National Health Education Enhancement Program, 20563-20568 [05-7888]
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Federal Register / Vol. 70, No. 75 / Wednesday, April 20, 2005 / Notices
Officer, Air Pollution and Respiratory
Health Branch, Division of
Environmental Hazards and Health
Effects, National Center for
Environmental Health, Centers for
Disease Control and Prevention, 1600
Clifton Road, NE, Mailstop E–17,
Atlanta, GA 30333, Telephone: 404–
498–1033, E-mail: mmercier@cdc.gov.
For financial, grants management, or
budget assistance, contact: Gary Teague,
Grants Management Specialist, CDC
Procurement and Grants Office, 2920
Brandywine Road, Atlanta, GA 30341,
Telephone: 770–488–1981, E-mail:
GTeague@cdc.gov.
VIII. Other Information
This and other CDC funding
opportunity announcements can be
found on the CDC Web site, Internet
address: https://www.cdc.gov. Click on
‘‘Funding’’ then ‘‘Grants and
Cooperative Agreements.’’
For additional reference materials,
please see Attachments I and II.
Dated: April 14, 2005.
William P. Nichols,
Director, Procurement and Grants Office,
Centers for Disease Control and Prevention.
Attachment I—References
‘‘National Asthma Training Curriculum’’ CD–
ROM educational resource, CDC National
Center for Environmental Health and the
Academy of Allergy, Asthma and
Immunology, August 2004.
‘‘Potentially Effective Interventions for
Asthma’’ https://www.cdc.gov/asthma/
interventions.htm.
Boss, L.; Kreutzer, R.; Luttinger, D.; Leighton,
J.; Wilcox, K.; and Redd, S. ‘‘The Public
Health Surveillance of Asthma,’’ Journal of
Asthma, 38(1), 83–89, 2001.
‘‘Framework for Program Evaluation in
Public Health,’’ Morbidity and Mortality
Weekly Report, September 17, 1999/
48(RR–11); 1–40 at https://www.cdc.gov/
mmwr/preview/mmwrhtml/rr4811a1.htm
or https://www.cdc.gov/eval/
framework.htm.
‘‘Surveillance of Work-Related Asthma in
Selected U.S. States Using Surveillance
Guidelines for State Health Departments—
California, Massachusetts, Michigan and
New Jersey, 1993–1995,’’ Morbidity and
Mortality Weekly Report, June 25, 1999/48
(SS03); 1–20 at https://www.cdc.gov/mmwr/
preview/mmwrhtml/ss4803a1.htm.
‘‘The Role of States in a Nationwide
Comprehensive Surveillance System for
Work-related Diseases, Injuries and
Hazards’’ at https://www.cste.org/
occupationalhealth.htm.
‘‘Minimum and Comprehensive State-Based
Activities in Occupational Safety and
Health,’’ June 1995—DHHS (NIOSH)
Publication No. 95–107 at https://
www.cdc.gov/niosh/95–107.html.
‘‘American Thoracic Society: Occupational
Contribution to the Burden of Airway
Disease,’’ American Journal of Respiratory
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and Critical Care Medicine, 167:787–797,
2003.
‘‘Updated Guidelines for Evaluating
Surveillance Systems, Recommendations
from the Guidelines Working Group,’’
Morbidity and Mortality Weekly Report,
July 27, 2001/(50)RR–13; 1–35 at https://
www.cdc.gov/mmwr/preview/mmwrhtml/
rr5013a1.htm.
Madden, J; Boss, L; Kownaski, M; Lambright,
L; Lee, C; Luttinger, D; Recer, G;
Wedemeyer, C. ‘‘Guide for State Health
Agencies in the Development of Asthma
Programs.’’ Atlanta, Georgia: U.S. Centers
for Disease Control and Prevention, 2003.
‘‘Guidelines for the Diagnosis and
Management of Asthma,’’ (Clinical Practice
Guidelines, Guidelines for the Diagnosis
and Management of Asthma. National
Institutes of Health (NIH), National Heart,
Lung and Blood Institute. NIH publication
No. 97–4051, April 1997) at https://
www.nhlbi.nih.gov/guidelines/asthma/
asthgdln.htm.
‘‘Key Clinical Activities for Quality Asthma
Care: Recommendations of the National
Asthma Education and Prevention
Program.’’ MMWR March 28, 2003;
52(RR06):1–84.
Strategies for addressing asthma in school
settings: https://www.cdc.gov/
HealthyYouth/asthma/.
Attachment II—BRFSS Asthma CallBack Survey
The National Asthma Survey (NAS) is a
comprehensive state/city level detailed
asthma survey. It is administered by phone
and includes respondents of all ages.
Previously the NAS was linked to the
National Immunization Survey (NIS) through
the State and Local Area Integrated
Telephone Survey (SLAITS) mechanism.
SLAITS is a function of the National Center
for Health Statistics. A full questionnaire for
that survey can be viewed on the SLAITS
Web site. https://www.cdc.gov/nchs/about/
major/slaits/nsa.htm.
The initial NAS field test occurred in 2002
in Alabama, California, Illinois and Texas.
This first field test did not achieve an
adequate response rate level. Consequently
additional field tests were implemented to
determine whether procedural changes could
improve the response rate. In 2003, the NAS
was conducted as a field test in the same four
states and also in a national sample.
There were four arms in the 2003 field test.
The national sample and the state sample
were the two main arms. The national sample
obtains demographic information about
respondents who do not have asthma in
order to estimate prevalence rates. The fourstate sample only solicited information from
households that had a member with asthma
and, consequently, prevalence rates cannot
be determined. Results from comparing the
four state results with the first field test will
determine if obtaining prevalence rates
resulted in a significantly lower response
rate. Comparing the national sample with the
first field test in the four states will
determine if the four selected states were
particularly difficult with respect to response
rates as was suggested from the results from
other surveys.
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20563
Each of the two main arms was also
divided into a NIS-connected sample and a
sample independent of the NIS procedures.
Comparisons between these two secondary
arms within each primary arm will determine
if restrictions related to the NIS survey
procedures were detrimental to the NAS
response rate. In addition, several other
modifications were made to simplify the
selection of a single respondent from the
household members.
During 2004 the data obtained were
weighted and scrutinized to determine the
best combination of methodological changes
to ensure that quality data result from further
implementation of the National Asthma
Survey.
In 2005 the NAS will be implemented as
a call-back survey in conjunction with the
Behavioral Risk Factor Surveillance System
(BRFSS) in three test states (Michigan,
Minnesota and Oregon). The child selection
module and the child prevalence module
must be conducted at the time of the BRFSS
interview. Adults and children who are
identified with lifetime asthma will be called
back approximately 2 weeks after the initial
BRFSS telephone interview. At the time of
the call-back the NAS interview will be
conducted. Draft questionnaires can be
obtained by contacting the Air Pollution and
Respiratory Health Branch (404–498–1000).
Prevalence figures for adults in all BRFSS
areas (50 states, DC and 3 territories) can be
obtained from the core BRFSS survey.
However, the child selection module and
child prevalence modules are needed for
state level child prevalence estimates from
BRFSS.
In 2006 funding to implement the BRFSS
asthma call-back survey will be provided to
BRFSS states, DC, or territories who
successfully apply for that funding in
conjunction with their BRFSS funding.
