Agency Information Collection Activities: Submission for OMB Review; Comment Request, 48440-48441 [2016-17411]
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Federal Register / Vol. 81, No. 142 / Monday, July 25, 2016 / Notices
Place: The Dupont Circle Hotel, 1500 New
Hampshire Avenue NW., Washington, DC
20036.
Contact Person: Susan Wohler Sunnarborg,
Ph.D., Scientific Review Officer, Office of
Scientific Review/DERA, National, Heart,
Lung, and Blood Institute 6701 Rockledge
Drive, Room 7182, Bethesda, MD 20892
sunnarborgsw@nhlbi.nih.gov
(Catalogue of Federal Domestic Assistance
Program Nos. 93.233, National Center for
Sleep Disorders Research; 93.837, Heart and
Vascular Diseases Research; 93.838, Lung
Diseases Research; 93.839, Blood Diseases
and Resources Research, National Institutes
of Health, HHS)
Dated: July 19, 2016.
Michelle Trout,
Program Analyst, Office of Federal Advisory
Committee Policy.
[FR Doc. 2016–17421 Filed 7–22–16; 8:45 am]
BILLING CODE 4140–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Dated: July 19, 2016.
Michelle Trout,
Program Analyst, Office of Federal Advisory
Committee Policy.
National Institutes of Health
National Heart, Lung, and Blood
Institute; Notice of Meeting
[FR Doc. 2016–17420 Filed 7–22–16; 8:45 am]
BILLING CODE 4140–01–P
Pursuant to section 10(d) of the
Federal Advisory Committee Act, as
amended (5 U.S.C. App.), notice is
hereby given of a meeting of the
National Heart, Lung, and Blood
Advisory Council.
The meeting 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
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 Heart, Lung,
and Blood Advisory Council.
Date: August 30, 2016.
Time: 1:00 p.m. to 3:00 p.m.
Agenda: To review and evaluate grant
applications.
Place: National Institutes of Health, 6701
Rockledge Drive, Room 9100, Bethesda, MD
20892 (Teleconference).
Contact Person: Valerie L. Prenger, Ph.D.,
MPH, Acting Division Director, Division of
mstockstill on DSK3G9T082PROD with NOTICES
Extramural Research Activities, National
Heart, Lung, and Blood Institute, 6701
Rockledge Drive, Room 7214, Bethesda, MD
20892–7924, 301–435–0270, prengerv@
nhlbi.nih.gov.
Any interested person may file written
comments with the committee by forwarding
the statement to the Contact Person listed on
this notice. The statement should include the
name, address, telephone number and when
applicable, the business or professional
affiliation of the interested person.
Information is also available on the
Institute’s/Center’s home page:
www.nhlbi.nih.gov/meetings/nhlbac/
index.htm, where an agenda and any
additional information for the meeting will
be posted when available.
(Catalogue of Federal Domestic Assistance
Program Nos. 93.233, National Center for
Sleep Disorders Research; 93.837, Heart and
Vascular Diseases Research; 93.838, Lung
Diseases Research; 93.839, Blood Diseases
and Resources Research, National Institutes
of Health, HHS)
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Substance Abuse and Mental Health
Services Administration
Agency Information Collection
Activities: Submission for OMB
Review; Comment Request
Periodically, the Substance Abuse and
Mental Health Services Administration
(SAMHSA) will publish a summary of
information collection requests under
OMB review, in compliance with the
Paperwork Reduction Act (44 U.S.C.
Chapter 35). To request a copy of these
documents, call the SAMHSA Reports
Clearance Officer on (240) 276–1243.
Project: Mental Health First Aid
Evaluation-NEW
The Substance Abuse and Mental
Health Services Administration’s
(SAMHSA) Center for Mental Health
Services (CMHS) is requesting approval
from the Office of Management and
Budget (OMB) for new data collection
Number of
respondents
Instrument/Activity
MHFA/YMHFA Pre-Training Survey ....................................
MHFA/YMHFA Post-Training Survey ..................................
MHFA/YMHFA 3-Month Follow-Up Survey .........................
MHFA/YMHFA 6-Month Follow-Up Survey .........................
Qualitative Interviews ...........................................................
VerDate Sep<11>2014
18:27 Jul 22, 2016
Jkt 238001
PO 00000
Frm 00066
Responses
per
respondent
22,800
22,800
19,380
17,100
23
Fmt 4703
Sfmt 4703
activities associated with its Mental
Health First Aid (MHFA) program.
