Proposed Data Collection Submitted for Public Comment and Recommendations, 55362-55364 [2015-23088]
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Federal Register / Vol. 80, No. 178 / Tuesday, September 15, 2015 / Notices
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Abstract: Section 208.63 of Regulation
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procedures reasonably designed to
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are no required reporting forms
associated with this information
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Board of Governors of the Federal Reserve
System, September 10, 2015.
Robert deV. Frierson,
Secretary of the Board.
[FR Doc. 2015–23103 Filed 9–14–15; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60Day–15–15BEZ; Docket No. CDC–2015–
0081]
Proposed Data Collection Submitted
for Public Comment and
Recommendations
Centers for Disease Control and
Prevention (CDC), Department of Health
and Human Services (HHS).
ACTION: Notice with comment period.
AGENCY:
The Centers for Disease
Control and Prevention (CDC), as part of
its continuing efforts to reduce public
burden and maximize the utility of
government information, invites the
general public and other Federal
agencies to take this opportunity to
comment on proposed and/or
continuing information collections, as
required by the Paperwork Reduction
Act of 1995. This notice invites
comment on a newly proposed
information collection request entitled
Improving Fetal Alcohol Spectrum
Disorders Prevention Practice through
Practice and Implementation Centers
and National Partnerships.
DATES: Written comments must be
received on or before November 16,
2015.
ADDRESSES: You may submit comments,
identified by Docket No. CDC–2015–
0081 by any of the following methods:
• Federal eRulemaking Portal:
Regulation.gov. Follow the instructions
for submitting comments.
• Mail: Leroy A. Richardson,
Information Collection Review Office,
Centers for Disease Control and
Prevention, 1600 Clifton Road NE., MS–
D74, Atlanta, Georgia 30329.
Instructions: All submissions received
must include the agency name and
Docket Number. All relevant comments
received will be posted without change
to Regulations.gov, including any
personal information provided. For
access to the docket to read background
documents or comments received, go to
Regulations.gov.
SUMMARY:
Please note: All public comment should be
submitted through the Federal eRulemaking
portal (Regulations.gov) or by U.S. mail to the
address listed above.
FOR FURTHER INFORMATION CONTACT:
To
request more information on the
proposed project or to obtain a copy of
the information collection plan and
instruments, contact the Information
Collection Review Office, Centers for
Disease Control and Prevention, 1600
VerDate Sep<11>2014
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Jkt 235001
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Clifton Road NE., MS–D74, Atlanta,
Georgia 30329; phone: 404–639–7570;
Email: omb@cdc.gov.
SUPPLEMENTARY INFORMATION: Under the
Paperwork Reduction Act of 1995 (PRA)
(44 U.S.C. 3501–3520), Federal agencies
must obtain approval from the Office of
Management and Budget (OMB) for each
collection of information they conduct
or sponsor. In addition, the PRA also
requires Federal agencies to provide a
60-day notice in the Federal Register
concerning each proposed collection of
information, including each new
proposed collection, each proposed
extension of existing collection of
information, and each reinstatement of
previously approved information
collection before submitting the
collection to OMB for approval. To
comply with this requirement, we are
publishing this notice of a proposed
data collection as described below.
Comments are invited on: (a) Whether
the proposed collection of information
is necessary for the proper performance
of the functions of the agency, including
whether the information shall have
practical utility; (b) the accuracy of the
agency’s estimate of the burden of the
proposed collection of information; (c)
ways to enhance the quality, utility, and
clarity of the information to be
collected; (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; and (e) estimates of capital
or start-up costs and costs of operation,
maintenance, and purchase of services
to provide information. Burden means
the total time, effort, or financial
resources expended by persons to
generate, maintain, retain, disclose or
provide information to or for a Federal
agency. This includes the time needed
to review instructions; to develop,
acquire, install and utilize technology
and systems for the purpose of
collecting, validating and verifying
information, processing and
maintaining information, and disclosing
and providing information; to train
personnel and to be able to respond to
a collection of information, to search
data sources, to complete and review
the collection of information; and to
transmit or otherwise disclose the
information.