Asthma program staff must work jointly with
their state’s BRFSS program coordinator
when submitting request for asthma call-back
funding to the National Center for Chronic
Disease Prevention and Health Promotion
(NCCDPHP).
[FR Doc. 05–7889 Filed 4–19–05; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
National Health Education
Enhancement Program
Announcement Type: Competing
Continuation.
Funding Opportunity Number: RFA
05072.
Catalog of Federal Domestic
Assistance Number: 93.283.
Letter of Intent Deadline: May 4, 2005.
Application Deadline: June 20, 2005.
Executive Summary: The purpose of
the program is to strengthen the nation’s
capacity to carry out public health
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activities in the area of asthma
education. More specifically, the
objective is to provide appropriate
resources for health education of
patients and others impacted by asthma.
I. Funding Opportunity Description
Authority: This program is authorized
under Sections 301 and 317 of the
Public Health Service Act, (42 U.S.C.
241 and 247b), as amended.
Background: Although there are many
asthma educational materials which
have been produced and disseminated,
there remain gaps in the availability and
dissemination of materials which are
targeted to adults, the elderly, rural
populations, non-English speaking
populations, adolescents, and other
underserved and disparately impacted
populations.
Purpose: The purpose of the program
is to strengthen the nation’s capacity to
carry out public health activities in the
area of asthma education. The objectives
are to: (1) Review and disseminate
currently available asthma educational
materials to reach community members
on a community, local and national
level; and (2) modify existing,
scientifically-proven-effective asthma
educational materials to make them
culturally and linguistically competent
for targeted populations, and
disseminate these materials on a
national level to families impacted by
asthma, particularly working with
underserved and disparately impacted
populations. This program addresses the
‘‘Healthy People 2010’’ focus area(s) of
reducing asthma hospitalizations,
deaths, and improving quality of life.
Measurable outcomes of the program
will be in alignment with one (or more)
of the following performance goal(s) for
the National Center for Environmental
Health (NCEH): To reduce the number
of asthma hospitalizations, deaths, and
emergency department visits.
This announcement is only for nonresearch activities supported by CDC. If
research is proposed, the application
will not be reviewed. For the definition
of research, please see the CDC Web site
at the following Internet address: http:/
/www.cdc.gov/od/ads/opspoll1.htm.
Activities: Awardee activities for this
program are as follows:
• Review and disseminate currently
available asthma educational materials
to reach applicant organization
members and other community
members on a national, local, and
community level. The materials must be
proven effective, and in accordance
with sound asthma management
practices and appropriate National
Asthma Education and Prevention
Program (NAEPP) Guidelines.
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• In cases where appropriate, asthma
educational materials do not exist for
populations which are underserved and
a need for such materials is identified,
applicants should adapt or modify
existing educational materials which
have been scientifically proven
effective, through appropriate,
published research results. Resulting
materials must be accurate, userfriendly, culturally and linguistically
appropriate, and be used to educate the
applicant organization’s members and
other members of the community, or
any targeted group for which a gap in
currently available educational
materials is identified. Literacy level
and appropriate demographics of your
target audience must be considered.
• Conduct interactive community
outreach education at the local level,
aimed at your members and community
members affected by asthma.
Present a plan by which you will
measure the effectiveness of your
proposed activities.
Collaborate with partners, including
CDC and appropriate asthma education
organizations, to ensure that best
practices are used in the adaptation/
modification and dissemination of
asthma education materials for your
target audiences.
In a cooperative agreement, CDC staff
is substantially involved in the program
activities, above and beyond routine
grant monitoring.
CDC Activities for this program are as
follows:
• Collaborate with recipients in the
modification and adaptation of existing
educational materials which have been
scientifically proven effective through
appropriate published research results.
Ensure coordination of this activity
among all recipients and facilitate
information sharing.
• Review recipients’ identification of
currently available educational
materials and gap analysis; and ensure
coordination of this activity among all
recipients, including information
sharing and elimination of duplication
of efforts among recipients.
• Facilitate and coordinate meetings
to bring together national groups as
collaborators, where appropriate.
• Collaborate with recipients on the
development of an appropriate
evaluation plan which measures the
effectiveness of recipient activities
involved in each step indicated, and
approve the plan.
• Coordinate recipient activities with
asthma education partners to ensure
duplication of activities and efforts does
not occur.
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II. Award Information
Type of Award: Cooperative
Agreement. CDC involvement in this
program is listed in the Activities
Section above.
Fiscal Year Funds: 2005.
Approximate Total Funding: $225,000
to $300,000. (This amount is an
estimate, and is subject to availability of
funds.)
Approximate Number of Awards:
Three.
Approximate Average Award: $75,000
to 100,000. (This amount is for the first
12-month budget period, and includes
both direct and indirect costs.)
Floor of Award Range: None.
Ceiling of Award Range: $100,000.
(This ceiling is for the first 12-month
budget period.)
Anticipated Award Date: August 31,
2005.
Budget Period Length: 12 months.
Project Period Length: 5 years.
Throughout the project period, CDC’s
commitment to continuation of awards
will be conditioned on the availability
of funds, evidence of satisfactory
progress by the recipient (as
documented in required reports), and
the determination that continued
funding is in the best interest of the
Federal Government.
III. Eligibility Information
III.1. Eligible Applicants
Applications may be submitted by
public and private nonprofit
organizations such as:
• Public nonprofit organizations.
• Private nonprofit organizations.
• Community-based organizations.
• Faith-based organizations.
Assistance will be provided only to
applicants that are well-established,
national, non-profit organizations with
experience in the development and
dissemination of asthma educational
materials; and whose membership
includes families of adults or children
with asthma, or others affected by the
disease.
The justification for the foregoing
limitation is the need for the applicant
to have immediate access to a national
audience, and existing expertise in the
modification and dissemination of
asthma educational materials to
community members impacted by
asthma, to insure they may access the
greatest number of people in the
shortest period of time.
To be eligible, applicants must:
1. Demonstrate that your
organization’s mission is explicitly
committed to improving the lives of
families impacted by asthma, or other
similar lung diseases, through the
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provision of timely, accurate, and useful
information about the disease and how
it can be controlled. You must have
experience providing asthma education
to a nationwide audience. The foregoing
may be demonstrated by submission of
your charter, articles of incorporation,
or other governing documents.
2. Demonstrate that your organization
is non-profit and recognized as taxexempt under Section 501(c)(3) of the
Internal Revenue Code. This may be
demonstrated through inclusion of your
Internal Revenue Service determination
letter.
3. Demonstrate that your organization
has the capacity for and experience in
providing educational services to
families with asthma on a nationwide
basis. This may be demonstrated
through letters of support.
4. Demonstrate that your organization
has the capacity for and experience
providing educational services to
families or a national network of local
organizations. This may be
demonstrated through a letter from your
organization’s leadership, which
describes your national network/
membership (number of members and
national coverage of the membership).
III.2. Cost Sharing or Matching
Matching funds are not required for
this program.
III.3. Other
If you request a funding amount
greater than the ceiling of the award
range, your application will be
considered non-responsive, and will not
be entered into the review process. You
will be notified that your application
did not meet the submission
requirements.
Special Requirements: If your
application is incomplete or nonresponsive to the special requirements
listed in this section, it will not be
entered into the review process. You
will be notified that your application
did not meet submission requirements.
• Late applications will be considered
non-responsive. See section ‘‘IV.3.
