Workshop to Discuss Development of a Women's Health Information Sharing Network, 45820 [E7-15944]
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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
Fmt 4703
Sfmt 4703
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]
[Page 45820]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E7-15944]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration
Workshop to Discuss Development of a Women's Health Information
Sharing Network
AGENCY: Food and Drug Administration, HHS.
ACTION: 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
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 community-based 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, 301-827-0350, FAX: 301-827-9194, e-mail:
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
