Meeting of the National Vaccine Advisory Committee, 62315-62316 [05-21611]
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Federal Register / Vol. 70, No. 209 / Monday, October 31, 2005 / Notices
comment on ways to enhance the
quality of the information that the
Commission proposes to collect, and on
ways to minimize the burden imposed
on tobacco companies in responding to
the Commission. Specifically, Philip
Morris suggested that the Commission:
(1) Identify the companies from which
it seeks data based on a particular sales
volume or market share, instead of from
a preset number of companies; (2) solicit
information from the tobacco companies
on a predetermined schedule; (3)
increase from 60 days to 90 days the
amount of time provided to the
companies to submit the requested data;
(4) announce in advance any changes in
the kinds of data to be collected or in
the ways that specific data should be
reported; (5) allow advertising and
promotional expenditure data to be
reported to the nearest $1,000, rather
than to the dollar; and (6) allow
expenses to be reported based on
generally accepted accounting
principles.
Philip Morris suggests that the FTC
use sales volume or market share
benchmarks to identify those companies
to whom it will send information
requests. The FTC does, in fact, consider
changes in industry market share in
determining whether requests should be
issued to new companies that have not
previously received them, but does not
believe it must adopt any one specific
mechanism for determining to whom it
will issue information requests. Insofar
as the FTC is asking for clearance from
OMB under the PRA to send
information requests to up to 15
companies, it will retain the flexibility
to adapt to major changes in either
industry.
Philip Morris suggests several
reasonable ways to decrease the burden
on the cigarette and smokeless tobacco
companies. Accordingly, after the first
set of 6(b) orders, which will be issued
after the FTC obtains OMB clearance to
do so, the FTC will attempt to issue its
6(b) orders in the second calendar
quarter of the year; unforeseen events
may, however, change this schedule in
any particular year. The FTC will also
extend the time period for companies to
submit their responses from 60 days to
90 days, and permit advertising and
promotional expenditure data to be
reported to the nearest $1,000.
Furthermore, the FTC intends that
expenses be reported based on generally
accepted accounting principles, and
Philip Morris’s suggestion provides an
opportunity to clear up any confusion
on this issue.
Philip Morris states that it would like
advance notice of any changes to the
information requirements in the 6(b)
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orders. The FTC provided advance
notice of certain relatively significant
changes to the cigarette and smokeless
tobacco 6(b) orders in 2002, so that the
companies would have additional time
to prepare for these changes. The FTC
will consider whether any additional
burden on the companies from
relatively minor changes in the
reporting requirements will be
outweighed by the costs of the
significant delay in obtaining the data
that would result from providing
advance notice.
Estimated hours burden: The FTC
staff’s estimate of the hours burden is
based on the time required to respond
to each information request. Although
the FTC intends to issue the information
requests only to the five largest cigarette
companies and the five largest
smokeless tobacco companies (for a total
of ten information requests), the burden
estimate is based on up to 15
information requests being issued per
year to take into account any future
changes in these industries. Because
these companies vary greatly in size, in
the number of products that they sell,
and in the extent and variety of their
advertising and promotion, the staff has
provided a range of the estimated hours
burden. Based upon its knowledge of
the industries, the staff estimates that
the time required to gather, organize,
format, and produce their responses
ranges between 30 and 80 hours per
information request for all but the very
largest companies. The very largest
companies could require hundreds of
hours per year. Thus, the staff estimates
a total of 1,800 hours per year, with an
average burden per company for each of
the intended ten recipients of 180 hours.
The staff estimates that for possible
additional recipients, which would be
smaller companies, the burden should
not exceed 300 hours (60 hours per
company × 5 companies). Thus the
staff’s estimate of the total burden is
2,100 hours. These estimates include
any time spent by separately
incorporated subsidiaries and other
entities affiliated with the ultimate
parent company that has received the
information request.4
Estimated cost burden: It is not
possible to calculate with precision the
labor costs associated with this data
production, as they entail varying
compensation levels of management
and/or support staff among companies
of different sizes. Financial, legal,
marketing, and clerical personnel may
be involved in the information
4 The staff’s burden estimate takes into account
that the first request to the five smokeless tobacco
companies may cover data for three calendar years.
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62315
collection process. The staff assumes
that professional personnel will handle
most of the tasks involved in gathering
and producing responsive information,
and have applied an average hourly
wage of $150/hour for their labor. The
staff’s best estimate for the total labor
costs for up to 15 information requests
is $315,000.
The staff estimates that the capital or
other non-labor costs associated with
the information requests are minimal.
