Vaccine Adverse Event Reporting; Revised Form VAERS-2; Withdrawal of Proposed Revised Form, 20708 [E6-5970]
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20708
Federal Register / Vol. 71, No. 77 / Friday, April 21, 2006 / Notices
stakeholders. The MAQC project will
work with participating scientists to
develop baseline practices for the
analysis of hybridization data. Original
datasets, analyses, and conclusions from
this project will be made available to the
public throughout the project. For more
information about the MAQC project,
please visit https://www.fda.gov/nctr/
science/centers/toxicoinformatics/
maqc/.
Dated: April 13, 2006.
Jeffrey Shuren,
Assistant Commissioner for Policy.
[FR Doc. E6–5995 Filed 4–20–06; 8:45 am]
ACTION:
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. 2001N–0464 (formerly Docket
No. 01N–0464)]
Vaccine Adverse Event Reporting;
Revised Form VAERS–2; Withdrawal of
Proposed Revised Form
Food and Drug Administration,
HHS.
ACTION:
Notice; withdrawal.
SUMMARY: The Food and Drug
Administration (FDA) is announcing the
withdrawal of a proposed revised form
that was issued in the Federal Register
on November 20, 2001.
DATES:
April 21, 2006.
FOR FURTHER INFORMATION CONTACT:
Joseph L. Okrasinski, Jr., Center for
Biologics Evaluation and Research
(HFM–17), Food and Drug
Administration, 1401 Rockville Pike,
Suite 200N, Rockville, MD 20852–1448,
301–827–6210.
In a notice
published in the Federal Register of
November 20, 2001 (66 FR 58153), FDA
announced the availability of a
proposed revised form entitled ‘‘Vaccine
Adverse Event Reporting System’’ (Form
VAERS–2) dated July 2001. This
proposed revised form is being
withdrawn because FDA is no longer
pursuing changes to the form.
rwilkins on PROD1PC63 with NOTICES
SUPPLEMENTARY INFORMATION:
Dated: April 12, 2006.
Jeffrey Shuren,
Assistant Commissioner for Policy.
[FR Doc. E6–5970 Filed 4–20–06; 8:45 am]
BILLING CODE 4160–01–S
VerDate Aug<31>2005
17:21 Apr 20, 2006
Jkt 208001
United States Visitor and Immigrant
Status Indicator Technology (US-VISIT)
Program; Notice of Availability of a
Final Programmatic Environmental
Assessment (PEA) and a Finding of No
Significant Impact (FONSI) on the USVISIT Plan for Potential Changes to
Immigration and Border Management
Processes
US-VISIT, DHS.
Notice of availability.
AGENCY:
BILLING CODE 4160–01–S
AGENCY:
DEPARTMENT OF HOMELAND
SECURITY
SUMMARY: A Final Programmatic
Environmental Assessment (PEA) and
Finding of No Significant Impact
(FONSI) for the United States Visitor
and Immigrant Status Indicator
Technology (US-VISIT) program are
available to the public for electronic
download. The Final PEA examines the
potential environmental impacts of four
strategic approaches to enhance
immigration and border management
processes and addresses the substantive
comments received on the Draft PEA
during the public comment period.
These four approaches are aimed at
improving information available to
determine the identity and immigration
status of individuals traveling to and
from the United States. The Final PEA
resulted in a FONSI that selected the
proposed action, or Hybrid Alternative,
as the approach to enhance the
immigration and border management
enterprise. The Final PEA and FONSI
are made available to the public in
accordance with the National
Environmental Policy Act of 1969
(NEPA) and the Council on
Environmental Quality (CEQ)
regulations for implementing NEPA.
DATES: The Final PEA and FONSI will
be available to the public on April 17,
2006.
ADDRESSES: Copies of the Final PEA and
FONSI may be obtained by download
through the Internet at https://
www.dhs.gov/us-visit.
