Agency Information Collection Activities: Proposed Collection: Comment Request, 19650-19651 [2010-8623]
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19650
Federal Register / Vol. 75, No. 72 / Thursday, April 15, 2010 / Notices
of regional and cross-cutting national
centers that conduct targeted, multidisciplinary education and training
programs for health care providers
treating persons with HIV/AIDS. The
AETCs’ purpose is to increase the
number of health care providers who are
effectively educated and motivated to
counsel, diagnose, treat, and medically
manage individuals with HIV infection,
and to help prevent high risk behaviors
that lead to HIV transmission.
As part of an ongoing effort to
evaluate AETC activities, information is
needed on AETC training sessions,
consultations, and technical assistance
activities. Each regional center collects
achieved through training events.
Collection of this information allows
HRSA and HAB to provide information
on training activities and types of
education and training provided to Ryan
White HIV/AIDS Program Grantees,
resource allocation, and capacity
expansion.
Trainees are asked to complete the
Participant Information Form (PIF) for
each activity they complete, and
trainers, are asked to complete the Event
Record (ER). The estimated annual
response burden to trainers as well as
attendees of training programs is as
follows:
forms on AETC training events, and the
centers are required to report aggregate
data on their activities to HRSA and the
HIV/AIDS Bureau (HAB). This data
collection provides information on the
number of training events, including
clinical trainings and consultations, as
well as technical assistance activities
conducted by each regional center, the
number of health care providers
receiving professional training or
consultation, and the time and effort
expended on different levels of training
and consultation activities. In addition,
information is obtained on the
populations served by the AETC
trainees, and the increase in capacity
Responses
per
respondent
Number of
respondents
Form
Total
responses
Hours per
response
Total burden
hours
PIF ....................................................................................
ER ....................................................................................
116,624
18,070
1
1
116,624
18,070
0.167
0.2
19,476.2
3,614
Total ..........................................................................
134,694
........................
134,694
..........................
23,090.2
Number of
respondents
Responses
per
respondent
Total
responses
Hours per
response
Total burden
hours
12
2
24
32
768
The estimated annual burden to
AETCs is as follows:
Aggregate data set ..............................................................
The total burden hours are 23,858.2.
Written comments and
recommendations concerning the
proposed information collection should
be sent within 30 days of this notice to
the desk officer for HRSA, either by email to OIRA_submission@omb.eop.gov
or by fax to 202–395–6974. Please direct
all correspondence to the ‘‘attention of
the desk officer for HRSA.’’
Dated: April 7, 2010.
Sahira Rafiullah,
Director, Division of Policy and Information
Coordination.
[FR Doc. 2010–8622 Filed 4–14–10; 8:45 am]
BILLING CODE 4165–15–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
mstockstill on DSKH9S0YB1PROD with NOTICES
Health Resources and Services
Administration
Agency Information Collection
Activities: Proposed Collection:
Comment Request
In compliance with the requirement
for opportunity for public comment on
proposed data collection projects
(section 350(c)(2)(A) of Title 44, United
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15:43 Apr 14, 2010
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States Code, as amended by the
Paperwork Reduction Act of 1995
Public Law 104–13, the Health
Resources and Services Administration
(HRSA) will publish periodic
summaries of proposed projects being
developed for submission to the Office
of Management and Budget (OMB)
under the Paperwork Reduction Act of
1995. To request more information on
the proposed project or to obtain a copy
of the data collection plans, call HRSA
Reports Clearance Officer at 301–443–
1129.
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 of
other forms of information technology.
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Proposed Project: Scholarships for
Disadvantaged Students Program (OMB
No. 0915–0149) Extension
The Scholarships for Disadvantaged
Students (SDS) Program has as its
purpose the provision of funds to
eligible schools to provide scholarships
to full-time students with financial need
from disadvantaged backgrounds
enrolled in health professions and
nursing programs.
