Attachment 2 - 60 day FRN

29169

Federal Register / Vol. 72, No. 100 / Thursday, May 24, 2007 / Notices
the occurrence of violence against
women through a survey administered
to a national sample of adult females
and males. The proposed study will
expand on this work by clarifying
definitions, expanding the categories of
sexual violence, and examining the
sexual violence event.
This study will focus on women and
will occur in two phases: Cognitive and
in-person interviews. In each of the
three communities, in-depth cognitive
interviews will be conducted with 12
adult women, for a total of 36 cognitive

total of 600 women. However, a total of
701 individuals will be screened.
Female respondents who are 18 years
old will be selected randomly from the
communities. Letters will be mailed to
each household in the sample. These
households will be contacted at a later
date in order to collect eligibility
information and to randomly select an
individual. Participants will complete a
45 minute interview.
There are no costs to respondents
except for their time to participate in the
interview.

interviews. However, a total of 66
individuals will be screened.
Respondents will be identified through
agencies working with victims of sexual
violence. Participants will be
interviewed (in either English or
Spanish) at the referral agency. The
primary purpose of this interview is to
assess the questions for the next phase
of the study.
In the next phase, researchers will
conduct face-to-face interviews with
approximately 200 women in each of
the three minority communities for a

ESTIMATE OF ANNUALIZED BURDEN HOURS
Number of
respondents

Respondents

Phase
Phase
Phase
Phase

One:
One:
Two:
Two:

Total burden
(in hours)

Screening for Cognitive Interview ...............................................
Cognitive Interview ......................................................................
Screening for Main Survey ..........................................................
Main Survey ................................................................................

66
36
701
600

1
1
1
1

3/60
2
5/60
45/60

3
72
58
450

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

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

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

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

583

Dated: May 18, 2007.
Maryam I. Daneshvar,
Acting Reports Clearance Officer, Centers for
Disease Control and Prevention.
[FR Doc. E7–10027 Filed 5–23–07; 8:45 am]
BILLING CODE 4163–18–P

DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60Day–07–0199]

Proposed Data Collections Submitted
for Public Comment and
Recommendations

rmajette on PROD1PC67 with NOTICES

Average
burden per
response
(in hours)

Number of
responses per
respondent

In compliance with the requirement
of Section 3506(c)(2)(A) of the
Paperwork Reduction Act of 1995 for
opportunity for public comment on
proposed data collection projects, the
Centers for Disease Control and
Prevention (CDC) will publish periodic
summaries of proposed projects. To
request more information on the
proposed projects or to obtain a copy of
the data collection plans and
instruments, call 404–639–5960 and
send comments to Maryam I. Daneshvar,
CDC Acting Reports Clearance Officer,
1600 Clifton Road, MS–D74, Atlanta,
GA 30333 or send an e-mail to
[email protected].
Comments are invited on: (a) Whether
the proposed collection of information
is necessary for the proper performance
of the functions of the agency, including

VerDate Aug<31>2005

15:52 May 23, 2007

Jkt 211001

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; and (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. Written comments should
be received within 60 days of this
notice.
Proposed Project
Importation of Etiologic Agents,
Hosts, and Vectors of Human Disease
(42 CFR 71.54)—(OMB Control No.
0920–0199)—Extension—Office of the
Director (OD), Centers for Disease
Control and Prevention (CDC).
Background and Brief Description
The Foreign Quarantine Regulations
(42 CFR part 71) set forth provisions to
prevent the introduction, transmission,
and spread of communicable disease
from foreign countries into the United
States. Subpart F—Importations—
contains provisions for importation of
etiologic agents, hosts, and vectors (42
CFR 71.54), requiring persons that
import or distribute after importation
these materials to obtain a permit issued
by the CDC. This request is for the
information collection requirements
contained in 42 CFR 71.54 for issuance
of permits by CDC to importers or
distributors after importation of

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Fmt 4703

Sfmt 4703

etiologic agents, hosts, or vectors of
human disease.
CDC is requesting continued OMB
approval to collect this information
through the use of two separate forms.
These forms are: (1) Application for
Permit to Import or Transport Etiologic
Agents, Hosts, or Vectors of Human
Disease and (2) Application for Permit
to Import or Transport Live Bats.
The Application for Permit to Import
or Transport Etiologic Agents, Hosts, or
Vectors of Human Disease will be used
by laboratory facilities, such as those
operated by government agencies,
universities, research institutions, and
zoologic exhibitions, and also by
importers of nonhuman primate trophy
materials, such as hunters or
taxidermists, to request permits for the
importation and subsequent distribution
after importation of etiologic agents,
hosts, or vectors of human disease. The
Application for Permit to Import or
Transport Etiologic Agents, Hosts, or
Vectors of Human Disease requests
applicant and sender contact
information; description of material for
importation; facility isolation and
containment information; and personnel
qualifications. Estimated average time to
complete this form is 20 minutes.
The Application for Permit to Import
or Transport Live Bats will be used by
laboratory facilities such as those
operated by government agencies,
universities, research institutions, and
zoologic exhibitions entities to request
importation and subsequent distribution
after importation of live bats. The

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24MYN1

29170

Federal Register / Vol. 72, No. 100 / Thursday, May 24, 2007 / Notices

Application for Permit to Import or
Transport Live Bats requests applicant
and sender contact information; a
description and intended use of bats to

be imported; facility isolation and
containment information; and personnel
qualifications. Estimated average time to
complete this form is 20 minutes.

