National Institute for Occupational Safety and Health Advisory Board on Radiation and Worker Health, 2946 [E6-436]
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Federal Register / Vol. 71, No. 11 / Wednesday, January 18, 2006 / Notices
complete collection of diabetes program
progress information using the Internet.
The number of hours that DPCPs
users spend with the system usage has
increased since compared to the initial
baseline proposed in the last OMB
approval three years ago. This increase
in burden does not directly translate
into a greater reporting burden, but
facilitates better monitoring and
tracking of their programs and helps
create an organizational memory.
Consequently, they are using the System
to a great extent as an integral part of
their program compared to previous
years. DPCPs add updates about their
work plans and other activities into the
System on an ongoing basis. The hourburden estimates include the time for
reviewing instructions, searching
existing data sources, gathering and
maintaining the data needed, and
completing and reviewing the collection
of information. Based on input provided
by a representative sample for DPCPs,
the total annualized response burden
increased from 4 to 96 hours, changing
the total burden hours from 236 to
5,664. Even though there has been an
increase in the burden hours the
number of responses remains at one (1),
because the DPCPs are only required to
report annually to CDC.
MIS has improved upon the old data
collection system by:
• Improving accountability.
• Shortening the information cycle.
• Eliminating non-standard reporting.
• Minimizing unnecessary
duplication of data collection and entry.
• Reducing the reporting burden on
small state organizations.
• Using plain, coherent, and
unambiguous terminology that is
understandable to respondents.
• Implementing a consistent system
for progress reporting and record
keeping processes.
• Identifying the retention periods for
record keeping requirements.
• Utilizing modern information
technology for data collection and
transfer.
• Significantly reducing the amount
of paper reports that diabetes prevention
and control programs are required to
submit.
MIS has allowed CDC to more rapidly
respond to outside inquiries concerning
a specific diabetes control activity
occurring in the state diabetes
prevention and control programs. The
data collection requirement has
formalized the format and the content of
diabetes data reported from the DPCPs
and provides an electronic means for
efficient collection and transmission to
the CDC headquarters.
MIS has facilitated the staff’s ability at
CDC to fulfill its obligations under the
cooperative agreements; to monitor,
evaluate, and compare individual
programs; and to assess and report
aggregate information regarding the
overall effectiveness of the DCP
program. It has also supported DDT’s
broader mission of reducing the burden
of diabetes by enabling DDT staff to
more effectively identify the strengths
and weaknesses of individual DPCPs
and to disseminate information related
to successful public health interventions
implemented by these organizations to
prevent and control diabetes.
Implementation of MIS has provided for
efficient collection of state-level
diabetes program data. The respondent’s
average Internet cost is $1,080 per year.
ESTIMATED ANNUALIZED BURDEN TABLE
Respondents
Number of
respondents
Number of
responses per
respondent
Average burden
per response
(in hrs.)
Total burden
(hours)
State Program Control Officers ...............................................................
59
1
96
5664
Dated: January 10, 2006.
Joan F. Karr,
Acting Reports Clearance Officer, Centers for
Disease Control and Prevention.
[FR Doc. E6–442 Filed 1–17–06; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
erjones on PROD1PC68 with NOTICES
National Institute for Occupational
Safety and Health Advisory Board on
Radiation and Worker Health
In accordance with section 10(a)(2) of
the Federal Advisory Committee Act
(Pub. L. 92–463), the Centers for Disease
Control and Prevention (CDC)
announces the following committee
meeting:
Correction: This notice was published
in the Federal Register on January 3,
2006, volume 71, Number 1, Page 120–
121. The meeting times/dates and
‘‘matters to be discussed’’ have been
changed.
VerDate Aug<31>2005
15:06 Jan 17, 2006
Jkt 208001
Subcommittee Meeting Time and
Date: 9 a.m.–2 p.m., January 24, 2006.
Committee Meeting Times and Dates:
2:30 a.m.–5 p.m., January 24, 2006. 8:30
a.m.–5 p.m., January 25, 2006. 8:30
a.m.–4:30 p.m., January 26, 2006.
