Request for Information (RFI): Change in Grant Appendix Materials, 43204-43205 [E6-12230]
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43204
Federal Register / Vol. 71, No. 146 / Monday, July 31, 2006 / Notices
SUPPLEMENTARY INFORMATION:
Intended Recipient of the Award:
Home Safety Council.
Amount of the Award: $100,000.
Authority: Section 1271 et seq. of the
Public Health Service Act, 42 U.S.C.
Section 300d–71 et seq. as amended by
the Poison Center Stabilization and
Enhancement Grant Program.
Project Period: The period of the
award will begin on September 1, 2006,
through August 31, 2007.
Justification for the Exception to
Competition
This project will be implemented
through a single source cooperative
agreement because the HSC is uniquely
positioned to immediately undertake
and complete the activities within one
year. The HSC has existing
organizational knowledge and
experience in developing materials for
the low literacy population through its
Home Safety Literacy Project, which
this project will be a component; the
HSC has an existing relationship with
key stakeholders in place for reaching
this vulnerable population; and the HSC
project director has extensive expertise
in poison prevention education.
Dated: July 3, 2006.
Elizabeth M. Duke,
Administrator.
[FR Doc. E6–12178 Filed 7–28–06; 8:45 am]
BILLING CODE 4165–15–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
Request for Information (RFI): Change
in Grant Appendix Materials
sroberts on PROD1PC70 with NOTICES
ACTION:
Notice.
SUMMARY: The National Institutes of
Health (NIH) and the Agency for
Healthcare Research and Quality
(AHRQ) are evaluating guidelines for
grant application appendixes in an
effort to streamline the application and
review processes. This RFI requests
input from interested applicants,
reviewers and other members of the
research community regarding the way
appendix materials should be used in
the grant submission, review and
management process. Comments will be
considered in the development of new
policies on appendix materials for
various grant programs.
DATES: Reponses must be received by
September 14, 2006 in order to ensure
that NIH and AHRQ will be able to
consider the comments in developing
VerDate Aug<31>2005
17:34 Jul 28, 2006
Jkt 208001
new policies on appendix materials for
various grant programs.
FOR FURTHER INFORMATION CONTACT: Email inquiries will be accepted at
appendix_comments@od.nih.gov.
SUPPLEMENTARY INFORMATION:
Background
The goal of changing the guidelines
for grant application appendix materials
is to encourage applications to be as
concise as possible while containing the
information needed for expert scientific
review. These changes should make
application preparation and handling
easier for both applicants and reviewers.
Current NIH and AHRQ policy
indicates that the Appendix may not be
used to circumvent the page limitations
of the Research Plan. Appended
publications may not be used to provide
further details of methodologies or
preliminary data described in the
Research Plan. All applications and
proposals for NIH and AHRQ funding
must be self-contained. NIH application
guide instructions note that the
Appendix is sent only to those members
of the Scientific Review Group (SRG)
assigned as primary reviewers of the
application. Currently, unless otherwise
stated in the solicitation, the following
materials may be included in a grant
application Appendix:
• Up to 10 publications or
manuscripts accepted for publication,
using URL links to publicly accessible
journal articles.
• Surveys, questionnaires, data
collection instruments, clinical
protocols, and informed consent
documents.
• Photographs or color images of gels,
micrographs, etc., provided that a
photocopy (may be reduced in size) is
also included within the 25-page limit
of Items a–d of the research plan. No
photographs or color images may be
included in the Appendix that are not
also represented within the Research
Plan.
Investigators spend much time and
energy developing applications to
Federal Agencies. It is unclear whether
appendix material which may or may
not be read by members of the SRG
improves current applications.
Submission of unnecessary materials
with grant applications wastes the time,
energy and resources of investigators,
applicant institutions, reviewers, and
the NIH and AHRQ.
Proposed Changes
The following changes are being
considered for implementation
concurrent with NIH/AHRQ’s transition
to the electronic grant application
process and the SF–424 (R&R):
PO 00000
Frm 00111
Fmt 4703
Sfmt 4703
• Submission of photographs or color
images of gels, micrographs, etc., will
not be allowed in the Appendix. Use of
the SF–424 (R&R) electronic grant
application will permit insertion into
the body of the Research Plan high
resolution images of the same quality
found in scientific publications.
• Materials currently submitted in the
Appendix which are essential to the
review of the application will be
submitted as part of the grant
application itself. For example,
documents such as clinical protocols,
informed consent forms, key
questionnaires, surveys, and similar
items which are needed by the SRG to
adequately assess human subjects issues
will be submitted as part of the
’Protection of Human Subjects’ section
of the grant application.
