Agency Information Collection Activities; Announcement of Office of Management and Budget Approval; MedWatch-The Food and Drug Administration Safety Information and Adverse Event Reporting Program; Proposal to Survey MedWatch Partners Organizations, 47498 [E6-13503]
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47498
Federal Register / Vol. 71, No. 159 / Thursday, August 17, 2006 / Notices
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
Centers for Disease Control and
Prevention
Food and Drug Administration
Decision To Evaluate a Petition To
Designate a Class of Employees at Los
Alamos National Laboratory, Los
Alamos, NM, To Be Included in the
Special Exposure Cohort
Disease, Disability, and Injury
Prevention and Control Special
Emphasis Panel: State-Based
Occupational Safety and Health
Surveillance, Program Announcement
With Special Receipt Date Program
Announcement Number (PAR) 04–106
[Docket No. 2006N–0166]
Centers for Disease Control and
Prevention (CDC), Department of Health
and Human Services (HHS).
AGENCY:
ACTION:
Notice.
SUMMARY: The Department of Health and
Human Services (HHS) gives notice as
required by 42 CFR 83.12(e) of a
decision to evaluate a petition to
designate a class of employees at the Los
Alamos National Laboratory, Los
Alamos, New Mexico, to be included in
the Special Exposure Cohort under the
Energy Employees Occupational Illness
Compensation Program Act of 2000. The
initial proposed definition for the class
being evaluated, subject to revision as
warranted by the evaluation, is as
follows:
Facility: Los Alamos National
Laboratory.
Location: Los Alamos, New Mexico.
Job Titles and/or Job Duties: All
Department of Energy employees,
contractors, and subcontractors
employed in all Tech areas.
Period of Employment: 1943–1975.
FOR FURTHER INFORMATION CONTACT:
Larry Elliott, Director, Office of
Compensation Analysis and Support,
National Institute for Occupational
Safety and Health, 4676 Columbia
Parkway, MS C–46, Cincinnati, OH
45226, Telephone 513–533–6800 (this is
not a toll-free number). Information
requests can also be submitted by e-mail
to OCAS@CDC.GOV.
Dated: August 11, 2006.
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 meeting:
Name: Disease, Disability, and Injury
Prevention and Control.
Special Emphasis Panel: State-Based
Occupational Safety and Health Surveillance,
Program Announcement with Special Receipt
Date PAR 04–106.
Time and Date: 12 p.m.–2 p.m., September
1, 2006 (Closed).
Place: Teleconference, 2400 Century
Parkway, NE., 4th Floor, Atlanta, GA 30345.
Status: The meeting will be closed to the
public in accordance with provisions set
forth in section 552b(c)(4) and (6), Title 5
U.S.C., and the Determination of the Director,
Management Analysis and Services Office,
CDC, pursuant to Public Law 92–463.
Matters to be Discussed: The meeting will
include the review, discussion, and
evaluation of research grants in response to
PAR 04–106, ‘‘State-Based Occupational
Safety and Health Surveillance,’’ Program
Announcement with Special Receipt Date.
Contact Person for More Information: M.
Chris Langub, Ph.D., Scientific Review
Administrator, National Institute for
Occupational Safety and Health, Centers for
Disease Control and Prevention, 1600 Clifton
Road, Mailstop E–74, Atlanta, Georgia 30333,
phone (404) 498–2543.
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.
Director, National Institute for Occupational
Safety and Health, Centers for Disease Control
and Prevention.
[FR Doc. 06–6986 Filed 8–16–06; 8:45 am]
Dated: August 10, 2006.
Alvin Hall,
Director, Management Analysis and Services
Office, Centers for Disease Control and
Prevention.
[FR Doc. E6–13555 Filed 8–16–06; 8:45 am]
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Agency Information Collection
Activities; Announcement of Office of
Management and Budget Approval;
MedWatch—The Food and Drug
Administration Safety Information and
Adverse Event Reporting Program;
Proposal to Survey MedWatch
Partners Organizations
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Notice.
SUMMARY: The Food and Drug
Administration (FDA) is announcing
that a collection of information entitled
‘‘MedWatch—The Food and Drug
Administration Safety Information and
Adverse event Reporting Program;
Proposal to Survey MedWatch Partners
Organizations’’ has been approved by
the Office of Management and Budget
(OMB) under the Paperwork Reduction
Act of 1995.
FOR FURTHER INFORMATION CONTACT: Liz
Berbakos, Office of Management
Programs (HFA–250), Food and Drug
Administration, 5600 Fishers Lane,
Rockville, MD 20857, 301–827–1482.
SUPPLEMENTARY INFORMATION: In the
Federal Register of May 1, 2006 (71 FR
25591), the agency announced that the
proposed information collection had
been submitted to OMB for review and
clearance under 44 U.S.C. 3507. An
agency may not conduct or sponsor, and
a person is not required to respond to,
a collection of information unless it
displays a currently valid OMB control
number. OMB has now approved the
information collection and has assigned
OMB control number 0910–0593. The
approval expires on December 31, 2006.
A copy of the supporting statement for
this information collection is available
on the Internet at https://www.fda.gov/
ohrms/dockets.
Dated: August 10, 2006.
Jeffrey Shuren,
Assistant Commissioner for Policy.
[FR Doc. E6–13503 Filed 8–16–06; 8:45 am]
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Agencies
[Federal Register Volume 71, Number 159 (Thursday, August 17, 2006)]
[Notices]
[Page 47498]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E6-13503]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration
[Docket No. 2006N-0166]
Agency Information Collection Activities; Announcement of Office
of Management and Budget Approval; MedWatch--The Food and Drug
Administration Safety Information and Adverse Event Reporting Program;
Proposal to Survey MedWatch Partners Organizations
AGENCY: Food and Drug Administration, HHS.
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: The Food and Drug Administration (FDA) is announcing that a
collection of information entitled ``MedWatch--The Food and Drug
Administration Safety Information and Adverse event Reporting Program;
Proposal to Survey MedWatch Partners Organizations'' has been approved
by the Office of Management and Budget (OMB) under the Paperwork
Reduction Act of 1995.
FOR FURTHER INFORMATION CONTACT: Liz Berbakos, Office of Management
Programs (HFA-250), Food and Drug Administration, 5600 Fishers Lane,
Rockville, MD 20857, 301-827-1482.
SUPPLEMENTARY INFORMATION: In the Federal Register of May 1, 2006 (71
FR 25591), the agency announced that the proposed information
collection had been submitted to OMB for review and clearance under 44
U.S.C. 3507. An agency may not conduct or sponsor, and a person is not
required to respond to, a collection of information unless it displays
a currently valid OMB control number. OMB has now approved the
information collection and has assigned OMB control number 0910-0593.
The approval expires on December 31, 2006. A copy of the supporting
statement for this information collection is available on the Internet
at https://www.fda.gov/ohrms/dockets.
Dated: August 10, 2006.
Jeffrey Shuren,
Assistant Commissioner for Policy.
[FR Doc. E6-13503 Filed 8-16-06; 8:45 am]
BILLING CODE 4160-01-S