Agency Information Collection Activities; Submission for Office of Management and Budget Review; Comment Request; Control of Communicable Diseases; Restrictions on African Rodents, Prairie Dogs, and Certain Other Animals, 45819-45820 [E7-15939]
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Federal Register / Vol. 72, No. 157 / Wednesday, August 15, 2007 / Notices
7,500 ineligible screened persons during
a 3-year period. Data collection will
rotate such that interviews will be
conducted among one group per year:
MSM in year 1, IDU in year 2, and HET
in year 3. The type of data collected for
each group will vary slightly due to
different sampling methods and risk
characteristics of the group.
Participation of respondents is
voluntary and there is no cost to the
respondents other than their time. The
total estimated annualized burden hours
is 9,931.
ESTIMATED ANNUALIZED BURDEN HOURS
Number of
respondents
Respondents
Number of
responses per
respondent
Average
burden per
response (in
hours)
NHBS–MSM
Screener ......................................................................................................................................
Survey ..........................................................................................................................................
17,500
12,500
1
1
5/60
30/60
13,750
12,500
1
1
5/60
55/60
13,750
12,500
1
1
5/60
40/60
NHBS–IDU
Screener ......................................................................................................................................
Survey ..........................................................................................................................................
NHBS–HET
Screener ......................................................................................................................................
Survey ..........................................................................................................................................
Dated: August 9, 2007.
Maryam I. Daneshvar,
Acting Reports Clearance Officer, Centers for
Disease Control and Prevention.
[FR Doc. E7–15983 Filed 8–14–07; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration for Children and
Families
President’s Committee for People With
Intellectual Disabilities; Notice of
Meeting
President’s Committee for
People with Intellectual Disabilities
(PCPID), Administration for Children
and Families, HHS.
ACTION: Notice of quarterly meeting.
AGENCY:
Thursday, September 6, 2007,
from 9 a.m.–5 p.m. EST, and Friday,
September 7, 2007, from 9 a.m.–2 p.m.
EST. The meeting will be open to the
public.
DATES:
The meeting will be held in
Room 800 of the Hubert H. Humphrey
Building, 200 Independence Ave., SW.,
Washington, DC 20201. Individuals who
will need accommodations for a
disability in order to attend the meeting
(e.g., sign language interpreting services,
assistive listening devices, materials in
alternative format such as large print or
Braille) should notify MJ Karimi via email at
Madjid.KarimieAsl@ACF.hhs.gov, or via
telephone at 202–619–0634 no later
ebenthall on PROD1PC69 with NOTICES
ADDRESSES:
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15:00 Aug 14, 2007
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than August 24, 2007. PCPID will
attempt to meet requests made after that
date, but cannot guarantee availability.
All meeting sites are barrier free.
Meeting Registration: The meeting is
open to the public, but attendance is
limited to the space available. Persons
wishing to attend this meeting must
register by contacting MJ Karimi at the
e-mail address or telephone number
listed in the ADDRESSES section of this
notice by 12 p.m. EST on September 5,
2007. For those unable to participate in
person, audio of the proceedings may be
accessed via telephone. Please use the
above contact information for MJ Karimi
to obtain telephone and passcode
information.
Agenda: PCPID will meet to discuss
the 2007 Report to the President. They
will also discuss possible content areas
for the 2008 Report to the President and
will divide into subcommittees for that
purpose.
FOR FURTHER INFORMATION CONTACT:
Sally D. Atwater, Executive Director,
President’s Committee for People with
Intellectual Disabilities, The Aerospace
Center, Suite 210, 370 L’Enfant
Promenade, SW., Washington, DC
20447. Telephone: 202–619–0634, fax:
202–205–9591. E-mail:
satwater@acf.hhs.gov.
PCPID
acts in an advisory capacity to the
President and the Secretary of Health
and Human Services on a broad range
of topics relating to programs, services
and supports for persons with
intellectual disabilities. PCPID, by
Executive Order, is responsible for
SUPPLEMENTARY INFORMATION:
PO 00000
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evaluating the adequacy of current
practices in programs, services and
supports for persons with intellectual
disabilities, and for reviewing legislative
proposals that impact the quality of life
experienced by citizens with
intellectual disabilities and their
families.
Dated: August 1, 2007.
Sally D. Atwater,
Executive Director, President’s Committee for
People with Intellectual Disabilities.
[FR Doc. E7–15974 Filed 8–14–07; 8:45 am]
BILLING CODE 4184–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. 2007N–0073]
Agency Information Collection
Activities; Submission for Office of
Management and Budget Review;
Comment Request; Control of
Communicable Diseases; Restrictions
on African Rodents, Prairie Dogs, and
Certain Other Animals
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Notice.
SUMMARY: The Food and Drug
Administration (FDA) is announcing
that a proposed collection of
information has been submitted to the
Office of Management and Budget
(OMB) for review and clearance under
the Paperwork Reduction Act of 1995.
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45820
Federal Register / Vol. 72, No. 157 / Wednesday, August 15, 2007 / Notices
Fax written comments on the
collection of information by September
14, 2007.
