Agency Information Collection Activities: Proposed Collection; Comment Request, 59191-59193 [E9-27523]
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59191
Federal Register / Vol. 74, No. 220 / Tuesday, November 17, 2009 / Notices
ESTIMATED ANNUALIZED BURDEN HOURS
Number of respondents
Instrument/Activity
Number of responses per
respondent
1400
450
750
750
750
750
750
750
750
135
1
1
1
1
12
1
1
1
3
1
0.17
0.03
0.17
0.33
0.08
0.02
0.02
0.03
0.08
0.03
238
14
128
248
720
15
15
23
180
4
100
50
50
50
50
50
50
50
15
7,700
1
1
1
12
1
1
1
3
1
45
0.17
0.17
0.33
0.08
0.02
0.02
0.03
0.08
0.03
—
17
9
17
48
1
1
2
12
1
1,693
Client Surveys: Children 0–7.
Screening and Diagnosis Tool ........................................................................
Positive Monitor Tracking .........................................................................
Services Child is Receiving at the time of the FASD Diagnosis .............
Services Planned and Provided based on Diagnostic Evaluation ...........
Services Delivery Tracking Form .............................................................
End of Intervention/Program Improvement Measure—Case Manager ....
End of Intervention/Program Improvement Measure—Parent/Guardian
End of Intervention/Program Customer Satisfaction with Service ...........
Outcome Measures (Children 0–7 years) ................................................
Lost to follow-up .......................................................................................
Client Surveys: Children 8–18:
Screening and Diagnosis Tool .................................................................
Services Child is Receiving at the time of the FASD Diagnosis .............
Services Planned and Provided based on Diagnostic Evaluation ...........
Services Delivery Tracking Form .............................................................
End of Intervention/Program Improvement Measure—Case Manager ....
End of Intervention/Program Improvement Measure—Parent/Guardian
End of Intervention/Program Customer Satisfaction with Service ...........
Outcome Measures (Children 8–18 years) ..............................................
Lost to follow-up .......................................................................................
TOTAL ...................................................................................................
Send comments to Summer King,
SAMHSA Reports Clearance Officer,
Room 7–1044, One Choke Cherry Road,
Rockville, MD 20857 AND e-mail her a
copy at summer.king@samhsa.hhs.gov.
Written comments should be received
within 60 days of this notice.
Dated: November 4, 2009.
Elaine Parry,
Director, Office of Program Services.
[FR Doc. E9–27524 Filed 11–16–09; 8:45 am]
BILLING CODE 4162–20–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Substance Abuse and Mental Health
Services Administration
mstockstill on DSKH9S0YB1PROD with NOTICES
Agency Information Collection
Activities: Proposed Collection;
Comment Request
In compliance with Section
3506(c)(2)(A) of the Paperwork
Reduction Act of 1995 concerning
opportunity for public comment on
proposed collections of information, the
Substance Abuse and Mental Health
Services Administration (SAMHSA)
will publish periodic summaries of
proposed projects. To request more
information on the proposed projects or
to obtain a copy of the information
collection plans, call the SAMHSA
Reports Clearance Officer on (240) 276–
1243.
Comments are invited on: (a) Whether
the proposed collections of information
are necessary for the proper
VerDate Nov<24>2008
20:50 Nov 16, 2009
Jkt 220001
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 or
other forms of information technology.
Proposed Project: Substance Abuse
Prevention and Treatment (SAPT)
Block Grant Uniform Application
Guidance and Instructions FY 2011–
2013 and Regulations (OMB No. 0930–
0080)—Revision
Sections 1921 through 1935 of the
Public Health Service Act (U.S.C. 300x–
21 to 300x–35) provide for annual
allotments to assist States to plan, carry
out and evaluate activities to prevent
and treat substance abuse and for
related activities. Under the provisions
of the law, States may receive
allotments only after an application is
submitted and approved by the
Secretary, DHHS. For the Federal fiscal
years (FY) 2011–FY 2013 Substance
Abuse Prevention and Treatment
(SAPT) Block Grant application cycles,
SAMHSA will provide States with
revised application guidance and
instructions to implement changes made
in accordance with recommendations
from the National Association of State
Alcohol and Drug Abuse Directors
(NASADAD) and their member States in
PO 00000
Frm 00079
Fmt 4703
Sfmt 4703
Average burden per response
Total burden
hours per collection
the revisions and clarification of data
reporting requirements and instructions.