FOR FURTHER INFORMATION CONTACT: Lisa
Mahoney, US–VISIT Environmental
Program Manager, at (202) 298–5245,
Monday–Friday, 8 a.m.—5 p.m. EDT.
SUPPLEMENTARY INFORMATION: US-VISIT
published a Notice of Availability of a
Draft Programmatic Environmental
Assessment (PEA) on the US-VISIT Plan
for Potential Changes to Immigration
and Border Management Processes in
the Federal Register (71 FR 8602,
February 17, 2006). The Notice briefly
discussed four strategic approaches
analyzed in the Draft PEA, informed the
public on how to obtain a copy of the
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Draft PEA, requested comments from
the public on the Draft PEA during the
public commenting period, and
informed the public on the location and
time of public meetings in seven
locations in the United States during the
public comment period. The comment
period ended on March 18, 2006.
Thirty-two (32) comments were received
and considered by US-VISIT.
The proposed action, or Hybrid
Alternative, has been selected as the
approach by which enhancements will
be made to immigration and border
management processes. This approach
was selected after careful review of the
environmental assessment and
consideration of input received from the
public and other federal and state
agencies during the public comment
period. The Hybrid Alternative was
chosen because it provides the most
opportunity for the entities responsible
for immigration and border management
to incorporate and balance the most
useful components of the virtual and
physical border alternatives to achieve
security, facilitation, individual privacy,
and immigration system integrity goals.
A review of the relative impacts showed
that no alternative would result in a
significant impact and that the Hybrid
Alternative ranked second in terms of
environmental preference. As
warranted, tiered environmental
analyses for specific initiatives at the
land border ports of entry resulting from
selection of the Hybrid Alternative will
be conducted and these tiered analyses
will be made available to the public. A
collection or ‘‘toolbox’’ of strategies and
information for monitoring, mitigation,
and environmental stewardship will
also be developed to be used in
implementing the Hybrid Alternative.
Juan Reyes,
Director, Office of Safety and Environmental
Programs, Department of Homeland Security.
[FR Doc. E6–5971 Filed 4–20–06; 8:45 am]
BILLING CODE 4410–10–P
DEPARTMENT OF HOMELAND
SECURITY
Office of the Secretary
[DHS–2005–0053]
Privacy Act of 1974; Systems of
Records
Department of Homeland
Security; United States Customs and
Border Protection.
ACTION: Notice of revision to and
expansion of Privacy Act system of
records.
AGENCY:
E:\FR\FM\21APN1.SGM
21APN1
]]>Agencies
[Federal Register Volume 71, Number 77 (Friday, April 21, 2006)]
[Notices]
[Page 20708]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E6-5970]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration
[Docket No. 2001N-0464 (formerly Docket No. 01N-0464)]
Vaccine Adverse Event Reporting; Revised Form VAERS-2; Withdrawal
of Proposed Revised Form
AGENCY: Food and Drug Administration, HHS.
ACTION: Notice; withdrawal.
-----------------------------------------------------------------------
SUMMARY: The Food and Drug Administration (FDA) is announcing the
withdrawal of a proposed revised form that was issued in the Federal
Register on November 20, 2001.
DATES: April 21, 2006.
FOR FURTHER INFORMATION CONTACT: Joseph L. Okrasinski, Jr., Center for
Biologics Evaluation and Research (HFM-17), Food and Drug
Administration, 1401 Rockville Pike, Suite 200N, Rockville, MD 20852-
1448, 301-827-6210.
SUPPLEMENTARY INFORMATION: In a notice published in the Federal
Register of November 20, 2001 (66 FR 58153), FDA announced the
availability of a proposed revised form entitled ``Vaccine Adverse
Event Reporting System'' (Form VAERS-2) dated July 2001. This proposed
revised form is being withdrawn because FDA is no longer pursuing
changes to the form.
Dated: April 12, 2006.
Jeffrey Shuren,
Assistant Commissioner for Policy.
[FR Doc. E6-5970 Filed 4-20-06; 8:45 am]
BILLING CODE 4160-01-S
