Agency Forms Undergoing Paperwork Reduction Act Review, 54828-54829 [E6-15504]
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54828
Federal Register / Vol. 71, No. 181 / Tuesday, September 19, 2006 / Notices
such objectives were not met, a
statement of why they were not met.
• Specific action(s) that the grantee
would like the OGHA/HHS to undertake
to alleviate a problem.
• Other pertinent information that
will permit monitoring and overview of
project operations.
• A quarterly financial report
describing the current financial status of
the funds used under this award. The
awardee and OGHA will agree at the
time of award for the format of this
portion of the report.
Within 90 days following the end of
the project period a final report
containing information and data of
interest to the Department of Health and
Human Services, Congress, and other
countries must be submitted to OGHA/
HHS. The specifics as to the format and
content of the final report and the
summary will be sent to the successful
applicant. At minimum, the report
should contain:
• A summary of the major activities
supported under the agreement and the
major accomplishments resulting from
activities to improve mortality in
partner country.
• An analysis of the project based on
the problem(s) described in the
application and needs assessments,
performed prior to or during the project
period, including a description of the
specific objectives stated in the grant
application and the accomplishments
and failures resulting from activities
during the grant period.
Quarterly performance reports and
annual reports may be submitted to: Mr.
DeWayne Wynn, Grants Management
Specialist, Office of Grants
Management, OPHS, HHS, 1101
Wootton Parkway, Suite 550, Rockville,
MD 20852, phone (240) 453–8822.
A Financial Status Report (FSR) SF–
269 is due 90 days after the close of each
12-month budget period and submitted
to OPHS—Office of Grants Management.
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VII. Agency Contacts
For assistance on administrative and
budgetary requirements, please contact:
Mr. DeWayne Wynn, Grants
Management Specialist, Office of Grants
Management, OPHS, HHS, 1101
Wootton Parkway, Suite 550, Rockville,
MD 20852, phone (240) 453–8822.
For assistance with questions
regarding program requirements, please
contact: Dr. Amar Bhat, Office of Global
Health Affairs, Asia-Pacific Division,
Office of the Secretary, Department of
Health and Human Services, 5600
Fishers Lane, Suite 18–101, Rockville,
MD 20857, phone: (301) 443–1410.
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VIII. Tips for Writing a Strong
Application
Include DUNS Number. You must
include a DUNS Number to have your
application reviewed. An application
will not be reviewed without a DUNS
number. To obtain a DUNS number,
access https://
www.dunandbradstreet.com or call 1–
866–705–5711. Please include the
DUNS number next to the OMB
Approval Number on the application
face page.
Keep your audience in mind.
Reviewers will use only the information
contained in the application to assess
the application. Be sure the application
and responses to the program
requirements and expectations are
complete and clearly written. Do not
assume that reviewers are familiar with
the applicant organization. Keep the
review criteria in mind when writing
the application.
Start preparing the application early.
Allow plenty of time to gather required
information from various sources.
Follow the instructions in this
guidance carefully. Place all information
in the order requested in the guidance.
If the information is not placed in the
requested order, you may receive a
lower score.
Be brief, concise, and clear. Make
your points understandable. Provide
accurate and honest information,
including candid accounts of problems
and realistic plans to address them. If
any required information or data is
omitted, explain why. Make sure the
information provided in each table,
chart, attachment, etc., is consistent
with the proposal narrative and
information in other tables.
Be organized and logical. Many
applications fail to receive a high score
because the reviewers cannot follow the
thought process of the applicant or
because parts of the application do not
fit together.
Be careful in the use of appendices.
Do not use the appendices for
information that is required in the body
of the application. Be sure to crossreference all tables and attachments
located in the appendices to the
appropriate text in the application.
Carefully proofread the application.
Misspellings and grammatical errors
will impede reviewers in understanding
the application. Be sure pages are
numbered (including appendices) and
that page limits are followed. Limit the
use of abbreviations and acronyms, and
define each one at its first use and
periodically throughout application.
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Dated: September 12, 2006.
Sandra R. Manning,
Deputy Director for Operations and
Management, Office of Global Health Affairs.
[FR Doc. E6–15503 Filed 9–18–06; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[30Day–06–0199]
Agency Forms Undergoing Paperwork
Reduction Act Review
The Centers for Disease Control and
Prevention (CDC) publishes a list of
information collection requests under
review by the Office of Management and
Budget (OMB) in compliance with the
Paperwork Reduction Act (44 U.S.C.
Chapter 35). To request a copy of these
requests, call the CDC Reports Clearance
Officer at (404) 639–5960 or send an email to omb@cdc.gov. Send written
comments to CDC Desk Officer, Office of
Management and Budget, Washington,
DC or by fax to (202) 395–6974. Written
comments should be received within 30
days of this notice.
Proposed Project
Importation of Etiologic Agents,
Hosts, and Vectors of Human Disease
(42 CFR 71.54)—(OMB Control No.