Submission Dates and Times’’ for more
information on deadlines.
• Note: Title 2 of the United States
Code Section 1611 states that an
organization described in Section
501(c)(4) of the Internal Revenue Code
that engages in lobbying activities is not
eligible to receive Federal funds
constituting an award, grant, or loan.
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IV. Application and Submission
Information
IV.1. Address To Request Application
Package
To apply for this funding opportunity
use application form PHS 5161–1.
CDC strongly encourages you to
submit your application electronically
by utilizing the forms and instructions
posted for this announcement at
https://www.grants.gov.
Application forms and instructions
are available on the CDC Web site, at the
following Internet address: https://
www.cdc.gov/od/pgo/forminfo.htm.
If you do not have access to the
Internet, or if you have difficulty
accessing the forms on-line, you may
contact the CDC Procurement and
Grants Office Technical Information
Management Section (PGO–TIM) staff
at: 770–488–2700. Application forms
can be mailed to you.
IV.2. Content and Form of Submission
Letter of Intent (LOI): Your LOI must
be written in the following format:
• Maximum number of pages: One.
• Font size: 12-point unreduced.
• Single spaced.
• Paper size: 8.5 by 11 inches.
• Page margin size: One inch.
• Printed only on one side of page.
• Written in plain language, avoid
jargon.
Your LOI must contain the following
information:
• Name and address of organization.
• Name, address, telephone number,
fax number and e-mail address of the
organization’s primary contact for
writing and submitting the application.
• A brief summary of the proposed
project.
Application: You must submit a
project narrative with your application
forms. The narrative must be submitted
in the following format:
• Maximum number of pages: 25
pages (not including attachments for
purposes of establishing eligibility). If
your narrative exceeds the page limit,
only the first pages which are within the
page limit will be reviewed.
• Font size: 12 point unreduced.
• Double spaced.
• Paper size: 8.5 by 11 inches.
• Page margin size: One inch.
• Printed only on one side of page.
• Pages shall be numbered
sequentially, including your narrative
and any appendices.
• Held together only by rubber bands
or metal clips; not bound in any other
way.
Your narrative should address
activities to be conducted over the
entire project period, and must include
the following items in the order listed:
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20565
• History and Experience.
• Proposed Program.
• Evaluation Plan.
• Facilities, Staff and Resources.
• Budget and Justification.
• Documentation of eligibility, as
follows:
a. Submit your charter, articles of
incorporation, or other governing
documents to demonstrate your
organization’s mission is explicitly
committed to improving the lives of
families impacted by asthma, or other
similar lung diseases, through the
provision of timely, accurate, and useful
information about the disease and how
it can be controlled.
b. Submit your Internal Revenue
Service determination letter which will
demonstrate your organization is nonprofit and recognized as tax-exempt
under Section 501(c)(3) of the Internal
Revenue Code.
c. Submit letters of support, which
will demonstrate that your organization
has the capacity for and experience in
providing educational services to
families with asthma on a nationwide
basis.
d. Submit a letter from your
organization’s leadership, which
describes your national network/
membership (number of members and
national coverage of the membership).
The budget justification and
documentation to establish eligibility
will NOT be counted in the stated page
limit.
Additional information may be
included in the application appendices.
The appendices will not be counted
toward the narrative page limit. This
additional information includes:
• Curriculum Vitae (of key staff
positions).
• Letters of Support.
You are required to have a Dun and
Bradstreet Data Universal Numbering
System (DUNS) number to apply for a
grant or cooperative agreement from the
Federal government. The DUNS number
is a nine-digit identification number,
which uniquely identifies business
entities. Obtaining a DUNS number is
easy and there is no charge. To obtain
a DUNS number, access https://
www.dunandbradstreet.com or call 1–
866–705–5711.
For more information, see the CDC
Web site at: https://www.cdc.gov/od/pgo/
funding/pubcommt.htm.
If your application form does not have
a DUNS number field, please write your
DUNS number at the top of the first
page of your application, and/or include
your DUNS number in your application
cover letter.
Additional requirements that may
require you to submit additional
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documentation with your application
are listed in section ‘‘VI.2.
Administrative and National Policy
Requirements.’’
IV.3. Submission Dates and Times
LOI Deadline Date: May 4, 2005.
CDC requests that you send a LOI if
you intend to apply for this program.
Although the LOI is not required, not
binding, and does not enter into the
review of your subsequent application,
the LOI will be used to gauge the level
of interest in this program, and to allow
CDC to plan the application review.
Application Deadline Date: June 20,
2005.
Explanation of Deadlines:
Applications must be received in the
CDC Procurement and Grants Office by
4 p.m. eastern time on the deadline
date.
You may submit your application
electronically at https://www.grants.gov.
Applications completed online through
Grants.gov are considered formally
submitted when the applicant
organization’s Authorizing Official
electronically submits the application to
https://www.grants.gov. Electronic
applications will be considered as
having met the deadline if the
application has been submitted
electronically by the applicant
organization’s Authorizing Official to
Grants.gov on or before the deadline
date and time.
If you submit your application
electronically with Grants.gov, your
application will be electronically time/
date stamped, which will serve as
receipt of submission. You will receive
an e-mail notice of receipt when CDC
receives the application.
If you submit your application by the
United States Postal Service or
commercial delivery service, you must
ensure that the carrier will be able to
guarantee delivery by the closing date
and time. If CDC receives your
submission after closing due to: (1)
Carrier error, when the carrier accepted
the package with a guarantee for
delivery by the closing date and time, or
(2) significant weather delays or natural
disasters, you will be given the
opportunity to submit documentation of
the carriers guarantee. If the
documentation verifies a carrier
problem, CDC will consider the
submission as having been received by
the deadline.
If you submit a hard copy application,
CDC will not notify you upon receipt of
your submission. If you have a question
about the receipt of your LOI or
application, first contact your courier. If
you still have a question, contact the
PGO–TIM staff at: 770–488–2700. Before
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calling, please wait two to three days
after the submission deadline. This will
allow time for submissions to be
processed and logged.
This announcement is the definitive
guide on LOI and application content,
submission address, and deadline. It
supersedes information provided in the
application instructions. If your
submission does not meet the deadline
above, it will not be eligible for review,
and will be discarded. You will be
notified that you did not meet the
submission requirements.
IV.4. Intergovernmental Review of
Applications
Your application is subject to
Intergovernmental Review of Federal
Programs, as governed by Executive
Order (EO) 12372. This order sets up a
system for state and local governmental
review of proposed federal assistance
applications. You should contact your
state single point of contact (SPOC) as
early as possible to alert the SPOC to
prospective applications, and to receive
instructions on your state’s process.
Click on the following link to get the
current SPOC list: https://
www.whitehouse.gov/omb/grants/
spoc.html.
IV.5. Funding Restrictions
Restrictions, which must be taken into
account while writing your budget, are
as follows:
• Funds may not be used for research.
• Reimbursement of pre-award costs
is not allowed.
If you are requesting indirect costs in
your budget, you must include a copy
of your federally approved indirect cost
rate agreement. If your indirect cost rate
is a provisional rate, the agreement
should be less than 12 months of age.
Guidance for completing your budget
can be found on the CDC Web site, at
the following Internet address: https://
www.cdc.gov/od/pgo/funding/
budgetguide.htm.
