Agency Information Collection Activities; Submission to OMB for Review and Approval; Comment Request; NESHAP for Pharmaceutical Production (Renewal), EPA ICR Number 1781.05, OMB Control Number 2060-0358, 28605-28606 [2010-12273]
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Federal Register / Vol. 75, No. 98 / Friday, May 21, 2010 / Notices
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Comment Date: 5 p.m. Eastern Time
on June 11, 2010.
Kimberly D. Bose,
Secretary.
[FR Doc. 2010–12230 Filed 5–20–10; 8:45 am]
BILLING CODE 6717–01–P
ENVIRONMENTAL PROTECTION
AGENCY
[EPA–HQ–OECA–2009–0381; FRL–9143–9]
Agency Information Collection
Activities; Submission to OMB for
Review and Approval; Comment
Request; NESHAP for Pharmaceutical
Production (Renewal), EPA ICR
Number 1781.05, OMB Control Number
2060–0358
emcdonald on DSK2BSOYB1PROD with NOTICES
AGENCY: Environmental Protection
Agency (EPA).
ACTION: Notice.
SUMMARY: In compliance with the
Paperwork Reduction Act (44 U.S.C.
3501 et seq.), this document announces
that an Information Collection Request
(ICR) has been forwarded to the Office
of Management and Budget (OMB) for
review and approval. This is a request
to renew an existing approved
collection. The ICR which is abstracted
below describes the nature of the
collection and the estimated burden and
cost.
DATES: Additional comments may be
submitted on or before June 21, 2010.
ADDRESSES: Submit your comments,
referencing docket ID number EPA–HQ–
OECA–2009–0381 to (1) EPA online
using https://www.regulations.gov (our
preferred method), or by e-mail to
docket.oeca@epa.gov, or by mail to: EPA
Docket Center (EPA/DC), Environmental
Protection Agency, Enforcement and
Compliance Docket and Information
Center, mail code 28221T, 1200
Pennsylvania Avenue, NW.,
Washington, DC 20460, and (2) OMB at:
Office of Information and Regulatory
Affairs, Office of Management and
Budget (OMB), Attention: Desk Officer
for EPA, 725 17th Street, NW.,
Washington, DC 20503.
VerDate Mar<15>2010
16:40 May 20, 2010
Jkt 220001
FOR FURTHER INFORMATION CONTACT:
Learia Williams, Compliance
Assessment and Media Programs
Division, Office of Compliance, Mail
Code 2223A, Environmental Protection
Agency, 1200 Pennsylvania Avenue,
NW., Washington, DC 20460; telephone
number: (202) 564–4113; fax number:
(202) 564–0050; e-mail address:
williams.learia@epa.gov.
EPA has
submitted the following ICR to OMB for
review and approval according to the
procedures prescribed in 5 CFR 1320.12.
On July 8, 2009 (74 FR 32580), EPA
sought comments on this ICR pursuant
to 5 CFR 1320.8(d). EPA received no
comments. Any additional comments on
this ICR should be submitted to EPA
and OMB within 30 days of this notice.
EPA has established a public docket
for this ICR under docket ID number
EPA–HQ–OECA–2009–0381, which is
available for public viewing online at
https://www.regulations.gov, in person
viewing at the Enforcement and
Compliance Docket in the EPA Docket
Center (EPA/DC), EPA West, Room
3334, 1301 Constitution Avenue, NW.,
Washington, DC. The EPA Docket
Center Public Reading Room is open
from 8:30 a.m. to 4:30 p.m., Monday
through Friday, excluding legal
holidays. The telephone number for the
Reading Room is (202) 566–1744, and
the telephone number for the
Enforcement and Compliance Docket is
(202) 566–1752.
Use EPA’s electronic docket and
comment system at https://
www.regulations.gov, to submit or view
public comments, to access the index
listing of the contents of the docket, and
to access those documents in the docket
that are available electronically. Once in
the system, select ‘‘docket search,’’ then
key in the docket ID number identified
above. Please note that EPA’s policy is
that public comments, whether
submitted electronically or on paper,
will be made available for public
viewing at https://www.regulations.gov,
as EPA receives them and without
change, unless the comment contains
copyrighted material, Confidential
Business Information (CBI), or other
information whose public disclosure is
restricted by statute. For further
information about the electronic docket,
go to https://www.regulations.gov.
Title: NESHAP for Pharmaceutical
Production (Renewal).
