Att 2 - 60 day FRN

51270

Federal Register / Vol. 75, No. 160 / Thursday, August 19, 2010 / Notices
ESTIMATE OF ANNUALIZED BURDEN HOURS—Continued
Type of respondent

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

Maryam I. Daneshvar,
Reports Clearance Officer, Centers for Disease
Control and Prevention.
[FR Doc. 2010–20569 Filed 8–18–10; 8:45 am]
BILLING CODE 4163–18–P

DEPARTMENT OF HEALTH AND
HUMAN SERVICES

Number of
responses per
respondent

Number of
respondents

Form name

5

48

12/60

48

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

40

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

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

8,568

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.
Behavioral Assessment Component of
the Behavioral Assessment and Rapid
Testing (BART) Project—New—National
Center for HIV/AIDS, Viral Hepatitis,
STD, and TB Prevention, (NCHHSTP),
Centers for Disease Control and
Prevention, (CDC).

[60Day–10–10GT]

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 or send
comments to Maryam Daneshvar, CDC
Reports Clearance Officer, 1600 Clifton
Road, MS–D74, Atlanta, GA 30333 or
send an e-mail to omb@cdc.gov.
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

Total annual
burden
(in hours)

Form 3 .............

Proposed Project

Centers for Disease Control and
Prevention

Average burden
per response
(in hours)

Background and Brief Description
This Behavioral Assessment and
Rapid Testing project will involve
conducting behavioral assessments and
rapid HIV testing at a variety of events
serving groups at high risk for acquiring
or transmitting HIV infection.
Behavioral assessments will be
conducted using one protocol and one
research agenda but at events serving
different minority and hard-to-reach
populations. This project will address
the increasing rates of HIV infection
among African Americans (AAs) and
men who have sex with men as well as
the need for early detection and linkage
to health care for HIV-infected persons.
The behavioral assessment component
will provide the opportunity to describe
the risk profiles and prevalence of
unrecognized infection among
individuals reachable for HIV
counseling and testing at these events.
Collected data will be used to develop
risk reduction interventions that are

appropriate for the attendees of future
events that attract persons who may be
at high risk for HIV infection. The
proposed project addresses ‘‘Healthy
People 2010’’ priority area(s) of
identifying new HIV infections and is in
alignment with NCHHSTP performance
goal(s) to strengthen the capacity
nationwide to monitor the HIV
epidemic, develop and implement
effective HIV prevention interventions,
and evaluate prevention programs.
The purpose of the proposed data
collection is to collect behavioral data at
selected public events serving specific
high-risk populations and to increase
the proportion of at-risk persons who
are aware of their HIV status. The
behavioral assessment component of the
project addresses the need for increased
behavioral data among some high-risk
groups that are more difficult to access
or represent increasingly greater
proportions of the HIV epidemic.
A convenience sample will be used to
select attendees at (1) Gay Pride; (2)
Minority Gay Pride; (3) black spring
break; and (4) cultural and social events
attracting large numbers of African
Americans. Trained interviewers will
select and approach event attendees. A
screener questionnaire will be used to
determine participation eligibility and
obtain oral consent. Approximately
7,000 individuals will be approached
and screened (through a 2-minute
interview) for eligibility to participate
each year. Approximately 5,600
individuals are expected to be eligible
and participate in the 5- to 15-minute
behavioral assessment interview each
year. There is no cost to respondents
other than their time.

emcdonald on DSK2BSOYB1PROD with NOTICES

ESTIMATE OF ANNUALIZED BURDEN TABLE
Number of
responses per
espondent

Number of
respondents

Average burden
per response
(hours)

Total burden
(in hours)

Respondent

Form

—African American males and females
(18+ yrs) at cultural/social events.
—Males (18+ yrs) at gay pride events
—Racial/ethnic minority males (18+ yrs) at
minority gay pride events
—African American males and females
(18–35 yrs) at spring break festivals
—African American males and females
(18+ yrs) at cultural/social events.

Eligibility Screener ...

7,000

1

2/60

233

Behavioral Assessment.