• Reprints or preprints of
publications or their PDFs will no
longer be allowed as part of the
Appendix. Links (URLs) to PubMed
Central or publicly available on-line
journals will be permitted in the
Biographical Sketches, Bibliography &
References Cited, and the Research Plan
sections of the grant application. Critical
information and detail should be
included within the Research Plan and
cited in the Bibliography & References
Cited section and/or figure or table
legend(s) to indicate publication status.
• Materials specifically designated in
the Funding Opportunity
Announcement may be included in the
Appendix, within identified page limits.
It is anticipated that most FOAs will not
permit materials to be included in the
Appendix.
• All members of the SRG will
receive copies of the full application
including any permitted Appendix
materials thereby increasing the equity
of the review.
Information Requested
Information in the following areas
will assist the NIH and AHRQ in
developing new policies regarding
submission of appendix materials.
Respondents will be asked to indicate
what perspective(s) they represent, i.e.
reviewer and/or applicant, institutional
official, etc.
1. Is there a need to reduce the
material submitted in the Appendix? If
yes, please provide specific types of
material that could be eliminated.
2. Is there information essential to the
application’s review that cannot be
included in the body of a grant
application as proposed? If yes, please
describe the material and identify
applicable grant program(s).
E:\FR\FM\31JYN1.SGM
31JYN1
Federal Register / Vol. 71, No. 146 / Monday, July 31, 2006 / Notices
3. Is it necessary to include reprint
and preprint PDFs as appendix
material? If yes, please explain.
4. Do you have concerns about
discontinuing the submission of
photographs or color images in the
Appendix of electronic grant
applications? If yes, please explain.
5. Will the proposed changes favor or
disfavor any specific group of
investigators? If yes, please explain.
Responses
Responses must be submitted
electronically at https://grants.nih.gov/
grants/guide/rfi_files/
rfi_appendix_add.htm. The responses
for each item should be limited to 500
words. Acknowledgement of receipt of
responses will not be made, nor will
respondents be notified of the
Government’s assessment of the
information received. No basis for
claims against the Government shall
arise as a result of a response to this
request for information or the
Government’s use of such information
as either part of our evaluation process
or in developing specifications for any
subsequent announcement. Individual
responses will be confidential. Any
proprietary information should be so
marked.
Dated: July 24, 2006.
Norka Ruiz Bravo,
Deputy Director for Extramural Research,
National Institutes of Health.
[FR Doc. E6–12230 Filed 7–28–06; 8:45 am]
BILLING CODE 4140–01–P
DEPARTMENT OF HOUSING AND
URBAN DEVELOPMENT
[Docket No. FR–5039–N–03]
Notice of Proposed Information
Collection: Comment Request;
Affirmative Fair Housing Marketing
(AFHM) Plan
Office of the Assistant
Secretary for Fair Housing and Equal
Opportunity, HUD.
ACTION: Notice.
sroberts on PROD1PC70 with NOTICES
AGENCY:
SUMMARY: The proposed information
collection requirement described below
will be submitted to the Office of
Management and Budget (OMB) for
review, as required by the Paperwork
Reduction Act of 1995. The Department
is soliciting public comments on the
subject proposal.
DATES: Comments Due Date: September
29, 2006.
ADDRESSES: Interested persons are
invited to submit comments regarding
this proposed information collection
VerDate Aug<31>2005
17:34 Jul 28, 2006
Jkt 208001
requirement. Comments should refer to
the proposal by name and/or OMB
Control Number and should be sent to:
Surrell Silverman, Reports Liaison
Officer, Fair Housing and Equal
Opportunity, Department of Housing
and Urban Development, 451 7th Street,
SW., Room 5216, Washington, DC
20410–2000.
FOR FURTHER INFORMATION CONTACT:
Shaye Hardy, Program Standards and
Compliance Division, Office of
Programs, Department of Housing and
Urban Development, 451 7th Street,
SW., Room 5222, Washington, DC
20410–2000; telephone: (202) 708–2288
(this is not a toll-free number) for copies
of the proposed forms and other
available documents. Hearing- or
speech-impaired individuals may access
this number TTY by calling the toll-free
Federal Information Relay Service at 1–
800–877–8339.
SUPPLEMENTARY INFORMATION: The
Department is submitting the proposed
information collection to OMB for
review, as required by the Paperwork
Reduction Act of 1995.
