Agency Information Collection Activities: Proposed Collection; Comment Request, 51283-51285 [E9-24017]
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Federal Register / Vol. 74, No. 192 / Tuesday, October 6, 2009 / Notices
The regulations contain information
collection requirements. The Act
authorizes funds to support activities on
behalf of individuals with significant
(severe) mental illness (adults) or
emotional impairment (children/youth)
[42 U.S.C. 10802(4)]. Only entities that
are designated by the governor of each
State, the five (5) territories (American
Samoa, Guam, the Northern Mariana
Islands, Puerto Rico, and the U.S. Virgin
Islands), the American Indian
Consortium (the Hopi and Navajo
Nations in the Southwest), and the
Mayor of the District of Columbia to
protect and advocate the rights of
persons with developmental disabilities
under Title I, Subtitle C—Protection and
Advocacy of Individual Rights, the
Developmental Disabilities Assistance
and Bill of Rights Act of 2000 (42 U.S.C.
150041 et seq.) are eligible to receive
PAIMI Program grants [42 U.S.C. at
10802(2)]. These grants are based on a
formula prescribed by the Secretary at
42 U.S.C. at 10822(a)(1)(A).
On January 1, each eligible State
protection and advocacy (P&A) system
is required to prepare a report that
describes its activities,
accomplishments, and expenditures to
protect the rights of individuals with
mental illness supported with payments
from PAIMI Program allotments during
the most recently completed fiscal year.
• Specification of the number of
systems that are public and nonprofit
systems established with PAIMI
Program allotments;
• Recommendations for activities and
services to improve the protection and
advocacy of the rights of individuals
with mental illness and a description of
the need for such activities and services
that were not met by the State P&A
systems established under the PAIMI
Act due to resource or annual program
priority limitations.
** [The PAIMI Rules at 42 CFR Part
51 at section 51.32(b), state that P&A
systems may place restrictions on case
or client acceptance criteria developed
as part of its annual PAIMI priorities.
Each P&A system is required to inform
prospective clients of any such
restrictions when he/she requests a
service].
This PAIMI PPR summary must
include a separate section, prepared by
the PAIMI Advisory Council (PAC) that
describes the council’s activities and its
assessment of the operations of the State
P&A system at 42 U.S.C. 10805(7).
The burden estimate for the annual
State P&A system reporting
requirements for these regulations is as
follows:
The PAIMI Act at 42 U.S.C. 10824(a)
requires that each P&A system transmit
a copy of its annual report to the
Secretary (via SAMHSA/CMHS) and to
the State Mental Health Agency where
the system is located. These annual
PAIMI Program Performance Reports
(PPR) to the Secretary must include the
following information:
• The number of (PAIMI-eligible)
individuals with mental illness served;
• A description of the types of
activities undertaken;
• A description of the types of
facilities providing care or treatment to
which such activities are undertaken;
• A description of the manner in
which the activities are initiated;
• A description of the
accomplishments resulting from such
activities;
• A description of systems to protect
and advocate the rights of individuals
with mental illness supported with
payments from PAIMI Program
allotments;
• A description of activities
conducted by States to protect and
advocate such rights;
• A description of mechanisms
established by residential facilities for
individuals with mental illness to
protect such rights; and
• A description of the coordination
among such systems, activities and
mechanisms;
Number of
respondents
42 CFR citation
Responses
per
respondent
Burden per
response
(hrs.)
Total annual
burden
57
57
1
1
26.0
10.0
1 1,482
51.23(c) Reports, materials and fiscal data provided to the PAC ...................
51.25(b)(2) Grievance Procedures ..................................................................
6
6
57
57
1
3
1
1
8.0
2.0
1.0
.5
56
42
57
29
Total ...................................................................................................
126
........................
........................
184
51.(8)(a)(2) Program Performance Report ......................................................
51.8(8)(a)(8) Advisory Council Report .............................................................