Proposed Project
Improving Fetal Alcohol Spectrum
Disorders Prevention and Practice
through Practice and Implementation
Centers and National Partnerships—
New—National Center on Birth Defects
and Developmental Disabilities
E:\FR\FM\15SEN1.SGM
15SEN1
55363
Federal Register / Vol. 80, No. 178 / Tuesday, September 15, 2015 / Notices
(NCBDDD), Centers for Disease Control
and Prevention (CDC).
Background and Brief Description
The National Center on Birth Defects
and Developmental Disabilities seeks to
collect training evaluation data from
healthcare practitioners and staff in
health systems where FASD-related
practice and systems changes are
implemented, and grantees of Practice
and Implementation Centers and
national partner organizations related to
prevention, identification, and
treatment of fetal alcohol spectrum
disorders (FASDs).
Prenatal exposure to alcohol is a
leading preventable cause of birth
defects and developmental disabilities.
The term ‘‘fetal alcohol spectrum
disorders’’ describes the full continuum
of effects that can occur in an individual
exposed to alcohol in utero. These
effects include physical, mental,
behavioral, and learning disabilities. All
of these have lifelong implications.
The purpose of this program is to
expand previous efforts from FASD
training programs and shift the
perspective from individual training for
practicing health care professionals to
one that capitalizes on prevention
opportunities and the ability to impact
health care practice at the systems level.
Since 2002, CDC funded FASD
Regional Training Centers (RTCs) to
provide education and training to
healthcare professionals and students
about FASD prevention, identification,
and treatment. In July 2013, CDC
convened an expert review panel to
evaluate the effectiveness of the RTC
program overall and make
recommendations about the program.
The panel highlighted several
accomplishments of the RTCs and
proposed several changes for future
programming: (1) The panel identified a
need for more comprehensive coverage
nationally with discipline-specific
trainings, increased use of technology,
greater collaboration with medical
societies, and stronger linkages with
national partner organizations to
increase the reach of training
opportunities, and (2) The panel
suggested that the training centers focus
on demonstrable practice change and
sustainability and place a stronger
emphasis on primary prevention of
FASDs. In addition, it was
recommended that future initiatives
have stronger evaluation components.
Based on the recommendations of the
expert review panel, CDC is placing
increased focus on prevention,
demonstrating practice change,
achieving national coverage, and
strengthening partnerships between
FASD Practice and Implementation
Centers, or PICs (the newly redesigned
RTCs), and medical societies and
national partner organizations. The
National Organization on Fetal Alcohol
Syndrome (NOFAS) also participates in
this project as a resource to the PICS
and national partners. The PICs and
national partners are asked to closely
collaborate in discipline-specific
workgroups (DSWs) and identify
strategies that will increase the reach of
the program on a national level. While
a major focus of the grantees’ work will
be national, regional approaches will be
used to develop new content and ‘‘test
out’’ feasibility and acceptability of
materials, especially among health care
providers and medical societies. In
addition, CDC is placing a stronger
emphasis on evaluation, with both
individual DSW/NOFAS evaluations
and a cross-site evaluation.
CDC requests OMB approval to collect
program evaluation information from (1)
healthcare practitioners from disciplines
targeted by each DSW, including
training participants, (2) health system
staff, and (3) cooperative agreement
grantees over a three-year period.
• Healthcare practitioners will
complete surveys to provide
information on whether project
trainings impacted their knowledge and
practice behavior regarding FASD
identification, prevention, and
treatment. The information will be used
to improve future trainings and assess
whether knowledge and practice
changes occurred. Some participants
will also complete qualitative key
informant interviews to gain additional
information on practice change.
• Health system employees will be
interviewed as part of high impact
evaluation studies. The high impact
evaluation studies will be focused
assessments of two to three specific
grantee efforts that seem likely to result
in achievement of program objectives.
• Grantees will complete program
evaluation forms to track perceptions of
DSW collaboration and perceptions of
key successes and challenges
encountered by the DSW.
It is estimated that 20,554
respondents will participate in the
evaluation each year, for a total
estimated burden of 4528.0 hours
annually. There are no costs to
respondents other than their time.
ESTIMATED ANNUALIZED BURDEN HOURS
Number of
respondents
Type of respondents
DSW/
Organization
Form name
FASD Core Training Participants.
FASD Core Training Participants.
FASD Core Training Participants.
Project Grantee Staff .........
All ......................................
FASD Core Training Survey—Pre-Test.
FASD Core Training Survey—Post-Test.