IV.6. Other Submission Requirements
LOI Submission Address: Submit your
LOI by express mail, delivery service,
fax, or e-mail to: Sheri Disler, Centers
for Disease Control and Prevention,
National Center for Environmental
Health, 1600 Clifton Road, MS E–17,
Atlanta, GA 30303; telephone: 404–498–
1018, Facsimile: 404–498–1088, e-mail
address: SDisler@cdc.gov.
Application Submission Address:
CDC strongly encourages applicants to
submit electronically at: https://
www.grants.gov. You will be able to
download a copy of the application
package from https://www.grants.gov,
complete it offline, and then upload and
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submit the application via the
Grants.gov site. E-mail submissions will
not be accepted. If you are having
technical difficulties in Grants.gov, they
can be reached by e-mail at https://
www.support@grants.gov or by phone at
1–800–518–4726. The Customer
Support Center is open from 7 a.m. to
9 p.m. eastern time, Monday through
Friday.
CDC recommends that you submit
your application to Grants.gov early
enough to resolve any unanticipated
difficulties prior to the deadline. You
may also submit a back-up paper
submission of your application. Any
such paper submission must be received
in accordance with the requirements for
timely submission detailed in Section
IV.3. of the grant announcement. The
paper submission must be clearly
marked: ‘‘BACK-UP FOR ELECTRONIC
SUBMISSION.’’
The paper submission must conform
to all requirements for non-electronic
submissions. If both electronic and
back-up paper submissions are received
by the deadline, the electronic version
will be considered the official
submission.
It is strongly recommended that you
submit your grant application using
Microsoft Office products (e.g.,
Microsoft Word, Microsoft Excel, etc.). If
you do not have access to Microsoft
Office products, you may submit a PDF
file. Directions for creating PDF files can
be found on the Grants.gov Web site.
Use of file formats other than Microsoft
Office or PDF may result in your file
being unreadable by our staff.
Or
Submit the original and two hard
copies of your application by mail or
express delivery service to: Technical
Information Management—RFA 05072,
CDC Procurement and Grants Office,
2920 Brandywine Road, Atlanta, GA
30341.
V. Application Review Information
V.1. Criteria
Applicants are required to provide
measures of effectiveness that will
demonstrate the accomplishment of the
various identified objectives of the
cooperative agreement. Measures of
effectiveness must relate to the
performance goals stated in the
‘‘Purpose’’ section of this
announcement. Measures must be
objective and quantitative, and must
measure the intended outcome. These
measures of effectiveness must be
submitted with the application and will
be an element of evaluation.
Your application will be evaluated
against the following criteria:
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1. History and Experience (30 Points)
The extent to which the proposal
clearly demonstrates the applicant’s
solid reputation and history of serving
families affected by asthma. The
proposal should demonstrate that the
applicant has a broad range of
knowledge and expertise in the field of
asthma, as well as significant years of
experience in the dissemination and
application of this knowledge and
expertise. The proposal should also
demonstrate that the applicant’s
membership is comprised of families
affected by asthma, and that this
membership is national in scope.
2. Proposed Program (30 Points)
The extent to which the proposal
clearly demonstrates the applicant’s
understanding of the issues surrounding
asthma and asthma education activities,
and addresses gaps in the current state
of asthma educational materials and
activities. The proposal should
demonstrate that the applicant has a
clear understanding of the gaps and
needs, and has a clear plan of activities,
which will address these gaps. The
applicant must demonstrate that their
educational materials are in adherence
to the NAEPP guidelines and, when
these guidelines are updated, that
materials are appropriately updated.
3. Evaluation Plan (30 Points)
The extent to which the applicant
describes a realistic plan to accurately
measure the effectiveness of their
activities, and a plan to implement the
quality improvements indicated by this
method over the life of the project. This
may include a discussion of efforts
undertaken to measure the effectiveness
of the applicant’s existing outreach and
educational activities.
4. Facilities, Staff and Resources (10
Points)
The extent to which the applicant can
provide adequate facilities, staff,
collaborators, and resources to
accomplish the proposed goal(s) and
objectives during the project period. The
extent to which the applicant
demonstrates staff and collaborator
availability, expertise, previous
experience, and capacity to perform the
undertaking successfully.
5. Budget (Not Scored)
The extent to which the proposal
demonstrates appropriateness and
justification of the requested budget
relative to the activities proposed.
V.2. Review and Selection Process
Applications will be reviewed for
completeness by the Procurement and
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Grants Office (PGO) staff, and for
responsiveness by the NCEH.
Incomplete applications and
applications that are non-responsive to
the eligibility criteria will not advance
through the review process. Applicants
will be notified that their application
did not meet submission requirements.
An objective review panel will
evaluate complete and responsive
applications according to the criteria
listed in the ‘‘V.1. Criteria’’ section
above. The objective review panel
participants will be CDC employees, all
of whom work outside the NCEH.
Applications will be funded in order
by score and rank determined by the
review panel.
V.3. Anticipated Announcement and
Award Dates
Anticipated award date is August 31,
2005.
VI. Award Administration Information
VI.1. Award Notices
Successful applicants will receive a
Notice of Award (NoA) from the CDC
Procurement and Grants Office. The
NoA shall be the only binding,
authorizing document between the
recipient and CDC. The NoA will be
signed by an authorized Grants
Management Officer, and mailed to the
recipient fiscal officer identified in the
application.
Unsuccessful applicants will receive
notification of the results of the
application review by mail.
VI.2. Administrative and National
Policy Requirements
45 CFR Part 74 and Part 92. For more
information on the Code of Federal
Regulations, see the National Archives
and Records Administration at the
following Internet address: https://
www.access.gpo.gov/nara/cfr/cfr-tablesearch.html.
The following additional
requirements apply to this project:
• AR–7 Executive Order 12372.
• AR–8 Public Health System
Reporting Requirements.
• AR–10 Smoke-Free Workplace
Requirements.
• AR–11 Healthy People 2010.
• AR–12 Lobbying Restrictions.
• AR–14 Accounting System
Requirements.
• AR–23 States and Faith-Based
Organizations.
• AR–24 Health Insurance
Portability and Accountability Act
Requirements.
Additional information on these
requirements can be found on the CDC
Web site at the following Internet
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20567
address: https://www.cdc.gov/od/pgo/
funding/ARs.htm.
An additional Certifications form
from the PHS5161–1 application needs
to be included in your Grants.gov
electronic submission only. Refer to
https://www.grants.gov/od/pgo/funding/
PHS5161–1Certificates.pdf. Once the
form is filled out, attach it to your
Grants.gov submission as Other
Attachment Forms.
VI.3. Reporting Requirements
You must provide CDC with an
original, plus two hard copies of the
following reports:
1. Interim progress report, due no less
than 90 days before the end of the
budget period. The progress report will
serve as your non-competing
continuation application, and must
contain the following elements:
a. Current Budget Period Activities
Objectives.
b. Current Budget Period Financial
Progress.
c. New Budget Period Program
Proposed Activity Objectives.
d. Budget.
e. Measures of Effectiveness.
f. Additional Requested Information.
2. Annual progress report, due 30
days after the end of the budget period.
The annual progress report must contain
the following elements:
a. Current Budget Period Activities
Objectives.
b. Lessons Learned.
3. Financial status report and annual
progress report, no more than 90 days
after the end of the budget period.
