Impact of Implementation of the Chemical Weapons Convention on Commercial Activities Involving “Schedule 1” Chemicals Through Calendar Year 2009, 58003-58005 [E9-27053]
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Federal Register / Vol. 74, No. 216 / Tuesday, November 10, 2009 / Notices
Site 3, Port of Albany, expanding the
site from 35 acres to 277 acres. The
applicant has requested that Site 4,
Crossroads Industrial Park be removed
from FTZ 121. The applicant is also
requesting approval of the following
additional ‘‘magnet sites’’: Site 5, 281
acres, Saratoga Technology + Energy
Park, 10 Hermes Road, Malta, NY 12020;
Site 6, 1192 acres, Luther Forest
Technology Campus, 40 Rocket Test
Station Road, Malta, NY 12020; Site 7,
133 acres, Florida Business Park
Extension, State Highway 5S,
Amsterdam, NY 12010. The applicant
proposes that Site 6 be subject to a
seven-year ‘‘sunset’’ time limit, instead
of the standard five-year ‘‘sunset’’ time
limit that would otherwise apply to
magnet sites under the ASF.
In accordance with the Board’s
regulations, Maureen Hinman of the
FTZ staff is designated examiner to
evaluate and analyze the facts and
information presented in the application
and case record and to report findings
and recommendations to the Board.
Public comment is invited from
interested parties. Submissions (original
and 3 copies) shall be addressed to the
Board’s Executive Secretary at the
address listed below. The closing period
for their receipt is January 11, 2010.
Rebuttal comments in response to
material submitted during the foregoing
period may be submitted during the
subsequent 15-day period (to January
25, 2010)
A copy of the application will be
available for public inspection at the
Office of the Executive Secretary,
Foreign-Trade Zones Board, Room 2111,
U.S. Department of Commerce, 1401
Constitution Avenue, NW., Washington,
DC 20230–0002, and in the ‘‘Reading
Room’’ section of the Board’s Web site,
which is accessible via https://
www.trade.gov/ftz. For further
information, contact Maureen Hinman
at maureen.hinman@trade.gov or (202)
482–0627.
Dated: November 3, 2009.
Elizabeth Whiteman,
Acting Executive Secretary.
[FR Doc. E9–27094 Filed 11–9–09; 8:45 am]
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BILLING CODE 3510–DS–P
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DEPARTMENT OF COMMERCE
United States Patent and Trademark
Office
[Docket No. PTO–P–2009–0048]
Grant of Interim Extension of the Term
of U.S. Patent No. 4,971,802;
MIFAMURTIDE
AGENCY: United States Patent and
Trademark Office.
ACTION: Notice of interim patent term
extension.
SUMMARY: The United States Patent and
Trademark Office has issued a
certificate under 35 U.S.C. 156(d)(5) for
a third one-year interim extension of the
term of U.S. Patent No. 4,971,802.
FOR FURTHER INFORMATION CONTACT: Raul
Tamayo by telephone at (571) 272–7728;
by mail marked to his attention and
addressed to the Commissioner for
Patents, Mail Stop Hatch-Waxman PTE,
P.O. Box 1450, Alexandria, VA 22313–
1450; by fax marked to his attention at
(571) 273–7728, or by e-mail to
Raul.Tamayo@uspto.gov.
Section
156 of Title 35, United States Code,
generally provides that the term of a
patent may be extended for a period of
up to five years if the patent claims a
product, or a method of making or using
a product, that has been subject to
certain defined regulatory review, and
that the patent may be extended for
interim periods of up to a year if the
regulatory review is anticipated to
extend beyond the expiration date of the
patent.
On September 30, 2009, IDM Pharma,
agent/licensee of patent owner Novartis,
timely filed an application under 35
U.S.C. 156(d)(5) for a third interim
extension of the term of U.S. Patent No.
4,971,802. Claims of the patent cover
muramyl tripeptide phosphatidyl
ethanolamine, which is labeled as the
active ingredient in the human drug
product Mifamurtide. The application
indicates, and the Food and Drug
Administration has confirmed, that a
New Drug Application for the human
drug product Mifamurtide has been
filed and is currently undergoing
regulatory review before the Food and
Drug Administration for permission to
market or use the product commercially.
