60 day FRN

16391

Federal Register / Vol. 80, No. 59 / Friday, March 27, 2015 / Notices
The government intends to
accomplish the following as a result of
this data collection: (a) Identify high
priority opportunities for public health
and healthcare collaboration, (b) inform
a public health-healthcare strategic

agenda, (c) improve the use of clinical
preventive services, and (d) improve
capacity of healthcare systems to
incorporate public health practices and
principles. At the conclusion of this
study, a formal report, two issue briefs,

and potentially a manuscript for
publication will be produced.
There are no costs to respondents
other than their time. The total
estimated annualized burden hours are
234.

ESTIMATED ANNUALIZED BURDEN HOURS

Prevention and Wellness Assessment Survey ..

150

1

30/60

Coordinating & Identifying Activity .....................
Communication Coordination Activity ................
Telephone Interview ...........................................

150
150
9

1
1
1

30/60
30/60
1

Physician, Nurse, or Other Healthcare Professional (To Complete Survey).
Key Health Plan Contact ....................................
Administrative Support ........................................
Physician, Nurse, or Other Healthcare Professional (To Complete 1-hour Interview Post
Survey).

[FR Doc. 2015–07034 Filed 3–26–15; 8:45 am]
BILLING CODE 4163–18–P

DEPARTMENT OF HEALTH AND
HUMAN SERVICES

[30Day–15–15GD]

[FR Doc. 2015–07039 Filed 3–26–15; 8:45 am]

Withdrawal of Information Collection
National Institute for
Occupational Safety and Health
(NIOSH), Centers for Disease Control
and Prevention.
In compliance with the requirement
of Section 3506(c)(2)(A) of the
Paperwork Reduction Act of 1995.
[FR Doc. 2015–06655 Filed 3–23–15;
8:45 a.m.]
Subject: Emergency Self Escape for
Coal Miners.
Action: Notice withdrawal.
SUMMARY: The Centers for Disease
Control and Prevention requests
withdrawal from publication the 30-Day
Federal Register Notice (FRN) 15–15GD
concerning the Emergency Self Escape
for Coal Miners ([FR Doc. 2015–06655
Filed 3–23–15; 8:45 a.m.]), which was
submitted on March 19, 2015 for public
inspection in the Federal Register.
CDC published the notice as a
Proposed Data Collections Submitted for
Public Comment and
Recommendations, when, in fact, the
notice should have received publication
as Agency Forms Undergoing
Paperwork Reduction Act Review.
AGENCY:

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The 30-day FRN published on
[03/24/15] at [Vol. 80, No. 56 Page
15618–15619] is withdrawn as of [03/
24/15].
FOR FURTHER INFORMATION CONTACT:
(404) 639–7570 or send comments to
CDC Leroy Richardson, 1600 Clifton
Road, MS D–74, Atlanta, GA 30333 or
send an email to [email protected].
SUPPLEMENTARY INFORMATION: N/A.
DATES:

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.

Centers for Disease Control and
Prevention

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Number of
responses per
respondent

Form name

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.

Average
burden per
response
(in hours)

Number of
respondents

Type of respondent

BILLING CODE 4163–18–P

DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60Day–15–0914; Docket No. CDC–2015–
0012]

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

SUMMARY:

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Fmt 4703

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Act of 1995. This notice invites
comment on Workplace Violence
Prevention Programs in New Jersey
Healthcare Facilities (OMB No. 0920–
0914, expires 02/29/2016). The National
Institute for Occupational Safety and
Health (NIOSH) is requesting a two year
extension in order to complete nursing
home interviews.
DATES: Written comments must be
received on or before May 26, 2015.
ADDRESSES: You may submit comments,
identified by Docket No. CDC–2015–
0012 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].

FOR FURTHER INFORMATION CONTACT:

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16392

Federal Register / Vol. 80, No. 59 / Friday, March 27, 2015 / Notices

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
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.

mstockstill on DSK4VPTVN1PROD with NOTICES

SUPPLEMENTARY INFORMATION:

Proposed Project
Workplace Violence Prevention
Programs in New Jersey Healthcare
Facilities (OMB No. 0920–0914, expires
02/29/2016)—Extension—National
Institute for Occupational Safety and
Health (NIOSH), Centers for Disease
Control and Prevention (CDC).

