60 day FRN

Att 2a- 60-day FRN.pdf

(NNDSS) Rubella (Data Elements)

60 day FRN

OMB: 0920-0728

Document [pdf]
Download: pdf | pdf
27315

Federal Register / Vol. 80, No. 92 / Wednesday, May 13, 2015 / Notices
total estimated annual burden hours for
the proposed project are 4,250 hours.

ESTIMATED ANNUALIZED BURDEN HOURS
Avg. burden
per response
(in hrs.)

Total burden
(in hrs.)

Form name

Physicians ......................

Retrospective MRI Assessment for Acute Flaccid Myelitis: Patient Summary Form.

6

8,500

5/60

4,250

Total ........................

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

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

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

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

4,250

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. 2015–11513 Filed 5–12–15; 8:45 am]
BILLING CODE 4163–18–P

DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention

• 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.

[60Day–15–0728; Docket No. CDC–2015–
0033]

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.

Proposed Data Collection Submitted
for Public Comment and
Recommendations

FOR FURTHER INFORMATION CONTACT:

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 proposed revision of the
National Notifiable Diseases
Surveillance System (NNDSS)
information collection. The NNDSS is
the nation’s public health surveillance
system that monitors the occurrence and
spread of diseases and conditions that
are nationally notifiable or under
national surveillance.
DATES: Written comments must be
received on or before July 13, 2015.
ADDRESSES: You may submit comments,
identified by Docket No. CDC–2015–
0033 by any of the following methods:
• Federal eRulemaking Portal:
Regulation.gov. Follow the instructions
for submitting comments.
SUMMARY:

asabaliauskas on DSK5VPTVN1PROD with NOTICES

Number of
responses per
respondent

Number of
respondents

Type of respondents

VerDate Sep<11>2014

17:27 May 12, 2015

Jkt 235001

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

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Fmt 4703

Sfmt 4703

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
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
National Notifiable Diseases
Surveillance System (OMB Control No.
0920–0728, Expires 01/31/2017)—
Revision—Center for Surveillance,
Epidemiology and Laboratory Services
(CSELS), Centers for Disease Control
and Prevention (CDC).
Background and Brief Description
The Public Health Services Act (42
U.S.C. 241) authorizes CDC to
disseminate nationally notifiable
condition information. The Nationally
Notifiable Diseases Surveillance System
(NNDSS) is based on data collected at
the state, territorial and local levels as
a result of legislation and regulations in
those jurisdictions that require health
care providers, medical laboratories,
and other entities to submit healthrelated data on reportable conditions to
public health departments. These

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13MYN1

27316

Federal Register / Vol. 80, No. 92 / Wednesday, May 13, 2015 / Notices

reportable conditions, which include
infectious and non-infectious diseases,
vary by jurisdiction depending upon
each jurisdiction’s health priorities and
needs. Infectious disease agents and
environmental hazards often cross
geographical boundaries. Each year, the
Council of State and Territorial Disease
Epidemiologists (CSTE), supported by
CDC, determines which reportable
conditions should be designated
nationally notifiable and voluntarily
submitted to CDC so that information
can be shared across jurisdictional
boundaries and both surveillance and
prevention and control activities can be

average burden per response based on
the burden tables from all of the
consolidated applications has not
changed. The burden on the states and
cities is estimated to be 10 hours per
response and the burden on the
territories is estimated to be 5 hours per
response. The addition of new vaccine,
laboratory, and disease-specific data
elements do not add any additional
burden because the states, territories,
and cities already collect those data
elements. There will be no increase in
burden for the states, territories, and
cities to send those data elements to
CDC. The estimated annual burden is
28,340 hours.

coordinated at regional and national
levels.
CDC requests a three-year approval for
a revision the NNDSS information
collection. This Revision includes
requests for approval to receive: (1) Case
notification data for Chikungunya,
Dengue-like illness, Non-HPS
Hantavirus, and Acute Flaccid Myelitis;
(2) new laboratory and vaccine data
elements for all conditions; and (3) new
disease-specific data elements for
Mumps, Pertussis, and Sexually
Transmitted Diseases.
Although this Revision includes case
notifications that were not part of the
last NNDSS Revision, the estimate of the

ESTIMATED ANNUALIZED BURDEN HOURS
Avg. burden
per response
(in hrs.)

Total burden
(in hrs.)

Form name

States ................................................
Territories ..........................................
Cities .................................................

Weekly and Annual ..........................
Weekly and Annual ..........................
Weekly and Annual ..........................

50
5
2

52
52
52

10
5
10

26,000
1,300
1,040

Total ...........................................

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

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

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

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

28,340

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. 2015–11514 Filed 5–12–15; 8:45 am]
BILLING CODE 4163–18–P

DEPARTMENT OF HEALTH AND
HUMAN SERVICES

Written comments must be
received on or before July 13, 2015.

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 new information

VerDate Sep<11>2014

17:27 May 12, 2015

Jkt 235001

You may submit comments,
identified by Docket No. CDC–2015–
0032 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.

ADDRESSES:

[60 Day–15–15AGK; Docket No. CDC–2015–
0032]

SUMMARY:

collection request entitled,
‘‘Understanding Barriers and
Facilitators to HIV prevention for Men
Who Have Sex with Men (MSM)’’ to
conduct qualitative research with most
at risk HIV-negative MSM. The research
is intended to understand issues
surrounding HIV risk for MSM, identify
influences of high risk behaviors and to
investigate risk management and
resiliency among HIV-negative MSM.
DATES:

Centers for Disease Control and
Prevention

asabaliauskas on DSK5VPTVN1PROD with NOTICES

Number of
responses per
respondent

Number of
respondents

Type of respondents

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.

PO 00000

Frm 00033

Fmt 4703

Sfmt 4703

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)
FOR FURTHER INFORMATION CONTACT:

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13MYN1


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