FASD Core Training Survey—6 Month Follow-Up.
DSW Report .....................
All ......................................
Nurses ...............................
Westat (Cross-Site Evaluator).
Westat (Cross-Site Evaluator).
Westat (Cross-Site Evaluator).
Westat (Cross-Site Evaluator).
Nursing .............................
Nurses ...............................
Nursing .............................
Project Grantee Staff .........
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All ......................................
National Partner Staff ........
Health System Staff ..........
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Key Informant Interview—
DSW Project Director.
Key Informant Interview—
National Partner.
Key Informant Interview—
Health System Staff.
Key Informant Interviews
with Champions.
Online Survey with
‘‘Friends’’/Members of
the Network.
Frm 00042
Fmt 4703
Sfmt 4703
Number of
responses
per
respondent
Average
burden per
response
(in hours)
4,013
1
15/60
1,003
4,013
1
15/60
1,003
4,013
1
20/60
1,338
90
2
10/60
30
6
3
60/60
18
6
3
60/60
18
60
3
30/60
90
14
1
45/60
10
34
2
15/60
17
E:\FR\FM\15SEN1.SGM
15SEN1
Total
burden
hours
55364
Federal Register / Vol. 80, No. 178 / Tuesday, September 15, 2015 / Notices
ESTIMATED ANNUALIZED BURDEN HOURS—Continued
Number of
respondents
DSW/
Organization
Form name
Healthcare Organization
Representatives.
Nursing .............................
Nurses and Nursing Students.
Nursing .............................
Physicians and students in
allied health professions.
Students in allied health
professions.
Obstetrics & Gynecology ..
Physicians .........................
Obstetrics & Gynecology ..
Physicians .........................
Obstetrics & Gynecology ..
Physicians .........................
Obstetrics & Gynecology ..
Residency Directors, Training Coordinators, Clinic
Directors.
Residency Directors, Training Coordinators, Clinical
Directors, Physicians.
Physicians .........................
Obstetrics & Gynecology ..
Physicians .........................
Pediatrics ..........................
Physicians .........................
Pediatrics ..........................
Physicians .........................
Physicians .........................
Pediatrics ..........................
Social Work & Family Physicians.
Medical and allied health
professionals.
Medical and allied health
professionals.
General public ...................
TOTAL ........................
Number of
responses
per
respondent
Average
burden per
response
(in hours)
67
1
30/60
33
2,934
1
10/60
489
1,200
1
6/60
120
600
1
6/60
60
600
1
6/60
60
600
1
2/60
20
124
1
2/60
4
14
1
30/60
7
Online Survey with
Healthcare Organization
Representatives.
Brief Online Questionnaire
for Nursing Organization
Memberships.
Avatar Training Satisfaction Survey.
Proficiency Ratings
Scale—Standardized
Patient Version.
Proficiency Ratings
Scale—Provider—Baseline.
Proficiency Rating Scale—
Provider—1 Month Follow-Up.
FASD Training Event
Evaluation.
Pre- Assessment of Training Implementation.
Type of respondents
Obstetrics & Gynecology ..
Obstetrics & Gynecology ..
Post-Assessment of Training Implementation.
14
1
30/60
7
Pediatrics ..........................
120
1
15/60
30
535
1
4/60
36
535
1
4/60
36
50
62
1
1
15/60
8/60
13
8
National Organization on
Fetal Alcohol Syndrome.
National Organization on
Fetal Alcohol Syndrome.
National Organization on
Fetal Alcohol Syndrome.
FASD Core Training Survey—Pediatrics 3 Month
Follow-Up.
Pediatrics DSW Baseline
Survey.
Pediatrics DSW Year 4
Survey.
FASD Toolkit User Survey
Family Medicine Comprehensive Practice
Evaluation.
NOFAS Webinar Survey—
Post-Test.
NOFAS Webinar Survey—
3 Month Follow-Up.
NOFAS Outcomes Vignette.
400
1
5/60
33
400
1
5/60
33
50
1
10/60
8
...........................................
...........................................
....................
....................
....................
4,524
Leroy A. Richardson,
Chief, Information Collection Review Office,
Office of Scientific Integrity, Office of the
Associate Director for Science, Office of the
Director, Centers for Disease Control and
Prevention.