Review of the application indicates
that, except for permission to market or
use the product commercially, the
subject patent would be eligible for an
extension of the patent term under 35
U.S.C. 156, and that the patent should
be extended for an additional year as
required by 35 U.S.C. 156(d)(5)(B).
SUPPLEMENTARY INFORMATION:
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Because it is apparent that the
regulatory review period will continue
beyond the extended expiration date of
the patent (November 20, 2009), interim
extension of the patent term under 35
U.S.C. 156(d)(5) is appropriate.
A third interim extension under 35
U.S.C. 156(d)(5) of the term of U.S.
Patent No. 4,971,802 is granted for a
period of one year from the extended
expiration date of the patent, i.e., until
November 20, 2010.
Dated: October 30, 2009.
David J. Kappos,
Under Secretary of Commerce for Intellectual
Property and Director of the United States
Patent and Trademark Office.
[FR Doc. E9–26998 Filed 11–9–09; 8:45 am]
BILLING CODE 3510–16–P
DEPARTMENT OF COMMERCE
Bureau of Industry and Security
[Docket No. 0910271381–91382–01]
Impact of Implementation of the
Chemical Weapons Convention on
Commercial Activities Involving
‘‘Schedule 1’’ Chemicals Through
Calendar Year 2009
AGENCY: Bureau of Industry and
Security, Commerce.
ACTION: Notice of inquiry.
SUMMARY: The Bureau of Industry and
Security (BIS) is seeking public
comments on the impact that
implementation of the Chemical
Weapons Convention, through the
Chemical Weapons Convention
Implementation Act and the Chemical
Weapons Convention Regulations, has
had on commercial activities involving
‘‘Schedule 1’’ chemicals during calendar
year 2009. The purpose of this notice of
inquiry is to collect information to assist
BIS in its preparation of the annual
certification to the Congress, which is
required under Condition 9 of Senate
Resolution 75, April 24, 1997, in which
the Senate gave its advice and consent
to the ratification of the Chemical
Weapons Convention.
DATES: Comments must be received by
December 10, 2009.
ADDRESSES: You may submit comments
by any of the following methods:
• E-mail: wfisher@bis.doc.gov.
Include the phrase ‘‘Schedule 1 Notice
of Inquiry’’ in the subject line;
• Fax: (202) 482–3355 (Attn: Willard
Fisher);
• Mail or Hand Delivery/Courier:
Willard Fisher, U.S. Department of
Commerce, Bureau of Industry and
Security, Regulatory Policy Division,
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58004
Federal Register / Vol. 74, No. 216 / Tuesday, November 10, 2009 / Notices
srobinson on DSKHWCL6B1PROD with NOTICES
14th Street & Pennsylvania Avenue,
NW., Room 2705, Washington, DC
20230.
FOR FURTHER INFORMATION CONTACT: For
questions on the Chemical Weapons
Convention requirements for ‘‘Schedule
1’’ chemicals, contact James Truske,
Treaty Compliance Division, Office of
Nonproliferation and Treaty
Compliance, Bureau of Industry and
Security, U.S. Department of Commerce,
Phone: (202) 482–1001. For questions
on the submission of comments, contact
Willard Fisher, Regulatory Policy
Division, Office of Exporter Services,
Bureau of Industry and Security, U.S.
Department of Commerce, Phone: (202)
482–2440.
SUPPLEMENTARY INFORMATION:
Background
In providing its advice and consent to
the ratification of the Convention on the
Prohibition of the Development,
Production, Stockpiling, and Use of
Chemical Weapons and Their
Destruction, commonly called the
Chemical Weapons Convention (CWC)
(the Convention), the Senate included in
Senate Resolution 75 (S. Res. 75, April
24, 1997) several conditions to its
ratification. Condition 9, titled
‘‘Protection of Advanced
Biotechnology,’’ calls for the President
to certify to Congress on an annual basis
that ‘‘the legitimate commercial
activities and interests of chemical,
biotechnology, and pharmaceutical
firms in the United States are not being
significantly harmed by the limitations
of the Convention on access to, and
production of, those chemicals and
toxins listed in Schedule 1.’’ On July 8,
2004, President Bush, by Executive
Order 13346, delegated his authority to
make the annual certification to the
Secretary of Commerce.