To qualify for participation in the SDS
program, a school must be carrying out
a program for recruiting and retaining
students from disadvantaged
backgrounds, including students who
are members of racial and ethnic
minority groups (section 737(d)(1)(B) of
the Public Health Service (PHS) Act). A
school must meet the eligibility criteria
to demonstrate that the program has
achieved success based on the number
and/or percentage of disadvantaged
students who graduate from the school.
In awarding SDS funds to eligible
schools, funding priorities must be
given to schools based on the proportion
of graduating students going into
primary care, the proportion of
underrepresented minority students,
and the proportion of graduates working
E:\FR\FM\15APN1.SGM
15APN1
19651
Federal Register / Vol. 75, No. 72 / Thursday, April 15, 2010 / Notices
in medically underserved communities
(section 737(c) of the PHS Act).
The estimated response burden is as
follows:
Number of
respondents
Form
Responses
per
respondents
Hours per
response
Total burden
hours
SDS Application ...............................................................................................
SDS Report ......................................................................................................
600
600
1
1
13
1
7,800
600
Total ..........................................................................................................
600
1
14
8,400
E-mail comments to
paperwork@hrsa.gov or mail to the
HRSA Reports Clearance Officer, Room
10–33, Parklawn Building, 5600 Fishers
Lane, Rockville, MD 20857. Written
comments should be received within 60
days of this notice.
Dated: April 6, 2010.
Sahira Rafiullah,
Director, Division of Policy and Information
Coordination.
[FR Doc. 2010–8623 Filed 4–14–10; 8:45 am]
BILLING CODE 4165–15–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2010–N–0031]
Agency Information Collection
Activities; Submission for Office of
Management and Budget Review;
Comment Request; Export of Medical
Devices-Foreign Letters of Approval
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Notice.
SUMMARY: The Food and Drug
Administration (FDA) is announcing
that a proposed collection of
information has been submitted to the
Office of Management and Budget
(OMB) for review and clearance under
the Paperwork Reduction Act of 1995.
DATES: Fax written comments on the
collection of information by May 17,
2010.
ADDRESSES: To ensure that comments on
the information collection are received,
OMB recommends that written
comments be faxed to the Office of
Information and Regulatory Affairs,
OMB, Attn: FDA Desk Officer, FAX:
202–395–7285, or e-mailed to
oira_submission@omb.eop.gov. All
comments should be identified with the
OMB control number 0910–0264. Also
include the FDA docket number found
in brackets in the heading of this
document.
FOR FURTHER INFORMATION CONTACT:
Daniel Gittleson, Office of Information
Management, Food and Drug
Administration, 1350 Piccard Dr., PI50–
400B, Rockville, MD 20850, 301–796–
5156, Daniel.Gittleson@fda.hhs.gov.
SUPPLEMENTARY INFORMATION: In
compliance with 44 U.S.C. 3507, FDA
has submitted the following proposed
collection of information to OMB for
review and clearance.
Export of Medical Devices-Foreign
Letters of Approval (OMB Control
Number 0910–0264)—Extension
Section 801(e)(2) of the Federal Food,
Drug, and Cosmetic Act (the act) (21
U.S.C. 381(e)(2)) provides for the
exportation of an unapproved device
under certain circumstances if the
exportation is not contrary to the public
health and safety and it has the approval
of the foreign country to which it is
intended for export. Requesters
communicate (either directly or through
a business associate in the foreign
country) with a representative of the
foreign government to which they seek
exportation, and written authorization
must be obtained from the appropriate
office within the foreign government
approving the importation of the
medical device. An alternative to
obtaining written authorization from the
foreign government is to accept a
notarized certification from a
responsible company official in the
United States that the product is not in
conflict with the foreign country’s laws.