ICR Numbers: EPA ICR Number
1781.05, OMB Control Number 2060–
0358.
ICR Status: This ICR is scheduled to
expire on July 31, 2010. Under OMB
regulations, the Agency may continue to
SUPPLEMENTARY INFORMATION:
PO 00000
Frm 00064
Fmt 4703
Sfmt 4703
28605
conduct or sponsor the collection of
information while this submission is
pending at OMB. An Agency may not
conduct or sponsor, and a person is not
required to respond to, a collection of
information unless it displays a
currently valid OMB control number.
The OMB control numbers for EPA’s
regulations in title 40 of the CFR, after
appearing in the Federal Register when
approved, are listed in 40 CFR part 9,
and displayed either by publication in
the Federal Register or by other
appropriate means, such as on the
related collection instrument or form, if
applicable. The display of OMB control
numbers in certain EPA regulations is
consolidated in 40 CFR part 9.
Abstract: The National Emission
Standards for Hazardous Air Pollutants
(NESHAP) for Pharmaceutical
Production (40 CFR part 63, subpart
GGG) were proposed on April 2, 1997,
and promulgated on September 21,
1998. These standards apply to the
facilities in pharmaceutical production
that are major sources of hazardous air
pollutants (HAP). The affected facility is
all pharmaceutical manufacturing
operation, which includes process
vents, storage tanks, equipment
components, and wastewater systems
commencing construction or
reconstruction after the date of the
proposal. In general, all NESHAP
require initial notifications,
performance tests, and periodic reports.
Owners/operators of affected
pharmaceutical production are required
to maintain records of the occurrence
and duration of any startup, shutdown,
or malfunction in the operation of an
affected facility, or any period during
which the monitoring system is
inoperative. These notifications, reports
and records are essential in determining
compliance and, in general, are required
of all sources subject to NESHAP.
Semiannual reports are also required.
Any owner or operator subject to the
provisions of this part shall maintain a
file of these measurements, and retain
the records for at least five years
following the date of such
measurements, maintenance reports,
and records. Performance tests reports
are required as this is the Agency’s
record of a source’s initial capability to
comply with the emission standard, and
serve as a record of the operating
conditions under which compliance
was achieved.
All reports are sent to the delegated
state or local authority. In the event that
there is no such delegated authority, the
reports are sent directly to the EPA
regional office. This information is
being collected to assure compliance
with 40 CFR part 63, subpart GGG, as
E:\FR\FM\21MYN1.SGM
21MYN1
emcdonald on DSK2BSOYB1PROD with NOTICES
28606
Federal Register / Vol. 75, No. 98 / Friday, May 21, 2010 / Notices
authorized in sections 112 and 114(a) of
the Clean Air Act. The required
information consists of emissions data
and other information that have been
determined to be private.
An agency may not conduct or
sponsor, and a person is not required to
respond to, a collection of information
unless it displays a currently valid OMB
Control Number. The OMB Control
Number for EPA regulations listed in 40
CFR part 9 and 48 CFR chapter 15, are
identified on the form and/or
instrument, if applicable.
Burden Statement: The annual public
reporting and recordkeeping burden for
this collection of information estimated
to average 178 hours per response.
Burden means the total time, effort, or
financial resources expended by persons
to generate, maintain, retain, or disclose,
and provide information to or for a
Federal agency. This includes the time
needed to review instructions; develop,
acquire, install, and utilize technology
and systems for the purposes of
collecting, validating, and verifying
information, processing and
maintaining information, and disclosing
and providing information. All existing
ways will have to adjust to comply with
any previously applicable instructions
and requirements that have
subsequently changed; train personnel
to be able to respond to a collection of
information; search data sources;
complete and review the collection of
information; and transmit or otherwise
disclose the information.
Respondents/Affected Entities:
Pharmaceutical production facilities.
Estimated Number of Respondents:
27.
Frequency of Response: Initially,
quarterly, semiannually, and
occasionally.
Estimated Total Annual Hour Burden:
44,246.
Estimated Total Annual Cost:
$4,297,480 which includes $4,185,214
in labor costs, no capital/startup costs,
and $112,266 in operation and
maintenance (O&M) costs.
Changes in the Estimates: There is an
adjustment in the labor hours in this
ICR, compared to the previous ICR. The
labor burden is decreased compared to
the most recently approved ICR due to
a reduction in the number of sources.