51.10 Remedial Actions.
Corrective Action Plans Implementation Status Report ...........................
1 Burden
hours associated with these reports are approved under OMB Control No. 0930–0169.
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.
jlentini on DSKJ8SOYB1PROD with NOTICES
1 570
Dated: September 28, 2009.
Elaine Parry,
Director, Office of Program Services.
[FR Doc. E9–24019 Filed 10–5–09; 8:45 am]
BILLING CODE 4162–20–P
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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
PO 00000
Frm 00031
Fmt 4703
Sfmt 4703
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)
E:\FR\FM\06OCN1.SGM
06OCN1
51284
Federal Register / Vol. 74, No. 192 / Tuesday, October 6, 2009 / Notices
jlentini on DSKJ8SOYB1PROD with NOTICES
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.
Project: Addiction Technology Transfer
Centers (ATTC) Network Program
Monitoring (OMB No. 0930–0216)—
Revision
The Substance Abuse and Mental
Health Administration’s (SAMHSA)
Center for Substance Abuse Treatment
(CSAT) will continue to monitor
program performance of its Addiction
Technology Transfer Centers (ATTCs).
The ATTCs disseminate current health
services research from the National
Institute on Drug Abuse, National
Institute on Alcohol Abuse and
Alcoholism, National Institute of Mental
Health, Agency for Health Care Policy
and Research, National Institute of
Justice, and other sources, as well as
other SAMHSA programs. To
accomplish this, the ATTCs develop
and update State-of-the-art, researchbased curricula and professional
development training.
Each of the forms is described below.
SAMHSA/CSAT is proposing to revise
the Event Description and Post-Event
forms currently used by the ATTCs. The
Follow-Up forms will not be changed.
The Pre-Events forms currently in use
will be eliminated.
Sixty percent of the forms are
administered in person to participants
at educational and training events, who
complete the forms by paper and pencil.
Ten percent of the training courses are
online, and thus, those forms are
administered online. The remaining
thirty percent is made up of 30-day
follow-up forms that are distributed to
consenting participants via electronic
mail using an online survey tool.
(1) The Event Description Form will
be revised. The form collects event
information. It includes questions
regarding the SAMHSA priority areas
and cross-cutting principles covered by
the content of the event. SAMHSA’s
priority areas and cross-cutting
principles have been revised since this
form was approved, so the form will be
revised to match the updated priorities
and principles. In addition, the Event
Description Form asks which of
SAMHSA’s Technical Assistance
Publications (TAPs) and Treatment
Improvement Protocols (TIPs) were used
during the event. New TIPs and TAPs
have been published since the form was
approved. Those new TIPs and TAPs
will be added to the form.
(2) The Pre-Event Form for meetings,
technical assistance events, and training
events will be eliminated. The
VerDate Nov<24>2008
16:15 Oct 05, 2009
Jkt 220001
demographic information that was
collected on this form will be added to
the Post-Event Forms. By incorporating
this demographic information on the
Post-Event Forms, the Pre-Event Form
can be eliminated, thereby reducing the
response burden for participants.
(3) The Post-Event Form for all events
will be revised. The five current
demographic questions will be revised
to reflect a more current understanding
of the field, and five additional
demographic questions will be
included.
(4) The Follow-Up Form for all events
will remain the same as the ones
currently in use by the ATTCs.
Event Description: The event
description form asks approximately 10
questions of the ATTC faculty/staff for
each of the ATTC events. The approved
form asks the event focus, format, and
publications to be used in the event. As
noted above, it will be revised to reflect
updates to SAMHSA’s priority areas and
cross-cutting principles and the
publication of new TIPs and TAPs.