There is no cost to the respondents
other than their time to complete the
form.

ESTIMATED ANNUALIZED BURDEN HOURS
CFR section
71.54

Responses
per
respondent

Average
hourly burden

Total annual
burden
(in hours)

2,300

1

0.333

766

Application for Permit ..........................................................................

Dated: May 18, 2007.
Maryam I. Daneshvar,
Acting Reports Clearance Officer, Centers for
Disease Control and Prevention.
[FR Doc. E7–10029 Filed 5–23–07; 8:45 am]
BILLING CODE 4163–18–P

DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60Day–07–0566]

Proposed Data Collections Submitted
for Public Comment and
Recommendations
In compliance with the requirement
of Section 3506(c)(2)(A) of the
Paperwork Reduction Act of 1995 for
opportunity for public comment on
proposed data collection projects, the
Centers for Disease Control and
Prevention (CDC) will publish periodic
summaries of proposed projects. To
request more information on the
proposed projects or to obtain a copy of
the data collection plans and
instruments, call 404–639–5960 and
send comments to Maryam I. Daneshvar,
CDC Acting Reports Clearance Officer,
1600 Clifton Road, MS–D74, Atlanta,
GA 30333 or send an e-mail to
[email protected].
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; and (d) ways to minimize the
burden of the collection of information
on respondents, including through the
use of automated collection techniques
rmajette on PROD1PC67 with NOTICES

Number of
respondents

VerDate Aug<31>2005

15:52 May 23, 2007

Jkt 211001

or other forms of information
technology. Written comments should
be received within 60 days of this
notice.
Proposed Project
Use of a Reader Response Postcard for
Workers Notified of Results of
Epidemiologic Studies Conducted by
the National Institute for Occupational
Safety and Health (NIOSH)—
Reinstatement—National Institute for
Occupational Safety and Health
(NIOSH), Centers for Disease Control
and Prevention (CDC).
Background and Brief Description
NIOSH, under Section 20(a)(1), (a)(4),
(a)(7)(c), and Section 22 (d), (e)(5)(7) of
the Occupational Safety and Health Act
(29 U.S.C. 669), has the responsibility to
‘‘conduct (directly or by grants or
contracts) research, experiments, and
demonstrations relating to occupational
safety and health, including studies of
psychological factors involved, and
relating to innovative methods,
techniques, and approaches for dealing
with occupational safety and health
problems.’’ NIOSH also has the
responsibility to ‘‘conduct special
research, experiments, and
demonstrations relating to occupational
safety and health as are necessary to
explore new problems, including those
created by new technology in
occupational safety and health [e.g.,
worker notification], which may require
ameliorative action beyond that which
is otherwise provided for in the
operating provisions of the Act’’.
Since 1977, the National Institute for
Occupational Safety and Health
(NIOSH) has been developing methods
and materials for the notification of
subjects of its epidemiological studies.
NIOSH involvement in notifying
workers of past exposures relates
primarily to informing surviving cohort
members of the findings of retrospective

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cohort studies conducted by NIOSH.
Current policy within NIOSH is to
notify subjects of the results of its
epidemiologic studies. The extent of the
notification effort depends upon the
level of excess mortality or the extent of
the disease or illness found in the
cohort. Current notification efforts range
from posting results at the facilities
studied to mailing individual letter
notifications to surviving cohort
members and other stakeholders. The
Industry wide Studies Branch (IWSB) of
NIOSH, Division of Surveillance,
Hazard Evaluation, and Field Studies
(DSHEFS), usually conducts about two
or three notifications per year, which
typically require individual letters
mailed to cohorts ranging in size from
200–20,000 workers each. In order to
assess the effectiveness of the
notification materials received by the
recipients and to improve future
communication of risk information, the
evaluation instrument proposed was
developed.
The NIOSH Institute-wide Worker
Notification Program routinely notifies
subjects about the results of
epidemiologic studies and the
implications of the results. The overall
purpose of the proposed project is to
gain insight into the effectiveness of
NIOSH worker notification in order to
improve the quality and usefulness of
the Institute’s worker notification
activities. Researchers from the NIOSH
Division of Surveillance, Hazard
Evaluations and Field Studies (DSHEFS)
propose to provide notified workers
with a Reader Response postcard for
routinely assessing notified study
subjects’ responses to individual letter
notification materials sent to them by
NIOSH. We are requesting approval for
three years. Participation is voluntary
and there is no cost to respondents
except for their time.

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24MYN1