The CWC is an international arms
control treaty that contains certain
verification provisions. In order to
implement these verification provisions,
the CWC established the Organization
for the Prohibition of Chemical
Weapons (OPCW). The CWC imposes
certain obligations on countries that
have ratified the Convention (i.e., States
Parties), among which are the enactment
of legislation to prohibit the production,
storage, and use of chemical weapons,
and the establishment of a National
Authority to serve as the national focal
point for effective liaison with the
OPCW and other States Parties for the
purpose of achieving the object and
purpose of the Convention and the
implementation of its provisions. The
CWC also requires each State Party to
implement a comprehensive data
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16:45 Nov 09, 2009
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declaration and inspection regime to
provide transparency and to verify that
both the public and private sectors of
the State Party are not engaged in
activities prohibited under the CWC.
‘‘Schedule 1’’ chemicals consist of
those toxic chemicals and precursors set
forth in the CWC ‘‘Annex on
Chemicals’’ and in Supplement No. 1 to
part 712 of the Chemical Weapons
Convention Regulations (CWCR) (15
CFR parts 710–722). The CWC
identified these toxic chemicals and
precursors as posing a high risk to the
object and purpose of the Convention.
The CWC restricts the production of
‘‘Schedule 1’’ chemicals for protective
purposes to two facilities per State
Party. The CWC Article-by-Article
Analysis submitted to the Senate in
Treaty Doc. 103–21 defined the term
‘‘protective purposes’’ to mean ‘‘used for
determining the adequacy of defense
equipment and measures.’’ Consistent
with this definition, U.S.
implementation, as authorized via
Presidential Decision Directive (PDD)
70, December 17, 1999, assigned the
responsibility to operate these two
facilities to the Department of Defense
(DOD), thereby precluding commercial
production of ‘‘Schedule 1’’ chemicals
for protective purposes in the United
States. This action did not establish any
limitations on ‘‘Schedule 1’’ chemical
activities that are not prohibited by the
CWC. However, the Department of
Defense maintains strict controls on
‘‘Schedule 1’’ chemicals produced at its
facilities in order to ensure the
accountability and proper use of such
chemicals, consistent with the object
and purpose of the Convention.
The provisions of the CWC that affect
commercial activities involving
‘‘Schedule 1’’ chemicals are
implemented in the CWCR (see 15 CFR
part 712) and in the Export
Administration Regulations (EAR) (see
15 CFR 742.18 and 15 CFR part 745),
both of which are administered by the
Bureau of Industry and Security (BIS).
Pursuant to CWC requirements, the
CWCR restrict commercial production
of ‘‘Schedule 1’’ chemicals to research,
medical, or pharmaceutical purposes.
The CWCR also contain other
requirements and prohibitions that
apply to ‘‘Schedule 1’’ chemicals and/or
‘‘Schedule 1’’ facilities. Specifically, the
CWCR:
(1) Prohibit the import of ‘‘Schedule
1’’ chemicals from States not Party to
the Convention (15 CFR 712.2(b));
(2) Require annual declarations by
certain facilities engaged in the
production of ‘‘Schedule 1’’ chemicals
in excess of 100 grams aggregate per
calendar year (i.e., declared ‘‘Schedule
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1’’ facilities) for purposes not prohibited
by the Convention (15 CFR 712.5(a)(1)
and (a)(2));
(3) Require government approval of
‘‘declared Schedule 1’’ facilities (15 CFR
712.5(f));
(4) Provide that ‘‘declared Schedule
1’’ facilities are subject to initial and
routine inspection by the Organization
for the Prohibition of Chemical
Weapons (15 CFR 712.5(e) and
716.1(b)(1));
(5) Require 200 days advance
notification of establishment of new
‘‘Schedule 1’’ production facilities
producing greater than 100 grams
aggregate of ‘‘Schedule 1’’ chemicals per
calendar year (15 CFR 712.4);
(6) Require advance notification and
annual reporting of all imports and
exports of ‘‘Schedule 1’’ chemicals to, or
from, other States Parties to the
Convention (15 CFR 712.6, 742.18(a)(1)
and 745.1); and
(7) Prohibit the export of ‘‘Schedule
1’’ chemicals to States not Party to the
Convention (15 CFR 742.18(a)(1) and
(b)(1)(ii)).
