Att 2 60dy FRN

Att 2 60 Day FRN.pdf

Aggregate Reports for Tuberculosis Program Evaluation

Att 2 60dy FRN

OMB: 0920-0457

Document [pdf]
Download: pdf | pdf
43203

Federal Register / Vol. 81, No. 127 / Friday, July 1, 2016 / Notices
of burden hours requested is 1,824
hours.

ESTIMATED ANNUALIZED BURDEN HOURS
Form name

Person with ALS .....................

ALS Case Validation Questions .............................................
ALS Case Registration Form .................................................
Voluntary Survey Modules .....................................................
Disease Progression Survey ..................................................
ALS Biorepository Specimen Processing Form .....................
ALS Registry Research Application Form .............................
Annual Update ........................................................................
Chapter/District Outreach Reporting Form ............................
National Office Outreach Reporting Form .............................

Researchers ............................
ALS Service Organization ......

Jeffrey M. Zirger,
Health Scientist, Acting 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. 2016–15645 Filed 6–30–16; 8:45 am]
BILLING CODE 4163–18–P

DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60Day–16–0457: Docket No. CDC–206–
0058]

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 Aggregate Reports for
Tuberculosis Program Evaluation. The
goal of the study is to allow CDC to
collect and monitor indicators for key
program activities, such as finding
tuberculosis infections in recent
contacts of cases and in other persons
likely to be infected and providing
therapy for latent tuberculosis infection
in an effort to eliminate Tuberculosis in
the United States.

SUMMARY:

asabaliauskas on DSK3SPTVN1PROD with NOTICES

Number of
respondents

Type of respondents

VerDate Sep<11>2014

19:05 Jun 30, 2016

Jkt 238001

Written comments must be
received on or before August 30, 2016.
ADDRESSES: You may submit comments,
identified by Docket No. CDC–2016–
0058 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.
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.
DATES:

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)
(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
FOR FURTHER INFORMATION CONTACT:

PO 00000

Frm 00022

Fmt 4703

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1,670
1,500
750
750
325
36
24
135
2

Number of
responses per
respondent
1
1
1
3
1
1
1
12
12

Average
burden per
response
(in hours)
2/60
10/60
80/60
5/60
30/60
30/60
15/60
5/60
20/60

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
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.

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43204

Federal Register / Vol. 81, No. 127 / Friday, July 1, 2016 / Notices

Proposed Project
Aggregate Reports for Tuberculosis
Program Evaluation (0920–0457—Exp.
9–30–2016)—Extension—National
Center for HIV/AIDS, Viral Hepatitis,
STD, and TB Prevention (NCHHSTP),
Centers for Disease Control and
Prevention (CDC)
Background and Brief Description
CDC requests the extension of the
Aggregate Reports for Tuberculosis
Program Evaluation, previously
approved under OMB No. 0920–0457
for 3-years. There are no revisions to the
report forms, data definitions, or
reporting instructions.
To ensure the elimination of
tuberculosis in the United States, CDC
monitors indicators for key program
activities, such as finding tuberculosis

infections in recent contacts of cases
and in other persons likely to be
infected and providing therapy for
latent tuberculosis infection. In 2000,
CDC implemented two program
evaluation reports for annual
submission: Aggregate report of followup for contacts of tuberculosis, and
Aggregate report of screening and
preventive therapy for tuberculosis
infection (OMB No. 0920–0457). The
respondents for these reports are the 68
state and local tuberculosis control
programs receiving federal cooperative
agreement funding through the CDC
Division of Tuberculosis Elimination
(DTBE). These reports emphasize
treatment outcomes, high-priority target
populations vulnerable to tuberculosis,
and programmed electronic report entry,
which transitioned to the National
Tuberculosis Indicators Project (NTIP), a

secure web-based system for program
evaluation data, in 2010. No other
federal agency collects this type of
national tuberculosis data, and the
Aggregate report of follow-up for
contacts of tuberculosis, and Aggregate
report of screening and preventive
therapy for tuberculosis infection are
the only data source about latent
tuberculosis infection for monitoring
national progress toward tuberculosis
elimination with these activities. CDC
provides ongoing assistance in the
preparation and utilization of these
reports at the local and state levels of
public health jurisdiction. CDC also
provides respondents with technical
support for the NTIP software
(Electronic—100%, Use of Electronic
Signatures—No). There is no cost to
respondents.

ESTIMATED ANNUALIZED BURDEN HOURS
Type of respondent

Form name

Data clerks and Program Managers, electronic.
Program Managers, manual .....................

Follow-up and Treatment of Contacts to
Tuberculosis Cases Form (Att 3a).
Follow-up and Treatment of Contacts to
Tuberculosis Cases Form (Att 3a).
Follow-up and Treatment of Contacts to
Tuberculosis Cases Form (Att 3a).
Targeted Testing and Treatment for Latent Tuberculosis Infection (Att 3b).
Targeted Testing and Treatment for Latent Tuberculosis Infection (Att 3b).
Targeted Testing and Treatment for Latent Tuberculosis Infection (Att 3b).

Data clerks, (manual) ................................
Data clerks and Program Managers, electronic.
Program Managers, (manual) ...................
Data clerks, (manual) ................................
Total ...................................................

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

Jeffrey M. Zirger,
Health Scientist, Acting 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. 2016–15647 Filed 6–30–16; 8:45 am]
BILLING CODE 4163–18–P

DEPARTMENT OF HEALTH AND
HUMAN SERVICES

asabaliauskas on DSK3SPTVN1PROD with NOTICES

Centers for Disease Control and
Prevention
[60Day–16–16ATI; Docket No. CDC–2016–
0057]

Proposed Data Collection Submitted
for Public Comment and
Recommendations
Centers for Disease Control and
Prevention (CDC), Department of Health
and Human Services (HHS).

AGENCY:

VerDate Sep<11>2014

19:05 Jun 30, 2016

Jkt 238001

ACTION:

Number of
responses per
respondent

100

1

30/60

50

18

1

30/60

9

18

1

3

54

100

1

30/60

50

18

1

30/60

9

18

1

3

54

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

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

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

226

Notice with comment period.

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 Development of CDC’s Act
Against AIDS Social Marketing
Campaigns Targeting Consumers. CDC
is requesting approval for revision to the
previously approved project to continue
testing HIV/AIDS prevention and
treatment messages to be included in
social marketing campaigns targeting
consumers.

SUMMARY:

Written comments must be
received on or before August 30, 2016.

DATES:

PO 00000

Frm 00023

Fmt 4703

Sfmt 4703

Average
burden per
response
(in hours)

Number of
respondents

Total
burden
hours

You may submit comments,
identified by Docket No. CDC–2016–
0057 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:

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.

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