Federal Register Notice

Attachment B 60 day Federal Register Notice.pdf

Contact Investigation Outcome Reporting Forms

Federal Register Notice

OMB: 0920-0900

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Federal Register / Vol. 82, No. 197 / Friday, October 13, 2017 / Notices
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60Day–17–0900; Docket No. CDC–2017–
0091]

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 effort to reduce public
burden and maximize the utility of
government information, invites the
general public and other Federal
agencies the opportunity to comment on
a proposed and/or continuing
information collection, as required by
the Paperwork Reduction Act of 1995.
This notice invites comment on a
proposed information collection project
titled Contact Investigation Outcome
Reporting Forms, a collection that
facilitates CDC working with state and
local health departments in conducting
contact investigations of individuals
exposed to a communicable illness
during travel.
DATES: CDC must receive written
comments on or before December 12,
2017.
SUMMARY:

You may submit comments,
identified by Docket No. CDC–2017–
0091 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. CDC will post, without
change, all relevant comments to
Regulations.gov.
Please note: Submit all Federal
comments 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 Leroy A.
Richardson, Information Collection
Review Office, Centers for Disease
Control and Prevention, 1600 Clifton
Road NE., MS–D74, Atlanta, Georgia

asabaliauskas on DSKBBXCHB2PROD with NOTICES

ADDRESSES:

VerDate Sep<11>2014

18:05 Oct 12, 2017

Jkt 244001

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 the OMB for approval. To
comply with this requirement, we are
publishing this notice of a proposed
data collection as described below.
The OMB is particularly interested in
comments that will help:
1. 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;
2. Evaluate the accuracy of the
agency’s estimate of the burden of the
proposed collection of information,
including the validity of the
methodology and assumptions used;
3. Enhance the quality, utility, and
clarity of the information to be
collected; and
4. 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 submissions
of responses.
5. Assess information collection costs.
Proposed Project
Contact Investigation Outcome
Reporting Forms (OMB Control Number
0920–0900, Expiration 6/30/2018)—
Revision—National Center for Emerging
and Zoonotic Infectious Diseases
(NCEZID), Centers for Disease Control
and Prevention (CDC).
Background and Brief Description
This is a request for revision to a
currently approved information
collection, OMB Control Number 0920–
0900, Contact Investigation Outcome
Reporting Forms. CDC requests a threeyear approval for contact investigation
outcome reporting information
collection tools to continue the CDC
routine contact investigation activities.

PO 00000

Frm 00057

Fmt 4703

Sfmt 4703

47743

To understand which pieces of data
are critical to understanding outcomes,
CDC bases all revisions on
reassessments of data from the past
three years.
CDC proposes to collect passengerlevel, epidemiologic, demographic, and
health status data from state/local
Health Departments and maritime
operators at the conclusion of contact
investigations of individuals believed to
have had exposure to a communicable
disease during travel. The health
departments or maritime operators
would obtain the CDC requested
information while conducting the
contact investigation according to their
established policies and procedures,
and would report the information to
CDC on a voluntary basis. This
information will assist CDC in fulfilling
its regulatory responsibility to prevent
the importation of communicable
diseases from foreign countries (42 CFR
part 71) and interstate control of
communicable diseases in humans (42
CFR part 70).
CDC provides state and local health
departments and maritime conveyance
operators with information to notify and
contact individuals and further
investigate this exposure by contacting
others with potential exposure to
disease. However, there currently is no
standardized tool or form to collect
pertinent information regarding the
outcome of such investigations.
To address the need to inform CDC of
additional actions that may be needed to
further protect public health based on
the outcome of the contact
investigations, CDC has developed
forms to assist health departments and
maritime conveyance operators in
reporting to CDC. The forms are specific
to the nature of the investigation:
Tuberculosis (TB), Measles, Rubella, or
the General form for other diseases of
public health concern. The purpose of
the forms is the same: To collect
information to help CDC quarantine
officials fully understand the extent of
disease spread and transmission during
travel and to inform the development
and/or refinement of investigative
protocols aimed at reducing the spread
of communicable disease.
Respondents are state and local health
departments and maritime conveyance
operators. Respondents may use these
standardized forms to submit data
voluntarily to CDC for each individual
contacted via a secure means of their
choice, e.g., web-based application, fax,
or email.
In the past three years, CDC has used
these forms to investigate TB cases on
aircrafts and on cruise ships, as well as

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Federal Register / Vol. 82, No. 197 / Friday, October 13, 2017 / Notices

during measles cases that have occurred
in the U.S. associated with travel.

The respondents are Cruise Ship
Medical Staff/Cargo Ship Managers and
State/local health department staff.

There is no cost to respondents other
than their time to complete the form and
submit the data to CDC.

ESTIMATED ANNUALIZED BURDEN HOURS
Form name

Cruise Ship Physicians/
Cargo Ship Managers.

Clinically Active TB Contact Investigation Outcome Reporting Form—Maritime.
Varicella Investigation Outcome Reporting Form
Influenza Like Illness Investigation Outcome Reporting Form.
General Contact Investigation Outcome Reporting Form—Air.
TB Contact Investigation Outcome Reporting
Form—Air.
Measles Contact Investigation Outcome Reporting Form—Air.
Rubella Contact Investigation Outcome Reporting Form—Air.
General Contact Investigation Outcome Reporting Form—Land.
..............................................................................

State/Local public health
staff.

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. 2017–22206 Filed 10–12–17; 8:45 am]
BILLING CODE 4163–18–P

DEPARTMENT OF HEALTH AND
HUMAN SERVICES

[60Day–17–17BBV; Docket No. CDC–2017–
0085]

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 ‘‘Online training for law
enforcement to reduce risks associated
with shift work and long work hours’’.
This study will develop and pilot test a

SUMMARY:

VerDate Sep<11>2014

18:05 Oct 12, 2017

Jkt 244001

Fmt 4703

Total burden
(in hours)

20/60

5

29
45

1
1

20/60
20/60

10
15

34

1

5/60

3

547

1

5/60

46

324

1

5/60

27

27

1

5/60

3

15

1

5/60

2

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

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

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

111

You may submit comments,
identified by Docket No. CDC–2017–
0085 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. CDC will post, without
change, all relevant comments to
Regulations.gov.
Please note: Submit all comments
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 Leroy A.
Richardson, Information Collection
Review Office, Centers for Disease
Control and Prevention, 1600 Clifton
Road NE., MS–D74, Atlanta, Georgia

Frm 00058

Average
burden per
response
(in hours)

1

new, online, interactive training
program tailored for the law
enforcement community that relays the
health and safety risks associated with
shift work, long work hours, and related
workplace sleep issues and presents
strategies for managers and officers to
reduce these risks.
DATES: CDC must receive written
comments on or before December 12,
2017.

PO 00000

Number of
responses per
respondent

15

ADDRESSES:

Centers for Disease Control and
Prevention

asabaliauskas on DSKBBXCHB2PROD with NOTICES

Number of
respondents

Type of respondents

Sfmt 4703

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 the OMB for approval. To
comply with this requirement, we are
publishing this notice of a proposed
data collection as described below.
The OMB is particularly interested in
comments that will help:
1. 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;
2. Evaluate the accuracy of the
agency’s estimate of the burden of the
proposed collection of information,
including the validity of the
methodology and assumptions used;
3. Enhance the quality, utility, and
clarity of the information to be
collected; and
4. Minimize the burden of the
collection of information on those who
are to respond, including through the

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13OCN1


File Typeapplication/pdf
File Modified2017-10-13
File Created2017-10-13

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