4. Final financial and performance
reports, no more than 90 days after the
end of the project period.
These reports must be mailed to the
Grants Management or Contract
Specialist listed in the ‘‘Agency
Contacts’’ section of this announcement.
VII. Agency Contacts
We encourage inquiries concerning
this announcement.
For general questions, contact:
Technical Information Management
Section, CDC Procurement and Grants
Office, 2920 Brandywine Road, Atlanta,
GA 30341; telephone: 770–488–2700.
For program technical assistance,
contact: Sheri Disler, Project Officer,
1600 Clifton Road, NE, MS E–17,
Atlanta, GA 30303; telephone: 404–498–
1018, e-mail: SDisler@cdc.gov.
For financial, grants management, or
budget assistance, contact: Edna Green,
Grants Management Specialist, CDC
Procurement and Grants Office, 2920
Brandywine Road, Atlanta, GA 30341;
telephone: 770–488–2743, e-mail:
EGreen@cdc.gov.
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Federal Register / Vol. 70, No. 75 / Wednesday, April 20, 2005 / Notices
VIII. Other Information
This and other CDC funding
opportunity announcements can be
found on the CDC Web site, Internet
address: https://www.cdc.gov. Click on
‘‘Funding’’ then ‘‘Grants and
Cooperative Agreements.’’
Dated: April 14, 2005.
William P. Nichols,
Director, Procurement and Grants Office,
Centers for Disease Control and Prevention.
[FR Doc. 05–7888 Filed 4–19–05; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. 2004N–0486]
Agency Information Collection
Activities; Submission for Office of
Management and Budget Review;
Comment Request; Experimental
Study of Health Claims on Food
Packages
AGENCY:
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.
DATES: Fax written comments on the
collection of information by May 20,
2005.
ADDRESSES: OMB is still experiencing
significant delays in the regular mail,
including first class and express mail,
and messenger deliveries are not being
accepted. 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: Fumie Yokota, Desk Officer
for FDA, FAX: 202–395–6974.
FOR FURTHER INFORMATION CONTACT:
Peggy Robbins, Office of Management
Programs (HFA–250), Food and Drug
Administration, 5600 Fishers Lane,
Rockville, MD 20857, 301–827–1223.
SUPPLEMENTARY INFORMATION: In
compliance with 44 U.S.C. 3507, FDA
has submitted the following proposed
collection of information to OMB for
review and clearance.
Experimental Study of Health Claims
on Food Packages
The authority for FDA to collect the
information derives from the FDA
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Commissioner’s authority, as specified
in section 903(d)(2) of the Federal Food,
Drug, and Cosmetic Act (the act) (21
U.S.C. 393(d)(2)).
To help consumers reduce their risk
of disease and improve their health by
making sound dietary decisions, in the
Federal Register of November 25, 2003
(68 FR 66040), FDA issued an advance
notice of proposed rulemaking
(ANPRM) to request comments on
various issues related to health claims
on conventional food and dietary
supplement labels. One of the issues
that FDA raised in the ANPRM related
to whether the wording of a health
claim needs to refer to the substance (a
component of food, e.g., a nutrient) that
is the basis of the claim. (Hereinafter,
the term ‘‘health claim’’ will refer only
to a claim meeting the standard of
significant scientific agreement or, in
other words, an FDA- authorized claim.)
For instance, in the example of the
calcium-osteoporosis claim (‘‘Calcium
may reduce the risk of osteoporosis’’),
FDA currently requires that the
substance that is the basis of the claim
(in this case, calcium) be included in
the wording of the claim (21 CFR
101.72). The requirement that the
substance in a health claim be included
in the wording of the claim was
motivated by FDA’s experience that
most substances that are the subject of
an authorized health claim are, like
calcium, substances that can be found in
a number of foods. Therefore, FDA
requires that health claims refer to the
common substance to assist consumers
in their understanding of the nature of
the diet-health relationship and, more
importantly, to help consumers
recognize that they can construct
healthy diets by using a variety of foods
that contain the substance.
FDA requests comments on the
usefulness of such statements (e.g.,
‘‘Calcium-rich foods, such as yogurt,
may reduce the risk of osteoporosis’’)
versus ‘‘food-specific’’ claims that do
not specify the food component (e.g.,
‘‘Yogurt may reduce the risk of
osteoporosis’’). How consumers respond
to the two kinds of statements can
suggest how the explicit mention of a
food component in a claim affects
dietary choices which, in turn, informs
any policy initiative(s) that FDA may
undertake in the future to provide
information to consumers to help them
make informed food choices.
The purpose of the proposed
collection of information is to enhance
FDA’s understanding of consumer
responses to health claims and inform
any policy initiative(s) that FDA may
undertake in the future. The information
will be used to assess what differences,
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if any, the inclusion of the food
component in a health claim makes in
the following areas: (1) Consumer
recognition of the food component
underlying a diet-disease relationship;
(2) consumer recognition that, in
addition to the food product that carries
the claim, there are other foods from
which they can obtain the food
component; and (3) consumer
perceptions of, and attitudes toward, the
food.
The proposed collection of
information is a controlled randomized
experimental study. The study will use
a 6 x 3 within-subjects design (6 frontpanel health claims/health messages x 3
diet-disease relationships), with
participants randomly assigned to
experimental conditions. In total, the
study will examine 18 experimental
conditions (6 front-panel health claim/
health message conditions x 3 dietdisease relationships), each condition is
a combination of a front-panel condition
and a diet-disease relationship.
The term ‘‘health message’’ refers to
nutrient content claims, structure/
function claims, and dietary guidance
statements. Prior knowledge of foods,
components of food (e.g., nutrients), and
risks will be measured; such prior
knowledge will serve as covariates in
the analysis. There are two independent
variables, type of front-panel health
claim/health message and type of dietdisease relationship. Health claim/
health message conditions include the
following items:
1. A ‘‘food-specific’’ health claim, e.g.,
‘‘Yogurt may reduce the risk of
osteoporosis;’’
2. A ‘‘nutrient-specific’’ health claim,
e.g., ‘‘Calcium-rich foods, such as
yogurt, may reduce the risk of
osteoporosis;’’
3. A nutrient content claim, e.g., ‘‘a
good source of calcium;’’
4. A structure/function claim, e.g.,
‘‘Helps promote bone health;’’
5. A dietary guidance statement, e.g.,
‘‘Dairy products may reduce the risk of
osteoporosis;’’ and
6. No health claim/health message.
Claims on food labels must be truthful
and nonmisleading as required under
sections 201(n) and 403(a)(1) of the act
(21 U.S.C. 321(n) and 343(a)(1)).
Health messages other than the two
health claims are included solely for
methodological purposes. The ‘‘no
health claim/health message’’ condition
is included to examine what consumers
already know about nutrients or food
sources, even when neither of them is
mentioned on a label. Health messages
are frequently found on food product
packages and provide consumers
various amounts of information about
E:\FR\FM\20APN1.SGM
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[Federal Register Volume 70, Number 75 (Wednesday, April 20, 2005)]
[Notices]
[Pages 20563-20568]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 05-7888]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
National Health Education Enhancement Program
Announcement Type: Competing Continuation.
Funding Opportunity Number: RFA 05072.
Catalog of Federal Domestic Assistance Number: 93.283.
Letter of Intent Deadline: May 4, 2005.
Application Deadline: June 20, 2005.
