Advisory Commission on Childhood Vaccines; Notice of Meeting, 7750-7751 [05-2881]
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7750
Federal Register / Vol. 70, No. 30 / Tuesday, February 15, 2005 / Notices
Send comments to Susan G. Queen,
Ph.D., HRSA Reports Clearance Officer,
Room 10–33, Parklawn Building, 5600
Fishers Lane, Rockville, MD 20857.
Written comments should be received
within 60 days of this notice.
Dated: February 8, 2005.
Steven A. Pelovitz,
Associate Administrator for Administration
and Financial Management.
[FR Doc. 05–2819 Filed 2–14–05; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERViCES
Health Resources and Services
Administration
data collection plans and draft
instruments, call the HRSA Reports
Clearance Officer on (301) 443–1129.
Comments are invited on: (a) Whether
the proposed collection of information
is necessary for the proper performance
of the functions of the agency, including
whether the information shall have
practical utility; (b) the accuracy of the
agency’s estimate of the burden of the
proposed collection of information; (c)
ways to enhance the quality, utility, and
clarity of the information to be
collected; and (d) ways to minimize the
burden of the collection of information
on respondents, including through the
use of automated collection techniques
or other forms of information
technology.
Agency Information Collection
Activities: Proposed Collection:
Comment Request
In compliance with the requirement
for opportunity for public comment on
proposed data collection projects
(section 3506 (c)(2)(A) of Title 44,
United States Code, as amended by the
Paperwork Reduction Act of 1995,
Public Law 104–13), the Health
Resources and Services Administration
(HRSA) publishes periodic summaries
of proposed projects being developed
for submission to the Office of
Management and Budget (OMB) under
the Paperwork Reduction Act of 1995.
To request more information on the
proposed project or to obtain copy of the
Proposed Project: Health Resources and
Services Administration (HRSA)
Awardee Application and Reporting
Tool (AART): (New)
The Awardee Application and
Reporting Tool (AART) will be an
online system allowing the 62 Awardees
participating in the National
Bioterrorism Hospital Preparedness
Program (NBHPP) to electronically
submit a continuing cooperative
agreement application (CAA), mid-year
progress report on annual activities, a
final report on annual activities and
progress indicator report to HRSA’s
Healthcare Systems Bureau, Division of
Healthcare Preparedness. The CAA will
be a standardized application consisting
Number of
respondents
Submission type
Responses
per
Respondent
of 16 Critical Benchmarks (CBM). For
each CBM, Awardees will be required to
provide a goal, objectives, and a budget
outlining how funding provided by
HRSA will be spent during the coming
year. On the mid-year progress report,
Awardees will indicate the progress
they have made toward each of the
objectives they noted on their CAA. For
the final report on annual activities,
Awardees will provide additional
details on how their objectives were
being achieved and how the program
monies were spent. On the progress
indicator report, Awardees will indicate
the progress they have made to date
toward achieving the program’s CBM.
Currently, the submission of the CAA
and progress reports is a manual process
by which Awardees submit paper-based
submissions or electronically transmit
text files to HRSA project officers (POs).
These files are then reviewed manually
and data analysis is difficult. The AART
system will provide POs with the ability
to review and approve applications,
review progress reports, and generate
reports online. In addition, the reporting
interface will allow HRSA to quickly
and efficiently analyze data, identify
trends, make timely program decisions,
and provide the Department of Health
and Human Services (HHS), Congress,
or other Agencies with any specific data
or metrics requested.
The burden estimate for Awardees to
complete and submit a submission is as
follows:
Total number
of responses
Hours per
response
Total burden
hours
Cooperative Agreement Application ....................................
Mid-year Report ...................................................................
Final Report on Annual Activities ........................................
Progress Indicator Report ....................................................
62
62
62
62
1
1
1
1
62
62
62
62
120
124
124
124
7,440
7,688
7,688
7,688
Total ..............................................................................
62
4
248
........................
30,504
Send comments to Susan G. Queen,
Ph.D., HRSA Reports Clearance Officer,
Room 14–45, Parklawn Building, 5600
Fishers Lane, Rockville, MD 20857.
Written comments should be received
within 60 days of this notice.
Dated: February 8, 2005.
Steven A. Pelovitz,
Associate Administrator for Administration
and Financial Management.
[FR Doc. 05–2820 Filed 2–14–05; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Health Resources and Services
Administration
Advisory Commission on Childhood
Vaccines; Notice of Meeting
In accordance with section 10(a)(2) of
the Federal Advisory Committee Act
(Pub. L. 92–463), notice is hereby given
of the following meeting:
Name: Advisory Commission on
Childhood Vaccines (ACCV).
Dates and Times: March 9, 2005, 12 noon–
4:30 p.m., EST and March 10, 2005, 9 a.m.–
5 p.m., EST.
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Place: Audio Conference Call and
Parklawn Building, Conference Rooms G & H,
5600 Fishers Lane, Rockville, MD 20857.
Status: The meeting is open to the public.