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2014–D–0609]
[FR Doc. 2015–23088 Filed 9–14–15; 8:45 am]
Agency Information Collection
Activities; Submission for Office of
Management and Budget Review;
Comment Request; Guidance for
Industry on Drug Supply Chain
Security Act Implementation:
Identification of Suspect Product and
Notification
mstockstill on DSK4VPTVN1PROD with NOTICES
BILLING CODE 4163–18–P
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
VerDate Sep<11>2014
Total
burden
hours
19:04 Sep 14, 2015
Jkt 235001
PO 00000
Notice.
Frm 00043
Fmt 4703
Sfmt 4703
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
(the PRA).
DATES: Fax written comments on the
collection of information by October 15,
2015.
ADDRESSES: To ensure that comments on
the information collection are received,
OMB recommends that written
comments be faxed to the Office of
Information and Regulatory Affairs,
OMB, Attn: FDA Desk Officer, FAX:
202–395–7285, or emailed to oira_
submission@omb.eop.gov. All
comments should be identified with the
SUMMARY:
E:\FR\FM\15SEN1.SGM
15SEN1
]]>Agencies
[Federal Register Volume 80, Number 178 (Tuesday, September 15, 2015)]
[Notices]
[Pages 55362-55364]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2015-23088]
=======================================================================
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[60Day-15-15BEZ; Docket No. CDC-2015-0081]
Proposed Data Collection Submitted for Public Comment and
Recommendations
AGENCY: Centers for Disease Control and Prevention (CDC), Department of
Health and Human Services (HHS).
ACTION: Notice with comment period.
-----------------------------------------------------------------------
SUMMARY: The Centers for Disease Control and Prevention (CDC), as part
of its continuing efforts to reduce public burden and maximize the
utility of government information, invites the general public and other
Federal agencies to take this opportunity to comment on proposed and/or
continuing information collections, as required by the Paperwork
Reduction Act of 1995. This notice invites comment on a newly proposed
information collection request entitled Improving Fetal Alcohol
Spectrum Disorders Prevention Practice through Practice and
Implementation Centers and National Partnerships.
DATES: Written comments must be received on or before November 16,
2015.
ADDRESSES: You may submit comments, identified by Docket No. CDC-2015-
0081 by any of the following methods:
Federal eRulemaking Portal: Regulation.gov. Follow the
instructions for submitting comments.
Mail: Leroy A. Richardson, Information Collection Review
Office, Centers for Disease Control and Prevention, 1600 Clifton Road
NE., MS-D74, Atlanta, Georgia 30329.
Instructions: All submissions received must include the agency name
and Docket Number. All relevant comments received will be posted
without change to Regulations.gov, including any personal information
provided. For access to the docket to read background documents or
comments received, go to Regulations.gov.
Please note: All public comment should be submitted through the
Federal eRulemaking portal (Regulations.gov) or by U.S. mail to the
address listed above.
FOR FURTHER INFORMATION CONTACT: To request more information on the
proposed project or to obtain a copy of the information collection plan
and instruments, contact the Information Collection Review Office,
Centers for Disease Control and Prevention, 1600 Clifton Road NE., MS-
D74, Atlanta, Georgia 30329; phone: 404-639-7570; Email: omb@cdc.gov.
SUPPLEMENTARY INFORMATION: Under the Paperwork Reduction Act of 1995
(PRA) (44 U.S.C. 3501-3520), Federal agencies must obtain approval from
the Office of Management and Budget (OMB) for each collection of
information they conduct or sponsor. In addition, the PRA also requires
Federal agencies to provide a 60-day notice in the Federal Register
concerning each proposed collection of information, including each new
proposed collection, each proposed extension of existing collection of
information, and each reinstatement of previously approved information
collection before submitting the collection to OMB for approval. To
comply with this requirement, we are publishing this notice of a
proposed data collection as described below.
Comments are invited on: (a) Whether the proposed collection of
information is necessary for the proper performance of the functions of
the agency, including whether the information shall have practical
utility; (b) the accuracy of the agency's estimate of the burden of the
proposed collection of information; (c) ways to enhance the quality,
utility, and clarity of the information to be collected; (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; and (e) estimates of capital or start-
up costs and costs of operation, maintenance, and purchase of services
to provide information. Burden means the total time, effort, or
financial resources expended by persons to generate, maintain, retain,
disclose or provide information to or for a Federal agency. This
includes the time needed to review instructions; to develop, acquire,
install and utilize technology and systems for the purpose of
collecting, validating and verifying information, processing and
maintaining information, and disclosing and providing information; to
train personnel and to be able to respond to a collection of
information, to search data sources, to complete and review the
collection of information; and to transmit or otherwise disclose the
information.