0920–0199)—Revision—Office of the
Director (OD), Centers for Disease
Control and Prevention.
Background and Brief Description
The Foreign Quarantine Regulations
(42 CFR Part 71) set forth provisions to
prevent the introduction, transmission,
and spread of communicable disease
from foreign countries into the United
States. Subpart F—Importations—
contains provisions for importation of
etiologic agents, hosts, and vectors (42
CFR 71.54), requiring persons that
import or distribute after importation of
these materials to obtain a permit issued
by the CDC. This request is for the
information collection requirements
contained in 42 CFR 71.54 for issuance
of permits by CDC to importers or
distributors after importation of
etiologic agents, hosts, or vectors of
human disease.
CDC is requesting continued OMB
approval to collect this information
through the use of two separate forms.
These forms are: (1) Application for
Permit to Import or Transport Etiologic
Agents, Hosts, or Vectors of Human
Disease and (2) Application for Permit
to Import or Transport Live Bats.
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Federal Register / Vol. 71, No. 181 / Tuesday, September 19, 2006 / Notices
The Application for Permit to Import
or Transport Etiologic Agents, Hosts, or
Vectors of Human Disease will be used
by laboratory facilities, such as those
operated by government agencies,
universities, research institutions, and
zoologic exhibitions, and also by
importers of nonhuman primate trophy
materials, such as hunters or
taxidermists, to request permits for the
importation and subsequent distribution
after importation of etiologic agents,
hosts, or vectors of human disease. The
Application for Permit to Import or
Transport Etiologic Agents, Hosts, or
Vectors of Human Disease requests
applicant and sender contact
information; description of material for
importation; facility isolation and
containment information; and personnel
qualifications. Estimated average time to
complete this form is 20 minutes.
The Application for Permit to Import
or Transport Live Bats will be used by
laboratory facilities such as those
operated by government agencies,
universities, research institutions, and
54829
zoologic exhibitions entities to request
importation and subsequent distribution
after importation of live bats. The
Application for Permit to Import or
Transport Live Bats requests applicant
and sender contact information; a
description and intended use of bats to
be imported; facility isolation and
containment information; and personnel
qualifications.
There is no cost to the respondents
other than their time. The total
annualized burden is 766 hours.
ESTIMATE OF ANNUALIZED BURDEN HOURS
CFR section
Number of
respondents
Responses per
respondent
Average hourly
burden
71.54 Application for Permit ....................................................................................................
2,300
1
20/60
Dated: September 12, 2006.
Joan F. Karr,
Acting Reports Clearance Officer, Centers for
Disease Control and Prevention.
[FR Doc. E6–15504 Filed 9–18–06; 8:45 am]
Act, Title III, section 330(e)(1)(C), and
330(c)(1)(B) and 330(c)(1)(C).
Background
The Health Resources and Services
Administration (HRSA), an agency of
the U.S. Department of Health and
Human Services, is the primary Federal
agency for improving access to health
DEPARTMENT OF HEALTH AND
care services for people who are
HUMAN SERVICES
uninsured, isolated or medically
Health Resources and Services
vulnerable. Comprising five bureaus and
Administration
12 offices, HRSA provides leadership
and financial support to health care
Strategy To Support Health
providers in every State and U.S.
Information Technology Among
territory. HRSA grantees provide health
HRSA’s Safety Net Providers
care to uninsured people, people living
with HIV/AIDS, and pregnant women,
AGENCY: Health Resources and Services
mothers and children. They train health
Administration (HRSA), HHS.
professionals and improve systems of
ACTION: Solicitation of comments.
care in rural communities. HRSA is the
Nation’s access agency—improving
SUMMARY: HRSA is requesting comments health and saving lives by making sure
on the future direction and strategy
the right services are available in the
regarding investments in health
right places at the right time.
information technology (HIT) for section
The Office of Health Information
330 grantees and other HRSA safety-net Technology (OHIT) serves as the HRSA
providers through its Office of Health
Administrator’s principal advisor for
Information Technology (OHIT). OHIT
promoting the adoption of HIT in the
will evaluate all comments received
service of the medically uninsured,
during the public comment period to
underserved and other vulnerable
inform OHIT’s policy direction.
populations, and ensuring that key
issues affecting the public and private
DATES: To be considered, comments
adoption of HIT are addressed. The
must be received by October 10, 2006.
mission of OHIT is to promote quality
FOR FURTHER INFORMATION CONTACT:
of care and improvements in patient
Anthony Achampong, Division of
health outcomes through the adoption
Health Information Technology State
and effective use of health information
and Community Assistance, Office of
technology (HIT) in the safety-net
Health Information Technology, Health
community. OHIT is also responsible for
Resources and Services Administration,
administering the Telehealth and Health
5600 Fishers Lane, 7C–22, Rockville,
Center Controlled Network (HCCN)
Maryland 20857;
grant programs. OHIT’s goal is to
aachampong@hrsa.gov.
represent the HIT needs of the safety-net
community providers to ensure that a
SUPPLEMENTARY INFORMATION: In
digital divide does not separate care for
accordance with Public Health Service
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patients of HRSA grantees and those
receiving care in other sectors. OHIT’s
goal is also to provide leadership across
the Federal agencies in HIT adoption in
the safety-net community.