Matters to be Discussed: The agenda
for the Subcommittee meeting includes
Task 3 review; review of Bethlehem
Steel, Rocky Flats, and Y–12 site
profiles; and individual dose
reconstruction reviews. The agenda for
the Board meeting includes Reports
from the Subcommittee and Working
Groups; Pacific Proving Grounds
Special Exposure Cohort (SEC)
Evaluation Report and Supplement; Site
Profiles for Bethlehem Steel, Rocky
Flats, Y–12, Hanford, Nevada Test Site,
and Savannah River Site; Letter from
Steel Workers; SEC Rule rewrite; Task 3
review of SC&A Contract; Conflict of
Interest issues; Dose Reconstruction
Reviews; an update on Science Issues
which will include but not be limited to
Lymphoma—Dose Reconstruction
Target Organ Selection; future
schedules; procedures for the Board to
use in reviewing SEC petitions
PO 00000
Frm 00047
Fmt 4703
Sfmt 4703
(including a discussion of the Y–12 SEC
Petition). The evening public comment
sessions are scheduled for January 24
from 5:30 p.m.–6:30 p.m. and January
25 from 7 p.m.–8:30 p.m.
For Further Information Contact: Dr.
Lewis V. Wade, Executive Secretary,
NIOSH, CDC, 4676 Columbia Parkway,
Cincinnati, Ohio 45226, telephone 513–
533–6825, fax 513–533–6826.
The Director, Management Analysis
and Services Office, has been delegated
the authority to sign Federal Register
notices pertaining to announcements of
meetings and other committee
management activities for both CDC and
the Agency for Toxic Substances and
Disease Registry.
Dated: January 9, 2006.
Alvin Hall,
Director, Management Analysis and Services
Office, Centers for Disease Control and
Prevention.
[FR Doc. E6–436 Filed 1–17–06; 8:45 am]
BILLING CODE 4163–18–P
E:\FR\FM\18JAN1.SGM
18JAN1
Agencies
[Federal Register Volume 71, Number 11 (Wednesday, January 18, 2006)]
[Notices]
[Page 2946]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E6-436]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
National Institute for Occupational Safety and Health Advisory
Board on Radiation and Worker Health
In accordance with section 10(a)(2) of the Federal Advisory
Committee Act (Pub. L. 92-463), the Centers for Disease Control and
Prevention (CDC) announces the following committee meeting:
Correction: This notice was published in the Federal Register on
January 3, 2006, volume 71, Number 1, Page 120-121. The meeting times/
dates and ``matters to be discussed'' have been changed.
Subcommittee Meeting Time and Date: 9 a.m.-2 p.m., January 24,
2006.
Committee Meeting Times and Dates: 2:30 a.m.-5 p.m., January 24,
2006. 8:30 a.m.-5 p.m., January 25, 2006. 8:30 a.m.-4:30 p.m., January
26, 2006.
Matters to be Discussed: The agenda for the Subcommittee meeting
includes Task 3 review; review of Bethlehem Steel, Rocky Flats, and Y-
12 site profiles; and individual dose reconstruction reviews. The
agenda for the Board meeting includes Reports from the Subcommittee and
Working Groups; Pacific Proving Grounds Special Exposure Cohort (SEC)
Evaluation Report and Supplement; Site Profiles for Bethlehem Steel,
Rocky Flats, Y-12, Hanford, Nevada Test Site, and Savannah River Site;
Letter from Steel Workers; SEC Rule rewrite; Task 3 review of SC&A
Contract; Conflict of Interest issues; Dose Reconstruction Reviews; an
update on Science Issues which will include but not be limited to
Lymphoma--Dose Reconstruction Target Organ Selection; future schedules;
procedures for the Board to use in reviewing SEC petitions (including a
discussion of the Y-12 SEC Petition). The evening public comment
sessions are scheduled for January 24 from 5:30 p.m.-6:30 p.m. and
January 25 from 7 p.m.-8:30 p.m.
For Further Information Contact: Dr. Lewis V. Wade, Executive
Secretary, NIOSH, CDC, 4676 Columbia Parkway, Cincinnati, Ohio 45226,
telephone 513-533-6825, fax 513-533-6826.
The Director, Management Analysis and Services Office, has been
delegated the authority to sign Federal Register notices pertaining to
announcements of meetings and other committee management activities for
both CDC and the Agency for Toxic Substances and Disease Registry.
Dated: January 9, 2006.
Alvin Hall,
Director, Management Analysis and Services Office, Centers for Disease
Control and Prevention.
[FR Doc. E6-436 Filed 1-17-06; 8:45 am]
BILLING CODE 4163-18-P