The notice solicits comments from
members of the public and affected
agencies concerning the proposed
information collection in order to:
(1) Evaluate whether the proposed
information collection is necessary for
the proper performance of the
Department’s program functions;
(2) Evaluate the accuracy of the
Department’s assessment of the
paperwork burden that may result from
the proposed information collection;
(3) Enhance the quality, utility, and
clarity of the information which must be
collected; and
(4) Minimize the burden of the
information collection on responders,
including the use of appropriate
automated collection techniques or
other forms of information technology
(e.g., electronic transmission of data).
Title of Regulation: Affirmative Fair
Housing Marketing Regulations and
Affirmative Fair Housing Marketing
Compliance Regulations.
OMB Control Number, if applicable;
2529–0013.
Description of the need for the
information and proposed use: HUD
uses this information to assess the
adequacy of the applicant’s proposed
actions to carry out the Affirmative Fair
Housing Marketing requirements of 24
CFR 200.600 and review compliance
with these requirements under 24 CFR
part 108, the AFHM Compliance
Regulations.
Agency form numbers, if applicable:
HUD–935.2A Affirmative Fair Housing
Marketing Plan (Multifamily) and HUD–
PO 00000
Frm 00112
Fmt 4703
Sfmt 4703
43205
935.2B Affirmative Fair Housing
Marketing Plan (Single-Family).
Members of affected public:
Applicants for mortgage insurance
under the Department’s insured singlefamily and multifamily subsidized and
unsubsidized programs.
Estimation of the total numbers of
hours needed to prepare the
information, collection including
number of respondents, frequency of
response, and hours of response: On an
annual basis, there are approximately
6,530 respondents, 1 response per
respondent, which equals 6,530 total
responses for both forms. Each new
respondent (300 multifamily + 30
single-family = 330 new respondents
annually) should take approximately 3
hours to complete, which equals
approximately 990 hours for new
respondents annually. HUD has
approximately 31,000 multifamily
housing insured and subsidized projects
in its inventory. Since multifamily
housing projects’ Affirmative Fair
Housing Marketing Plans (Multifamily)
(HUD 935.2A) should be reviewed and
updated every 5 years, it is estimated
that 20 percent of the multifamily
housing project inventory (6,200) will
review their plans each year. This
review will take approximately 1 hour
to complete, which equals 6,200 hours
for the review of these plans annually.
It is also estimated that slightly less than
20 percent of the reviewed plans
(approximately 1,200) will need to be
updated. The updating of these plans
will take approximately 1 hour to
complete, which equals approximately
1,200 hours for the updating of these
plans annually. The total estimated
number of hours needed to prepare this
information collection is 8,390 hours.
Status of the proposed information
collection: HUD revised Form HUD–
935.2 Affirmative Fair Housing Plan.
This revision consists of creating a form
to be used by Multifamily Housing
(MFH) and a second form to be used by
Single-Family Housing (SFH). This
action was taken to make the
completion of the form clearer for the
MFH and SFH user. The current form
has several instances where there are
alternative directions. The major
difference in the proposed form is that
the Office of Fair Housing and Equal
Opportunity will have approval
authority for the Form HUD–935.2A to
be completed by MFH users and the
Office of Housing-Single-Family
Housing will have approval authority
for the Form HUD–935.2B to be
completed by SFH users.
Authority: Section 3506 of the Paperwork
Reduction Act of 1995, 44 U.S.C. Chapter 35,
as amended.
E:\FR\FM\31JYN1.SGM
31JYN1
Agencies
[Federal Register Volume 71, Number 146 (Monday, July 31, 2006)]
[Notices]
[Pages 43204-43205]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E6-12230]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
National Institutes of Health
Request for Information (RFI): Change in Grant Appendix Materials
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: The National Institutes of Health (NIH) and the Agency for
Healthcare Research and Quality (AHRQ) are evaluating guidelines for
grant application appendixes in an effort to streamline the application
and review processes. This RFI requests input from interested
applicants, reviewers and other members of the research community
regarding the way appendix materials should be used in the grant
submission, review and management process. Comments will be considered
in the development of new policies on appendix materials for various
grant programs.
DATES: Reponses must be received by September 14, 2006 in order to
ensure that NIH and AHRQ will be able to consider the comments in
developing new policies on appendix materials for various grant
programs.
FOR FURTHER INFORMATION CONTACT: E-mail inquiries will be accepted at
appendix_comments@od.nih.gov.