This information is needed to
evaluate implementation of MHFA and
Youth Mental Health First Aid in three
distinct grant programs: Project
Advancing Wellness and Resilience in
Education (AWARE) State Education
Agency (SEA) Cooperative Agreements,
which provide funding to support
MHFA and YMHFA training to state
education agencies; Project AWARE
Local Education Agency (LEA) Grants,
which provide funding to school
districts; and Project AWARE
Community (C), a new funding
opportunity in fiscal year 2015 that is
intended to support MHFA and YMHFA
training through a wide range of
community organizations.
The MHFA/YMHFA evaluation will
address both overarching and programspecific questions related to the
implementation and effectiveness of
widespread dissemination of mental
health literacy programs through these
three distinct funding mechanisms and
increase SAMHSA’s understanding of
training, referral benefits, and issues in
varied milieu (e.g., implementation
climate, leadership). These evaluation
questions are essential to address
because, although MHFA/YMHFA has a
track record and well-articulated theory
of action, it is vital for SAMHSA to be
able to identify factors that are expected
to increase or decrease the extent
MHFA/YMHFA is disseminated and
implemented with quality.
This data collection is covered under
the requirements of Public Law 103–62,
the Government Performance and
Results Act (GPRA) of 1993, Title 38,
section 527, Evaluation and Data
Collection, as well as 38 CFR 1.15,
Standards for Program Evaluation.
SAMHSA is requesting clearance for
four data collection instruments:
(1) MHFA/YMHFA Pre-Training
Survey
(2) MHFA/YMHFA Post-Training
Survey
(3) MHFA/YMHFA 3-Month and 6Month Follow-Up Survey
(4) Qualitative protocol for interviews
with site coordinators
The table below reflects the
annualized hourly burden.
Total
responses
1
1
1
1
1
E:\FR\FM\25JYN1.SGM
22,800
22,800
19,380
17,100
23
25JYN1
Hours per
response
.33
.25
.17
.17
.75
Total burden
hours
7,524
5,700
3,294
2,907
17.25
Federal Register / Vol. 81, No. 142 / Monday, July 25, 2016 / Notices
Number of
respondents
Instrument/Activity
Total ..............................................................................
Written comments and
recommendations concerning the
proposed information collection should
be sent by August 24, 2016 to the
SAMHSA Desk Officer at the Office of
Information and Regulatory Affairs,
Office of Management and Budget
(OMB). To ensure timely receipt of
comments, and to avoid potential delays
in OMB’s receipt and processing of mail
sent through the U.S. Postal Service,
commenters are encouraged to submit
their comments to OMB via email to:
OIRA_Submission@omb.eop.gov.
Although commenters are encouraged to
send their comments via email,
commenters may also fax their
comments to: 202–395–7285.
Commenters may also mail them to:
Office of Management and Budget,
Office of Information and Regulatory
Affairs, New Executive Office Building,
Room 10102, Washington, DC 20503.
Summer King,
Statistician.
[FR Doc. 2016–17411 Filed 7–22–16; 8:45 am]
BILLING CODE 4162–20–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Substance Abuse and Mental Health
Services Administration
Current List of HHS-Certified
Laboratories and Instrumented Initial
Testing Facilities Which Meet Minimum
Standards To Engage in Urine Drug
Testing for Federal Agencies
Substance Abuse and Mental
Health Services Administration, HHS.
AGENCY:
ACTION:
Notice.
The Department of Health and
Human Services (HHS) notifies federal
agencies of the laboratories and
Instrumented Initial Testing Facilities
(IITF) currently certified to meet the
standards of the Mandatory Guidelines
for Federal Workplace Drug Testing
Programs (Mandatory Guidelines). The
Mandatory Guidelines were first
published in the Federal Register on
April 11, 1988 (53 FR 11970), and
subsequently revised in the Federal
Register on June 9, 1994 (59 FR 29908);
September 30, 1997 (62 FR 51118);
April 13, 2004 (69 FR 19644); November
25, 2008 (73 FR 71858); December 10,
mstockstill on DSK3G9T082PROD with NOTICES
SUMMARY:
VerDate Sep<11>2014
18:27 Jul 22, 2016
Jkt 238001
22,823
Responses
per
respondent
........................
2008 (73 FR 75122); and on April 30,
2010 (75 FR 22809).