Executive Summary: The purpose of the program is to strengthen the
nation's capacity to carry out public health
[[Page 20564]]
activities in the area of asthma education. More specifically, the
objective is to provide appropriate resources for health education of
patients and others impacted by asthma.
I. Funding Opportunity Description
Authority: This program is authorized under Sections 301 and 317 of
the Public Health Service Act, (42 U.S.C. 241 and 247b), as amended.
Background: Although there are many asthma educational materials
which have been produced and disseminated, there remain gaps in the
availability and dissemination of materials which are targeted to
adults, the elderly, rural populations, non-English speaking
populations, adolescents, and other underserved and disparately
impacted populations.
Purpose: The purpose of the program is to strengthen the nation's
capacity to carry out public health activities in the area of asthma
education. The objectives are to: (1) Review and disseminate currently
available asthma educational materials to reach community members on a
community, local and national level; and (2) modify existing,
scientifically-proven-effective asthma educational materials to make
them culturally and linguistically competent for targeted populations,
and disseminate these materials on a national level to families
impacted by asthma, particularly working with underserved and
disparately impacted populations. This program addresses the ``Healthy
People 2010'' focus area(s) of reducing asthma hospitalizations,
deaths, and improving quality of life.
Measurable outcomes of the program will be in alignment with one
(or more) of the following performance goal(s) for the National Center
for Environmental Health (NCEH): To reduce the number of asthma
hospitalizations, deaths, and emergency department visits.
This announcement is only for non-research activities supported by
CDC. If research is proposed, the application will not be reviewed. For
the definition of research, please see the CDC Web site at the
following Internet address: https://www.cdc.gov/od/ads/opspoll1.htm.
Activities: Awardee activities for this program are as follows:
Review and disseminate currently available asthma
educational materials to reach applicant organization members and other
community members on a national, local, and community level. The
materials must be proven effective, and in accordance with sound asthma
management practices and appropriate National Asthma Education and
Prevention Program (NAEPP) Guidelines.
In cases where appropriate, asthma educational materials
do not exist for populations which are underserved and a need for such
materials is identified, applicants should adapt or modify existing
educational materials which have been scientifically proven effective,
through appropriate, published research results. Resulting materials
must be accurate, user-friendly, culturally and linguistically
appropriate, and be used to educate the applicant organization's
members and other members of the community, or any targeted group for
which a gap in currently available educational materials is identified.
Literacy level and appropriate demographics of your target audience
must be considered.
Conduct interactive community outreach education at the
local level, aimed at your members and community members affected by
asthma.
Present a plan by which you will measure the effectiveness of your
proposed activities.
Collaborate with partners, including CDC and appropriate asthma
education organizations, to ensure that best practices are used in the
adaptation/modification and dissemination of asthma education materials
for your target audiences.
In a cooperative agreement, CDC staff is substantially involved in
the program activities, above and beyond routine grant monitoring.
CDC Activities for this program are as follows:
Collaborate with recipients in the modification and
adaptation of existing educational materials which have been
scientifically proven effective through appropriate published research
results. Ensure coordination of this activity among all recipients and
facilitate information sharing.
Review recipients' identification of currently available
educational materials and gap analysis; and ensure coordination of this
activity among all recipients, including information sharing and
elimination of duplication of efforts among recipients.
Facilitate and coordinate meetings to bring together
national groups as collaborators, where appropriate.
Collaborate with recipients on the development of an
appropriate evaluation plan which measures the effectiveness of
recipient activities involved in each step indicated, and approve the
plan.
Coordinate recipient activities with asthma education
partners to ensure duplication of activities and efforts does not
occur.
II. Award Information
Type of Award: Cooperative Agreement. CDC involvement in this
program is listed in the Activities Section above.
Fiscal Year Funds: 2005.
Approximate Total Funding: $225,000 to $300,000. (This amount is an
estimate, and is subject to availability of funds.)
Approximate Number of Awards: Three.
Approximate Average Award: $75,000 to 100,000. (This amount is for
the first 12-month budget period, and includes both direct and indirect
costs.)
Floor of Award Range: None.
Ceiling of Award Range: $100,000. (This ceiling is for the first
12-month budget period.)
Anticipated Award Date: August 31, 2005.
Budget Period Length: 12 months.
Project Period Length: 5 years.
Throughout the project period, CDC's commitment to continuation of
awards will be conditioned on the availability of funds, evidence of
satisfactory progress by the recipient (as documented in required
reports), and the determination that continued funding is in the best
interest of the Federal Government.
III. Eligibility Information
III.1. Eligible Applicants
Applications may be submitted by public and private nonprofit
organizations such as:
Public nonprofit organizations.
Private nonprofit organizations.
Community-based organizations.
Faith-based organizations.
Assistance will be provided only to applicants that are well-
established, national, non-profit organizations with experience in the
development and dissemination of asthma educational materials; and
whose membership includes families of adults or children with asthma,
or others affected by the disease.
The justification for the foregoing limitation is the need for the
applicant to have immediate access to a national audience, and existing
expertise in the modification and dissemination of asthma educational
materials to community members impacted by asthma, to insure they may
access the greatest number of people in the shortest period of time.
To be eligible, applicants must:
1. Demonstrate that your organization's mission is explicitly
committed to improving the lives of families impacted by asthma, or
other similar lung diseases, through the
[[Page 20565]]
provision of timely, accurate, and useful information about the disease
and how it can be controlled. You must have experience providing asthma
education to a nationwide audience. The foregoing may be demonstrated
by submission of your charter, articles of incorporation, or other
governing documents.
2. Demonstrate that your organization is non-profit and recognized
as tax-exempt under Section 501(c)(3) of the Internal Revenue Code.
This may be demonstrated through inclusion of your Internal Revenue
Service determination letter.
3. Demonstrate that your organization has the capacity for and
experience in providing educational services to families with asthma on
a nationwide basis. This may be demonstrated through letters of
support.
4. Demonstrate that your organization has the capacity for and
experience providing educational services to families or a national
network of local organizations. This may be demonstrated through a
letter from your organization's leadership, which describes your
national network/membership (number of members and national coverage of
the membership).
III.2. Cost Sharing or Matching
Matching funds are not required for this program.
III.3. Other
If you request a funding amount greater than the ceiling of the
award range, your application will be considered non-responsive, and
will not be entered into the review process. You will be notified that
your application did not meet the submission requirements.
Special Requirements: If your application is incomplete or non-
responsive to the special requirements listed in this section, it will
not be entered into the review process. You will be notified that your
application did not meet submission requirements.
Late applications will be considered non-responsive. See
section ``IV.3. Submission Dates and Times'' for more information on
deadlines.
Note: Title 2 of the United States Code Section 1611
states that an organization described in Section 501(c)(4) of the
Internal Revenue Code that engages in lobbying activities is not
eligible to receive Federal funds constituting an award, grant, or
loan.
IV. Application and Submission Information
IV.1. Address To Request Application Package
To apply for this funding opportunity use application form PHS
5161-1.
CDC strongly encourages you to submit your application
electronically by utilizing the forms and instructions posted for this
announcement at https://www.grants.gov.
Application forms and instructions are available on the CDC Web
site, at the following Internet address: https://www.cdc.gov/od/pgo/
forminfo.htm.
