12 June 2006
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[Federal Register: June 12, 2006 (Volume 71, Number 112)]
[Rules and Regulations]
[Page 33614-33622]
From the Federal Register Online via GPO Access [wais.access.gpo.gov]
[DOCID:fr12jn06-10]
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DEPARTMENT OF COMMERCE
Bureau of Industry and Security
15 CFR Parts 738, 742, 745, and 774
[Docket No. 060228055-6055-01]
RIN 0694-AD62
Implementation of Unilateral Chemical/Biological (CB) Controls on
Certain Biological Agents and Toxins; Clarification of Controls on
Medical Products Containing Certain Toxins on the Australia Group (AG)
Common Control Lists; Additions to the List of States Parties to the
Chemical Weapons Convention (CWC)
AGENCY: Bureau of Industry and Security, Commerce.
ACTION: Final rule.
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SUMMARY: The Bureau of Industry and Security (BIS) is publishing this
final rule to amend the Export Administration Regulations (EAR) to
expand export and reexport controls on certain biological agents and
toxins (referred to, herein, as ``select agents and toxins'') that have
been determined by the Centers for Disease Control and Prevention
(CDC), U.S. Department of Health and Human Services, and the Animal and
Plant Health Inspection Service (APHIS), U.S. Department of
Agriculture, to have the potential to pose a severe threat to human,
animal and plant life, as well as certain sectors of the U.S. economy
(e.g., agriculture). Prior to the publication of this rule, twenty-two
of these agents were not listed on the Commerce Control List (CCL) and
one of these agents was incompletely specified therein. By amending the
EAR to add a new CCL entry that controls CDC and/or APHIS select agents
and toxins (including associated genetic elements, recombinant nucleic
acids, and recombinant organisms) not previously specified on the CCL,
this rule complements the controls that CDC and AHPIS have imposed on
the possession, use, and transfer of these select agents and toxins
within the United States. The addition of these items to the CCL is
expected to have a minimal impact on U.S. industry, since the volume of
exports and reexports is extremely limited.
This rule also amends the EAR to clarify controls on certain
medical products containing AG-controlled toxins, other than ricin or
saxitoxin, by revising the definition of such products to clearly
indicate that they include pharmaceutical formulations, prepackaged for
distribution as clinical or medical products, that have been approved
by the Food and Drug Administration (FDA) for use as an
``Investigational New Drug'' (IND). Specifically, this rule clarifies
that FDA-approved IND products containing AG-controlled toxins (except
ricin or saxitoxin) are considered to be ``medical products'' as
described in the CCL entry that controls vaccines, immunotoxins,
medical products, and diagnostic and food testing kits. BIS is making
this clarification because the previous revision to the definition of
medical products inadvertently failed to specify that such products
include IND items. Furthermore, this clarification is consistent with
the language in the AG exemption for clinical and medical products
containing botulinum toxins and conotoxins, since the AG exemption
applies when such products are designed for ``testing,'' as well as
human administration, in the treatment of medical conditions.
In addition, this rule removes the license requirements for exports
and
[[Page 33615]]
reexports to St. Kitts and Nevis of items that require a license for
export or reexport only to countries of concern for chemical and
biological weapons proliferation (CB) reasons. This change is being
made because St. Kitts and Nevis is not listed in Country Group D:3. As
a result of this change, there is now a one-to-one correspondence
between the countries included in Country Group D:3 and the countries
for which a license requirement is indicated under CB Column 3 of the
Commerce Country Chart.
Finally, this rule updates the list of countries that currently are
States Parties to the Chemical Weapons Convention (CWC) by adding
Antigua and Barbuda, Bhutan, Cambodia, the Democratic Republic of the
Congo, Djibouti, Grenada, Haiti, Honduras, Liberia, and Vanuatu, which
recently became States Parties. As a result of this change, the CW
(Chemical Weapons) license requirements and policies in the EAR that
apply to these countries now conform with those applicable to other CWC
States Parties.
DATES: This rule is effective June 12, 2006. Although there is no
formal comment period, public comments on this regulation are welcome
on a continuing basis.