Although the information requests may
necessitate that industry members
maintain the requested information
provided to the Commission, they
should already have in place the means
to compile and maintain business
records.
William Blumenthal,
General Counsel.
[FR Doc. 05–21592 Filed 10–28–05; 8:45 am]
BILLING CODE 6750–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Meeting of the National Vaccine
Advisory Committee
Department of Health and
Human Services, Office of the Secretary.
ACTION: Notice.
AGENCY:
SUMMARY: As stipulated by the Federal
Advisory Committee Act, the
Department of Health and Human
Services (DHHS) is hereby giving notice
that the National Vaccine Advisory
Committee (NVAC) will hold a meeting.
The meeting is open to the public.
DATES: The meeting will be held on
November 29, 2005, from 9 a.m. to 5
p.m., and on November 30, 2005, from
9 a.m. to 3:30 p.m.
ADDRESSES: Department of Health and
Human Services; Hubert H. Humphrey
Building, Room 705–A; 200
Independence Avenue, SW.,
Washington, DC 20201.
FOR FURTHER INFORMATION CONTACT: Ms.
Emma English, Program Analyst,
National Vaccine Program Office,
Department of Health and Human
Services, Room 443–H Hubert H.
Humphrey Building, 200 Independence
Avenue, SW., Washington, DC 20201;
(202) 690–5566, nvac@osophs.dhhs.gov.
SUPPLEMENTARY INFORMATION: Pursuant
to section 2101 of the Public Service Act
(42 U.S.C. 300aa–1), the Secretary of
Health and Human Services was
mandated to establish the National
Vaccine Program to achieve optimal
prevention of human infectious diseases
through immunization and to achieve
optimal prevention against adverse
E:\FR\FM\31OCN1.SGM
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62316
Federal Register / Vol. 70, No. 209 / Monday, October 31, 2005 / Notices
reactions to vaccines. The National
Vaccine Advisory Committee was
established to provide advice and make
recommendations to the Assistant
Secretary for Health, as the Director of
the National Vaccine Program, on
matters related to the program’s
responsibilities.
Topics to be discussed at the meeting
include the 2005–2006 influenza
season, pandemic influenza
preparedness, and the financing of
vaccines. New liaison representatives
and ex-officio members will be
welcomed to the Committee and
updates will be given by various
subcommittees and working groups. A
tentative agenda will be made available
on or about November 14, 2005 for
review on the NVAC Web site: https://
www.hhs.gov/nvpo/nvac.
Public attendance at the meeting is
limited to space available. Individuals
must provide a photo ID for entry into
the Humphrey Building. Individuals
who plan to attend and need special
assistance, such as sign language
interpretation or other reasonable
accommodations, should notify the
designated contact person. Members of
the public will have the opportunity to
provide comments at the meeting.
Public comment will be limited to five
minutes per speaker. Any members of
the public who wish to have printed
material distributed to NVAC members
should submit materials to the
Executive Secretary, NVAC, through the
contact person listed above prior to
close of business November 24, 2005.
Preregistration is required for both
public attendance and comment. Any
individual who wishes to attend the
meeting and/or participate in the public
comment session should e-mail
nvac@osophs.dhhs.gov or call 202–690–
5566.
Dated: October 26, 2005.
Bruce Gellin,
Director, National Vaccine Program Office.
[FR Doc. 05–21611 Filed 10–28–05; 8:45 am]
Centers for Disease Control and
Prevention (CDC).
CDC is requesting approval from the
Office of Management and Budget
(OMB) to interview 1,000 randomly
selected HIV-infected persons in the
United States who are not receiving care
to determine: (1) Their reasons for not
being in care; (2) information about any
barriers to receiving care; and (3)
treatment, and their clinical status (i.e.,
CD4 and HIV viral load levels). There
are approximately 1 million HIVinfected persons in the United States. Of
these, an estimated 75 percent know
they are infected, but approximately
half of those who know they are
infected do not have evidence of having
received any medical care for their HIV
infection.
For this proposed data collection,
areas participating in CDC’s Morbidity
Monitoring Project (MMP) will identify
HIV-infected people using their state’s
HIV/AIDS surveillance and
supplemental laboratory databases.
Once HIV-infected people who are not
in care are identified, an interview will
be conducted. The information to be
collected includes demographic data,
HIV testing history, high-risk drug use
and sexual behaviors, and reasons for
not using health care and treatment.
Results from this study will be used
in conjunction with data from the
Morbidity Monitoring Project to
determine the extent of medical services
and resources needed for persons who
are infected with HIV, but who have not
received medical care and treatment.
