26094 Federal Register / Vol. 71, No.
85 / Wednesday, May 3, 2006 / Notices
number, OMB number, and OS
document identifier, to
naomi.cook@hhs.gov, or call the Reports
Clearance Office on (202) 690–6162.
Written comments and
recommendations for the proposed
information collections must be
received within 30 days, and directed to
the Desk Officer at the address below:
OMB Desk Officer: John Kraemer, OMB
Human Resources and Housing Branch,
Attention: (OMB (0990–0269), New
Executive Office Building, Room 10235,
Washington DC 20503.
Dated: April 21, 2006.
Robert E. Polson,
Office of the Secretary, Paperwork Reduction
Act Reports Clearance Officer.
[FR Doc. E6–6688 Filed 5–2–06; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Office of the Secretary
[Document Identifier: OS–0990–New; 30-day
notice]
Agency Information Collection
Activities: Proposed Collection;
Comment Request
AGENCY: Office of the Secretary, Office
of Women’s Health.
In compliance with the requirement
of section 3506(c)(2)(A) of the
Paperwork Reduction Act of 1995, the
Office of the Secretary (OS), Department
of Health and Human Services, is
publishing the following summary of a
proposed collection for public
comment. Interested persons are invited
to send comments regarding this burden
estimate or any other aspect of this
collection of information, including any
of the following subjects: (1) The
necessity and utility of the proposed
information collection for the proper
performance of the agency’s functions;
(2) the accuracy of the estimated
burden; (3) ways to enhance the quality,
utility, and clarity of the information to
be collected; and (4) the use of
automated collection techniques or
other forms of information technology to
minimize the information collection
burden.
Type of Information Collection
Request: Regular Clearance, New
collection;
Title of Information Collection:
National Women’s Health Week
(NWHW) Survey;
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Form/OMB No.: OS–0990–New;
Use: The Office of Women’s Health
will evaluate how National Women’s
Health Week (NWHW) is implemented
across the country, and to assess
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whether or not NWHW is reaching its
program objectives, with an emphasis
on messages, delivery mechanisms,
levels of outreach and contact, and
partnership strategies.
Frequency: Reporting, on occasion;
Affected Public: Business or other for-
profit, not-for-profit institutions,
Federal, State, local or tribal
government;
Annual Number of Respondents:
1,400;
Total Annual Responses: 2,800;
Average Burden Per Response: 1 hour;
Total Annual Hours: 700.
To obtain copies of the supporting
statement and any related forms for the
proposed paperwork collections
referenced above, access the HHS Web
site address at http://www.hhs.gov/ocio/
infocollect/pending/ or e-mail your
request, including your address, phone
number, OMB number, and OS
document identifier, to
naomi.cook@hhs.gov, or call the Reports
Clearance Office on (202) 690–6162.
Written comments and
recommendations for the proposed
information collections must be
received within 30 days, of this notice
directly to the Desk Officer at the
address below: OMB Desk Officer: John
Kraemer, OMB Human Resources and
Housing Branch, Attention: (OMB
#0990–New), New Executive Office
Building, Room 10235, Washington DC
20503.
Dated: April 21, 2006.
Robert E. Polson,
Office of the Secretary, Paperwork Reduction
Act Reports Clearance Officer.
[FR Doc. E6–6689 Filed 5–2–06; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
Industry Exchange Workshop to
Celebrate Food and Drug
Administration Centennial: Past,
Present, and Future of Regulated
Food, Drugs, Nutritional Supplements,
and Medical Devices; Public Workshop
AGENCY: Food and Drug Administration,
HHS.
ACTION: Notice of public workshop.
SUMMARY: The Food and Drug
Administration (FDA) Philadelphia
District, in cooperation with the
Chemical Heritage Foundation (CHF), is
announcing a workshop on past,
current, and future issues and
challenges in FDA regulation as part of
the celebration of FDA’s 100-year
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anniversary. Topics for discussion
include: Turning points in FDA history;
the impact of changes in science and
technology on FDA regulation,
regulation in the globalized economy,
consumer access to information in the
regulatory environment; and a risk-
based approach to regulation as a model
for the future. The purpose of this 1-day
workshop for consumers, industry,
academia, and regulators is to promote
dialogue among regulators and these
stakeholders.
Date and Time: The public workshop
will be held on Tuesday, May 16, 2006,
from 9 a.m. to 5 p.m.
Location: The public workshop will
be held at the Chemical Heritage
Foundation, 315 Chestnut St.,
Philadelphia, PA 19106, 215–873–8214,
FAX: 215–629–5249.
Contact: Marie Falcone, Food and
Drug Administration, U.S.
