Agency Information Collection Activities: Submission for OMB Review; Comment Request, 3739-3740 [2010-1173]
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3739
Federal Register / Vol. 75, No. 14 / Friday, January 22, 2010 / Notices
www.cfsan.fda.gov/~comm/
expcllst.html, which identifies U.S.
dairy product manufacturers/processors
that have expressed interest to FDA in
exporting dairy products to Chile, are
subject to FDA jurisdiction, and are not
the subject of a pending judicial
enforcement action (i.e., an injunction
or seizure) or a pending warning letter.
The term ‘‘dairy products,’’ for purposes
of this list, is not intended to cover the
raw agricultural commodity raw milk.
Application for inclusion on the list is
voluntary. However, Chile has advised
that dairy products from firms not on
this list could be delayed or prevented
by Chilean authorities from entering
commerce in Chile. The guidance
explains what information firms should
submit to FDA in order to be considered
for inclusion on the list and what
criteria FDA intends to use to determine
eligibility for placement on the list. The
document also explains how FDA
intends to update the list and how FDA
intends to communicate any new
information to Chile. Finally, the
guidance notes that FDA considers the
information on this list, which is
provided voluntarily with the
understanding that it will be posted on
FDA’s Web site and communicated to,
and possibly further disseminated by,
Chile, to be information that is not
protected from disclosure under 5
U.S.C. 552(b)(4). Under the guidance,
FDA recommends that U.S. firms that
want to be placed on the list send the
following information to FDA: (1) Name
and address of the firm and the
manufacturing plant; (2) name,
telephone number, and e-mail address
(if available) of the contact person; (3)
a list of products presently shipped and
expected to be shipped in the next 3
years; (4) identities of agencies that
inspect the plant and the date of last
inspection; (5) plant number and copy
of last inspection notice; and (6) if other
than an FDA inspection, copy of last
inspection report. FDA requests that this
information be updated every 2 years.
In the Federal Register of June 4, 2009
(74 FR 26867), FDA published a 60-day
notice requesting public comment on
the proposed collection of information.
FDA received two letters in response,
each containing one or more comments.
The comments were outside the scope
of the comment request in the notice.
FDA estimates the burden of this
collection of information as follows:
TABLE 1.—ESTIMATED ANNUAL REPORTING BURDEN1
Activity
No. of
Respondents
Annual Frequency
per Response
Total Annual
Responses
Hours per
Response
Total Hours
New written requests to be
placed on the list
15
1
15
1.5
23
Biannual update
88
1
88
1.0
88
Occasional updates
25
1
25
0.5
13
Total
erowe on DSK5CLS3C1PROD with NOTICES
1 There
124
are no capital or operating and maintenance costs associated with this collection of information.
The estimate of the number of firms
that will submit new written requests to
be placed on the list, biannual updates
and occasional updates is based on the
FDA’s experience maintaining the list
over the past 4 years. The estimate of
the number of hours that it will take a
firm to gather the information needed to
be placed on the list or update its
information is based on FDA’s
experience with firms submitting
similar requests. FDA believes that the
information to be submitted will be
readily available to the firms.
To date, over 175 producers have
sought to be included on the list. FDA
estimates that, each year, approximately
15 new firms will apply to be added to
the list. We estimate that a firm will
require 1.5 hours to read the guidance,
gather the information needed, and to
prepare a communication to FDA that
contains the information and requests
that the firm be placed on the list for a
total of 22.5 hours, rounded to 23.
Under the guidance, every 2 years each
producer on the list must provide
updated information in order to remain
on the list. FDA estimates that each year
approximately half of the firms on the
list, 88 firms (175 x 0.5 = 87.5, rounded
to 88), will resubmit the information to
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14:43 Jan 21, 2010
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remain on the list. We estimate that a
firm already on the list will require 1.0
hours to biannually update and
resubmit the information to FDA,
including time reviewing the
information and corresponding with
FDA, for a total of 88 hours. In addition,
FDA expects that, each year,
approximately 25 firms will need to
submit an occasional update and each
firm will require 0.5 hours to prepare a
communication to FDA reporting the
change, for a total of 12.5 hours,
rounded to 13.
Dated: January 15, 2010.
David Dorsey
Acting Deputy Commissioner for Policy,
Planning and Budget.
[FR Doc. 2010–1153 Filed 1–21–10; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Health Resources and Services
Administration
Agency Information Collection
Activities: Submission for OMB
Review; Comment Request
Periodically, the Health Resources
and Services Administration (HRSA)
publishes abstracts of information
collection requests under review by the
Office of Management and Budget
(OMB), in compliance with the
Paperwork Reduction Act of 1995 (44
U.S.C. Chapter 35). To request a copy of
the clearance requests submitted to
OMB for review, e-mail
paperwork@hrsa.gov or call the HRSA
Reports Clearance Office on (301) 443–
1129.