Technical Assistance and Meeting
Events Forms
The ATTCs provide technical
assistance, which is a jointly planned
consultation generally involving a series
of contacts between the ATTC and an
outside organization/institution during
which the ATTC provides expertise and
gives direction toward resolving a
problem or improving conditions. The
ATTCs hold meetings, which are ATTC
sponsored or co-sponsored events in
which a group of people representing
one or more agencies other than the
ATTC work cooperatively on a project,
problem, and/or a policy. The ATTCs
will collect satisfaction measures after
each technical assistance and meeting
event. The ATTCs will base the PostEvent Form on the approved CSAT
Government Performance and Results
Act (GPRA) Customer Satisfaction form
(OMB #0930–0197). The only revision
to this GPRA form will be that the
ATTCs will revise the five current
demographic questions asked on this
form and include five additional
demographic questions. The ATTCs will
collect satisfaction measures 30 days
after each event by using the approved
CSAT Government Performance and
Results Act (GPRA) Customer
Satisfaction form (OMB #0930–0197).
The ATTCs are eliminating the
Technical Assistance and Meeting PreEvent Forms currently in use.
Post-Event Form for Technical
Assistance and Meetings: The PostEvent Information form for technical
assistance and meetings asks
approximately 25 questions of each
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Sfmt 4703
individual that participated in the
event. The current form asks the
participants to report satisfaction with
the quality of the event and event
materials, and to assess their level of
skills in the topic area. The five current
demographic questions on the form will
be revised to reflect a more current
understanding of the field, and five
additional demographic questions will
be included. The form will ask
participants to report demographic
information, education, profession, field
of study, status of certification or
licensure, workplace role, and
employment setting.
30-Day Follow-Up Form for Technical
Assistance and Meetings: The Followup Information Form for technical
assistance and meetings asks about 20
questions of about 25% of consenting
participants. The approved form asks
the participants to report satisfaction
with the quality of the event materials,
to assess their level of skills in the topic
area, and to report whether or not they
have shared information from the event
at their place of work. This form is
already approved by OMB and will not
be revised (OMB #0930–0197).
Training Forms
Trainings are defined as ATTC
sponsored or co-sponsored events,
mainly focusing on the enhancement of
knowledge and/or skills of counselors
and other professionals who work with
individuals with substance use
disorder-related problems. The ATTCs
will collect information from training
participants at the end of the training
event by using a revised version of the
currently approved Post-Event Form for
training. The current approval for this
form is under OMB #0930–0216. The
only revision to this Post-Event Form
will be that the ATTCs will revise the
five current demographic questions
asked and include five additional
demographic questions. The ATTCs will
collect information from training
participants 30 days after the training
event by using the same form currently
approved for this purpose under OMB
#0930–0216. The Pre-Event Form for
training will be eliminated.
Post-Event Form for Training: The
Post- Form for Training asks
approximately 25 questions of each
individual that participated in the
training. The approved form asks the
participants to report satisfaction with,
usefulness of, and quality of the training
and training materials as well as to
assess their level of skills in the topic
area. The five current demographic
questions on the form will be revised to
reflect a more current understanding of
the field, and five additional
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51285
Federal Register / Vol. 74, No. 192 / Tuesday, October 6, 2009 / Notices
demographic questions will be
included. The form will ask participants
to report demographic information,
education, profession, field of study,
status of certification or licensure,
workplace role, and employment
setting.
Follow-up Form for Training: The
Follow-up Information Form for
Training asks about 25 questions of
about 25% of consenting participants.
The approved form asks the participants
to report satisfaction with, usefulness of,
and quality of the training and training
materials as well as to assess their level
of skills in the topic area. The form also
asks participants to report whether or
not they have shared information from
the event at their place of work and
which, if any, barriers they have
encountered to applying the information
gained from the training. This form is
already approved by OMB and will not
be revised (OMB #0930–0216).
The information collected on the
ATTC forms will assist CSAT in
documenting the numbers and types of
participants in ATTC events, describing
Number of
respondents
Type of respondent
Faculty/staff Event Description Form ...............................................................
Meeting and Technical Assistance Participants:
Post-Event Form .......................................................................................
Follow-up Form .........................................................................................