Additionally, new data related to those
not receiving care will be used to design
effective interventions for linking
persons to care.
Participation in the data collection is
voluntary and there is no cost to
respondents to participate in the survey
other than their time.
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Proposed Project
BILLING CODE 4150–44–P
Centers for Disease Control and
Prevention
[60Day–06–05DA]
Proposed Data Collections Submitted
for Public Comment and
Recommendations
In compliance with the requirement
of section 3506(c)(2)(A) of the
Paperwork Reduction Act of 1995 for
opportunity for public comment on
proposed data collection projects, the
Centers for Disease Control and
Prevention (CDC) will publish periodic
summaries of proposed projects. To
request more information on the
proposed projects or to obtain a copy of
the data collection plans and
instruments, call 404–639–4766 and
send comments to Seleda Perryman,
CDC Assistant Reports Clearance
Officer, 1600 Clifton Road, MS–D74,
Atlanta, GA 30333 or send an e-mail to
omb@cdc.gov.
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. Written comments should
be received within 60 days of this
notice.
Surveillance of HIV/AIDS Related
Events Among Persons Not Receiving
Care—New—National Center for HIV,
STD, and TB Prevention (NCHSTP),
ESTIMATED ANNUALIZED BURDEN TABLE
Respondents
Number of respondents
Number of
responses per
respondent
Average burden per response
(in hours)
Total burden
(in hours)
HIV Positive Persons .......................................................................................
1,000
1
1
1,000
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31OCN1
Agencies
[Federal Register Volume 70, Number 209 (Monday, October 31, 2005)]
[Notices]
[Pages 62315-62316]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 05-21611]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Meeting of the National Vaccine Advisory Committee
AGENCY: Department of Health and Human Services, Office of the
Secretary.
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: As stipulated by the Federal Advisory Committee Act, the
Department of Health and Human Services (DHHS) is hereby giving notice
that the National Vaccine Advisory Committee (NVAC) will hold a
meeting. The meeting is open to the public.
DATES: The meeting will be held on November 29, 2005, from 9 a.m. to 5
p.m., and on November 30, 2005, from 9 a.m. to 3:30 p.m.
ADDRESSES: Department of Health and Human Services; Hubert H. Humphrey
Building, Room 705-A; 200 Independence Avenue, SW., Washington, DC
20201.
FOR FURTHER INFORMATION CONTACT: Ms. Emma English, Program Analyst,
National Vaccine Program Office, Department of Health and Human
Services, Room 443-H Hubert H. Humphrey Building, 200 Independence
Avenue, SW., Washington, DC 20201; (202) 690-5566,
nvac@osophs.dhhs.gov.
SUPPLEMENTARY INFORMATION: Pursuant to section 2101 of the Public
Service Act (42 U.S.C. 300aa-1), the Secretary of Health and Human
Services was mandated to establish the National Vaccine Program to
achieve optimal prevention of human infectious diseases through
immunization and to achieve optimal prevention against adverse
[[Page 62316]]
reactions to vaccines. The National Vaccine Advisory Committee was
established to provide advice and make recommendations to the Assistant
Secretary for Health, as the Director of the National Vaccine Program,
on matters related to the program's responsibilities.
Topics to be discussed at the meeting include the 2005-2006
influenza season, pandemic influenza preparedness, and the financing of
vaccines. New liaison representatives and ex-officio members will be
welcomed to the Committee and updates will be given by various
subcommittees and working groups. A tentative agenda will be made
available on or about November 14, 2005 for review on the NVAC Web
site: https://www.hhs.gov/nvpo/nvac.
Public attendance at the meeting is limited to space available.
Individuals must provide a photo ID for entry into the Humphrey
Building. Individuals who plan to attend and need special assistance,
such as sign language interpretation or other reasonable
accommodations, should notify the designated contact person. Members of
the public will have the opportunity to provide comments at the
meeting. Public comment will be limited to five minutes per speaker.
Any members of the public who wish to have printed material distributed
to NVAC members should submit materials to the Executive Secretary,
NVAC, through the contact person listed above prior to close of
business November 24, 2005. Preregistration is required for both public
attendance and comment. Any individual who wishes to attend the meeting
and/or participate in the public comment session should e-mail
nvac@osophs.dhhs.gov or call 202-690-5566.
Dated: October 26, 2005.
Bruce Gellin,
Director, National Vaccine Program Office.
[FR Doc. 05-21611 Filed 10-28-05; 8:45 am]
BILLING CODE 4150-44-P