ADDRESSES: You may submit comments, identified by RIN 0694-AD62, by any
of the following methods:
E-mail: public.comments@bis.doc.gov. Include ``RIN 0694-
AD62'' in the subject line of the message.
Fax: (202) 482-3355. Please alert the Regulatory Policy
Division, by calling (202) 482-2440, if you are faxing comments.
Mail or Hand Delivery/Courier: Willard Fisher, U.S.
Department of Commerce, Bureau of Industry and Security, Regulatory
Policy Division, 14th St. & Pennsylvania Avenue, NW., Room 2705,
Washington, DC 20230, ATTN: RIN 0694-AD62.
Send comments regarding this collection of information, including
suggestions for reducing the burden, to David Rostker, Office of
Management and Budget (OMB), by e-mail to David_Rostker@omb.eop.gov,
or by fax to (202) 395-7285; and to the Regulatory Policy Division,
Bureau of Industry and Security, Department of Commerce, P.O. Box 273,
Washington, DC 20044. Comments on this collection of information should
be submitted separately from comments on the final rule (i.e., RIN
0694-AD62)--all comments on the latter should be submitted by one of
the three methods outlined above.
FOR FURTHER INFORMATION CONTACT: Douglas Brown, Director, Chemical and
Biological Controls Division, Office of Nonproliferation and Treaty
Compliance, Bureau of Industry and Security, Telephone: (202) 482-5808.
SUPPLEMENTARY INFORMATION:
Background
A. Amendments to the EAR Establishing Export and Reexport Controls on
Certain Select Agents and Toxins
The Bureau of Industry and Security (BIS) is amending the Export
Administration Regulations (EAR) to expand export and reexport controls
on certain select agents and toxins (including associated genetic
elements, recombinant nucleic acids, and recombinant organisms) that
have been determined by the Centers for Disease Control and Prevention
(CDC) and the Animal and Plant Health Inspection Service (APHIS) to
have the potential to pose a severe threat to human, animal and plant
life and to certain sectors of the U.S. economy. APHIS and CDC regulate
the domestic possession, use, and transfer of these select agents and
toxins in accordance with the following regulations: 7 CFR part 331,
which contains the APHIS regulations regarding the Possession, Use, and
Transfer of PPQ (Plant Protection and Quarantine Programs) Select
Agents and Toxins; 9 CFR part 121, which contains the APHIS regulations
regarding the Possession, Use, and Transfer of VS (Veterinary Services
Programs) and Overlap Select Agents and Toxins; and 42 CFR part 73,
which contains the CDC regulations regarding HHS (Department of Health
and Human Services) and Overlap Select Agents and Toxins.
This rule amends the Commerce Control List (CCL) (Supplement No. 1
to Part 774 of the EAR) to include those CDC and/or APHIS select agents
and toxins (including associated genetic elements, recombinant nucleic
acids, and recombinant organisms) not previously specified on the CCL.
Prior to the publication of this rule, twenty-two of these agents and
toxins were not listed on the CCL and one was only partially specified
on the CCL. However, most of these agents and toxins were listed on the
CCL prior to the publication of this rule. Currently, they are
controlled under Export Control Classification Numbers (ECCNs) 1C351,
1C352, 1C353, and 1C354. Together, these four ECCNs control sixty items
identified as CDC and/or APHIS select agents and toxins, all of which
are included on the Australia Group (AG) Common Control Lists.
The export and reexport controls established by this rule will
complement the controls that CDC and APHIS have imposed on the
possession, use, and transfer of these select agents and toxins and
associated genetic elements, recombinant nucleic acids, and recombinant
organisms within the United States. BIS is taking this action with the
understanding that CDC and APHIS have not imposed controls on the
export and reexport of these items in recognition of the Department of
Commerce's role in regulating the export and reexport of biological
agents and toxins. Their regulations do, however, apply to imports of
select agents and toxins. Collectively, the controls administered by
BIS, CDC, and APHIS will significantly reduce the potential
availability of these items for use in unauthorized activities that
could pose a serious threat to human, animal or plant health and
disrupt certain sectors of the U.S. economy (e.g., agriculture).