ADDRESSES: To ensure that comments on
the information collection are received,
OMB recommends that written
comments be faxed to the Office of
Information and Regulatory Affairs,
OMB, Attn: FDA Desk Officer, FAX:
202–395–6974, or e-mailed to
baguilar@omb.eop.gov. All comments
should be identified with the OMB
control number 0910–0519. Also
include the FDA docket number found
in brackets in the heading of this
document.
FOR FURTHER INFORMATION CONTACT:
Jonna Capezzuto, Office of the Chief
Information Officer (HFA–250), Food
and Drug Administration, 5600 Fishers
Lane, Rockville, MD 20857, 301–827–
4659.
SUPPLEMENTARY INFORMATION: In
compliance with 44 U.S.C. 3507, FDA
has submitted the following proposed
collection of information to OMB for
review and clearance.
DATES:
Control of Communicable Diseases;
Restrictions on African Rodents, Prairie
Dogs, and Certain Other Animals (OMB
Control Number 0910–0519)—Extension
Under 21 CFR 1240.63(a)(2)(ii), an
individual must submit a written
request to seek permission to capture,
offer to capture, transport, offer to
transport, sell, barter, or exchange, offer
to sell, barter, or exchange, distribute,
offer to distribute, and/or release into
the environment any of the following
animals:
• Prairie dogs (Cynomys sp.),
• African Tree squirrels (Heliosciurus
sp.),
• Rope squirrels (Funisciurus sp.)
• African Dormice (Graphiurus sp.),
• Gambian giant pouched rats
(Cricetomys sp.),
• Brush-tailed porcupines (Atherurus
sp.),
• Striped mice (Hybomys sp.), or
Any other animal so prohibited by
order of the Commissioner of Food and
Drugs (the Commissioner) because of
that animal’s potential to transmit the
monkeypox virus.
The request cannot seek written
permission to sell, barter, or exchange,
or offer to sell, barter, or exchange, as
a pet, the animals listed previously or
any animal covered by an order by the
Commissioner.
The request must state the reasons
why an exemption is needed, describe
the animals involved, and explain why
an exemption will not result in the
spread of monkeypox within the United
States.
Our estimates are based on our
current experience with the interim
final rule. To estimate the number of
respondents, we examined the number
of requests we have received in fiscal
year 2006. There were 122 requests,
submitted by 65 individuals, in that
time, and this figure represents a minor
increase over the previous estimate of
120 annual responses (See 69 FR 7752,
February 19, 2004). As we cannot
determine whether the latest data
indicates a trend towards more requests
or is an anomaly, we have elected to
increase our estimate to 122 requests.
We also have revised the estimated
number of respondents to 65 (compared
to 120 in our previous estimate) and, as
a result, adjusted the annual frequency
per response to 1.88 (which represents
122 responses/65 respondents; the
actual result is 1.8769, which we have
rounded up to 1.88).
Furthermore, consistent with our
earlier Paperwork Reduction Act
submission, we will estimate that each
respondent will need 4 hours to
complete its request for an exemption.
Therefore, the total reporting burden
under 21 CFR 1240.63(a)(2)(ii)(A) and
(B) will be 488 hours (122 responses ×
4 hours per response = 488 hours).
In the Federal Register of March 13,
2007 (72 FR 11368), FDA published a
60-day notice requesting public
comment on the information collection
provisions. No comments were received.
TABLE 1.—ESTIMATED ANNUAL REPORTING BURDEN1
No. of
Respondents
21 CFR Section
1240.63(a)(2)(ii)(A) and (B)
1 There
65
BILLING CODE 4160–01–S
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
Workshop to Discuss Development of
a Women’s Health Information Sharing
Network
Food and Drug Administration,
ebenthall on PROD1PC69 with NOTICES
HHS.
ACTION:
Total Annual
Responses
1.88
Hours per
Response
122
Total Hours
4
488
are no capital costs or operating and maintenance costs associated with this collection of information.
Dated: August 8, 2007.
Jeffrey Shuren,
Assistant Commissioner for Policy.
[FR Doc. E7–15939 Filed 8–14–07; 8:45 am]
AGENCY:
Annual Frequency
per Response
Notice of workshop.
The Food and Drug Administration
(FDA), Office of Women’s Health is
announcing a workshop to develop a
women’s health information sharing
VerDate Aug<31>2005
15:00 Aug 14, 2007
Jkt 211001
network, with assistance from the FDA
Office of Women’s Health, and to
discuss opportunities for national
nursing/nurse practitioner organizations
to share information about their
women’s health education activities.
Representatives of national communitybased nursing and nurse practitioner
organizations are invited. A continental
breakfast will be provided.
Date and Time: The workshop will be
held on September 18, 2007, from 8:30
a.m. to 12 p.m.
Location: The workshop will be held
at the Association of Women’s Health,
Obstetric and Neonatal Nurses
Association (AWHONN), 2000 L. St.,
NW., Suite 740, Washington, DC 20036.
Contact Person: Susana Perry, Food
and Drug Administration, Office of
Women’s Health (HF–8), 5600 Fishers
Lane, Rm. 16–65, Rockville, MD 20857,
PO 00000
Frm 00098
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301–827–0350, FAX: 301–827–9194, email: susana.perry@fda.hhs.gov.
