Draft Manufactured Food Regulatory Program Standards; Availability; Correction, 43203 [E6-12179]
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Federal Register / Vol. 71, No. 146 / Monday, July 31, 2006 / Notices
new information to Chile. Finally, the
revised guidance notes that FDA
considers the information on this list,
which is provided voluntarily with the
understanding that it will be posted on
FDA’s Internet site and communicated
to, and possibly further disseminated
by, Chile, to be information that is not
protected from disclosure under 5
U.S.C. 552(b)(4). Under this guidance,
FDA recommends that U.S. firms that
want to be placed on the list send the
following information to FDA: Name
and address of the firm and the
manufacturing plant; name, telephone
number, and e-mail address (if
available) of the contact person; a list of
products presently shipped and
expected to be shipped in the next 3
years; identities of agencies that inspect
the plant and the date of last inspection;
plant number and copy of last
inspection notice; and, if other than an
FDA inspection, copy of last inspection
report. FDA requests that this
information be updated every 2 years.
FDA estimates the burden of this
collection of information as follows:
TABLE 1.—ESTIMATED ANNUAL REPORTING BURDEN1
Activity
No. of
Respondents
Annual Frequency
per Response
Total Annual
Responses
Hours per
Response
Total Hours
New written requests to be
placed on the list
15
1
15
1.5
22.5
Biannual update
55
1
55
1.0
55.0
Occasional updates
25
1
25
0.5
12.5
Total
sroberts on PROD1PC70 with NOTICES
1There
90
are no capital costs or operating and maintenance costs associated with this collection of information.
The estimate of the number of firms
that will submit new written requests to
be placed on the list, biannual updates
and occasional updates is based on the
FDA’s experience maintaining the list
over the past 3 years. The estimate of
the number of hours that it will take a
firm to gather the information needed to
be placed on the list or update its
information is based on FDA’s
experience with firms submitting
similar requests. FDA believes that the
information to be submitted will be
readily available to the firms.
To date, over 110 producers have
sought to be included on the list. FDA
estimates that, each year, approximately
15 new firms will apply to be added to
the list. We estimate that a firm will
require 1.5 hours to read the guidance,
gather the information needed, and to
prepare a communication to FDA that
contains the information and requests
that the firm be placed on the list.
Under the revised guidance, every 2
years each producer on the list must
provide updated information in order to
remain on the list. FDA estimates that
each year approximately half of the
firms on the list, 55 firms, will resubmit
the information to remain on the list.
We estimate that a firm already on the
list will require 1.0 hours to biannually
update and resubmit the information to
FDA, including time reviewing the
information and corresponding with
FDA. In addition, FDA expects that,
each year, approximately 25 firms will
need to submit an occasional update
and each firm will require 0.5 hours to
prepare a communication to FDA
reporting the change.
VerDate Aug<31>2005
19:33 Jul 28, 2006
Jkt 208001
Dated: July 21, 2006.
Jeffrey Shuren,
Assistant Commissioner for Policy.
[FR Doc. E6–12160 Filed 7–28–06; 8:45 am]
BILLING CODE 4160–01–S
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
the Internet address
‘‘http:www.fda.gov.ohrms/dockets/
default.htm’’ is corrected to read
‘‘https://www.fda.gov/ohrms/dockets/
98fr/06d-0246-gdl0001.pdf’’.
Dated: July 25, 2006.
Jeffrey Shuren,
Assistant Commissioner for Policy.
[FR Doc. E6–12179 Filed 7–28–06; 8:45 am]
BILLING CODE 4160–01–S
[Docket No. 2006D–0246]
Draft Manufactured Food Regulatory
Program Standards; Availability;
Correction
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Frm 00110
Fmt 4703
Sfmt 4703
Health Resources and Services
Administration
Cooperative Agreement for Poison
Prevention Education
Notice; correction.
SUMMARY: The Food and Drug
Administration is correcting a notice
that appeared in the Federal Register of
July 20, 2006. The document announced
the availability of a draft document
entitled ‘‘Manufactured Food Regulatory
Program Standards.’’ The document was
published with an incorrect Internet
address. This document corrects that
error.
FOR FURTHER INFORMATION CONTACT:
Beverly Kent, Division of Federal-State
Relations, Food and Drug
Administration, 300 Pearl St., suite 100,
Buffalo, NY 14202, 716–541–0331.
SUPPLEMENTARY INFORMATION: In FR Doc.
E6–11539, appearing on page 41221 in
the Federal Register of Thursday, July
20, 2006, the following correction is
made:
1. On page 41222, in the first column,
under the ‘‘Electronic Access’’ caption,
PO 00000
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Health Resources and Services
Administration (HRSA), HHS.
ACTION: Notice of Single Source Award.
AGENCY:
SUMMARY: HRSA will be forming a
partnership with the Home Safety
Council (HSC) to collaborate on
reaching America’s low literacy
population. Through this project, easy
to read and comprehend poison
prevention material will be developed
and distributed to the public, poison
centers, safety and injury prevention
professionals, health educators, and first
responders.
FOR FURTHER INFORMATION CONTACT:
Shkeda Johnson, Senior Public Health
Analyst, Healthcare Systems Bureau,
Division of Healthcare Preparedness,
Room 13–103, 5600 Fishers Lane,
Rockville, MD 20857. Telephone: 301–
443–1210 Email: sjohnson@hrsa.gov.
E:\FR\FM\31JYN1.SGM
31JYN1
]]>Agencies
[Federal Register Volume 71, Number 146 (Monday, July 31, 2006)]
[Notices]
[Page 43203]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E6-12179]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration
[Docket No. 2006D-0246]
Draft Manufactured Food Regulatory Program Standards;
Availability; Correction
AGENCY: Food and Drug Administration, HHS.
ACTION: Notice; correction.
-----------------------------------------------------------------------
SUMMARY: The Food and Drug Administration is correcting a notice that
appeared in the Federal Register of July 20, 2006. The document
announced the availability of a draft document entitled ``Manufactured
Food Regulatory Program Standards.'' The document was published with an
incorrect Internet address. This document corrects that error.
FOR FURTHER INFORMATION CONTACT: Beverly Kent, Division of Federal-
State Relations, Food and Drug Administration, 300 Pearl St., suite
100, Buffalo, NY 14202, 716-541-0331.
SUPPLEMENTARY INFORMATION: In FR Doc. E6-11539, appearing on page 41221
in the Federal Register of Thursday, July 20, 2006, the following
correction is made:
1. On page 41222, in the first column, under the ``Electronic
Access'' caption, the Internet address ``http:www.fda.gov.ohrms/
dockets/default.htm'' is corrected to read ``https://www.fda.gov/ohrms/
dockets/98fr/06d-0246-gdl0001.pdf''.
Dated: July 25, 2006.
Jeffrey Shuren,
Assistant Commissioner for Policy.
[FR Doc. E6-12179 Filed 7-28-06; 8:45 am]
BILLING CODE 4160-01-S