Although none of the 23 agents and toxins (and associated genetic
elements, recombinant nucleic acids, and recombinant organisms) are
currently identified on any of the AG Common Control Lists, the United
States intends to work in cooperation with the governments of other AG
participating countries to consider the addition of these items to the
appropriate AG control lists.
Specifically, this rule adds new ECCN 1C360 to the CCL and revises
ECCN 1C353 to control the select agents and toxins and associated
genetic elements, recombinant nucleic acids, and recombinant organisms
identified in 7 CFR part 331, 9 CFR part 121, and/or 42 CFR part 73
that are not specified elsewhere on the CCL. The current CDC/APHIS
select agents and toxins that are controlled under new ECCN 1C360 are
listed, below, under the categories human and zoonotic pathogens/
toxins, animal pathogens, and plant pathogens. One of these items is
specified elsewhere on the CCL, as indicated below.
A. Human and zoonotic pathogens and toxins:
1. Viruses:
a. Central European tick-borne encephalitis viruses:
i. Absettarov;
ii. Hanzalova;
iii. Hypr;
iv. Kumlinge;
b. Cercopithecine herpesvirus 1 (Herpes B virus);
c. Reconstructed replication competent forms of the 1918 pandemic
influenza virus containing any portion of the coding regions of all
eight gene segments;
[[Page 33616]]
2. Fungi:
a. Coccidioides immitis;
b. Coccidioides posadasii;
3. Toxins: Shiga-like ribosome inactivating proteins not controlled
under ECCN 1C351.d.10;
B Animal pathogens:
1. Viruses:
a. Akabane virus;
b. Bovine spongiform encephalopathy agent;
c. Camel pox virus;
d. Malignant catarrhal fever virus;
e. Menangle virus;
2. Mycoplasma:
a. Mycoplasma capricolum;
b. Mycoplasma F38;
3. Rickettsia: Erhlichia ruminantium (a.k.a. Cowdria ruminantium);
C. Plant pathogens:
1. Bacteria:
a. Candidatus Liberobacter africanus (a.k.a. Liberobacter
africanus);
b. Candidatus Liberobacter asiaticus (a.k.a. Liberobacter
asiaticus);
c. Xylella fastidiosa pv. citrus variegated chlorosis (CVC);
2. Fungi:
a. Peronosclerospora philippinensis;
b. Sclerophthora rayssiae var. zeae;
c. Synchytrium endobioticum.
New ECCN 1C360 controls these CDC/APHIS select agents and toxins
for chemical and biological weapons proliferation (CB) reasons (to
destinations indicated under CB Column 1) and anti-terrorism (AT)
reasons (to destinations indicated under AT Column 1). Items controlled
for CB Column 1 reasons require a license for export or reexport to all
destinations, worldwide, as set forth in Section 742.2(a)(1) of the EAR
and as indicated on the Commerce Country Chart (see Supplement No. 1 to
Part 738 of the EAR). Items controlled for AT Column 1 reasons require
a license to Libya, North Korea, Sudan, and Syria, as indicated on the
Commerce Country Chart. See Part 742 of the EAR for additional
information on these AT license requirements. Exports and reexports of
these ``select agents'' may also require a license for reasons
specified elsewhere in the EAR (e.g., the end-user/end-use license
requirements described in Part 744 of the EAR and the embargoes and
other special controls described in Part 746 of the EAR).
This final rule also amends ECCNs 1E001 and 1E351 to control
certain technology related to the select agents and toxins listed in
new ECCN 1C360. The License Requirements section of ECCN 1E001 is
revised to indicate that a license is required, for CB reasons, to
export technology for the ``development'' or ``production'' of these
items to all destinations, worldwide, as set forth in Section
742.2(a)(1) of the EAR and as indicated under CB Column 1 on the
Commerce Country Chart. Such technology also is controlled under ECCN
1E001 for AT reasons and requires a license to Libya, North Korea,
Sudan, and Syria, as indicated under AT Column 1 on the Commerce
Country Chart. The heading of ECCN 1E351 is revised to indicate that
this ECCN controls technology for the disposal of microbiological
materials listed in new ECCN 1C360. Such technology requires a license
under ECCN 1E351 for export or reexport to all destinations, worldwide,
as set forth in Section 742.2(a)(1) of the EAR and as indicated under
CB Column 1 on the Commerce Country Chart, and to Libya, North Korea,
Sudan, and Syria, as indicated under AT Column 1 on the Commerce
Country Chart. See Part 742 of the EAR for additional information on
the AT license requirements for these ECCNs. Exports and reexports of
this technology may also require a license for reasons specified
elsewhere in the EAR (e.g., the end-user/end-use license requirements
described in Part 744 of the EAR and the embargoes and other special
controls described in Part 746 of the EAR).