Registration: There is no fee, but
preregistration is required.
Seating is limited. If you require
special accommodations due to a
disability, please contact Susana Perry
at least 7 days in advance (September
11, 2007).
Dated: August 8, 2007.
Jeffrey Shuren,
Assistant Commissioner for Policy.
[FR Doc. E7–15944 Filed 8–14–07; 8:45 am]
BILLING CODE 4160–01–S
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]]>Agencies
[Federal Register Volume 72, Number 157 (Wednesday, August 15, 2007)]
[Notices]
[Pages 45819-45820]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E7-15939]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration
[Docket No. 2007N-0073]
Agency Information Collection Activities; Submission for Office
of Management and Budget Review; Comment Request; Control of
Communicable Diseases; Restrictions on African Rodents, Prairie Dogs,
and Certain Other Animals
AGENCY: Food and Drug Administration, HHS.
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: The Food and Drug Administration (FDA) is announcing that a
proposed collection of information has been submitted to the Office of
Management and Budget (OMB) for review and clearance under the
Paperwork Reduction Act of 1995.
[[Page 45820]]
DATES: Fax written comments on the collection of information by
September 14, 2007.
ADDRESSES: To ensure that comments on the information collection are
received, OMB recommends that written comments be faxed to the Office
of Information and Regulatory Affairs, OMB, Attn: FDA Desk Officer,
FAX: 202-395-6974, or e-mailed to baguilar@omb.eop.gov. All comments
should be identified with the OMB control number 0910-0519. Also
include the FDA docket number found in brackets in the heading of this
document.
FOR FURTHER INFORMATION CONTACT: Jonna Capezzuto, Office of the Chief
Information Officer (HFA-250), Food and Drug Administration, 5600
Fishers Lane, Rockville, MD 20857, 301-827-4659.
SUPPLEMENTARY INFORMATION: In compliance with 44 U.S.C. 3507, FDA has
submitted the following proposed collection of information to OMB for
review and clearance.
Control of Communicable Diseases; Restrictions on African Rodents,
Prairie Dogs, and Certain Other Animals (OMB Control Number 0910-
0519)--Extension
Under 21 CFR 1240.63(a)(2)(ii), an individual must submit a written
request to seek permission to capture, offer to capture, transport,
offer to transport, sell, barter, or exchange, offer to sell, barter,
or exchange, distribute, offer to distribute, and/or release into the
environment any of the following animals:
Prairie dogs (Cynomys sp.),
African Tree squirrels (Heliosciurus sp.),
Rope squirrels (Funisciurus sp.)
African Dormice (Graphiurus sp.),
Gambian giant pouched rats (Cricetomys sp.),
Brush-tailed porcupines (Atherurus sp.),
Striped mice (Hybomys sp.), or
Any other animal so prohibited by order of the Commissioner of Food
and Drugs (the Commissioner) because of that animal's potential to
transmit the monkeypox virus.
The request cannot seek written permission to sell, barter, or
exchange, or offer to sell, barter, or exchange, as a pet, the animals
listed previously or any animal covered by an order by the
Commissioner.
The request must state the reasons why an exemption is needed,
describe the animals involved, and explain why an exemption will not
result in the spread of monkeypox within the United States.
Our estimates are based on our current experience with the interim
final rule. To estimate the number of respondents, we examined the
number of requests we have received in fiscal year 2006. There were 122
requests, submitted by 65 individuals, in that time, and this figure
represents a minor increase over the previous estimate of 120 annual
responses (See 69 FR 7752, February 19, 2004). As we cannot determine
whether the latest data indicates a trend towards more requests or is
an anomaly, we have elected to increase our estimate to 122 requests.
We also have revised the estimated number of respondents to 65
(compared to 120 in our previous estimate) and, as a result, adjusted
the annual frequency per response to 1.88 (which represents 122
responses/65 respondents; the actual result is 1.8769, which we have
rounded up to 1.88).
Furthermore, consistent with our earlier Paperwork Reduction Act
submission, we will estimate that each respondent will need 4 hours to
complete its request for an exemption. Therefore, the total reporting
burden under 21 CFR 1240.63(a)(2)(ii)(A) and (B) will be 488 hours (122
responses x 4 hours per response = 488 hours).
In the Federal Register of March 13, 2007 (72 FR 11368), FDA
published a 60-day notice requesting public comment on the information
collection provisions. No comments were received.
Table 1.--Estimated Annual Reporting Burden\1\
----------------------------------------------------------------------------------------------------------------
No. of Annual Frequency Total Annual Hours per
21 CFR Section Respondents per Response Responses Response Total Hours
----------------------------------------------------------------------------------------------------------------
1240.63(a)(2)(ii) 65 1.88 122 4 488
(A) and (B)
----------------------------------------------------------------------------------------------------------------
\1\ There are no capital costs or operating and maintenance costs associated with this collection of
information.
Dated: August 8, 2007.
Jeffrey Shuren,
Assistant Commissioner for Policy.
[FR Doc. E7-15939 Filed 8-14-07; 8:45 am]
BILLING CODE 4160-01-S