Proposed Project
Improving Fetal Alcohol Spectrum Disorders Prevention and Practice
through Practice and Implementation Centers and National Partnerships--
New--National Center on Birth Defects and Developmental Disabilities
[[Page 55363]]
(NCBDDD), Centers for Disease Control and Prevention (CDC).
Background and Brief Description
The National Center on Birth Defects and Developmental Disabilities
seeks to collect training evaluation data from healthcare practitioners
and staff in health systems where FASD-related practice and systems
changes are implemented, and grantees of Practice and Implementation
Centers and national partner organizations related to prevention,
identification, and treatment of fetal alcohol spectrum disorders
(FASDs).
Prenatal exposure to alcohol is a leading preventable cause of
birth defects and developmental disabilities. The term ``fetal alcohol
spectrum disorders'' describes the full continuum of effects that can
occur in an individual exposed to alcohol in utero. These effects
include physical, mental, behavioral, and learning disabilities. All of
these have lifelong implications.
The purpose of this program is to expand previous efforts from FASD
training programs and shift the perspective from individual training
for practicing health care professionals to one that capitalizes on
prevention opportunities and the ability to impact health care practice
at the systems level.
Since 2002, CDC funded FASD Regional Training Centers (RTCs) to
provide education and training to healthcare professionals and students
about FASD prevention, identification, and treatment. In July 2013, CDC
convened an expert review panel to evaluate the effectiveness of the
RTC program overall and make recommendations about the program. The
panel highlighted several accomplishments of the RTCs and proposed
several changes for future programming: (1) The panel identified a need
for more comprehensive coverage nationally with discipline-specific
trainings, increased use of technology, greater collaboration with
medical societies, and stronger linkages with national partner
organizations to increase the reach of training opportunities, and (2)
The panel suggested that the training centers focus on demonstrable
practice change and sustainability and place a stronger emphasis on
primary prevention of FASDs. In addition, it was recommended that
future initiatives have stronger evaluation components.
Based on the recommendations of the expert review panel, CDC is
placing increased focus on prevention, demonstrating practice change,
achieving national coverage, and strengthening partnerships between
FASD Practice and Implementation Centers, or PICs (the newly redesigned
RTCs), and medical societies and national partner organizations. The
National Organization on Fetal Alcohol Syndrome (NOFAS) also
participates in this project as a resource to the PICS and national
partners. The PICs and national partners are asked to closely
collaborate in discipline-specific workgroups (DSWs) and identify
strategies that will increase the reach of the program on a national
level. While a major focus of the grantees' work will be national,
regional approaches will be used to develop new content and ``test
out'' feasibility and acceptability of materials, especially among
health care providers and medical societies. In addition, CDC is
placing a stronger emphasis on evaluation, with both individual DSW/
NOFAS evaluations and a cross-site evaluation.
CDC requests OMB approval to collect program evaluation information
from (1) healthcare practitioners from disciplines targeted by each
DSW, including training participants, (2) health system staff, and (3)
cooperative agreement grantees over a three-year period.
Healthcare practitioners will complete surveys to provide
information on whether project trainings impacted their knowledge and
practice behavior regarding FASD identification, prevention, and
treatment. The information will be used to improve future trainings and
assess whether knowledge and practice changes occurred. Some
participants will also complete qualitative key informant interviews to
gain additional information on practice change.
Health system employees will be interviewed as part of
high impact evaluation studies. The high impact evaluation studies will
be focused assessments of two to three specific grantee efforts that
seem likely to result in achievement of program objectives.
Grantees will complete program evaluation forms to track
perceptions of DSW collaboration and perceptions of key successes and
challenges encountered by the DSW.
It is estimated that 20,554 respondents will participate in the
evaluation each year, for a total estimated burden of 4528.0 hours
annually. There are no costs to respondents other than their time.