SUPPLEMENTARY INFORMATION:
Background
The goal of changing the guidelines for grant application appendix
materials is to encourage applications to be as concise as possible
while containing the information needed for expert scientific review.
These changes should make application preparation and handling easier
for both applicants and reviewers.
Current NIH and AHRQ policy indicates that the Appendix may not be
used to circumvent the page limitations of the Research Plan. Appended
publications may not be used to provide further details of
methodologies or preliminary data described in the Research Plan. All
applications and proposals for NIH and AHRQ funding must be self-
contained. NIH application guide instructions note that the Appendix is
sent only to those members of the Scientific Review Group (SRG)
assigned as primary reviewers of the application. Currently, unless
otherwise stated in the solicitation, the following materials may be
included in a grant application Appendix:
Up to 10 publications or manuscripts accepted for
publication, using URL links to publicly accessible journal articles.
Surveys, questionnaires, data collection instruments,
clinical protocols, and informed consent documents.
Photographs or color images of gels, micrographs, etc.,
provided that a photocopy (may be reduced in size) is also included
within the 25-page limit of Items a-d of the research plan. No
photographs or color images may be included in the Appendix that are
not also represented within the Research Plan.
Investigators spend much time and energy developing applications to
Federal Agencies. It is unclear whether appendix material which may or
may not be read by members of the SRG improves current applications.
Submission of unnecessary materials with grant applications wastes the
time, energy and resources of investigators, applicant institutions,
reviewers, and the NIH and AHRQ.
Proposed Changes
The following changes are being considered for implementation
concurrent with NIH/AHRQ's transition to the electronic grant
application process and the SF-424 (R&R):
Submission of photographs or color images of gels,
micrographs, etc., will not be allowed in the Appendix. Use of the SF-
424 (R&R) electronic grant application will permit insertion into the
body of the Research Plan high resolution images of the same quality
found in scientific publications.
Materials currently submitted in the Appendix which are
essential to the review of the application will be submitted as part of
the grant application itself. For example, documents such as clinical
protocols, informed consent forms, key questionnaires, surveys, and
similar items which are needed by the SRG to adequately assess human
subjects issues will be submitted as part of the 'Protection of Human
Subjects' section of the grant application.
Reprints or preprints of publications or their PDFs will
no longer be allowed as part of the Appendix. Links (URLs) to PubMed
Central or publicly available on-line journals will be permitted in the
Biographical Sketches, Bibliography & References Cited, and the
Research Plan sections of the grant application. Critical information
and detail should be included within the Research Plan and cited in the
Bibliography & References Cited section and/or figure or table
legend(s) to indicate publication status.
Materials specifically designated in the Funding
Opportunity Announcement may be included in the Appendix, within
identified page limits. It is anticipated that most FOAs will not
permit materials to be included in the Appendix.
All members of the SRG will receive copies of the full
application including any permitted Appendix materials thereby
increasing the equity of the review.
Information Requested
Information in the following areas will assist the NIH and AHRQ in
developing new policies regarding submission of appendix materials.
Respondents will be asked to indicate what perspective(s) they
represent, i.e. reviewer and/or applicant, institutional official, etc.
1. Is there a need to reduce the material submitted in the
Appendix? If yes, please provide specific types of material that could
be eliminated.
2. Is there information essential to the application's review that
cannot be included in the body of a grant application as proposed? If
yes, please describe the material and identify applicable grant
program(s).
[[Page 43205]]
3. Is it necessary to include reprint and preprint PDFs as appendix
material? If yes, please explain.
4. Do you have concerns about discontinuing the submission of
photographs or color images in the Appendix of electronic grant
applications? If yes, please explain.
5. Will the proposed changes favor or disfavor any specific group
of investigators? If yes, please explain.
Responses
Responses must be submitted electronically at https://
grants.nih.gov/grants/guide/rfi_files/rfi_appendix_add.htm. The
responses for each item should be limited to 500 words. Acknowledgement
of receipt of responses will not be made, nor will respondents be
notified of the Government's assessment of the information received. No
basis for claims against the Government shall arise as a result of a
response to this request for information or the Government's use of
such information as either part of our evaluation process or in
developing specifications for any subsequent announcement. Individual
responses will be confidential. Any proprietary information should be
so marked.
Dated: July 24, 2006.
Norka Ruiz Bravo,
Deputy Director for Extramural Research, National Institutes of Health.
[FR Doc. E6-12230 Filed 7-28-06; 8:45 am]
BILLING CODE 4140-01-P