A notice listing all currently HHScertified laboratories and IITFs is
published in the Federal Register
during the first week of each month. If
any laboratory or IITF certification is
suspended or revoked, the laboratory or
IITF will be omitted from subsequent
lists until such time as it is restored to
full certification under the Mandatory
Guidelines.
If any laboratory or IITF has
withdrawn from the HHS National
Laboratory Certification Program (NLCP)
during the past month, it will be listed
at the end and will be omitted from the
monthly listing thereafter.
This notice is also available on the
Internet at https://www.samhsa.gov/
workplace.
FOR FURTHER INFORMATION CONTACT:
Giselle Hersh, Division of Workplace
Programs, SAMHSA/CSAP, 5600
Fishers Lane, Room 16N03A, Rockville,
Maryland 20857; 240–276–2600 (voice).
SUPPLEMENTARY INFORMATION: The
Mandatory Guidelines were initially
developed in accordance with Executive
Order 12564 and section 503 of Public
Law 100–71. The ‘‘Mandatory
Guidelines for Federal Workplace Drug
Testing Programs,’’ as amended in the
revisions listed above, requires strict
standards that laboratories and IITFs
must meet in order to conduct drug and
specimen validity tests on urine
specimens for federal agencies.
To become certified, an applicant
laboratory or IITF must undergo three
rounds of performance testing plus an
on-site inspection. To maintain that
certification, a laboratory or IITF must
participate in a quarterly performance
testing program plus undergo periodic,
on-site inspections.
Laboratories and IITFs in the
applicant stage of certification are not to
be considered as meeting the minimum
requirements described in the HHS
Mandatory Guidelines. A HHS-certified
laboratory or IITF must have its letter of
certification from HHS/SAMHSA
(formerly: HHS/NIDA), which attests
that it has met minimum standards.
In accordance with the Mandatory
Guidelines dated November 25, 2008
(73 FR 71858), the following HHScertified laboratories and IITFs meet the
minimum standards to conduct drug
PO 00000
Frm 00067
Fmt 4703
Total
responses
Sfmt 4703
82,103
Hours per
response
........................
48441
Total burden
hours
19,442
and specimen validity tests on urine
specimens:
HHS-Certified Instrumented Initial
Testing Facilities
Dynacare, 6628 50th Street NW.,
Edmonton, AB Canada T6B 2N7, 780–
784–1190 (Formerly: GammaDynacare Medical Laboratories)
HHS-Certified Laboratories
ACM Medical Laboratory, Inc., 160
Elmgrove Park, Rochester, NY 14624,
585–429–2264
Aegis Analytical Laboratories, Inc., 345
Hill Ave., Nashville, TN 37210, 615–
255–2400 (Formerly: Aegis Sciences
Corporation, Aegis Analytical
Laboratories, Inc., Aegis Analytical
Laboratories)
Alere Toxicology Services, 1111 Newton
St., Gretna, LA 70053, 504–361–8989/
800–433–3823 (Formerly: Kroll
Laboratory Specialists, Inc.,
Laboratory Specialists, Inc.)
Alere Toxicology Services, 450
Southlake Blvd., Richmond, VA
23236, 804–378–9130 (Formerly:
Kroll Laboratory Specialists, Inc.,
Scientific Testing Laboratories, Inc.;
Kroll Scientific Testing Laboratories,
Inc.)
Baptist Medical Center-Toxicology
Laboratory, 11401 I–30, Little Rock,
AR 72209–7056, 501–202–2783
(Formerly: Forensic Toxicology
Laboratory Baptist Medical Center)
Clinical Reference Lab, 8433 Quivira
Road, Lenexa, KS 66215–2802, 800–
445–6917
DrugScan, Inc., 200 Precision Road,
Suite 200, Horsham, PA 19044, 800–
235–4890
Dynacare,* 245 Pall Mall Street,
London, ONT, Canada N6A 1P4, 519–
679–1630 (Formerly: GammaDynacare Medical Laboratories)
ElSohly Laboratories, Inc., 5 Industrial
Park Drive, Oxford, MS 38655, 662–
236–2609
Fortes Laboratories, Inc., 25749 SW.
Canyon Creek Road, Suite 600,
Wilsonville, OR 97070, 503–486–1023
Laboratory Corporation of America
Holdings, 7207 N. Gessner Road,
Houston, TX 77040, 713–856–8288/
800–800–2387
Laboratory Corporation of America
Holdings, 69 First Ave., Raritan, NJ
08869, 908–526–2400/800–437–4986
(Formerly: Roche Biomedical
Laboratories, Inc.)