Request for Comments
In order to assist in determining
whether the legitimate commercial
activities and interests of chemical,
biotechnology, and pharmaceutical
firms in the United States are
significantly harmed by the limitations
of the Convention on access to, and
production of, ‘‘Schedule 1’’ chemicals
as described in this notice, BIS is
seeking public comments on any effects
that implementation of the Chemical
Weapons Convention, through the
Chemical Weapons Convention
Implementation Act and the Chemical
Weapons Convention Regulations, has
had on commercial activities involving
‘‘Schedule 1’’ chemicals during calendar
year 2009. To allow BIS to properly
evaluate the significance of any harm to
commercial activities involving
‘‘Schedule 1’’ chemicals, public
comments submitted in response to this
notice of inquiry should include both a
quantitative and qualitative assessment
of the impact of the CWC on such
activities.
Submission of Comments
All comments must be submitted to
one of the addresses indicated in this
notice. The Department requires that all
comments be submitted in written form.
The Department encourages interested
persons who wish to comment to do so
at the earliest possible time. The period
for submission of comments will close
on December 10, 2009. The Department
will consider all comments received
before the close of the comment period.
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Federal Register / Vol. 74, No. 216 / Tuesday, November 10, 2009 / Notices
Comments received after the end of the
comment period will be considered if
possible, but their consideration cannot
be assured. The Department will not
accept comments accompanied by a
request that a part or all of the material
be treated confidentially because of its
business proprietary nature or for any
other reason. The Department will
return such comments and materials to
the persons submitting the comments
and will not consider them. All
comments submitted in response to this
notice will be a matter of public record
and will be available for public
inspection and copying.
The Office of Administration, Bureau
of Industry and Security, U.S.
Department of Commerce, displays
public comments on the BIS Freedom of
Information Act (FOIA) Web site at
https://www.bis.doc.gov/foia. This office
does not maintain a separate public
inspection facility. If you have technical
difficulties accessing this Web site,
please call BIS’s Office of
Administration, at (202) 482–1093, for
assistance.
Dated: November 4, 2009.
Matthew S. Borman,
Acting Assistant Secretary for Export
Administration.
[FR Doc. E9–27053 Filed 11–9–09; 8:45 am]
BILLING CODE 3510–33–P
DEPARTMENT OF DEFENSE
Defense Intelligence Agency National
Defense Intelligence College Board of
Visitors Closed Meeting
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AGENCY: National Defense Intelligence
College, Defense Intelligence Agency,
DoD.
ACTION: Notice of closed meeting.
SUMMARY: Pursuant to the provisions of
subsection (d) of section 10 of Public
Law 92–463, as amended by section 5 of
Public Law 94–409, notice is hereby
given that a closed meeting of the
Defense Intelligence Agency National
Defense Intelligence College Board of
Visitors has been scheduled for January
12 and 13, 2010.
DATES: The meeting will be held on
Tuesday, January 12, 2010 (from 8 a.m.
to 5 p.m.) and on Wednesday, January
13, 2010 (from 8 a.m. to 12 p.m.).
ADDRESSES: The meeting will be held at
the National Defense Intelligence
College, Washington, DC 20340–5100.
FOR FURTHER INFORMATION CONTACT: Dr.
David R. Ellison, President, DIA
National Defense Intelligence College,
16:45 Nov 09, 2009
Dated: November 5, 2009.
Mitchell S. Bryman,
Alternate OSD Federal Register Liaison
Officer, Department of Defense.
[FR Doc. E9–26996 Filed 11–9–09; 8:45 am]
BILLING CODE 5001–06–P
DEPARTMENT OF EDUCATION
Office of Postsecondary Education;
Overview Information; International
Research and Studies (IRS) Program;
Notice Inviting Applications for New
Awards for Fiscal Year (FY) 2010
Catalog of Federal Domestic
Assistance (CFDA) Numbers: 84.017A–1
and 84.017A–3.
DATES:
Applications Available: November 10,
2009.
Deadline for Transmittal of
Applications: January 12, 2010.
Full Text of Announcement
Office of the Secretary
VerDate Nov<24>2008
Washington, DC 20340–5100 (202/231–
3344).
SUPPLEMENTARY INFORMATION: The entire
meeting is devoted to the discussion of
classified information as defined in
section 552b(c)(1), title 5 of the U.S.
Code and therefore will be closed. The
Board will discuss several current
critical intelligence issues and advise
the Director, DIA, as to the successful
accomplishment of the mission assigned
to the National Defense Intelligence
College.