5,600

1

15/60

1,400

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Federal Register / Vol. 75, No. 160 / Thursday, August 19, 2010 / Notices

51271

ESTIMATE OF ANNUALIZED BURDEN TABLE—Continued
Form

Number of
respondents

Number of
responses per
espondent

Average burden
per response
(hours)

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

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

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

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

Respondent

Total burden
(in hours)

—Males (18+ yrs) at gay pride events
—Racial/ethnic minority males (18+ yrs) at
minority gay pride events
—African American males and females
(18–35 yrs) at spring break festivals
Total ....................................................

Dated: August 13, 2010.
Thelma Sims,
Acting Reports Clearance Officer, Centers for
Disease Control and Prevention.
[FR Doc. 2010–20568 Filed 8–18–10; 8:45 am]
BILLING CODE 4163–18–P

FOR FURTHER INFORMATION CONTACT:
Denver Presley, Jr., Office of Information
Management, Food and Drug
Administration, 1350 Piccard Dr., P150–
400B, Rockville, MD 20850, 301–796–
3793.

DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2010–N–0420]

Agency Information Collection
Activities; Proposed Collection;
Comment Request; Testing
Communications on the Food and
Drug Administration/Center for
Veterinary Medicine’s Regulated
Products Used in Animals
AGENCY:

Food and Drug Administration,

emcdonald on DSK2BSOYB1PROD with NOTICES

Notice.

SUMMARY: 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 and to allow 60 days for
public comment in response to the
notice. This notice solicits comments on
communication studies involving FDA/
Center for Veterinary Medicine (CVM)
regulated products intended for use in
animals. This information will be used
to explore concepts of interest and assist
in the development and modification of
communication messages and
campaigns to fulfill the Agency’s
mission in protecting the public health.
DATES: Submit either electronic or
written comments on the collection of
information by October 18, 2010.
ADDRESSES: Submit electronic
comments on the collection of
information to http://
www.regulations.gov. Submit written
comments on the collection of

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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
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.
With respect to the following
collection of information, FDA invites
comments on these topics: (1) Whether
the proposed collection of information
is necessary for the proper performance
of FDA’s functions, including whether
the information will have practical
utility; (2) the accuracy of FDA’s
estimate of the burden of the proposed
collection of information, including the
validity of the methodology and
assumptions used; (3) ways to enhance
the quality, utility, and clarity of the
information to be collected; and (4)
ways to minimize the burden of the
collection of information on
respondents, including through the use
of automated collection techniques,
SUPPLEMENTARY INFORMATION:

HHS.
ACTION:

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.

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when appropriate, and other forms of
information technology.
Testing Communications on the Food
and Drug Administration/Center for
Veterinary Medicine’s Regulated
Products Used in Animals—21 U.S.C.
393 (d)(2)(D)—(OMB Control Number–
0910–NEW )
CVM has authorization under section
903(d)(2)(D) of the Federal Food, Drug,
and Cosmetic Act (21 U.S.C.
393(d)(2)(D) to conduct educational and
public information programs relating to
the safety of CVM-regulated products.
Further, CVM is authorized to conduct
this needed research to ensure that these
programs have the highest likelihood of
being effective. Thus, CVM concludes
that improving communications about
the safety of regulated animal drugs,
feed, food additives, and devices will
involve many research methods,
including individual indepth
interviews, mall-intercept interviews,
focus groups, self-administered surveys,
gatekeeper reviews, and omnibus
telephone surveys.
The information collected will serve
three major purposes. First, as formative
research, it will provide critical
knowledge needed about target
audiences to develop messages and
campaigns about the use of animal
drugs, feed, food additives, and devices.
Knowledge of both the consumer and
the veterinary professional
decisionmaking processes will provide a
better understanding of target audiences
that FDA will need in order to design
effective communication strategies,
messages, and labels. These
communications will aim to improve
public understanding of the risks and
benefits of using regulated animal drugs,
feed, food additives, and devices by
providing users with a better context in
which to place risk information more
completely. Second, as initial testing, it
will allow FDA to assess the potential
effectiveness of messages and materials
in reaching and successfully
communicating with their intended
audiences. Testing messages with a
sample of the target audience will allow

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