The reduction was caused by a number
of sources becoming synthetic area
minor sources before the compliance
date. All of the sources subject to the
standard are major sources.
There is a decrease in the capital/
startup and operations and maintenance
(O&M) costs from the previous ICR due
to the decrease in the number of
sources.
VerDate Mar<15>2010
16:40 May 20, 2010
Jkt 220001
Dated: May 17, 2010.
John Moses,
Director, Collection Strategies Division.
[FR Doc. 2010–12273 Filed 5–20–10; 8:45 am]
BILLING CODE 6560–50–P
ENVIRONMENTAL PROTECTION
AGENCY
[EPA–HQ–OECA–2009–0534; FRL–9153–7]
Agency Information Collection
Activities; Submission to OMB for
Review and Approval; Comment
Request; NESHAP for Off-Site Waste
and Recovery Operations (Renewal),
EPA ICR Number 1717.07, OMB
Control Number 2060–0313
AGENCY: Environmental Protection
Agency (EPA).
ACTION: Notice.
SUMMARY: In compliance with the
Paperwork Reduction Act (44 U.S.C.
3501 et seq.), this document announces
that an Information Collection Request
(ICR) has been forwarded to the Office
of Management and Budget (OMB) for
review and approval. This is a request
to renew an existing approved
collection. The ICR which is abstracted
below describes the nature of the
collection and the estimated burden and
cost.
DATES: Additional comments may be
submitted on or before June 21, 2010.
ADDRESSES: Submit your comments,
referencing docket ID number EPA–HQ–
OECA–2009–0534, to (1) EPA online
using https://www.regulations.gov (our
preferred method), or by e-mail to
docket.oeca@epa.gov, or by mail to: EPA
Docket Center (EPA/DC), Environmental
Protection Agency, Enforcement and
Compliance Docket and Information
Center, Mail Code 28221T, 1200
Pennsylvania Avenue, NW.,
Washington, DC 20460, and (2) OMB at:
Office of Information and Regulatory
Affairs, Office of Management and
Budget (OMB), Attention: Desk Officer
for EPA, 725 17th Street, NW.,
Washington, DC 20503.
FOR FURTHER INFORMATION CONTACT:
Robert C. Marshall, Jr. of the Office of
Compliance, Environmental Protection
Agency, 1200 Pennsylvania Avenue,
NW., Washington, DC 20460; telephone
number: (202) 564–7021; fax number:
(202) 564–0050; e-mail address:
marshall.robert@epa.gov.
SUPPLEMENTARY INFORMATION: EPA has
submitted the following ICR to OMB for
review and approval according to the
procedures prescribed in 5 CFR 1320.12.
On July 30, 2009 (74 FR 38005), EPA
sought comments on this ICR pursuant
PO 00000
Frm 00065
Fmt 4703
Sfmt 4703
to 5 CFR 1320.8(d). EPA received no
comments. Any additional comments on
this ICR should be submitted to EPA
and OMB within 30 days of this notice.
EPA has established a public docket
for this ICR under docket ID number
EPA–HQ–OECA–2009–0534, which is
available for public viewing online at
https://www.regulations.gov, in person
viewing at the Enforcement and
Compliance Docket in the EPA Docket
Center (EPA/DC), EPA West, Room
3334, 1301 Constitution Avenue, NW.,
Washington, DC. The EPA Docket
Center Public Reading Room is open
from 8:30 a.m. to 4:30 p.m., Monday
through Friday, excluding legal
holidays. The telephone number for the
Reading Room is (202) 566–1744, and
the telephone number for the
Enforcement and Compliance Docket is
(202) 566–1752.
Use EPA’s electronic docket and
comment system at https://
www.regulations.gov, to submit or view
public comments, access the index
listing of the contents of the docket, and
to access those documents in the docket
that are available electronically. Once in
the system, select ‘‘docket search,’’ then
key in the docket ID number identified
above. Please note that EPA’s policy is
that public comments, whether
submitted electronically or in paper,
will be made available for public
viewing at https://www.regulations.gov,
as EPA receives them and without
change, unless the comment contains
copyrighted material, Confidential
Business Information (CBI), or other
information whose public disclosure is
restricted by statute. For further
information about the electronic docket,
go to https://www.regulations.gov.
Title: NESHAP for Off-Site Waste and
Recovery Operations (Renewal).
ICR Numbers: EPA ICR Number
1717.07, OMB Control Number 2060–
0313.
