey errors
(such as missing rates, item nonresponse, and don’t know rates), these
pilot tests can be used to run
experimental designs in order to capture
how different questions function in a
field setting.
There are no costs to respondents
other than their time. The total
estimated annual burden hours are
4,383.

survey response error and the survey
response process.
In addition to these qualitative
methods, NCHS also uses various tools
to obtain quantitative data, which can
be analyzed alone or analyzed alongside
qualitative data to give a much fuller
accounting of the survey response
process. For instance, phone, internet,
mail, and in-person follow-up
interviews of previous NCHS survey
respondents may be used to test the
validity of survey questions and
questionnaires and to obtain more
detailed information that cannot be
gathered on the original survey.

ESTIMATED ANNUALIZED BURDEN HOURS
Form name

Individuals or households ..............................
Individuals or households ..............................
Individuals or households ..............................

Eligibility Screeners .......................................
Developmental Questionnaires .....................
Focus group documents ...............................

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. 2015–14786 Filed 6–16–15; 8:45 am]
BILLING CODE 4163–18–P

DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60-Day–15–0134; Docket No. CDC–2015–
0039]

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 to several of the
information collections pertaining to the
importation of dogs as outlined in the
currently approved information

SUMMARY:

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Number of
respondents

Type of respondents

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collection entitled ‘‘Foreign Quarantine
Regulations (42 CFR part 71)’’.
DATES: Written comments must be
received on or before August 17, 2015.
ADDRESSES: You may submit comments,
identified by Docket No. CDC–2015–
0039 by any of the following methods:
• Federal eRulemaking Portal:
Regulation.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 comment should be
submitted through the Federal eRulemaking
portal (Regulations.gov) or by U.S. mail to the
address listed above.

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)
FOR FURTHER INFORMATION CONTACT:

PO 00000

Frm 00040

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Sfmt 4703

4,000
3,900
100

Number of
responses per
respondent

Average burden
per response
(in hrs.)

1
1
1

5/60
1
1.5

(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

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Federal Register / Vol. 80, No. 116 / Wednesday, June 17, 2015 / Notices

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 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
Foreign Quarantine Regulations (42
CFR part 71)—Revision—(OMB Control
No. 0920–0134, Expires September 30,
2017), National Center for Emerging and
Zoonotic Infections Diseases (NCEZID),
Centers for Disease Control and
Prevention (CDC).
Background and Brief Description
This information collection revision
request is an effort to provide greater
clarity surrounding paperwork
requirements and focuses exclusively on
certain information collections that

• CDC will include one modified IC:
‘‘71.51(c)(2), (d) Application For
Permission To Import A Dog
Unimmunized Against Rabies’’. This
will include a reduced estimate of the
numbers of these permits, formerly CDC
form 75.37 NOTICE TO OWNERS AND
IMPORTERS OF DOGS: Requirement for
Dog Confinement, issued each year.
• CDC will include a separate IC
pertaining to 71.51(c)(1), (d). The title
for this IC is Valid Rabies Vaccination
Certificate, which will include only the
burden associated with rabies
vaccination certificates.
• CDC is also including an
information collection for 71.51(c)(i),
(ii), and (iii) which provides exemption
criteria for the importation of a dog
without a rabies vaccination certificate.
CDC is not requesting changes to any
of the other information collections
included under OMB control number
0920–0134.
The total requested burden hours is
307,613. There is no burden to
respondents other than the time taken to
complete the reports or documentation
for CDC.

pertain to importation of dogs into the
United States. Specifically, CDC seeks to
make the following changes:
• CDC is asking to correct a
transcription error in the burden tables
in section 12. Currently, the relevant IC
reads: 71.51(b)(2) Dogs/cats:
Certification of Confinement,
Vaccination (CDC form 75.37). It should
have been: 71.51(c)(2) Dogs:
Certification of Confinement,
Vaccination (CDC form 75.37).
• CDC is also proposing to replace the
CDC form 75.37 NOTICE TO OWNERS
AND IMPORTERS OF DOGS:
Requirement for Dog Confinement with
a new Application For Permission To
Import A Dog Unimmunized Against
Rabies, which, if the importer meets the
criteria for importation, will be followed
by a CDC-completed Permit to
Conditionally Import a Dog
Inadequately Immunized against
Rabies—Single Entry
• CDC is also requesting approval to
change and split the current information
collection (IC) ‘‘71.51(c)(2) Dogs/cats:
Certification of Confinement,
Vaccination (CDC form 75.37)’’ into two
separate ICs.

ESTIMATED ANNUALIZED BURDEN HOURS
Form name/CFR reference

Maritime conveyance operators ........

71.21(a) Radio Report of death/illness—illness reports from ships
(fillable PDF (individual case and
cumulative report), phone, transcribed email).
71.21(b) Death/Illness reports from
aircrafts (verbal, no form).
71.21(c) Gastrointestinal Illnesses
reports 24 and 4 hours before arrival (MIDRS).
71.21(c)
Recordkeeping—Medical
logs (no form, captains provide
logs).
71.33(c) Report by persons in isolation or surveillance (verbal, no
form).
71.35 Report of death/illness during
stay in port (verbal, no form).
Locator Form used in an outbreak
of public health significance.
Locator Form used for reporting of
an ill passenger(s).
71.51(c)(1), (d)—Valid Rabies Vaccination Certificates.
71.51(c)(i), (ii), and (iii) exemption
criteria for the importation of a
dog without a rabies vaccination
certificate.
71.51(c)(2), (d) Application For Permission To Import A Dog
Unimmunized Against Rabies.
71.51(b) (3) Dogs/cats: Record of
sickness or deaths (no form,
record review).