If you do not have access to the Internet, or if you have
difficulty accessing the forms on-line, you may contact the CDC
Procurement and Grants Office Technical Information Management Section
(PGO-TIM) staff at: 770-488-2700. Application forms can be mailed to
you.
IV.2. Content and Form of Submission
Letter of Intent (LOI): Your LOI must be written in the following
format:
Maximum number of pages: One.
Font size: 12-point unreduced.
Single spaced.
Paper size: 8.5 by 11 inches.
Page margin size: One inch.
Printed only on one side of page.
Written in plain language, avoid jargon.
Your LOI must contain the following information:
Name and address of organization.
Name, address, telephone number, fax number and e-mail
address of the organization's primary contact for writing and
submitting the application.
A brief summary of the proposed project.
Application: You must submit a project narrative with your
application forms. The narrative must be submitted in the following
format:
Maximum number of pages: 25 pages (not including
attachments for purposes of establishing eligibility). If your
narrative exceeds the page limit, only the first pages which are within
the page limit will be reviewed.
Font size: 12 point unreduced.
Double spaced.
Paper size: 8.5 by 11 inches.
Page margin size: One inch.
Printed only on one side of page.
Pages shall be numbered sequentially, including your
narrative and any appendices.
Held together only by rubber bands or metal clips; not
bound in any other way.
Your narrative should address activities to be conducted over the
entire project period, and must include the following items in the
order listed:
History and Experience.
Proposed Program.
Evaluation Plan.
Facilities, Staff and Resources.
Budget and Justification.
Documentation of eligibility, as follows:
a. Submit your charter, articles of incorporation, or other
governing documents to demonstrate your organization's mission is
explicitly committed to improving the lives of families impacted by
asthma, or other similar lung diseases, through the provision of
timely, accurate, and useful information about the disease and how it
can be controlled.
b. Submit your Internal Revenue Service determination letter which
will demonstrate your organization is non-profit and recognized as tax-
exempt under Section 501(c)(3) of the Internal Revenue Code.
c. Submit letters of support, which will demonstrate that your
organization has the capacity for and experience in providing
educational services to families with asthma on a nationwide basis.
d. Submit a letter from your organization's leadership, which
describes your national network/membership (number of members and
national coverage of the membership).
The budget justification and documentation to establish eligibility
will NOT be counted in the stated page limit.
Additional information may be included in the application
appendices. The appendices will not be counted toward the narrative
page limit. This additional information includes:
Curriculum Vitae (of key staff positions).
Letters of Support.
You are required to have a Dun and Bradstreet Data Universal
Numbering System (DUNS) number to apply for a grant or cooperative
agreement from the Federal government. The DUNS number is a nine-digit
identification number, which uniquely identifies business entities.
Obtaining a DUNS number is easy and there is no charge. To obtain a
DUNS number, access https://www.dunandbradstreet.com or call 1-866-705-
5711.
For more information, see the CDC Web site at: https://www.cdc.gov/
od/pgo/funding/pubcommt.htm.
If your application form does not have a DUNS number field, please
write your DUNS number at the top of the first page of your
application, and/or include your DUNS number in your application cover
letter.
Additional requirements that may require you to submit additional
[[Page 20566]]
documentation with your application are listed in section ``VI.2.
Administrative and National Policy Requirements.''
IV.3. Submission Dates and Times
LOI Deadline Date: May 4, 2005.
CDC requests that you send a LOI if you intend to apply for this
program. Although the LOI is not required, not binding, and does not
enter into the review of your subsequent application, the LOI will be
used to gauge the level of interest in this program, and to allow CDC
to plan the application review.
Application Deadline Date: June 20, 2005.
Explanation of Deadlines: Applications must be received in the CDC
Procurement and Grants Office by 4 p.m. eastern time on the deadline
date.
You may submit your application electronically at https://
www.grants.gov. Applications completed online through Grants.gov are
considered formally submitted when the applicant organization's
Authorizing Official electronically submits the application to https://
www.grants.gov. Electronic applications will be considered as having
met the deadline if the application has been submitted electronically
by the applicant organization's Authorizing Official to Grants.gov on
or before the deadline date and time.
If you submit your application electronically with Grants.gov, your
application will be electronically time/date stamped, which will serve
as receipt of submission. You will receive an e-mail notice of receipt
when CDC receives the application.
If you submit your application by the United States Postal Service
or commercial delivery service, you must ensure that the carrier will
be able to guarantee delivery by the closing date and time. If CDC
receives your submission after closing due to: (1) Carrier error, when
the carrier accepted the package with a guarantee for delivery by the
closing date and time, or (2) significant weather delays or natural
disasters, you will be given the opportunity to submit documentation of
the carriers guarantee. If the documentation verifies a carrier
problem, CDC will consider the submission as having been received by
the deadline.
If you submit a hard copy application, CDC will not notify you upon
receipt of your submission. If you have a question about the receipt of
your LOI or application, first contact your courier. If you still have
a question, contact the PGO-TIM staff at: 770-488-2700. Before calling,
please wait two to three days after the submission deadline. This will
allow time for submissions to be processed and logged.
This announcement is the definitive guide on LOI and application
content, submission address, and deadline. It supersedes information
provided in the application instructions. If your submission does not
meet the deadline above, it will not be eligible for review, and will
be discarded. You will be notified that you did not meet the submission
requirements.
IV.4. Intergovernmental Review of Applications
Your application is subject to Intergovernmental Review of Federal
Programs, as governed by Executive Order (EO) 12372. This order sets up
a system for state and local governmental review of proposed federal
assistance applications. You should contact your state single point of
contact (SPOC) as early as possible to alert the SPOC to prospective
applications, and to receive instructions on your state's process.
Click on the following link to get the current SPOC list: https://
www.whitehouse.gov/omb/grants/spoc.html.
IV.5. Funding Restrictions
Restrictions, which must be taken into account while writing your
budget, are as follows:
Funds may not be used for research.
Reimbursement of pre-award costs is not allowed.
If you are requesting indirect costs in your budget, you must
include a copy of your federally approved indirect cost rate agreement.
If your indirect cost rate is a provisional rate, the agreement should
be less than 12 months of age.
Guidance for completing your budget can be found on the CDC Web
site, at the following Internet address: https://www.cdc.gov/od/pgo/
funding/budgetguide.htm.
IV.6. Other Submission Requirements
LOI Submission Address: Submit your LOI by express mail, delivery
service, fax, or e-mail to: Sheri Disler, Centers for Disease Control
and Prevention, National Center for Environmental Health, 1600 Clifton
Road, MS E-17, Atlanta, GA 30303; telephone: 404-498-1018, Facsimile:
404-498-1088, e-mail address: SDisler@cdc.gov.
Application Submission Address: CDC strongly encourages applicants
to submit electronically at: https://www.grants.gov. You will be able to
download a copy of the application package from https://www.grants.gov,
complete it offline, and then upload and submit the application via the
Grants.gov site. E-mail submissions will not be accepted. If you are
having technical difficulties in Grants.gov, they can be reached by e-
mail at http:www.support@grants.gov">//www.support@grants.gov or by phone at 1-800-518-4726.
The Customer Support Center is open from 7 a.m. to 9 p.m. eastern time,
Monday through Friday.
CDC recommends that you submit your application to Grants.gov early
enough to resolve any unanticipated difficulties prior to the deadline.