ICR Status: This ICR is scheduled to
expire on July 31, 2010. Under OMB
regulations, the Agency may continue to
conduct or sponsor the collection of
information while this submission is
pending at OMB. An agency may not
conduct or sponsor, and a person is not
required to respond to, a collection of
information unless it displays a
currently valid OMB control number.
The OMB control numbers for EPA’s
regulations in title 40 of the CFR, after
appearing in the Federal Register when
approved, are listed in 40 CFR part 9,
and displayed either by publication in
the Federal Register or by other
appropriate means, such as on the
related collection instrument or form, if
applicable. The display of OMB control
E:\FR\FM\21MYN1.SGM
21MYN1
]]>Agencies
[Federal Register Volume 75, Number 98 (Friday, May 21, 2010)]
[Notices]
[Pages 28605-28606]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2010-12273]
=======================================================================
-----------------------------------------------------------------------
ENVIRONMENTAL PROTECTION AGENCY
[EPA-HQ-OECA-2009-0381; FRL-9143-9]
Agency Information Collection Activities; Submission to OMB for
Review and Approval; Comment Request; NESHAP for Pharmaceutical
Production (Renewal), EPA ICR Number 1781.05, OMB Control Number 2060-
0358
AGENCY: Environmental Protection Agency (EPA).
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: In compliance with the Paperwork Reduction Act (44 U.S.C. 3501
et seq.), this document announces that an Information Collection
Request (ICR) has been forwarded to the Office of Management and Budget
(OMB) for review and approval. This is a request to renew an existing
approved collection. The ICR which is abstracted below describes the
nature of the collection and the estimated burden and cost.
DATES: Additional comments may be submitted on or before June 21, 2010.
ADDRESSES: Submit your comments, referencing docket ID number EPA-HQ-
OECA-2009-0381 to (1) EPA online using https://www.regulations.gov (our
preferred method), or by e-mail to docket.oeca@epa.gov, or by mail to:
EPA Docket Center (EPA/DC), Environmental Protection Agency,
Enforcement and Compliance Docket and Information Center, mail code
28221T, 1200 Pennsylvania Avenue, NW., Washington, DC 20460, and (2)
OMB at: Office of Information and Regulatory Affairs, Office of
Management and Budget (OMB), Attention: Desk Officer for EPA, 725 17th
Street, NW., Washington, DC 20503.
FOR FURTHER INFORMATION CONTACT: Learia Williams, Compliance Assessment
and Media Programs Division, Office of Compliance, Mail Code 2223A,
Environmental Protection Agency, 1200 Pennsylvania Avenue, NW.,
Washington, DC 20460; telephone number: (202) 564-4113; fax number:
(202) 564-0050; e-mail address: williams.learia@epa.gov.
SUPPLEMENTARY INFORMATION: EPA has submitted the following ICR to OMB
for review and approval according to the procedures prescribed in 5 CFR
1320.12. On July 8, 2009 (74 FR 32580), EPA sought comments on this ICR
pursuant to 5 CFR 1320.8(d). EPA received no comments. Any additional
comments on this ICR should be submitted to EPA and OMB within 30 days
of this notice.
EPA has established a public docket for this ICR under docket ID
number EPA-HQ-OECA-2009-0381, which is available for public viewing
online at https://www.regulations.gov, in person viewing at the
Enforcement and Compliance Docket in the EPA Docket Center (EPA/DC),
EPA West, Room 3334, 1301 Constitution Avenue, NW., Washington, DC. The
EPA Docket Center Public Reading Room is open from 8:30 a.m. to 4:30
p.m., Monday through Friday, excluding legal holidays. The telephone
number for the Reading Room is (202) 566-1744, and the telephone number
for the Enforcement and Compliance Docket is (202) 566-1752.
Use EPA's electronic docket and comment system at https://www.regulations.gov, to submit or view public comments, to access the
index listing of the contents of the docket, and to access those
documents in the docket that are available electronically. Once in the
system, select ``docket search,'' then key in the docket ID number
identified above. Please note that EPA's policy is that public
comments, whether submitted electronically or on paper, will be made
available for public viewing at https://www.regulations.gov, as EPA
receives them and without change, unless the comment contains
copyrighted material, Confidential Business Information (CBI), or other
information whose public disclosure is restricted by statute. For
further information about the electronic docket, go to https://www.regulations.gov.