E:\FR\FM\25JYN1.SGM
25JYN1
Agencies
[Federal Register Volume 81, Number 142 (Monday, July 25, 2016)]
[Notices]
[Pages 48440-48441]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2016-17411]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Substance Abuse and Mental Health Services Administration
Agency Information Collection Activities: Submission for OMB
Review; Comment Request
Periodically, the Substance Abuse and Mental Health Services
Administration (SAMHSA) will publish a summary of information
collection requests under OMB review, in compliance with the Paperwork
Reduction Act (44 U.S.C. Chapter 35). To request a copy of these
documents, call the SAMHSA Reports Clearance Officer on (240) 276-1243.
Project: Mental Health First Aid Evaluation-NEW
The Substance Abuse and Mental Health Services Administration's
(SAMHSA) Center for Mental Health Services (CMHS) is requesting
approval from the Office of Management and Budget (OMB) for new data
collection activities associated with its Mental Health First Aid
(MHFA) program.
This information is needed to evaluate implementation of MHFA and
Youth Mental Health First Aid in three distinct grant programs: Project
Advancing Wellness and Resilience in Education (AWARE) State Education
Agency (SEA) Cooperative Agreements, which provide funding to support
MHFA and YMHFA training to state education agencies; Project AWARE
Local Education Agency (LEA) Grants, which provide funding to school
districts; and Project AWARE Community (C), a new funding opportunity
in fiscal year 2015 that is intended to support MHFA and YMHFA training
through a wide range of community organizations.
The MHFA/YMHFA evaluation will address both overarching and
program-specific questions related to the implementation and
effectiveness of widespread dissemination of mental health literacy
programs through these three distinct funding mechanisms and increase
SAMHSA's understanding of training, referral benefits, and issues in
varied milieu (e.g., implementation climate, leadership). These
evaluation questions are essential to address because, although MHFA/
YMHFA has a track record and well-articulated theory of action, it is
vital for SAMHSA to be able to identify factors that are expected to
increase or decrease the extent MHFA/YMHFA is disseminated and
implemented with quality.
This data collection is covered under the requirements of Public
Law 103-62, the Government Performance and Results Act (GPRA) of 1993,
Title 38, section 527, Evaluation and Data Collection, as well as 38
CFR 1.15, Standards for Program Evaluation.
SAMHSA is requesting clearance for four data collection
instruments:
(1) MHFA/YMHFA Pre-Training Survey
(2) MHFA/YMHFA Post-Training Survey
(3) MHFA/YMHFA 3-Month and 6-Month Follow-Up Survey
(4) Qualitative protocol for interviews with site coordinators
The table below reflects the annualized hourly burden.
----------------------------------------------------------------------------------------------------------------
Number of Responses per Total Hours per Total burden
Instrument/Activity respondents respondent responses response hours
----------------------------------------------------------------------------------------------------------------
MHFA/YMHFA Pre-Training Survey.. 22,800 1 22,800 .33 7,524
MHFA/YMHFA Post-Training Survey. 22,800 1 22,800 .25 5,700
MHFA/YMHFA 3-Month Follow-Up 19,380 1 19,380 .17 3,294
Survey.........................
MHFA/YMHFA 6-Month Follow-Up 17,100 1 17,100 .17 2,907
Survey.........................
Qualitative Interviews.......... 23 1 23 .75 17.25
[[Page 48441]]
Total....................... 22,823 .............. 82,103 .............. 19,442
----------------------------------------------------------------------------------------------------------------
Written comments and recommendations concerning the proposed
information collection should be sent by August 24, 2016 to the SAMHSA
Desk Officer at the Office of Information and Regulatory Affairs,
Office of Management and Budget (OMB). To ensure timely receipt of
comments, and to avoid potential delays in OMB's receipt and processing
of mail sent through the U.S. Postal Service, commenters are encouraged
to submit their comments to OMB via email to:
OIRA_Submission@omb.eop.gov. Although commenters are encouraged to send
their comments via email, commenters may also fax their comments to:
202-395-7285. Commenters may also mail them to: Office of Management
and Budget, Office of Information and Regulatory Affairs, New Executive
Office Building, Room 10102, Washington, DC 20503.
Summer King,
Statistician.
[FR Doc. 2016-17411 Filed 7-22-16; 8:45 am]
BILLING CODE 4162-20-P