During negotiations with the States
resulting in agreement on the National
Outcome Measures (NOMs) for
substance abuse treatment and
prevention, SAMHSA pledged to the
States to:
1. Reduce respondent burden;
2. Work with the States to improve
performance management of the SAPT
Block Grant;
3. Improve the availability, timeliness,
and quality of data available to Federal,
State, and provider administrators of
block grant funded programs.
This revision of the Uniform
Application and Regulation for the
SAPT Block Grant takes additional steps
toward implementing these
commitments. SAMHSA, in
consultation with NASADAD, has
provided States the ability to reduce
their application burden by
consolidating the FY 2011–FY 2013
State Plan into a 3-year plan. With the
exception of the projected annual
budget form, States only would be
expected to submit any proposed
revisions to its approved three-year plan
but would otherwise not have to
resubmit a State Plan during FY 2012
and FY 2013. Individual States may
reduce their respondent burden further
by selecting the option of using
SAMHSA pre-populated tables for
Section IVa and IVb. The data for these
tables would be drawn from SAMHSA
data sets known as Drug and Alcohol
Services Information System (DASIS)
Treatment Episode Data Set (TEDS) and
E:\FR\FM\17NON1.SGM
17NON1
59192
Federal Register / Vol. 74, No. 220 / Tuesday, November 17, 2009 / Notices
National Survey on Drug Use and
Health (NSDUH) by SAMHSA and
provided to the States. In addition, the
Web-based Block Grant Application
System now facilitates completion of
the provider entity table through added
pre-populated data items. The data for
this table would be drawn from
SAMHSA data set known as DASIS
National Survey of Substance Abuse
Treatment Services (N–SSATS).
SAMHSA will continue to work with
NASADAD and the States to assess the
feasibility and usefulness of prepopulating additional sections of the
application with data extracted from
SAMHSA data sets to further reduce
respondent burden.
SAMHSA continues to provide the
States with the option of reporting on
prevention expenditures utilizing the
six primary prevention strategies or
utilizing the Institute of Medicine
classification of Universal, Selective or
Indicated. SAMHSA has designed the
State Prevention Framework State
Incentive Grant (SPF SIG) competitive
program and funded contracts in States
without an SPF SIG to support data
driven prevention planning by the
Single State Agencies for Substance
Abuse. States are expected to use the
State level data collected with support
from these programs in the planning in
section II of the Uniform Application.
The Uniform Application has been
modified to move needs assessment,
planning narrative and future year
budget forms into Section II, the FY
2011–FY 2013 Plan section.
In December 2004, SAMHSA and the
States agreed on the goal of having all
States reporting the NOMs measures as
defined at the meeting by the end of a
3-year implementation period starting in
FY 2005 and concluding at the end of
FY 2007. By January 2006, supportive
technical assistance on information
technology design and payment for data
submitted became available by the State
Outcomes Measurement and
Management System (SOMMS)
program. States who have participated
in the SOMMS/NOMs subcontracts may
choose to have their data pre-populated
which would significantly reduce their
reporting burden for this application.
During the subsequent three years,
SAMHSA in partnership with the States
and all other SAPT Block Grant
stakeholders have continued to work
towards improving standards for
analyzing and responding to the results
of NOMs data appropriate to each level
of block grant funded administration
including Federal, State, and Provider
roles and responsibilities.
SAMHSA realigned resources to
address the need for technical assistance
in information technology (IT) and
software purchasing to implement and
maintain NOMs data standards. This
technical assistance first became
available in September 2006 and IT
support continues.
Revisions to the previously-approved
Uniform Application resulting from
such stakeholder input reflect the
following changes: (1) Section I, Form 2,
‘‘Table of Contents,’’ was revised to
appropriately enumerate the specific
items within each section; (2) In Section
II, the former single year ‘‘Intended Use
Plan’’ is aggregated into a ‘‘Three Year
State Plan’’ to reduce the States’ annual
plan reporting burden. The first ‘‘Three
Year Plan’’ will cover FYs 2011–2013.