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I. Funding Opportunity Description
Purpose of Program: The IRS Program
provides grants to conduct research and
studies to improve and strengthen
instruction in modern foreign languages,
area studies, and other international
fields.
Priorities: In accordance with 34 CFR
75.105(b)(2)(ii), these priorities are from
the regulations for this program (34 CFR
660.10 and 660.34).
Competitive Preference Priorities: For
FY 2010, these priorities are competitive
preference priorities. Under 34 CFR
75.105(c)(2)(i), we award an additional
five points to an application that meets
one or more of these priorities.
These priorities are:
Competitive Preference Priority 1—
Instructional Materials Applications.
The development of specialized
instructional or assessment materials
focused on any of the following seventyeight (78) languages selected from the
U.S. Department of Education’s list of
Less Commonly Taught Languages
(LCTLs):
Akan (Twi-Fante), Albanian,
Amharic, Arabic (all dialects),
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58005
Armenian, Azeri (Azerbaijani), Balochi,
Bamanakan (Bamana, Bambara,
Mandikan, Mandingo, Maninka, Dyula),
Belarusian, Bengali (Bangla), Berber (all
languages), Bosnian, Bulgarian,
Burmese, Cebuano (Visayan), Chechen,
Chinese (Cantonese), Chinese (Gan),
Chinese (Mandarin), Chinese (Min),
Chinese (Wu), Croatian, Dari, Dinka,
Georgian, Gujarati, Hausa, Hebrew
(Modern), Hindi, Igbo, Indonesian,
Japanese, Javanese, Kannada, Kashmiri,
Kazakh, Khmer (Cambodian), Kirghiz,
Korean, Kurdish (Kurmanji), Kurdish
(Sorani), Lao, Malay (Bahasa Melayu or
Malaysian), Malayalam, Marathi,
Mongolian, Nepali, Oromo, Panjabi,
Pashto, Persian (Farsi), Polish,
Portuguese (all varieties), Quechua,
Romanian, Russian, Serbian, Sinhala
(Sinhalese), Somali, Swahili, Tagalog,
Tajik, Tamil, Telugu, Thai, Tibetan,
Tigrigna, Turkish, Turkmen, Ukrainian,
Urdu, Uyghur/Uigur, Uzbek,
Vietnamese, Wolof, Xhosa, Yoruba, and
Zulu.
Competitive Preference Priority 2—
Research, Surveys, and Studies
Applications.
Research, surveys, or studies relating
to current needs for improving
internationalization (including foreign
language instruction, area studies, and
international studies) in Historically
Black Colleges and Universities
(HBCUs), Predominantly Black
Institutions (PBIs), Hispanic Serving
Institutions (HSIs), Tribally Controlled
Colleges and Universities (TCCUs),
Asian American and Native American
Pacific Islander-serving Institutions
(AANAPISIs), Native American-serving
Nontribal Institutions (NASNTIs), or
Alaskan Native and/or Native Hawaiian
institutions (as defined in Title III and
Title V of the Higher Education Act of
1965, as amended).
Note: You will receive an additional five
points for meeting a competitive preference
priority in your application. Applicants are
expected to address only one competitive
preference priority in each application, but
regardless of how many priorities are
addressed, no more than five points in total
can be awarded to a single application.
Program Authority: 20 U.S.C. 1125.
Applicable Regulations: (a) The
Education Department General
Administrative Regulations (EDGAR) in
34 CFR parts 74, 75, 77, 80, 82, 84, 85,
86, 97, 98, and 99. (b) The regulations
for this program in 34 CFR parts 655
and 660.
Note: The regulations in 34 CFR part 86
apply to institutions of higher education
only.
Areas of National Need: In
accordance with section 601(c) of the
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Agencies
[Federal Register Volume 74, Number 216 (Tuesday, November 10, 2009)]
[Notices]
[Pages 58003-58005]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E9-27053]
-----------------------------------------------------------------------
DEPARTMENT OF COMMERCE
Bureau of Industry and Security
[Docket No. 0910271381-91382-01]
Impact of Implementation of the Chemical Weapons Convention on
Commercial Activities Involving ``Schedule 1'' Chemicals Through
Calendar Year 2009
AGENCY: Bureau of Industry and Security, Commerce.
ACTION: Notice of inquiry.