This rule also makes conforming changes to ECCNs 1C351 and 1C353 to
reflect the addition of new ECCN 1C360 to the CCL. This rule amends
ECCN 1C351 to clarify the scope of controls on verotoxins in 1C351.d.10
by adding a new Technical Note, at the end of the List of Items
Controlled, to indicate that verotoxins are Shiga-like ribosome
inactivating proteins, which are among the select agents and toxins
subject to the domestic controls administered by CDC and APHIS (see new
ECCN 1C360.a.3.a). In addition, this rule amends ECCN 1C353 by revising
the List of Items Controlled to indicate that this ECCN controls
genetic elements and genetically modified organisms containing nucleic
acid sequences associated with the pathogenicity of microorganisms
controlled by new ECCN 1C360 (i.e., genetic elements, recombinant
nucleic acids, and recombinant organisms associated with the CDC and/or
APHIS select agents and toxins controlled by new ECCN 1C360), as well
as microorganisms controlled by ECCN 1C351.a to .c, 1C352, or 1C354.
This rule also revises the List of Items Controlled in ECCN 1C353 to
indicate that this ECCN controls genetically modified organisms that
contain nucleic acid sequences coding for any of the ``toxins''
controlled by new ECCN 1C360, or ``sub-units of toxins'' thereof. Items
controlled under ECCN 1C351 or ECCN 1C353 are subject to the same CCL-
based license requirements (i.e., CB Column 1 and AT Column 1), as
described above, for items controlled under new ECCN 1C360.
This rule also amends ECCNs 1C351, 1C352, 1C353, and 1C354 by
revising the ``Related Controls'' paragraph in the List of Items
Controlled for each entry to indicate that APHIS and/or CDC maintain
controls on the transfer and possession within the United States of
certain items controlled by the ECCN. These changes reflect the fact
that most of the select agents and toxins subject to the domestic
controls of APHIS and/or CDC are already included on the control lists
maintained by the AG.
This rule amends the List of Items Controlled in ECCN 1C991 by
expanding the scope of this ECCN to control vaccines against items in
new ECCN 1C360, immunotoxins containing items in 1C360.a.3 (currently,
these include Shiga-like ribosome inactivating proteins not controlled
under ECCN 1C351.d.10), medical products containing items in 1C360.a.3,
and diagnostic and food testing kits containing items in 1C360.a.3.
Controlling these specific vaccines, immunotoxins, medical products,
and diagnostic and food testing kits under ECCN 1C991, instead of new
ECCN 1C360, means that they generally may be exported or reexported,
without a license, to all destinations, except embargoed destinations
and countries indicated under AT Column 1 on the Commerce Country Chart
(Supplement No. 1 to Part 738 of the EAR)--see Parts 742 and 746 of the
EAR for additional information on these license requirements. A license
also may be required to export or reexport these items for reasons
specified elsewhere in the EAR (e.g., Part 744 of the EAR).
In addition, this rule makes conforming changes to Section 742.2 of
the EAR to reflect the addition of new ECCN 1C360 to the CCL. A
reference to new ECCN 1C360 is added to paragraph (a)(1)(i), which
identifies the ECCNs containing human and zoonotic pathogens/toxins,
animal pathogens, plant pathogens, genetic elements, and genetically
modified microorganisms that require a license for CB reasons to
destinations indicated under CB Column 1 on the Commerce Country Chart
(i.e., all destinations, worldwide).