Responses
per
respondent
250
Hours per
response
1
30,000
7,500
Total ...................................................................................................
42,750
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: September 28, 2009.
Elaine Parry,
Director, Office of Program Services.
[FR Doc. E9–24017 Filed 10–5–09; 8:45 am]
BILLING CODE 4162–20–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
[Docket No. FDA–2009–N–0163]
Agency Information Collection
Activities; Submission for Office of
Management and Budget Review;
Comment Request; Draft Guidance,
Emergency Use Authorization of
Medical Products
AGENCY:
In
compliance with 44 U.S.C. 3507, FDA
has submitted the following proposed
collection of information to OMB for
review and clearance.
SUPPLEMENTARY INFORMATION:
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.
VerDate Nov<24>2008
16:15 Oct 05, 2009
Jkt 220001
DATES: Fax written comments on the
collection of information by November
5, 2009.
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:
202–395–6974, or e-mailed to
oira_submission@omb.eop.gov. All
comments should be identified with the
OMB Control Number 0910–0595. Also
include the FDA docket number found
in brackets in the heading of this
document.
FOR FURTHER INFORMATION CONTACT:
Jonna Capezzuto, Office of Information
Management (HFA–710), Food and Drug
Administration, 5600 Fishers Lane,
Rockville, MD 20857, 301–796–3794,
JonnaLynn.Capezzuto@fda.hhs.gov.
Food and Drug Administration
Draft Guidance, Emergency Use
Authorization of Medical Products—
(OMB Control Number 0910–0595)—
Extension
The draft guidance describes the
agency’s general recommendations and
procedures for issuance of emergency
use authorizations (EUA) under section
564 of the Federal Food, Drug, and
Cosmetic Act (the act) (21 U.S.C.
PO 00000
Frm 00033
Fmt 4703
.25
Total annual
burden hours
62.50
5,000
1
.12
600
Covered under CSAT Government Performance and Results Act
(GPRA) Customer Satisfaction form (OMB #0930–0197)
Training Participants:
Post-Event Form .......................................................................................
Follow-up Form .........................................................................................
jlentini on DSKJ8SOYB1PROD with NOTICES
the extent to which participants report
improvement in their clinical
competency, and which method is most
effective in disseminating knowledge to
various audiences. This type of
information is crucial to support CSAT
in complying with GPRA reporting
requirements and will inform future
development of knowledge
dissemination activities.
The chart below summarizes the
annualized burden for this project.
Sfmt 4703
1
1
.16
.16
4,800
1,200
6,662.50
360bbb–3), which was amended by the
Project BioShield Act of 2004 (Pub. L.
108–276). The act permits the FDA
Commissioner (the Commissioner) to
authorize the use of unapproved
medical products or unapproved uses of
approved medical products during an
emergency declared under section 564
of the act. The data to support issuance
of an EUA must demonstrate that, based
on the totality of the scientific evidence
available to the Commissioner,
including data from adequate and wellcontrolled clinical trials (if available), it
is reasonable to believe that the product
may be effective in diagnosing, treating,
or preventing a serious or lifethreatening disease or condition (21
U.S.C. 360bbb–3(c)). Although the exact
type and amount of data needed to
support an EUA may vary depending on
the nature of the declared emergency
and the nature of the candidate product,
FDA recommends that a request for
consideration for an EUA include
scientific evidence evaluating the
product’s safety and effectiveness,
including the adverse event profile for
diagnosis, treatment, or prevention of
the serious or life-threatening disease or
condition, as well as data and other
information on safety, effectiveness,
risks and benefits, and (to the extent
available) alternatives.
Under section 564 of the act, the FDA
Commissioner may establish conditions
on the approval of an EUA. Section
564(e) requires the FDA Commissioner
(to the extent practicable given the
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]]>Agencies
[Federal Register Volume 74, Number 192 (Tuesday, October 6, 2009)]
[Notices]
[Pages 51283-51285]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E9-24017]
-----------------------------------------------------------------------
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)
[[Page 51284]]
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.