-----------------------------------------------------------------------
SUMMARY: The Bureau of Industry and Security (BIS) is seeking public
comments on the impact that implementation of the Chemical Weapons
Convention, through the Chemical Weapons Convention Implementation Act
and the Chemical Weapons Convention Regulations, has had on commercial
activities involving ``Schedule 1'' chemicals during calendar year
2009. The purpose of this notice of inquiry is to collect information
to assist BIS in its preparation of the annual certification to the
Congress, which is required under Condition 9 of Senate Resolution 75,
April 24, 1997, in which the Senate gave its advice and consent to the
ratification of the Chemical Weapons Convention.
DATES: Comments must be received by December 10, 2009.
ADDRESSES: You may submit comments by any of the following methods:
E-mail: wfisher@bis.doc.gov. Include the phrase ``Schedule
1 Notice of Inquiry'' in the subject line;
Fax: (202) 482-3355 (Attn: Willard Fisher);
Mail or Hand Delivery/Courier: Willard Fisher, U.S.
Department of Commerce, Bureau of Industry and Security, Regulatory
Policy Division,
[[Page 58004]]
14th Street & Pennsylvania Avenue, NW., Room 2705, Washington, DC
20230.
FOR FURTHER INFORMATION CONTACT: For questions on the Chemical Weapons
Convention requirements for ``Schedule 1'' chemicals, contact James
Truske, Treaty Compliance Division, Office of Nonproliferation and
Treaty Compliance, Bureau of Industry and Security, U.S. Department of
Commerce, Phone: (202) 482-1001. For questions on the submission of
comments, contact Willard Fisher, Regulatory Policy Division, Office of
Exporter Services, Bureau of Industry and Security, U.S. Department of
Commerce, Phone: (202) 482-2440.
SUPPLEMENTARY INFORMATION:
Background
In providing its advice and consent to the ratification of the
Convention on the Prohibition of the Development, Production,
Stockpiling, and Use of Chemical Weapons and Their Destruction,
commonly called the Chemical Weapons Convention (CWC) (the Convention),
the Senate included in Senate Resolution 75 (S. Res. 75, April 24,
1997) several conditions to its ratification. Condition 9, titled
``Protection of Advanced Biotechnology,'' calls for the President to
certify to Congress on an annual basis that ``the legitimate commercial
activities and interests of chemical, biotechnology, and pharmaceutical
firms in the United States are not being significantly harmed by the
limitations of the Convention on access to, and production of, those
chemicals and toxins listed in Schedule 1.'' On July 8, 2004, President
Bush, by Executive Order 13346, delegated his authority to make the
annual certification to the Secretary of Commerce.
The CWC is an international arms control treaty that contains
certain verification provisions. In order to implement these
verification provisions, the CWC established the Organization for the
Prohibition of Chemical Weapons (OPCW). The CWC imposes certain
obligations on countries that have ratified the Convention (i.e.,
States Parties), among which are the enactment of legislation to
prohibit the production, storage, and use of chemical weapons, and the
establishment of a National Authority to serve as the national focal
point for effective liaison with the OPCW and other States Parties for
the purpose of achieving the object and purpose of the Convention and
the implementation of its provisions. The CWC also requires each State
Party to implement a comprehensive data declaration and inspection
regime to provide transparency and to verify that both the public and
private sectors of the State Party are not engaged in activities
prohibited under the CWC.
``Schedule 1'' chemicals consist of those toxic chemicals and
precursors set forth in the CWC ``Annex on Chemicals'' and in
Supplement No. 1 to part 712 of the Chemical Weapons Convention
Regulations (CWCR) (15 CFR parts 710-722). The CWC identified these
toxic chemicals and precursors as posing a high risk to the object and
purpose of the Convention.
The CWC restricts the production of ``Schedule 1'' chemicals for
protective purposes to two facilities per State Party. The CWC Article-
by-Article Analysis submitted to the Senate in Treaty Doc. 103-21
defined the term ``protective purposes'' to mean ``used for determining
the adequacy of defense equipment and measures.'' Consistent with this
definition, U.S. implementation, as authorized via Presidential
Decision Directive (PDD) 70, December 17, 1999, assigned the
responsibility to operate these two facilities to the Department of
Defense (DOD), thereby precluding commercial production of ``Schedule
1'' chemicals for protective purposes in the United States. This action
did not establish any limitations on ``Schedule 1'' chemical activities
that are not prohibited by the CWC. However, the Department of Defense
maintains strict controls on ``Schedule 1'' chemicals produced at its
facilities in order to ensure the accountability and proper use of such
chemicals, consistent with the object and purpose of the Convention.