In the next two subsequent years, only
revisions or updates to the 3-year plan
will be required in the States’ FY 2012
and FY 2013 Uniform Applications.
Planned expenditures of each Federal
Fiscal Year award will still be collected
annually; (3) In Section II, the Form
formerly specified as Form 12 has been
removed; (4) In Section III, Narratives
covering the Federal requirements,
financial expenditure reports and
services utilization reports are
consolidated into the ‘‘Annual Report
Section’’; (5) In Section IV subparts IVa
and IVb, Treatment and Prevention
Performance Reporting Forms are
maintained and are to be completed
annually.
The total annual reporting burden
estimate is shown below:
FY 2011
Number of respondents
Responses
per respondent
Number of
hours per response
Total hours
Sections I–III—States and Territories ..............................................................
Section IV–A ....................................................................................................
Section IV–B ....................................................................................................
Recordkeeping .................................................................................................
60
60
60
60
1
1
1
1
* 480
40
42.75
16
28,800
2,400
2,565
960
Total ..........................................................................................................
60
........................
........................
34,725
* (additional 10 hours per completion of Section II per State due to addition of FYs 2012 and 2013 in ‘‘Three Year Plan’’).
FY 2012 AND FY 2013
[Due to the reduction in section II]
Number of respondents
Responses
per respondent
Number hours
per response
Total hours
mstockstill on DSKH9S0YB1PROD with NOTICES
Sections I–III—States and Territories ..............................................................
Section IVa ......................................................................................................
Section IVb ......................................................................................................
Recordkeeping .................................................................................................
60
60
60
60
1
1
1
1
440
40
42.75
16
26,400
2,400
2,565
960
Total ..........................................................................................................
60
........................
........................
32,325
* (reduction of approximately 40 hours per respondent due to reductions in response burden for Section II, ‘‘Three Year Plan’’).
Average Annual Total Burden is
projected to be 33,125 or a decrease of
about 800 hours.
VerDate Nov<24>2008
20:50 Nov 16, 2009
Jkt 220001
Send comments to Summer King,
SAMHSA Reports Clearance Officer,
Room 7–1044, One Choke Cherry Road,
PO 00000
Frm 00080
Fmt 4703
Sfmt 4703
Rockville, MD 20857 and e-mail a copy
to summer.king@samhsa.hhs.gov.
E:\FR\FM\17NON1.SGM
17NON1
Federal Register / Vol. 74, No. 220 / Tuesday, November 17, 2009 / Notices
Written comments should be received
within 60 days of this notice.
Dated: November 10, 2009.
Elaine Parry,
Director, Office of Program Services.
[FR Doc. E9–27523 Filed 11–16–09; 8:45 am]
BILLING CODE 4162–20–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2009–N–0664]
National Mammography Quality
Assurance Advisory Committee;
Notice of Meeting
AGENCY:
Food and Drug Administration,
HHS.
mstockstill on DSKH9S0YB1PROD with NOTICES
ACTION:
Notice.
This notice announces a forthcoming
meeting of a public advisory committee
of the Food and Drug Administration
(FDA). The meeting will be open to the
public.
Name of Committee: National
Mammography Quality Assurance
Advisory Committee.
General Function of the Committee:
To provide advice and
recommendations to the agency on
FDA’s regulatory issues.
Date and Time: The meeting will be
held on January 25, 2010, from 9 a.m.
to 5 p.m.
Location: Holiday Inn, WalkerWhetstone Ballroom, Two Montgomery
Village Ave., Gaithersburg, MD.
Contact Person: Normica Facey, Food
and Drug Administration, 10903 New
Hampshire Ave., Silver Spring, MD
20993, 301–796–5914, or FDA Advisory
Committee Information Line, 1–800–
741–8138 (301–443–0572 in the
Washington, DC area), code
3014512397. Please call the Information
Line for up-to-date information on this
meeting. A notice in the Federal
Register about last minute modifications
that impact a previously announced
advisory committee meeting cannot
always be published quickly enough to
provide timely notice. Therefore, you
should always check the agency’s Web
site and call the appropriate advisory
committee hot line/phone line to learn
about possible modifications before
coming to the meeting.