Customhouse, 200 Chestnut St., rm. 900,
Philadelphia, PA 19106, 215–717–3703,
FAX: 215–597–5798, e-mail:
Marie.Falcone@fda.hhs.gov.
Registration: Send registration
information (including name, title, firm
name, address, telephone, fax number)
and the registration fee of $20.00
payable to the Chemical Heritage
Foundation, 315 Chestnut St.,
Philadelphia, PA 19106. To register via
the Internet go to http://
www.chemheritage.org/events/fda/
index.html. (FDA has verified the Web
site address, but is not responsible for
subsequent changes to the Web site after
this document publishes in the Federal
Register.) The registrar will also accept
payment by major credit cards. The
registration fee for FDA Philadelphia
District employees is waived.
For more information on the meeting,
or for questions about registration,
contact the Chemical Heritage
Foundation (CHF) at 215–873–8214,
FAX: 215–629–5249, or via e-mail:
arthurd@chemheritage.org.
Attendees are responsible for their
own accommodations.
The registration fee will be used to
offset the expenses of hosting the
conference, including meals,
refreshments, meeting rooms, and
materials. Space is limited, therefore
interested parties are encouraged to
register early. Limited onsite registration
may be available. Please arrive early to
ensure prompt registration.
If you need special accommodations
due to a disability, please contact Marie
Falcone (see Contact) at least 7 days in
advance of the workshop.
SUPPLEMENTARY INFORMATION: The ‘‘FDA
Past, Present, and Future of Regulating
Food, Drugs, Medical Devices, and
03MYN1
 Federal Register / Vol. 71, No. 85 / Wednesday, May 3, 2006 / Notices
Nutritional Supplements’’ workshop
helps fulfill the Department of Health
and Human Services’ and FDA’s
important mission to protect the public
health by encouraging informed
dialogue on the future direction of FDA
regulation in the context of its historical
accomplishments.
The workshop will also help to
implement the objectives of section 406
of the FDA Modernization Act (21
U.S.C. 393) and the FDA Plan for
Statutory Compliance, which include
working more closely with stakeholders
and providing access to scientific and
technical expertise. Finally, the
workshop furthers the goals of the Small
Business Regulatory Enforcement
Fairness Act (Public Law 104–121) by
providing outreach activities by
Government agencies directed to small
businesses.
Dated: April 28, 2006.
Jeffrey Shuren,
Assistant Commissioner for Policy.
[FR Doc. 06–4185 Filed 5–1–06; 10:37 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[FDA 225–06–8400]
Memorandum of Understanding
Between the Food and Drug
Administration, United States
Department of Health and Human
Services, the Animal and Plant Health
Inspection Service, the United States
Department of Agriculture, and The
National Institutes of Health, United
States Department of Health and
Human Services Concerning
Laboratory Animal Welfare
AGENCY: Food and Drug Administration,
HHS.
ACTION: Notice.
SUMMARY: The purpose of this
Memorandum of Understanding (MOU)
is to set forth an agreement between the
Animal and Plant Health Inspection
Service, U.S. Department of Agriculture,
and the National Institutes of Health,
U.S. Department of Health and Human
Services concerning Laboratory Animal
Welfare and FDA (collectively ‘‘the
Parties’’, or individually as a ‘‘Party’’)
regarding the framework for reciprocal
cooperation which will assist each
agency in meeting its responsibilities in
promoting proper laboratory animal care
and welfare. This MOU replaces 225–
83–8400.
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26095
DATES: The agreement became effective
February 14, 2006.
FOR FURTHER INFORMATION CONTACT:
For FDA: Rodney T. Allnut, Office of
Enforcement, Office of Regulatory
Affairs, Food and Drug
Administration, HFC–230, rm. 126,
15800 Crabbs Branch, Rockville,
MD 20855, 240–632–6848, FAX:
240–632–6861.
For USDA: Chester Gipson, Animal
and Plant Health Inspection
Service, U.S. Department of
Agriculture, 4700 River Rd., Unit
97, rm. 6A–16, Riverdale, MD
20737–1234, 301–734–4980, FAX:
301–734–4993.
For NIH: Carol Wigglesworth, Office
of Laboratory Animal Welfare,
Office of Extramural Research,
National Institutes of Health,
Rockwall I, suite 1050, MSC 7982,
6705 Rockledge Dr., Bethesda, MD
20892–7982, 301–496–7163, FAX:
301–402–2803.
SUPPLEMENTARY INFORMATION: In
accordance with 21 CFR 20.108(c),
which states that all written agreements
and MOUs between FDA and others
shall be published in the Federal
Register, the agency is publishing notice
of this MOU.
Dated: April 26, 2006.
Jeffrey Shuren,
Assistant Commissioner for Policy.
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03MYN1