The public can join the meeting in person at
the address listed above or by audio
conference call by dialing 1–888–913–9965
on March 9–10 and providing the following
information:
Leader’s Name: Joyce Somsak.
Password: ACCV.
Agenda: The agenda items will include,
but are not limited to: a summary of the
Causation in Fact session at the U.S. Court
of Federal Claims’ 17th Judicial Conference;
a report and discussion from the ACCV
Workgroup on changes to the Vaccine Injury
Table; and updates from the Division of
Vaccine Injury Compensation (DVIC), the
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Federal Register / Vol. 70, No. 30 / Tuesday, February 15, 2005 / Notices
Department of Justice, and the National
Vaccine Program Office. Agenda items are
subject to change as priorities dictate.
Public Comments: Persons interested in
providing an oral presentation should submit
a written request, along with a copy of their
presentation to: Ms. Cheryl Lee, Principal
Staff Liaison, DVIC, Healthcare Systems
Bureau (HSB), Health Resources and Services
Administration (HRSA), Room 11C–26, 5600
Fishers Lane, Rockville, MD 20857 or e-mail
clee@hrsa.gov. Requests should contain the
name, address, telephone number, and any
business or professional affiliation of the
person desiring to make an oral presentation.
Groups having similar interests are requested
to combine their comments and present them
through a single representative. The
allocation of time may be adjusted to
accommodate the level of expressed interest.
DVIC will notify each presenter by mail or
telephone of their assigned presentation time.
Persons who do not file an advance request
for a presentation, but desire to make an oral
statement, may announce it at the time of the
comment period. These persons will be
allocated time as it permits.
For further information contact: Anyone
requiring information regarding the ACCV,
should contact Ms. Cheryl Lee, Principal
Staff Liaison, DVIC, HSB, HRSA, Room 11C–
26, 5600 Fishers Lane, Rockville, MD 20857;
telephone (301) 443–2124 or e-mail
clee@hrsa.gov.
Dated: February 9, 2005.
Tina M. Cheatham,
Director, Division of Policy Review and
Coordination.
[FR Doc. 05–2881 Filed 2–14–05; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health/National
Institute of Environmental Health
Sciences; Division of Extramural
Research and Training
Submission for OMB Review;
Comment Request; Hazardous Waste
Worker Training
Summary: Under the provisions of
Section 3507(a)(1)(D) of the Paperwork
Reduction Act of 1995, the National
Institute of Environmental Health
Sciences (NIEHS), the National
Institutes of Health (NIH) has submitted
to the Office of Management and Budget
(OMB) a request to review and approve
the information collection listed below.
This proposed information collection
was previously published in the Federal
Register on December 8, 2004, pages
71061–71062, and allowed 60-days for
public comment. No public comments
were received. The purpose of this
notice is to allow an additional 30 days
for public comment. The National
Institutes of Health may not conduct or
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17:50 Feb 14, 2005
Jkt 205001
sponsor, and the respondent is not
required to respond to, an information
collection that has been extended,
revised, or implemented on or after
October 1, 1995, unless it displays a
currently valid OMB control number.
Proposed Collection: Title: Hazardous
Waste Worker Training—42 CFR Part
65. Type of Information Collection
Request: Revision of OMB No. 0925–
0348, expiration date February 28, 2005.
Need and Use of Information Collection:
This request for OMB review and
approval of the information collection is
required by regulation 42 CFR part
65(a)(6). The National Institute of
Environmental Health Sciences (NIEHS)
has been given major responsibility for
initiating a worker safety and health
training program under Section 126 of
the Superfund Amendments and
Reauthorization Act of 1986 (SARA) for
hazardous waste workers and
emergency responders. A network of
non-profit organizations that are
committed to protecting working and
their communities by delivering highquality, peer-reviewed safety and health
curricula to target populations of
hazardous waste workers and
emergency responders has been
developed. In seventeen years (FY
1987–2004), the NIEHS Worker Training
program has successfully supported 20
primary grantees that have trained more
than 1.3 million workers across the
country and presented over 69,000
classroom and hands-on training
courses, which have accounted for
nearly 18 million contact hours of actual
training. Generally, the grant will
initially be for one year, and subsequent
continuation awards are also for one
year at a time. Grantees must submit a
separate application to have the support
continued for each subsequent year.
Grantees are to provide information in
accordance with S65.4 (a), (b), (c) and
65.6 (b) on the nature, duration, and
purpose of the training, selection
criteria for trainees’ qualifications and
competency of the project director and
staff, cooperative agreements in the case
of joint applications, the adequacy of
training plans and resources, including
budget and curriculum, and response to
meeting training criteria in OSHA’s
Hazardous Waste Operations and
Emergency Response Regulations (29
CFR 1910.120). As a cooperative
agreement, there are additional
requirements for the progress report
section of the application. Grantees are
to provide their information in hard
copy as well as enter information into
the WETP Grantee Data Management
System. The information collected is
used by the Director through officers,
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7751
employees, experts, and consultants to
evaluate applications based on technical
merit to determine whether to make
awards. Frequency of Response:
Biannual. Affected Public: Non-profit
organizations. Type of Respondents:
Grantees. The annual reporting burden
is as follows: Estimated Number of
Respondents: 18; Estimated Number of
Responses per Respondent: 2; Average
Burden Hours Per Response: 10; and
Estimated Total Annual Burden Hours
Requested: 360. The annualized cost to
respondents is estimated at: $10,764.