The provisions of the CWC that affect commercial activities
involving ``Schedule 1'' chemicals are implemented in the CWCR (see 15
CFR part 712) and in the Export Administration Regulations (EAR) (see
15 CFR 742.18 and 15 CFR part 745), both of which are administered by
the Bureau of Industry and Security (BIS). Pursuant to CWC
requirements, the CWCR restrict commercial production of ``Schedule 1''
chemicals to research, medical, or pharmaceutical purposes. The CWCR
also contain other requirements and prohibitions that apply to
``Schedule 1'' chemicals and/or ``Schedule 1'' facilities.
Specifically, the CWCR:
(1) Prohibit the import of ``Schedule 1'' chemicals from States not
Party to the Convention (15 CFR 712.2(b));
(2) Require annual declarations by certain facilities engaged in
the production of ``Schedule 1'' chemicals in excess of 100 grams
aggregate per calendar year (i.e., declared ``Schedule 1'' facilities)
for purposes not prohibited by the Convention (15 CFR 712.5(a)(1) and
(a)(2));
(3) Require government approval of ``declared Schedule 1''
facilities (15 CFR 712.5(f));
(4) Provide that ``declared Schedule 1'' facilities are subject to
initial and routine inspection by the Organization for the Prohibition
of Chemical Weapons (15 CFR 712.5(e) and 716.1(b)(1));
(5) Require 200 days advance notification of establishment of new
``Schedule 1'' production facilities producing greater than 100 grams
aggregate of ``Schedule 1'' chemicals per calendar year (15 CFR 712.4);
(6) Require advance notification and annual reporting of all
imports and exports of ``Schedule 1'' chemicals to, or from, other
States Parties to the Convention (15 CFR 712.6, 742.18(a)(1) and
745.1); and
(7) Prohibit the export of ``Schedule 1'' chemicals to States not
Party to the Convention (15 CFR 742.18(a)(1) and (b)(1)(ii)).
Request for Comments
In order to assist in determining whether the legitimate commercial
activities and interests of chemical, biotechnology, and pharmaceutical
firms in the United States are significantly harmed by the limitations
of the Convention on access to, and production of, ``Schedule 1''
chemicals as described in this notice, BIS is seeking public comments
on any effects that implementation of the Chemical Weapons Convention,
through the Chemical Weapons Convention Implementation Act and the
Chemical Weapons Convention Regulations, has had on commercial
activities involving ``Schedule 1'' chemicals during calendar year
2009. To allow BIS to properly evaluate the significance of any harm to
commercial activities involving ``Schedule 1'' chemicals, public
comments submitted in response to this notice of inquiry should include
both a quantitative and qualitative assessment of the impact of the CWC
on such activities.
Submission of Comments
All comments must be submitted to one of the addresses indicated in
this notice. The Department requires that all comments be submitted in
written form.
The Department encourages interested persons who wish to comment to
do so at the earliest possible time. The period for submission of
comments will close on December 10, 2009. The Department will consider
all comments received before the close of the comment period.
[[Page 58005]]
Comments received after the end of the comment period will be
considered if possible, but their consideration cannot be assured. The
Department will not accept comments accompanied by a request that a
part or all of the material be treated confidentially because of its
business proprietary nature or for any other reason. The Department
will return such comments and materials to the persons submitting the
comments and will not consider them. All comments submitted in response
to this notice will be a matter of public record and will be available
for public inspection and copying.
The Office of Administration, Bureau of Industry and Security, U.S.
Department of Commerce, displays public comments on the BIS Freedom of
Information Act (FOIA) Web site at https://www.bis.doc.gov/foia. This
office does not maintain a separate public inspection facility. If you
have technical difficulties accessing this Web site, please call BIS's
Office of Administration, at (202) 482-1093, for assistance.
Dated: November 4, 2009.
Matthew S. Borman,
Acting Assistant Secretary for Export Administration.
[FR Doc. E9-27053 Filed 11-9-09; 8:45 am]
BILLING CODE 3510-33-P