Project: Addiction Technology Transfer Centers (ATTC) Network Program
Monitoring (OMB No. 0930-0216)--Revision
The Substance Abuse and Mental Health Administration's (SAMHSA)
Center for Substance Abuse Treatment (CSAT) will continue to monitor
program performance of its Addiction Technology Transfer Centers
(ATTCs). The ATTCs disseminate current health services research from
the National Institute on Drug Abuse, National Institute on Alcohol
Abuse and Alcoholism, National Institute of Mental Health, Agency for
Health Care Policy and Research, National Institute of Justice, and
other sources, as well as other SAMHSA programs. To accomplish this,
the ATTCs develop and update State-of-the-art, research-based curricula
and professional development training.
Each of the forms is described below. SAMHSA/CSAT is proposing to
revise the Event Description and Post-Event forms currently used by the
ATTCs. The Follow-Up forms will not be changed. The Pre-Events forms
currently in use will be eliminated.
Sixty percent of the forms are administered in person to
participants at educational and training events, who complete the forms
by paper and pencil. Ten percent of the training courses are online,
and thus, those forms are administered online. The remaining thirty
percent is made up of 30-day follow-up forms that are distributed to
consenting participants via electronic mail using an online survey
tool.
(1) The Event Description Form will be revised. The form collects
event information. It includes questions regarding the SAMHSA priority
areas and cross-cutting principles covered by the content of the event.
SAMHSA's priority areas and cross-cutting principles have been revised
since this form was approved, so the form will be revised to match the
updated priorities and principles. In addition, the Event Description
Form asks which of SAMHSA's Technical Assistance Publications (TAPs)
and Treatment Improvement Protocols (TIPs) were used during the event.
New TIPs and TAPs have been published since the form was approved.
Those new TIPs and TAPs will be added to the form.
(2) The Pre-Event Form for meetings, technical assistance events,
and training events will be eliminated. The demographic information
that was collected on this form will be added to the Post-Event Forms.
By incorporating this demographic information on the Post-Event Forms,
the Pre-Event Form can be eliminated, thereby reducing the response
burden for participants.
(3) The Post-Event Form for all events will be revised. The five
current demographic questions will be revised to reflect a more current
understanding of the field, and five additional demographic questions
will be included.
(4) The Follow-Up Form for all events will remain the same as the
ones currently in use by the ATTCs.
Event Description: The event description form asks approximately 10
questions of the ATTC faculty/staff for each of the ATTC events. The
approved form asks the event focus, format, and publications to be used
in the event. As noted above, it will be revised to reflect updates to
SAMHSA's priority areas and cross-cutting principles and the
publication of new TIPs and TAPs.
Technical Assistance and Meeting Events Forms
The ATTCs provide technical assistance, which is a jointly planned
consultation generally involving a series of contacts between the ATTC
and an outside organization/institution during which the ATTC provides
expertise and gives direction toward resolving a problem or improving
conditions. The ATTCs hold meetings, which are ATTC sponsored or co-
sponsored events in which a group of people representing one or more
agencies other than the ATTC work cooperatively on a project, problem,
and/or a policy. The ATTCs will collect satisfaction measures after
each technical assistance and meeting event. The ATTCs will base the
Post-Event Form on the approved CSAT Government Performance and Results
Act (GPRA) Customer Satisfaction form (OMB 0930-0197). The
only revision to this GPRA form will be that the ATTCs will revise the
five current demographic questions asked on this form and include five
additional demographic questions. The ATTCs will collect satisfaction
measures 30 days after each event by using the approved CSAT Government
Performance and Results Act (GPRA) Customer Satisfaction form (OMB
0930-0197). The ATTCs are eliminating the Technical Assistance
and Meeting Pre-Event Forms currently in use.