You may also submit a back-up paper submission of your application. Any
such paper submission must be received in accordance with the
requirements for timely submission detailed in Section IV.3. of the
grant announcement. The paper submission must be clearly marked:
``BACK-UP FOR ELECTRONIC SUBMISSION.''
The paper submission must conform to all requirements for non-
electronic submissions. If both electronic and back-up paper
submissions are received by the deadline, the electronic version will
be considered the official submission.
It is strongly recommended that you submit your grant application
using Microsoft Office products (e.g., Microsoft Word, Microsoft Excel,
etc.). If you do not have access to Microsoft Office products, you may
submit a PDF file. Directions for creating PDF files can be found on
the Grants.gov Web site. Use of file formats other than Microsoft
Office or PDF may result in your file being unreadable by our staff.
Or
Submit the original and two hard copies of your application by mail
or express delivery service to: Technical Information Management--RFA
05072, CDC Procurement and Grants Office, 2920 Brandywine Road,
Atlanta, GA 30341.
V. Application Review Information
V.1. Criteria
Applicants are required to provide measures of effectiveness that
will demonstrate the accomplishment of the various identified
objectives of the cooperative agreement. Measures of effectiveness must
relate to the performance goals stated in the ``Purpose'' section of
this announcement. Measures must be objective and quantitative, and
must measure the intended outcome. These measures of effectiveness must
be submitted with the application and will be an element of evaluation.
Your application will be evaluated against the following criteria:
[[Page 20567]]
1. History and Experience (30 Points)
The extent to which the proposal clearly demonstrates the
applicant's solid reputation and history of serving families affected
by asthma. The proposal should demonstrate that the applicant has a
broad range of knowledge and expertise in the field of asthma, as well
as significant years of experience in the dissemination and application
of this knowledge and expertise. The proposal should also demonstrate
that the applicant's membership is comprised of families affected by
asthma, and that this membership is national in scope.
2. Proposed Program (30 Points)
The extent to which the proposal clearly demonstrates the
applicant's understanding of the issues surrounding asthma and asthma
education activities, and addresses gaps in the current state of asthma
educational materials and activities. The proposal should demonstrate
that the applicant has a clear understanding of the gaps and needs, and
has a clear plan of activities, which will address these gaps. The
applicant must demonstrate that their educational materials are in
adherence to the NAEPP guidelines and, when these guidelines are
updated, that materials are appropriately updated.
3. Evaluation Plan (30 Points)
The extent to which the applicant describes a realistic plan to
accurately measure the effectiveness of their activities, and a plan to
implement the quality improvements indicated by this method over the
life of the project. This may include a discussion of efforts
undertaken to measure the effectiveness of the applicant's existing
outreach and educational activities.
4. Facilities, Staff and Resources (10 Points)
The extent to which the applicant can provide adequate facilities,
staff, collaborators, and resources to accomplish the proposed goal(s)
and objectives during the project period. The extent to which the
applicant demonstrates staff and collaborator availability, expertise,
previous experience, and capacity to perform the undertaking
successfully.
5. Budget (Not Scored)
The extent to which the proposal demonstrates appropriateness and
justification of the requested budget relative to the activities
proposed.
V.2. Review and Selection Process
Applications will be reviewed for completeness by the Procurement
and Grants Office (PGO) staff, and for responsiveness by the NCEH.
Incomplete applications and applications that are non-responsive to the
eligibility criteria will not advance through the review process.
Applicants will be notified that their application did not meet
submission requirements.
An objective review panel will evaluate complete and responsive
applications according to the criteria listed in the ``V.1. Criteria''
section above. The objective review panel participants will be CDC
employees, all of whom work outside the NCEH.
Applications will be funded in order by score and rank determined
by the review panel.
V.3. Anticipated Announcement and Award Dates
Anticipated award date is August 31, 2005.
VI. Award Administration Information
VI.1. Award Notices
Successful applicants will receive a Notice of Award (NoA) from the
CDC Procurement and Grants Office. The NoA shall be the only binding,
authorizing document between the recipient and CDC. The NoA will be
signed by an authorized Grants Management Officer, and mailed to the
recipient fiscal officer identified in the application.
Unsuccessful applicants will receive notification of the results of
the application review by mail.
VI.2. Administrative and National Policy Requirements
45 CFR Part 74 and Part 92. For more information on the Code of
Federal Regulations, see the National Archives and Records
Administration at the following Internet address: https://
www.access.gpo.gov/nara/cfr/cfr-table-search.html.
The following additional requirements apply to this project:
AR-7 Executive Order 12372.
AR-8 Public Health System Reporting Requirements.
AR-10 Smoke-Free Workplace Requirements.
AR-11 Healthy People 2010.
AR-12 Lobbying Restrictions.
AR-14 Accounting System Requirements.
AR-23 States and Faith-Based Organizations.
AR-24 Health Insurance Portability and Accountability Act
Requirements.
Additional information on these requirements can be found on the
CDC Web site at the following Internet address: https://www.cdc.gov/od/
pgo/funding/ARs.htm.
An additional Certifications form from the PHS5161-1 application
needs to be included in your Grants.gov electronic submission only.
Refer to https://www.grants.gov/od/pgo/funding/PHS5161-
1Certificates.pdf. Once the form is filled out, attach it to your
Grants.gov submission as Other Attachment Forms.
VI.3. Reporting Requirements
You must provide CDC with an original, plus two hard copies of the
following reports:
1. Interim progress report, due no less than 90 days before the end
of the budget period. The progress report will serve as your non-
competing continuation application, and must contain the following
elements:
a. Current Budget Period Activities Objectives.
b. Current Budget Period Financial Progress.
c. New Budget Period Program Proposed Activity Objectives.
d. Budget.
e. Measures of Effectiveness.
f. Additional Requested Information.
2. Annual progress report, due 30 days after the end of the budget
period. The annual progress report must contain the following elements:
a. Current Budget Period Activities Objectives.
b. Lessons Learned.
3. Financial status report and annual progress report, no more than
90 days after the end of the budget period.
4. Final financial and performance reports, no more than 90 days
after the end of the project period.
These reports must be mailed to the Grants Management or Contract
Specialist listed in the ``Agency Contacts'' section of this
announcement.
VII. Agency Contacts
We encourage inquiries concerning this announcement.
For general questions, contact: Technical Information Management
Section, CDC Procurement and Grants Office, 2920 Brandywine Road,
Atlanta, GA 30341; telephone: 770-488-2700.
For program technical assistance, contact: Sheri Disler, Project
Officer, 1600 Clifton Road, NE, MS E-17, Atlanta, GA 30303; telephone:
404-498-1018, e-mail: SDisler@cdc.gov.
For financial, grants management, or budget assistance, contact:
Edna Green, Grants Management Specialist, CDC Procurement and Grants
Office, 2920 Brandywine Road, Atlanta, GA 30341; telephone: 770-488-
2743, e-mail: EGreen@cdc.gov.
[[Page 20568]]
VIII. Other Information
This and other CDC funding opportunity announcements can be found
on the CDC Web site, Internet address: https://www.cdc.gov. Click on
``Funding'' then ``Grants and Cooperative Agreements.''
Dated: April 14, 2005.
William P. Nichols,
Director, Procurement and Grants Office, Centers for Disease Control
and Prevention.
[FR Doc. 05-7888 Filed 4-19-05; 8:45 am]
BILLING CODE 4163-18-P