Estimated Annualized Burden Hours
--------------------------------------------------------------------------------------------------------------------------------------------------------
Number of Average
Number of responses burden per Total
Type of respondents DSW/ Organization Form name respondents per response burden
respondent (in hours) hours
--------------------------------------------------------------------------------------------------------------------------------------------------------
FASD Core Training Participants.......... All......................... FASD Core Training Survey-- 4,013 1 15/60 1,003
Pre-Test.
FASD Core Training Participants.......... All......................... FASD Core Training Survey-- 4,013 1 15/60 1,003
Post-Test.
FASD Core Training Participants.......... All......................... FASD Core Training Survey-- 4,013 1 20/60 1,338
6 Month Follow-Up.
Project Grantee Staff.................... Westat (Cross-Site DSW Report................. 90 2 10/60 30
Evaluator).
Project Grantee Staff.................... Westat (Cross-Site Key Informant Interview-- 6 3 60/60 18
Evaluator). DSW Project Director.
National Partner Staff................... Westat (Cross-Site Key Informant Interview-- 6 3 60/60 18
Evaluator). National Partner.
Health System Staff...................... Westat (Cross-Site Key Informant Interview-- 60 3 30/60 90
Evaluator). Health System Staff.
Nurses................................... Nursing..................... Key Informant Interviews 14 1 45/60 10
with Champions.
Nurses................................... Nursing..................... Online Survey with 34 2 15/60 17
``Friends''/Members of the
Network.
[[Page 55364]]
Healthcare Organization Representatives.. Nursing..................... Online Survey with 67 1 30/60 33
Healthcare Organization
Representatives.
Nurses and Nursing Students.............. Nursing..................... Brief Online Questionnaire 2,934 1 10/60 489
for Nursing Organization
Memberships.
Physicians and students in allied health Obstetrics & Gynecology..... Avatar Training 1,200 1 6/60 120
professions. Satisfaction Survey.
Students in allied health professions.... Obstetrics & Gynecology..... Proficiency Ratings Scale-- 600 1 6/60 60
Standardized Patient
Version.
Physicians............................... Obstetrics & Gynecology..... Proficiency Ratings Scale-- 600 1 6/60 60
Provider--Baseline.
Physicians............................... Obstetrics & Gynecology..... Proficiency Rating Scale-- 600 1 2/60 20
Provider--1 Month Follow-
Up.
Physicians............................... Obstetrics & Gynecology..... FASD Training Event 124 1 2/60 4
Evaluation.
Residency Directors, Training Obstetrics & Gynecology..... Pre- Assessment of Training 14 1 30/60 7
Coordinators, Clinic Directors. Implementation.
Residency Directors, Training Obstetrics & Gynecology..... Post-Assessment of Training 14 1 30/60 7
Coordinators, Clinical Directors, Implementation.
Physicians.
Physicians............................... Pediatrics.................. FASD Core Training Survey-- 120 1 15/60 30
Pediatrics 3 Month Follow-
Up.
Physicians............................... Pediatrics.................. Pediatrics DSW Baseline 535 1 4/60 36
Survey.
Physicians............................... Pediatrics.................. Pediatrics DSW Year 4 535 1 4/60 36
Survey.
Physicians............................... Pediatrics.................. FASD Toolkit User Survey... 50 1 15/60 13
Physicians............................... Social Work & Family Family Medicine 62 1 8/60 8
Physicians. Comprehensive Practice
Evaluation.
Medical and allied health professionals.. National Organization on NOFAS Webinar Survey--Post- 400 1 5/60 33
Fetal Alcohol Syndrome. Test.
Medical and allied health professionals.. National Organization on NOFAS Webinar Survey--3 400 1 5/60 33
Fetal Alcohol Syndrome. Month Follow-Up.
General public........................... National Organization on NOFAS Outcomes Vignette.... 50 1 10/60 8
Fetal Alcohol Syndrome.
------------
TOTAL................................ ............................ ........................... ........... ........... ........... 4,524
--------------------------------------------------------------------------------------------------------------------------------------------------------
Leroy A. Richardson,
Chief, Information Collection Review Office, Office of Scientific
Integrity, Office of the Associate Director for Science, Office of the
Director, Centers for Disease Control and Prevention.
[FR Doc. 2015-23088 Filed 9-14-15; 8:45 am]
BILLING CODE 4163-18-P