Agenda: On January 25, 2010, the
committee will discuss guidance
documents issued since the last
meeting. The committee will also
receive updates on: Interventional
mammography accreditation programs,
recently approved alternative standards,
VerDate Nov<24>2008
20:50 Nov 16, 2009
Jkt 220001
facility inspection findings, the status of
current inspection followup actions,
and the radiological health program.
FDA intends to make background
material available to the public no later
than 2 business days before the meeting.
If FDA is unable to post the background
material on its Web site prior to the
meeting, the background material will
be made publicly available at the
location of the advisory committee
meeting, and the background material
will be posted on FDA’s Web site after
the meeting. Background material is
available at https://www.fda.gov/
AdvisoryCommittees/Calendar/
default.htm. Scroll down to the
appropriate advisory committee link.
Procedure: Interested persons may
present data, information, or views,
orally or in writing, on issues pending
before the committee. Written
submissions may be made to the contact
person on or before January 4, 2010.
Oral presentations from the public will
be scheduled between approximately
9:30 a.m. and 10:30 a.m. Those desiring
to make formal oral presentations
should notify the contact person and
submit a brief statement of the general
nature of the evidence or arguments
they wish to present, the names and
addresses of proposed participants, and
an indication of the approximate time
requested to make their presentation on
or before December 28, 2009. Time
allotted for each presentation may be
limited. If the number of registrants
requesting to speak is greater than can
be reasonably accommodated during the
scheduled open public hearing session,
FDA may conduct a lottery to determine
the speakers for the scheduled open
public hearing session. The contact
person will notify interested persons
regarding their request to speak by
December 29, 2009.
Persons attending FDA’s advisory
committee meetings are advised that the
agency is not responsible for providing
access to electrical outlets.
FDA welcomes the attendance of the
public at its advisory committee
meetings and will make every effort to
accommodate persons with physical
disabilities or special needs. If you
require special accommodations due to
a disability, please contact AnnMarie
Williams, 301–796–5996, at least 7 days
in advance of the meeting.
FDA is committed to the orderly
conduct of its advisory committee
meetings. Please visit our Web site at
https://www.fda.gov/
AdvisoryCommittees/AboutAdvisory
Committees/ucm111462.htm for
procedures on public conduct during
advisory committee meetings.
PO 00000
Frm 00081
Fmt 4703
Sfmt 4703
59193
Notice of this meeting is given under
the Federal Advisory Committee Act (5
U.S.C. app. 2).
Dated: November 10, 2009.
David Horowitz,
Assistant Commissioner for Policy.
[FR Doc. E9–27492 Filed 11–16–09; 8:45 am]
BILLING CODE 4160–01–S
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2009–N–0664]
Oncologic Drugs Advisory Committee;
Notice of Meeting
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Notice.
This notice announces a forthcoming
meeting of a public advisory committee
of the Food and Drug Administration
(FDA). The meeting will be open to the
public.
Name of Committee: Oncologic Drugs
Advisory Committee.
General Function of the Committee:
To provide advice and
recommendations to the agency on
FDA’s regulatory issues.
Date and Time: The meeting will be
held on December 17, 2009, from 8 a.m.
to 1 p.m.
Location: Hilton Washington DC
North/Gaithersburg, The Ballrooms, 620
Perry Pkwy., Gaithersburg, MD. The
hotel phone number is 301–977–8900.
Contact Person: Nicole Vesely, Center
for Drug Evaluation and Research (HFD–
21), Food and Drug Administration,
5600 Fishers Lane, (for express delivery,
5630 Fishers Lane, rm. 1093) Rockville,
MD 20857, 301–827–6793, fax: 301–
827–6776, e-mail:
nicole.vesely@fda.hhs.gov, or FDA
Advisory Committee Information Line,
1–800–741–8138 (301–443–0572 in the
Washington, DC area), code
3014512542. Please call the Information
Line for up-to-date information on this
meeting. A notice in the Federal
Register about last minute modifications
that impact a previously announced
advisory committee meeting cannot
always be published quickly enough to
provide timely notice. Therefore, you
should always check the agency’s Web
site and call the appropriate advisory
committee hot line/phone line to learn
about possible modifications before
coming to the meeting.