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Background and Brief Description
The National Institute for
Occupational Safety and Health
(NIOSH) is requesting a two-year
extension to complete the nursing home
interviews for the project entitled
‘‘Workplace Violence Prevention
Programs in New Jersey Healthcare
Facilities’’. The long-term goal of the
proposed project is to reduce violence
against healthcare workers. The
objective of the proposed study is twofold: (1) To examine healthcare facility
compliance with the New Jersey
Violence Prevention in Health Care
Facilities Act, and (2) to evaluate the
effectiveness of the regulations in this
Act in reducing assault injuries to
workers.
Our central hypothesis is that
facilities with high compliance with the
regulations will have lower rates of
employee violence-related injury.
NIOSH received OMB approval (0920–
0914) to evaluate the legislation at
hospitals and at nursing homes, to
conduct a nurse survey and to conduct
a home healthcare aide survey. Data
collection is complete for the hospitals,
the nurse survey, and the home
healthcare aide survey. We are
requesting an extension to evaluate the
legislation at nursing homes.
First, we will conduct face-to-face
interviews with the Chairs of the
Violence Prevention Committees in 40
nursing homes (20 in New Jersey and 20
in Virginia) who are in charge of
overseeing compliance efforts. The
purpose of the interviews is to measure
compliance to the state regulations
(violence prevention policies, reporting
systems for violent events, violence
prevention committee, written violence
prevention plan, violence risk
assessments, post incident response and
violence prevention training). The
details of their Workplace Violence
Prevention Program are in their existing
policies and procedures. Second, we
will also collect assault injury data from
nursing home’s violent event reports
three years pre-regulation (2009–2011)
and three years post-regulation (2012–
2014). This data is captured in existing
Occupational Safety and Health
Administration (OSHA) logs and is
publicly available. The purpose of
collecting these data is to evaluate
changes in assault injury rates before
and after enactment of the regulations.
A contractor will conduct the
interviews, collect the nursing home’s
policies and procedures, and collect the
assault injury data (OSHA logs).
Healthcare workers are nearly five
times more likely to be victims of
violence than workers in all industries

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combined. While healthcare workers are
not at particularly high risk for jobrelated homicide, nearly 60% of all
nonfatal assaults occurring in private
industry are experienced in healthcare
occupations.
Six states have enacted laws to reduce
violence against healthcare workers by
requiring workplace violence
prevention programs. However, little is
understood about how effective these
laws are in reducing violence against
healthcare workers. We will test our
central hypothesis by accomplishing the
following specific aims:
1. Compare the comprehensiveness of
nursing home workplace violence
prevention programs before and after
enactment of the New Jersey regulations
in nursing homes; Working hypothesis:
Based on our preliminary research, we
hypothesize that enactment of the
regulations will improve the
comprehensiveness of nursing home
workplace violence prevention program
policies, procedures and training.
2. Examine patterns of assault injuries
to nursing home workers before and
after enactment of the regulations;
Working hypothesis: Based on our
preliminary research, we hypothesize
that rates of assault injuries to nursing
home workers will decrease following
enactment of the regulations.
Healthcare facilities falling under the
regulations are eligible for study
inclusion (i.e., nursing homes). A
contractor will conduct face-to-face
interviews with the chairs of the
Violence Prevention Committees at 40
nursing homes, who as stated in
regulations, are in charge of overseeing
compliance efforts. These individuals
will include nursing home
administrators. The purpose of the
interviews is to measure compliance to
the state regulations (Aim 1). The
interview form was pilot-tested by the
study team in the fall 2010 and includes
the following components as mandated
in the regulations: Violence prevention
policies, reporting systems for violent
events, violence prevention committee,
written violence prevention plan,
violence risk assessments, post incident
response and violence prevention
training. The nursing home’s policy and
procedures documents will be obtained
by the contractor to provide details
about their workplace violence
prevention program; a NIOSH employee
will complete the abstraction form from
the policy and procedures documents
received from the contractor. Questions
will also be asked about barriers and
facilitators to developing the violence
prevention program. These data will be
collected in the post-regulation time
period.