The following request has been
submitted to the Office of Management
and Budget for review under the
Paperwork Reduction Act of 1995:
E:\FR\FM\22JAN1.SGM
22JAN1
3740
Federal Register / Vol. 75, No. 14 / Friday, January 22, 2010 / Notices
Proposed Project: Advanced Education
Nursing Traineeship (AENT) and Nurse
Anesthetist Traineeship (NAT) (OMB
No. 0915–0305) [Extension]
The Health Resources and Services
Administration (HRSA) provides
training grants to educational
institutions to increase the number of
advanced education nurses through the
Advanced Education Nursing
Traineeship (AENT) Program and the
Nurse Anesthetist Traineeship (NAT)
Program.
HRSA developed the AENT and NAT
tables for the application guidances and
the Nurse Traineeship Database for the
two nursing traineeship programs. The
AENT and NAT tables are used
annually by grant applicants that are
applying for AENT and NAT funding.
The funds appropriated for the AENT
and NAT programs are distributed
among eligible institutions based on a
formula. Award amounts are based on
enrollment and graduate data reported
on the tables and two funding factors
(Statutory Funding Preference and
Statutory Special Consideration).
The AENT and NAT tables include
information on program participants
such as the number of enrollees,
projected data on enrollees and
graduates for the following academic
year, number of trainees supported,
number of graduates, number of
graduates supported and the types of
programs they are enrolling into and/or
from which they are graduating. AENT
and NAT applicants will have a single
access point to submit their grant
applications including the tables.
Applications are submitted in two
phases: Grants.gov (Phase 1) and the
HRSA Electronic Handbooks (Phase 2).
These tables will be available
electronically through the HRSA
Electronic Handbooks (Phase 2) for
applicants to submit their AENT and/or
Number of
respondents
Instrument
Responses
per
respondent
NAT grant application(s). The tables are
also used in the Nurse Traineeship
Database which is used by Division of
Nursing staff and not the applicants.
Data from the tables will be used in
the award determination and validation
process. Additionally, the data will be
used to ensure programmatic
compliance, report to Congress and
policymakers on the program
accomplishments, and formulate and
justify future budgets for these activities
submitted to OMB and Congress.
The burden estimate for this project is
as follows: AENT increased from 1 hour
to 1.5 hours due to the revisions of
AENT Tables 1, 2, 3 and 4 to capture
comprehensive data to provide for more
detailed data analysis of the AENT
Program. NAT burden estimate is
increased from 1 hour to 1.5 hours in
fiscal year 2011 due to the additional
data collection.
Total
responses
Hours per
response
Total burden
hours
AENT ....................................................................................
NAT ......................................................................................
500
100
1
1
500
100
1.5
1.5
750
150
Total ..............................................................................
600
........................
600
........................
900
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: January 14, 2010.
Sahira Rafiullah,
Deputy Director, Division of Policy Review
and Coordination.
[FR Doc. 2010–1173 Filed 1–21–10; 8:45 am]
BILLING CODE 4165–15–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
erowe on DSK5CLS3C1PROD with NOTICES
National Institute of Mental Health;
Notice of Closed Meetings
Pursuant to section 10(d) of the
Federal Advisory Committee Act, as
amended (5 U.S.C. App.), notice is
hereby given of the following meetings.
The meetings will be closed to the
public in accordance with the
provisions set forth in sections
552b(c)(4) and 552b(c)(6), Title 5 U.S.C.,
as amended. The grant applications and
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the discussions could disclose
confidential trade secrets or commercial
property such as patentable material,
and personal information concerning
individuals associated with the grant
applications, the disclosure of which
would constitute a clearly unwarranted
invasion of personal privacy.
Name of Committee: National Institute of
Mental Health Special Emphasis Panel,
Translational Research Center in Behavioral
Science.
Date: February 19, 2010.
Time: 12 p.m. to 4 p.m.
Agenda: To review and evaluate grant
applications.
Place: National Institutes of Health,
Neuroscience Center, 6001 Executive
Boulevard, Rockville, MD 20852. (Telephone
Conference Call.)
Contact Person: Serena P. Chu, PhD,
Scientific Review Officer, Division of
Extramural Activities, National Institute of
Mental Health, NIH, Neuroscience Center,
6001 Executive Blvd., Room 6154, MSC 9609,
Rockville, MD 20892–9609. 301–443–0004.
sechu@mail.nih.gov.
Name of Committee: National Institute of
Mental Health Special Emphasis Panel,
Identification and Characterization of
Sensitive Periods for Neurodevelopment in
Studies of Mental Illness. Date: February 22–
23, 2010. Time: 8:30 a.m. to 5 p.m.
Agenda: To review and evaluate grant
applications.
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Place: Four Seasons Hotel DTRS
Washington, LLC, 2800 Pennsylvania
Avenue, NW., Washington, DC 20007.