Post-Event Form for Technical Assistance and Meetings: The Post-
Event Information form for technical assistance and meetings asks
approximately 25 questions of each individual that participated in the
event. The current form asks the participants to report satisfaction
with the quality of the event and event materials, and to assess their
level of skills in the topic area. The five current demographic
questions on the form will be revised to reflect a more current
understanding of the field, and five additional demographic questions
will be included. The form will ask participants to report demographic
information, education, profession, field of study, status of
certification or licensure, workplace role, and employment setting.
30-Day Follow-Up Form for Technical Assistance and Meetings: The
Follow-up Information Form for technical assistance and meetings asks
about 20 questions of about 25% of consenting participants. The
approved form asks the participants to report satisfaction with the
quality of the event materials, to assess their level of skills in the
topic area, and to report whether or not they have shared information
from the event at their place of work. This form is already approved by
OMB and will not be revised (OMB 0930-0197).
Training Forms
Trainings are defined as ATTC sponsored or co-sponsored events,
mainly focusing on the enhancement of knowledge and/or skills of
counselors and other professionals who work with individuals with
substance use disorder-related problems. The ATTCs will collect
information from training participants at the end of the training event
by using a revised version of the currently approved Post-Event Form
for training. The current approval for this form is under OMB
0930-0216. The only revision to this Post-Event Form will be
that the ATTCs will revise the five current demographic questions asked
and include five additional demographic questions. The ATTCs will
collect information from training participants 30 days after the
training event by using the same form currently approved for this
purpose under OMB 0930-0216. The Pre-Event Form for training
will be eliminated.
Post-Event Form for Training: The Post- Form for Training asks
approximately 25 questions of each individual that participated in the
training. The approved form asks the participants to report
satisfaction with, usefulness of, and quality of the training and
training materials as well as to assess their level of skills in the
topic area. The five current demographic questions on the form will be
revised to reflect a more current understanding of the field, and five
additional
[[Page 51285]]
demographic questions will be included. The form will ask participants
to report demographic information, education, profession, field of
study, status of certification or licensure, workplace role, and
employment setting.
Follow-up Form for Training: The Follow-up Information Form for
Training asks about 25 questions of about 25% of consenting
participants. The approved form asks the participants to report
satisfaction with, usefulness of, and quality of the training and
training materials as well as to assess their level of skills in the
topic area. The form also asks participants to report whether or not
they have shared information from the event at their place of work and
which, if any, barriers they have encountered to applying the
information gained from the training. This form is already approved by
OMB and will not be revised (OMB 0930-0216).
The information collected on the ATTC forms will assist CSAT in
documenting the numbers and types of participants in ATTC events,
describing the extent to which participants report improvement in their
clinical competency, and which method is most effective in
disseminating knowledge to various audiences. This type of information
is crucial to support CSAT in complying with GPRA reporting
requirements and will inform future development of knowledge
dissemination activities.
The chart below summarizes the annualized burden for this project.
----------------------------------------------------------------------------------------------------------------
Number of Responses per Hours per Total annual
Type of respondent respondents respondent response burden hours
----------------------------------------------------------------------------------------------------------------
Faculty/staff Event Description Form............ 250 1 .25 62.50
Meeting and Technical Assistance Participants: .............. .............. .............. ..............
Post-Event Form............................. 5,000 1 .12 600
Follow-up Form.............................. Covered under CSAT Government Performance and Results Act
(GPRA) Customer Satisfaction form (OMB 0930-0197)
Training Participants: .............. .............. .............. ..............
Post-Event Form............................. 30,000 1 .16 4,800
Follow-up Form.............................. 7,500 1 .16 1,200
---------------------------------------------------------------
Total................................... 42,750 .............. .............. 6,662.50
----------------------------------------------------------------------------------------------------------------
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: September 28, 2009.
Elaine Parry,
Director, Office of Program Services.
[FR Doc. E9-24017 Filed 10-5-09; 8:45 am]
BILLING CODE 4162-20-P