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16393

Federal Register / Vol. 80, No. 59 / Friday, March 27, 2015 / Notices
A contractor will also collect assault
injury data from nursing home violent
event reports three years pre-regulation
(2009–2011) and three years postregulation (2012–2014). This data will
be collected from existing OSHA logs; a
NIOSH employee will fill out the
Employee Incident Form from the
OSHA logs received from the contractor.
The purpose of collecting these data is
to evaluate changes in assault injury

rates before and after enactment of the
regulations (Aim 2). The following
information will be abstracted from the
OSHA logs: Date, time and location of
the incident; identity, job title and job
task of the victim; identity of the
perpetrator; description of the violent
act, including whether a weapon was
used; description of physical injuries;
number of employees in the vicinity
when the incident occurred, and their

actions in response to the incident;
recommendations of police advisors,
employees or consultants, and; actions
taken by the facility in response to the
incident. No employee or perpetrator
identifiable information will be
collected.
There are no costs to respondents
other than their time. The total
estimated burden hours are 120.

ESTIMATED ANNUALIZED BURDEN HOURS
Number of
respondents

Total burden
(in hours)

Form name

Nursing Home Administrator ..................
Nursing Home Administrator ..................
Nursing Home Administrator ..................

Interview ......................................
Abstraction Form .........................
Employee Incident Form .............

40
40
40

1
1
1

1
1
1

40
40
40

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

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

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

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

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

120

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.

Dated: March 20, 2015.
Francis S. Collins,
Director, NIH.
[FR Doc. 2015–07064 Filed 3–26–15; 8:45 am]
BILLING CODE 4140–01–P

BILLING CODE 4163–18–P

DEPARTMENT OF HEALTH AND
HUMAN SERVICES

DEPARTMENT OF HEALTH AND
HUMAN SERVICES

Food and Drug Administration
[Docket No. FDA–2012–N–0114]

National Institutes of Health Statement
of Organization, Functions, and
Delegations of Authority
Part N, National Institutes of Health
(NIH), of the Statement of Organization,
Functions, and Delegations of Authority
for the Department of Health and
Human Services (40 FR 22859, May 27,
1975, as amended most recently at 77
FR 1941, January 12, 2012, and
redesignated from Part HN as Part N at
60 FR 56605, November 9, 1995), is
amended as set forth below to rename
the National Center for Complementary
and Alternative Medicine (NCCAM).
Section N–D, Organization and
Functions, under the heading National
Center for Complementary and
Alternative Medicine (NCCAM), is
renamed to the National Center for
Complementary and Integrative Health
(NCCIH).
Delegations of Authority Statement:
All delegations and redelegations of
authority to officers and employees of
NIH that were in effect immediately
prior to the effective date of this
reorganization and are consistent with
this reorganization shall continue in
effect, pending further redelegation.

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20:59 Mar 26, 2015

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Agency Information Collection
Activities; Proposed Collection;
Comment Request; Request for
Samples and Protocols
AGENCY:

Food and Drug Administration,

HHS.
ACTION:

The Food and Drug
Administration (FDA) is announcing an
opportunity for public comment on the
proposed collection of certain
information by the Agency. 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 of an existing collection of
information, and to allow 60 days for
public comment in response to the
notice. This notice solicits comments on
the information collection requirements
relating to the regulations which state
that protocols for samples of biological
products must be submitted to the
Agency.
DATES: Submit either electronic or
written comments on the collection of
information by May 26, 2015.

Frm 00035

Fmt 4703

FDA
PRA Staff, Office of Operations, Food
and Drug Administration, 8455
Colesville Rd., COLE–14526, Silver
Spring, MD 20993–0002, PRAStaff@
fda.hhs.gov.

FOR FURTHER INFORMATION CONTACT:

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.
‘‘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 (44
U.S.C. 3506(c)(2)(A)) requires Federal
Agencies to provide a 60-day notice in
the Federal Register concerning each
proposed collection of information,
including each proposed extension of an
existing collection of information,
before submitting the collection to OMB
for approval. To comply with this
requirement, FDA is publishing notice
of the proposed collection of
information set forth in this document.

SUPPLEMENTARY INFORMATION:

Notice.

SUMMARY:

PO 00000

Submit electronic
comments on the collection of
information to http://
www.regulations.gov. Submit written
comments on the collection of
information to the Division of Dockets
Management (HFA–305), Food and Drug
Administration, 5630 Fishers Lane, Rm.
1061, Rockville, MD 20852. All
comments should be identified with the
docket number found in brackets in the
heading of this document.

ADDRESSES:

[FR Doc. 2015–07038 Filed 3–26–15; 8:45 am]

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Average
burden per
esponse
(in hours)

Number of
responses per
respondent

Type of respondents

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