Contact Person: Megan Libbey, PhD,
Scientific Review Officer, Division of
Extramural Activities, National Institute of
Mental Health, NIH, Neuroscience Center,
6001 Executive Blvd., Room 6148, MSC 9609,
Rockville, MD 20852–9609. 301–402–6807.
libbeym@mail.nih.gov.
Name of Committee: National Institute of
Mental Health Special Emphasis Panel,
Eating Disorders.
Date: February 23, 2010.
Time: 1:30 p.m. to 4 p.m.
Agenda: To review and evaluate grant
applications.
Place: National Institutes of Health,
Neuroscience Center, 6001 Executive
Boulevard, Rockville, MD 20852. (Telephone
Conference Call.)
Contact Person: Serena P. Chu, PhD,
Scientific Review Officer, Division of
Extramural Activities, National Institute of
Mental Health, NIH, Neuroscience Center,
6001 Executive Blvd., Room 6154, MSC 9609,
Rockville, MD 20892–9609. 301–443–0004.
sechu@mail.nih.gov.
(Catalogue of Federal Domestic Assistance
Program Nos. 93.242, Mental Health Research
Grants; 93.281, Scientist Development
Award, Scientist Development Award for
Clinicians, and Research Scientist Award;
93.282, Mental Health National Research
Service Awards for Research Training,
National Institutes of Health, HHS)
E:\FR\FM\22JAN1.SGM
22JAN1
]]>Agencies
[Federal Register Volume 75, Number 14 (Friday, January 22, 2010)]
[Notices]
[Pages 3739-3740]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2010-1173]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Health Resources and Services Administration
Agency Information Collection Activities: Submission for OMB
Review; Comment Request
Periodically, the Health Resources and Services Administration
(HRSA) publishes abstracts of information collection requests under
review by the Office of Management and Budget (OMB), in compliance with
the Paperwork Reduction Act of 1995 (44 U.S.C. Chapter 35). To request
a copy of the clearance requests submitted to OMB for review, e-mail
paperwork@hrsa.gov or call the HRSA Reports Clearance Office on (301)
443-1129.
The following request has been submitted to the Office of
Management and Budget for review under the Paperwork Reduction Act of
1995:
[[Page 3740]]
Proposed Project: Advanced Education Nursing Traineeship (AENT) and
Nurse Anesthetist Traineeship (NAT) (OMB No. 0915-0305) [Extension]
The Health Resources and Services Administration (HRSA) provides
training grants to educational institutions to increase the number of
advanced education nurses through the Advanced Education Nursing
Traineeship (AENT) Program and the Nurse Anesthetist Traineeship (NAT)
Program.
HRSA developed the AENT and NAT tables for the application
guidances and the Nurse Traineeship Database for the two nursing
traineeship programs. The AENT and NAT tables are used annually by
grant applicants that are applying for AENT and NAT funding. The funds
appropriated for the AENT and NAT programs are distributed among
eligible institutions based on a formula. Award amounts are based on
enrollment and graduate data reported on the tables and two funding
factors (Statutory Funding Preference and Statutory Special
Consideration).
The AENT and NAT tables include information on program participants
such as the number of enrollees, projected data on enrollees and
graduates for the following academic year, number of trainees
supported, number of graduates, number of graduates supported and the
types of programs they are enrolling into and/or from which they are
graduating. AENT and NAT applicants will have a single access point to
submit their grant applications including the tables. Applications are
submitted in two phases: Grants.gov (Phase 1) and the HRSA Electronic
Handbooks (Phase 2). These tables will be available electronically
through the HRSA Electronic Handbooks (Phase 2) for applicants to
submit their AENT and/or NAT grant application(s). The tables are also
used in the Nurse Traineeship Database which is used by Division of
Nursing staff and not the applicants.
Data from the tables will be used in the award determination and
validation process. Additionally, the data will be used to ensure
programmatic compliance, report to Congress and policymakers on the
program accomplishments, and formulate and justify future budgets for
these activities submitted to OMB and Congress.
The burden estimate for this project is as follows: AENT increased
from 1 hour to 1.5 hours due to the revisions of AENT Tables 1, 2, 3
and 4 to capture comprehensive data to provide for more detailed data
analysis of the AENT Program. NAT burden estimate is increased from 1
hour to 1.5 hours in fiscal year 2011 due to the additional data
collection.
----------------------------------------------------------------------------------------------------------------
Number of Responses per Total Hours per Total burden
Instrument respondents respondent responses response hours
----------------------------------------------------------------------------------------------------------------
AENT............................ 500 1 500 1.5 750
NAT............................. 100 1 100 1.5 150
-------------------------------------------------------------------------------
Total....................... 600 .............. 600 .............. 900
----------------------------------------------------------------------------------------------------------------
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 e-mail 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: January 14, 2010.
Sahira Rafiullah,
Deputy Director, Division of Policy Review and Coordination.
[FR Doc. 2010-1173 Filed 1-21-10; 8:45 am]
BILLING CODE 4165-15-P