Aircraft commander or operators ......
Maritime conveyance operators ........

Maritime conveyance operators ........

Isolated or Quarantined individuals ..

Maritime conveyance operators ........
Traveler .............................................
Traveler .............................................

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Importer .............................................
Importer .............................................

Importer .............................................

Importer .............................................

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Number of
responses per
respondent

Number of
respondents

Type of respondent

Sfmt 4703

Average
burden per
response
(in hours)

Total burden
hours

2,000

1

2/60

67

1,700

1

2/60

57

17,000

1

3/60

850

17,000

1

3/60

850

11

1

3/60

1

5

1

30/60

3

2,700,000

1

5/60

225,000

800

1

5/60

67

245,310

1

15/60

61,328

43,290

1

15/60

10,823

1,400

1

15/60

350

20

1

15/60

5

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Federal Register / Vol. 80, No. 116 / Wednesday, June 17, 2015 / Notices
ESTIMATED ANNUALIZED BURDEN HOURS—Continued
Average
burden per
response
(in hours)

Total burden
hours

Form name/CFR reference

Importer/Filer .....................................

CDC PGA Message Set for Importing Cats and Dogs.
71.52(d) Turtle Importation Permits
(no form, just written request).
71.56(a)(2) African Rodents—Request for exemption ( no form,
written request only).
CDC PGA Message Set for Importing African Rodents.
71.55 Dead bodies (death certificates submitted).
71.56(a)(iii) Appeal (no form, written
request only).
Statement or documentation of Noninfectiousness (Documented, no
form; authority under 71.32(b)).
CDC PGA Message Set for Importing African Rodent and All Family
Viverridae Products.

30,000

1

15/60

7,500

5

1

30/60

3

20

1

1

20

60

1

15/60

15

5

1

1

5

2

1

1

2

2,000

1

5/60

167

2,000

1

15/60

500

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

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

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

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

307,613

Importer .............................................
Importer .............................................
Importer/Filer .....................................
Importers ...........................................
Filer ...................................................
Filer/Importer .....................................
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. 2015–14787 Filed 6–16–15; 8:45 am]
BILLING CODE 4163–18–P

DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services

Agency Information Collection
Activities: Proposed Collection;
Comment Request
Centers for Medicare &
Medicaid Services, HHS.
ACTION: Notice.
AGENCY:

The Centers for Medicare &
Medicaid Services (CMS) is announcing
an opportunity for the public to
comment on CMS’ intention to collect
information from the public. Under the
Paperwork Reduction Act of 1995 (the
PRA), federal agencies are required to
publish notice in the Federal Register
concerning each proposed collection of
information (including each proposed
extension or reinstatement of an existing
collection of information) and to allow
60 days for public comment on the
proposed action. Interested persons are
invited to send comments regarding our
burden estimates or any other aspect of
this collection of information, including

SUMMARY:

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any of the following subjects: (1) The
necessity and utility of the proposed
information collection for the proper
performance of the agency’s functions;
(2) the accuracy of the estimated
burden; (3) ways to enhance the quality,
utility, and clarity of the information to
be collected; and (4) the use of
automated collection techniques or
other forms of information technology to
minimize the information collection
burden.
Comments must be received by
August 17, 2015:
ADDRESSES: When commenting, please
reference the document identifier or
OMB control number. To be assured
consideration, comments and
recommendations must be submitted in
any one of the following ways:
1. Electronically. You may send your
comments electronically to http://
www.regulations.gov. Follow the
instructions for ‘‘Comment or
Submission’’ or ‘‘More Search Options’’
to find the information collection
document(s) that are accepting
comments.
2. By regular mail. You may mail
written comments to the following
address: CMS, Office of Strategic
Operations and Regulatory Affairs,
Division of Regulations Development,
Attention: Document Identifier/OMB
Control Number ll, Room C4–26–05,
7500 Security Boulevard, Baltimore,
Maryland 21244–1850.
To obtain copies of a supporting
statement and any related forms for the
proposed collection(s) summarized in
DATES:

[Document Identifier: CMS–10565]

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Type of respondent

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this notice, you may make your request
using one of following:
1. Access CMS’ Web site address at
http://www.cms.hhs.gov/
PaperworkReductionActof1995.
2. Email your request, including your
address, phone number, OMB number,
and CMS document identifier, to
[email protected].
3. Call the Reports Clearance Office at
(410) 786–1326.
FOR FURTHER INFORMATION CONTACT:
Reports Clearance Office at (410) 786–
1326.
SUPPLEMENTARY INFORMATION:
Contents
This notice sets out a summary of the
use and burden associated with the
following information collections. More
detailed information can be found in
each collection’s supporting statement
and associated materials (see
ADDRESSES).
CMS–10565 Off-Cycle Submission of
Summaries of Model of Care Changes
Under the 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.
The term ‘‘collection of information’’ is
defined in 44 U.S.C. 3502(3) and 5 CFR
1320.3(c) and includes agency requests
or requirements that members of the
public submit reports, keep records, or
provide information to a third party.
Section 3506(c)(2)(A) of the PRA
requires federal agencies to publish a
60-day notice in the Federal Register

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