There are no Capital Costs, Operating
Costs and/or Maintenance Costs to
report.
Request for Comments: Written
comments and/or suggestions from the
public and affected agencies are invited
on one or more of the following points:
(1) Whether the proposed collection of
information is necessary for the proper
performance of the function of the
agency, including whether the
information will have practical utility;
(2) The accuracy of the agency’s
estimate of the burden of the proposed
collection of information, including the
validity of the methodology and
assumptions used; (3) Ways to enhance
the quality, utility, and clarity of the
information to be collected; and (4)
Ways to minimize the burden of the
collection of information on those who
are to respond, including the use of
appropriate automated, electronic,
mechanical, or other technological
collection techniques or other forms of
information technology.
Direct Comments to OMB: Written
comments and/or suggestions regarding
the item(s) contained in this notice,
especially regarding the estimated
public burden and associated response
time, should be directed to the: Office
of Management and Budget, Office of
Regulatory Affairs, New Executive
Office Building, Room 10235,
Washington, DC 20503, Attention: Desk
Officer for NIH. To request more
information on the proposed project or
to obtain a copy of the data collection
plans and instruments, contact: Joseph
T. Hughes, Jr., Director, Worker
Education and Training Program,
Division of Extramural Research and
Training, NIEHS, P.O. Box 12233,
Research Triangle Park, NC 27709 or
call non-toll-free number (919) 541–
0217 or E-mail your request, including
your address to wetp@niehs.nih.gov.
Comments Due Date: Comments
regarding this information collection are
best assured of having their full effect if
received within 30-days of the date of
this publication.
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Agencies
[Federal Register Volume 70, Number 30 (Tuesday, February 15, 2005)]
[Notices]
[Pages 7750-7751]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 05-2881]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Health Resources and Services Administration
Advisory Commission on Childhood Vaccines; Notice of Meeting
In accordance with section 10(a)(2) of the Federal Advisory
Committee Act (Pub. L. 92-463), notice is hereby given of the following
meeting:
Name: Advisory Commission on Childhood Vaccines (ACCV).
Dates and Times: March 9, 2005, 12 noon-4:30 p.m., EST and March
10, 2005, 9 a.m.-5 p.m., EST.
Place: Audio Conference Call and Parklawn Building, Conference
Rooms G & H, 5600 Fishers Lane, Rockville, MD 20857.
Status: The meeting is open to the public. The public can join
the meeting in person at the address listed above or by audio
conference call by dialing 1-888-913-9965 on March 9-10 and
providing the following information:
Leader's Name: Joyce Somsak.
Password: ACCV.
Agenda: The agenda items will include, but are not limited to: a
summary of the Causation in Fact session at the U.S. Court of
Federal Claims' 17th Judicial Conference; a report and discussion
from the ACCV Workgroup on changes to the Vaccine Injury Table; and
updates from the Division of Vaccine Injury Compensation (DVIC), the
[[Page 7751]]
Department of Justice, and the National Vaccine Program Office.
Agenda items are subject to change as priorities dictate.
Public Comments: Persons interested in providing an oral
presentation should submit a written request, along with a copy of
their presentation to: Ms. Cheryl Lee, Principal Staff Liaison,
DVIC, Healthcare Systems Bureau (HSB), Health Resources and Services
Administration (HRSA), Room 11C-26, 5600 Fishers Lane, Rockville, MD
20857 or e-mail clee@hrsa.gov. Requests should contain the name,
address, telephone number, and any business or professional
affiliation of the person desiring to make an oral presentation.
Groups having similar interests are requested to combine their
comments and present them through a single representative. The
allocation of time may be adjusted to accommodate the level of
expressed interest. DVIC will notify each presenter by mail or
telephone of their assigned presentation time.
Persons who do not file an advance request for a presentation,
but desire to make an oral statement, may announce it at the time of
the comment period. These persons will be allocated time as it
permits.
For further information contact: Anyone requiring information
regarding the ACCV, should contact Ms. Cheryl Lee, Principal Staff
Liaison, DVIC, HSB, HRSA, Room 11C-26, 5600 Fishers Lane, Rockville,
MD 20857; telephone (301) 443-2124 or e-mail clee@hrsa.gov.
Dated: February 9, 2005.
Tina M. Cheatham,
Director, Division of Policy Review and Coordination.
[FR Doc. 05-2881 Filed 2-14-05; 8:45 am]
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