Title: NESHAP for Pharmaceutical Production (Renewal).
ICR Numbers: EPA ICR Number 1781.05, OMB Control Number 2060-0358.
ICR Status: This ICR is scheduled to expire on July 31, 2010. Under
OMB regulations, the Agency may continue to conduct or sponsor the
collection of information while this submission is pending at OMB. An
Agency may not conduct or sponsor, and a person is not required to
respond to, a collection of information unless it displays a currently
valid OMB control number. The OMB control numbers for EPA's regulations
in title 40 of the CFR, after appearing in the Federal Register when
approved, are listed in 40 CFR part 9, and displayed either by
publication in the Federal Register or by other appropriate means, such
as on the related collection instrument or form, if applicable. The
display of OMB control numbers in certain EPA regulations is
consolidated in 40 CFR part 9.
Abstract: The National Emission Standards for Hazardous Air
Pollutants (NESHAP) for Pharmaceutical Production (40 CFR part 63,
subpart GGG) were proposed on April 2, 1997, and promulgated on
September 21, 1998. These standards apply to the facilities in
pharmaceutical production that are major sources of hazardous air
pollutants (HAP). The affected facility is all pharmaceutical
manufacturing operation, which includes process vents, storage tanks,
equipment components, and wastewater systems commencing construction or
reconstruction after the date of the proposal. In general, all NESHAP
require initial notifications, performance tests, and periodic reports.
Owners/operators of affected pharmaceutical production are required
to maintain records of the occurrence and duration of any startup,
shutdown, or malfunction in the operation of an affected facility, or
any period during which the monitoring system is inoperative. These
notifications, reports and records are essential in determining
compliance and, in general, are required of all sources subject to
NESHAP. Semiannual reports are also required.
Any owner or operator subject to the provisions of this part shall
maintain a file of these measurements, and retain the records for at
least five years following the date of such measurements, maintenance
reports, and records. Performance tests reports are required as this is
the Agency's record of a source's initial capability to comply with the
emission standard, and serve as a record of the operating conditions
under which compliance was achieved.
All reports are sent to the delegated state or local authority. In
the event that there is no such delegated authority, the reports are
sent directly to the EPA regional office. This information is being
collected to assure compliance with 40 CFR part 63, subpart GGG, as
[[Page 28606]]
authorized in sections 112 and 114(a) of the Clean Air Act. The
required information consists of emissions data and other information
that have been determined to be private.
An agency may not conduct or sponsor, and a person is not required
to respond to, a collection of information unless it displays a
currently valid OMB Control Number. The OMB Control Number for EPA
regulations listed in 40 CFR part 9 and 48 CFR chapter 15, are
identified on the form and/or instrument, if applicable.
Burden Statement: The annual public reporting and recordkeeping
burden for this collection of information estimated to average 178
hours per response. Burden means the total time, effort, or financial
resources expended by persons to generate, maintain, retain, or
disclose, and provide information to or for a Federal agency. This
includes the time needed to review instructions; develop, acquire,
install, and utilize technology and systems for the purposes of
collecting, validating, and verifying information, processing and
maintaining information, and disclosing and providing information. All
existing ways will have to adjust to comply with any previously
applicable instructions and requirements that have subsequently
changed; train personnel to be able to respond to a collection of
information; search data sources; complete and review the collection of
information; and transmit or otherwise disclose the information.
Respondents/Affected Entities: Pharmaceutical production
facilities.
Estimated Number of Respondents: 27.
Frequency of Response: Initially, quarterly, semiannually, and
occasionally.
Estimated Total Annual Hour Burden: 44,246.
Estimated Total Annual Cost: $4,297,480 which includes $4,185,214
in labor costs, no capital/startup costs, and $112,266 in operation and
maintenance (O&M) costs.
Changes in the Estimates: There is an adjustment in the labor hours
in this ICR, compared to the previous ICR. The labor burden is
decreased compared to the most recently approved ICR due to a reduction
in the number of sources. The reduction was caused by a number of
sources becoming synthetic area minor sources before the compliance
date. All of the sources subject to the standard are major sources.
There is a decrease in the capital/startup and operations and
maintenance (O&M) costs from the previous ICR due to the decrease in
the number of sources.
Dated: May 17, 2010.
John Moses,
Director, Collection Strategies Division.
[FR Doc. 2010-12273 Filed 5-20-10; 8:45 am]
BILLING CODE 6560-50-P