Agenda: On December 17, 2009, the
committee will discuss new drug
application (NDA) 022–555, proposed
E:\FR\FM\17NON1.SGM
17NON1
]]>Agencies
[Federal Register Volume 74, Number 220 (Tuesday, November 17, 2009)]
[Notices]
[Pages 59191-59193]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E9-27523]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Substance Abuse and Mental Health Services Administration
Agency Information Collection Activities: Proposed Collection;
Comment Request
In compliance with Section 3506(c)(2)(A) of the Paperwork Reduction
Act of 1995 concerning opportunity for public comment on proposed
collections of information, the Substance Abuse and Mental Health
Services Administration (SAMHSA) will publish periodic summaries of
proposed projects. To request more information on the proposed projects
or to obtain a copy of the information collection plans, call the
SAMHSA Reports Clearance Officer on (240) 276-1243.
Comments are invited on: (a) Whether the proposed collections of
information are 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 or other
forms of information technology.
Proposed Project: Substance Abuse Prevention and Treatment (SAPT) Block
Grant Uniform Application Guidance and Instructions FY 2011-2013 and
Regulations (OMB No. 0930-0080)--Revision
Sections 1921 through 1935 of the Public Health Service Act (U.S.C.
300x-21 to 300x-35) provide for annual allotments to assist States to
plan, carry out and evaluate activities to prevent and treat substance
abuse and for related activities. Under the provisions of the law,
States may receive allotments only after an application is submitted
and approved by the Secretary, DHHS. For the Federal fiscal years (FY)
2011-FY 2013 Substance Abuse Prevention and Treatment (SAPT) Block
Grant application cycles, SAMHSA will provide States with revised
application guidance and instructions to implement changes made in
accordance with recommendations from the National Association of State
Alcohol and Drug Abuse Directors (NASADAD) and their member States in
the revisions and clarification of data reporting requirements and
instructions.
During negotiations with the States resulting in agreement on the
National Outcome Measures (NOMs) for substance abuse treatment and
prevention, SAMHSA pledged to the States to:
1. Reduce respondent burden;
2. Work with the States to improve performance management of the
SAPT Block Grant;
3. Improve the availability, timeliness, and quality of data
available to Federal, State, and provider administrators of block grant
funded programs.
This revision of the Uniform Application and Regulation for the
SAPT Block Grant takes additional steps toward implementing these
commitments. SAMHSA, in consultation with NASADAD, has provided States
the ability to reduce their application burden by consolidating the FY
2011-FY 2013 State Plan into a 3-year plan. With the exception of the
projected annual budget form, States only would be expected to submit
any proposed revisions to its approved three-year plan but would
otherwise not have to resubmit a State Plan during FY 2012 and FY 2013.
Individual States may reduce their respondent burden further by
selecting the option of using SAMHSA pre-populated tables for Section
IVa and IVb. The data for these tables would be drawn from SAMHSA data
sets known as Drug and Alcohol Services Information System (DASIS)
Treatment Episode Data Set (TEDS) and
[[Page 59192]]
National Survey on Drug Use and Health (NSDUH) by SAMHSA and provided
to the States. In addition, the Web-based Block Grant Application
System now facilitates completion of the provider entity table through
added pre-populated data items. The data for this table would be drawn
from SAMHSA data set known as DASIS National Survey of Substance Abuse
Treatment Services (N-SSATS). SAMHSA will continue to work with NASADAD
and the States to assess the feasibility and usefulness of pre-
populating additional sections of the application with data extracted
from SAMHSA data sets to further reduce respondent burden.
SAMHSA continues to provide the States with the option of reporting
on prevention expenditures utilizing the six primary prevention
strategies or utilizing the Institute of Medicine classification of
Universal, Selective or Indicated. SAMHSA has designed the State
Prevention Framework State Incentive Grant (SPF SIG) competitive
program and funded contracts in States without an SPF SIG to support
data driven prevention planning by the Single State Agencies for
Substance Abuse. States are expected to use the State level data
collected with support from these programs in the planning in section
II of the Uniform Application.