This certification must include a
statement acknowledging that the
responsible company official making the
certification is subject to the provisions
of 18 U.S.C. 1001. This statutory
provision makes it a criminal offense to
knowingly and willingly make a false or
fraudulent statement, or make or use a
false document, in any manner within
the jurisdiction of a department or
agency of the United States. The
respondents to this collection of
information are companies that seek to
export medical devices. FDA’s estimate
of the reporting burden is based on the
experience of FDA’s medical device
program personnel.
In the Federal Register of January 26,
2010 (75 FR 4086), FDA published a 60day notice requesting public comment
on the proposed collection of
information. No comments were
received.
FDA estimates the burden of this
collection of information as follows:
TABLE 1.—ESTIMATED ANNUAL REPORTING BURDEN1
Section of the
Federal Food,
Drug, and
Cosmetic Act
No. of
Respondents
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801(e)(2)
Annual Frequency
per Response
38
Total Annual
Responses
1
Hours
per Response
38
Total Hours
3
114
1 There
Total Operating
and Maintenance
Costs2
$6,250
are no capital costs or operating and maintenance costs associated with this collection of information.
to a clerical error, the operating and maintenance costs that appeared in the notice issued in the FEDERAL REGISTER of January 26, 2010,
were reported as zero. The correct figure is in Table 1 of this document.
2Due
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15APN1
Agencies
[Federal Register Volume 75, Number 72 (Thursday, April 15, 2010)]
[Notices]
[Pages 19650-19651]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2010-8623]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Health Resources and Services Administration
Agency Information Collection Activities: Proposed Collection:
Comment Request
In compliance with the requirement for opportunity for public
comment on proposed data collection projects (section 350(c)(2)(A) of
Title 44, United States Code, as amended by the Paperwork Reduction Act
of 1995 Public Law 104-13, the Health Resources and Services
Administration (HRSA) will publish periodic summaries of proposed
projects being developed for submission to the Office of Management and
Budget (OMB) under the Paperwork Reduction Act of 1995. To request more
information on the proposed project or to obtain a copy of the data
collection plans, call HRSA Reports Clearance Officer at 301-443-1129.
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 of other
forms of information technology.
Proposed Project: Scholarships for Disadvantaged Students Program (OMB
No. 0915-0149) Extension
The Scholarships for Disadvantaged Students (SDS) Program has as
its purpose the provision of funds to eligible schools to provide
scholarships to full-time students with financial need from
disadvantaged backgrounds enrolled in health professions and nursing
programs.
To qualify for participation in the SDS program, a school must be
carrying out a program for recruiting and retaining students from
disadvantaged backgrounds, including students who are members of racial
and ethnic minority groups (section 737(d)(1)(B) of the Public Health
Service (PHS) Act). A school must meet the eligibility criteria to
demonstrate that the program has achieved success based on the number
and/or percentage of disadvantaged students who graduate from the
school. In awarding SDS funds to eligible schools, funding priorities
must be given to schools based on the proportion of graduating students
going into primary care, the proportion of underrepresented minority
students, and the proportion of graduates working
[[Page 19651]]
in medically underserved communities (section 737(c) of the PHS Act).
The estimated response burden is as follows:
----------------------------------------------------------------------------------------------------------------
Number of Responses per Hours per Total burden
Form respondents respondents response hours
----------------------------------------------------------------------------------------------------------------
SDS Application................................. 600 1 13 7,800
SDS Report...................................... 600 1 1 600
---------------------------------------------------------------
Total....................................... 600 1 14 8,400
----------------------------------------------------------------------------------------------------------------
E-mail comments to paperwork@hrsa.gov or mail to the HRSA Reports
Clearance Officer, Room 10-33, Parklawn Building, 5600 Fishers Lane,
Rockville, MD 20857. Written comments should be received within 60 days
of this notice.
Dated: April 6, 2010.
Sahira Rafiullah,
Director, Division of Policy and Information Coordination.
[FR Doc. 2010-8623 Filed 4-14-10; 8:45 am]
BILLING CODE 4165-15-P