HCCNs are the potential foundation
for a HRSA strategy on HIT adoption
and use by section 330 grantees. The
HCCN grant program was developed in
1994 to support the creation,
development, and operation of
networks, controlled by health centers,
to ensure access to health care for the
medically underserved populations
through the enhancement of health
center operations. The HCCNs routinely
perform core business functions across
their marketplace, State, or region. The
core business functions range from
electronic health records, credentialing
and privileging programs, utilization
review and management, and clinical
quality improvement. They provide
these functions at or below marketplace
cost to their members to increase
efficiencies, reduce costs, and improve
health care quality for underserved and
uninsured populations. As such, the
HCCNs are vital to achieving the
President’s goal of assuring that every
American in the Nation will have an
Electronic Health Record (EHR) by 2014.
HRSA’S Quality Initiative
In May 2006, HRSA reconfirmed its
goal to improve the quality of health
service and health outcomes for all the
patients served by HRSA grantees
including the 14.5 million patients
served by health centers, and
announced a commitment to develop
new reporting requirements to measure
and document clinical outcomes. It is
expected that further development of
the HIT infrastructure used by health
centers and other HRSA grantees will
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]]>Agencies
[Federal Register Volume 71, Number 181 (Tuesday, September 19, 2006)]
[Notices]
[Pages 54828-54829]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E6-15504]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[30Day-06-0199]
Agency Forms Undergoing Paperwork Reduction Act Review
The Centers for Disease Control and Prevention (CDC) publishes a
list of information collection requests under review by the Office of
Management and Budget (OMB) in compliance with the Paperwork Reduction
Act (44 U.S.C. Chapter 35). To request a copy of these requests, call
the CDC Reports Clearance Officer at (404) 639-5960 or send an e-mail
to omb@cdc.gov. Send written comments to CDC Desk Officer, Office of
Management and Budget, Washington, DC or by fax to (202) 395-6974.
Written comments should be received within 30 days of this notice.
Proposed Project
Importation of Etiologic Agents, Hosts, and Vectors of Human
Disease (42 CFR 71.54)--(OMB Control No. 0920-0199)--Revision--Office
of the Director (OD), Centers for Disease Control and Prevention.
Background and Brief Description
The Foreign Quarantine Regulations (42 CFR Part 71) set forth
provisions to prevent the introduction, transmission, and spread of
communicable disease from foreign countries into the United States.
Subpart F--Importations--contains provisions for importation of
etiologic agents, hosts, and vectors (42 CFR 71.54), requiring persons
that import or distribute after importation of these materials to
obtain a permit issued by the CDC. This request is for the information
collection requirements contained in 42 CFR 71.54 for issuance of
permits by CDC to importers or distributors after importation of
etiologic agents, hosts, or vectors of human disease.
CDC is requesting continued OMB approval to collect this
information through the use of two separate forms. These forms are: (1)
Application for Permit to Import or Transport Etiologic Agents, Hosts,
or Vectors of Human Disease and (2) Application for Permit to Import or
Transport Live Bats.
[[Page 54829]]
The Application for Permit to Import or Transport Etiologic Agents,
Hosts, or Vectors of Human Disease will be used by laboratory
facilities, such as those operated by government agencies,
universities, research institutions, and zoologic exhibitions, and also
by importers of nonhuman primate trophy materials, such as hunters or
taxidermists, to request permits for the importation and subsequent
distribution after importation of etiologic agents, hosts, or vectors
of human disease. The Application for Permit to Import or Transport
Etiologic Agents, Hosts, or Vectors of Human Disease requests applicant
and sender contact information; description of material for
importation; facility isolation and containment information; and
personnel qualifications. Estimated average time to complete this form
is 20 minutes.
The Application for Permit to Import or Transport Live Bats will be
used by laboratory facilities such as those operated by government
agencies, universities, research institutions, and zoologic exhibitions
entities to request importation and subsequent distribution after
importation of live bats. The Application for Permit to Import or
Transport Live Bats requests applicant and sender contact information;
a description and intended use of bats to be imported; facility
isolation and containment information; and personnel qualifications.
There is no cost to the respondents other than their time. The
total annualized burden is 766 hours.
Estimate of Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
Number of Responses per Average hourly
CFR section respondents respondent burden
----------------------------------------------------------------------------------------------------------------
71.54 Application for Permit.............................. 2,300 1 20/60
----------------------------------------------------------------------------------------------------------------
Dated: September 12, 2006.
Joan F. Karr,
Acting Reports Clearance Officer, Centers for Disease Control and
Prevention.
[FR Doc. E6-15504 Filed 9-18-06; 8:45 am]
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