The Uniform Application has been modified to move needs assessment,
planning narrative and future year budget forms into Section II, the FY
2011-FY 2013 Plan section.
In December 2004, SAMHSA and the States agreed on the goal of
having all States reporting the NOMs measures as defined at the meeting
by the end of a 3-year implementation period starting in FY 2005 and
concluding at the end of FY 2007. By January 2006, supportive technical
assistance on information technology design and payment for data
submitted became available by the State Outcomes Measurement and
Management System (SOMMS) program. States who have participated in the
SOMMS/NOMs subcontracts may choose to have their data pre-populated
which would significantly reduce their reporting burden for this
application. During the subsequent three years, SAMHSA in partnership
with the States and all other SAPT Block Grant stakeholders have
continued to work towards improving standards for analyzing and
responding to the results of NOMs data appropriate to each level of
block grant funded administration including Federal, State, and
Provider roles and responsibilities.
SAMHSA realigned resources to address the need for technical
assistance in information technology (IT) and software purchasing to
implement and maintain NOMs data standards. This technical assistance
first became available in September 2006 and IT support continues.
Revisions to the previously-approved Uniform Application resulting
from such stakeholder input reflect the following changes: (1) Section
I, Form 2, ``Table of Contents,'' was revised to appropriately
enumerate the specific items within each section; (2) In Section II,
the former single year ``Intended Use Plan'' is aggregated into a
``Three Year State Plan'' to reduce the States' annual plan reporting
burden. The first ``Three Year Plan'' will cover FYs 2011-2013. In the
next two subsequent years, only revisions or updates to the 3-year plan
will be required in the States' FY 2012 and FY 2013 Uniform
Applications. Planned expenditures of each Federal Fiscal Year award
will still be collected annually; (3) In Section II, the Form formerly
specified as Form 12 has been removed; (4) In Section III, Narratives
covering the Federal requirements, financial expenditure reports and
services utilization reports are consolidated into the ``Annual Report
Section''; (5) In Section IV subparts IVa and IVb, Treatment and
Prevention Performance Reporting Forms are maintained and are to be
completed annually.
The total annual reporting burden estimate is shown below:
FY 2011
----------------------------------------------------------------------------------------------------------------
Number of
Number of Responses per hours per Total hours
respondents respondent response
----------------------------------------------------------------------------------------------------------------
Sections I-III--States and Territories.......... 60 1 * 480 28,800
Section IV-A.................................... 60 1 40 2,400
Section IV-B.................................... 60 1 42.75 2,565
Recordkeeping................................... 60 1 16 960
---------------------------------------------------------------
Total....................................... 60 .............. .............. 34,725
----------------------------------------------------------------------------------------------------------------
* (additional 10 hours per completion of Section II per State due to addition of FYs 2012 and 2013 in ``Three
Year Plan'').
FY 2012 and FY 2013
[Due to the reduction in section II]
----------------------------------------------------------------------------------------------------------------
Number of Responses per Number hours
respondents respondent per response Total hours
----------------------------------------------------------------------------------------------------------------
Sections I-III--States and Territories.......... 60 1 440 26,400
Section IVa..................................... 60 1 40 2,400
Section IVb..................................... 60 1 42.75 2,565
Recordkeeping................................... 60 1 16 960
---------------------------------------------------------------
Total....................................... 60 .............. .............. 32,325
----------------------------------------------------------------------------------------------------------------
* (reduction of approximately 40 hours per respondent due to reductions in response burden for Section II,
``Three Year Plan'').
Average Annual Total Burden is projected to be 33,125 or a decrease
of about 800 hours.
Send comments to Summer King, SAMHSA Reports Clearance Officer,
Room 7-1044, One Choke Cherry Road, Rockville, MD 20857 and e-mail a
copy to summer.king@samhsa.hhs.gov.
[[Page 59193]]
Written comments should be received within 60 days of this notice.
Dated: November 10, 2009.
Elaine Parry,
Director, Office of Program Services.
[FR Doc. E9-27523 Filed 11-16-09; 8:45 am]
BILLING CODE 4162-20-P