The changes described above are expected to have a minimal impact
on U.S. industry, since the volume of exports and reexports of the
select agents and toxins (controlled under new ECCN 1C360), associated
genetic elements, recombinant nucleic acids, and recombinant organisms
(controlled under ECCN 1C353) and the related
[[Page 33617]]
technology for these items (controlled under ECCN 1E001 or 1E351) is
extremely limited.
B. Amendments to the EAR Clarifying Controls on Medical Products
Containing Certain AG-Controlled Toxins
This rule amends ECCN 1C991 on the CCL to clarify the controls on
medical products containing AG-controlled toxins other than ricin and
saxitoxin. Specifically, this rule clarifies that the ``medical
products'' controlled by ECCN 1C991 include pharmaceutical
formulations, prepackaged for distribution as clinical or medical
products, that have been approved by the U.S. Food and Drug
Administration (FDA) for use as an ``Investigational New Drug'' (IND).
Consistent with this definition, FDA-approved IND products containing
any of the toxins in ECCN 1C351.d, except those controlled for Chemical
Weapons Convention (CW) reasons under 1C351.d.5 or .d.6 (i.e., ricin
and saxitoxin), are treated as ``medical products'' controlled under
ECCN 1C991.c. or .d. This clarification is intended to eliminate any
uncertainty concerning the control status of these IND products since
the publication of the final rule that revised the definition of
``medical products'' in ECCN 1C991 on October 3, 2000 (65 FR 58911).
Furthermore, this clarification is consistent with language in the AG
exemption for clinical and medical products containing botulinum toxins
and conotoxins, since the AG exemption applies when such products are
designed for ``testing,'' as well as human administration, in the
treatment of medical conditions. Such medical products, when exported
for the legitimate medical treatment for which they are intended, pose
no significant proliferation concerns.
This rule further clarifies the types of medical products
controlled under ECCN 1C991 by revising the ``Related Definitions''
paragraph in the List of Items Controlled for that ECCN to indicate
that ECCN 1C991 controls FDA-approved ``clinical'' or medical products,
having the characteristics in 1C991.c or .d, that are: (1) designed for
``testing,'' as well as human administration, in the treatment of
medical conditions, and (2) prepackaged for distribution as either
``clinical'' products or medical products. This clarification is
intended to make the description of medical products, in the Related
Definitions paragraph of ECCN 1C991, more consistent with the language
of the AG exemption for clinical and medical products containing
botulinum toxins and conotoxins.
Medical products specified in 1C991.c generally may be exported or
reexported without a license to all destinations, except embargoed
destinations and countries indicated under AT Column 1 on the Commerce
Country Chart (Supplement No. 1 to Part 738 of the EAR). Medical
products specified in 1C991.d require a license for export or reexport
to countries of concern for CB reasons (i.e., Country Group D:3), as
set forth in Section 742.2(a)(3) of the EAR and as indicated under CB
Column 3 on the Commerce Country Chart, and to countries indicated
under AT Column 1 on the Commerce Country Chart. See Part 742 of the
EAR for additional information on these AT license requirements. A
license also may be required to export or reexport these items for
reasons specified elsewhere in the EAR (e.g., the end-user/end-use
license requirements described in Part 744 of the EAR and the embargoes
and other special controls described in Part 746 of the EAR). Medical
products intended for export or reexport in any configuration other
than ``prepackaged units applicable to the intended medical treatment''
(e.g., bulk shipments), or intended for any end-uses other than medical
treatment, are controlled under ECCN 1C351 or ECCN 1C360.
In addition to the export requirements described in the EAR, the
export of an IND, as defined in FDA regulations set forth in 21 CFR
312.3, is subject to certain FDA requirements pursuant to 21 CFR
312.110. These FDA requirements are independent of the export
requirements described in the EAR, and exporters must satisfy them in
addition to any requirements specified in the EAR.
Finally, note that, in accordance with the policy set forth in the
General Technology Note in Supplement No. 2 to Part 774 of the EAR
(i.e., ```technology' `required' for the `development,' `production,'
or `use' of a controlled product remains controlled even when
applicable to a product controlled at a lower level''), technology for
the ``development'' or ``production'' of items controlled under ECCN
1C351, 1C352, 1C353, 1C354, or 1C360, which is controlled under ECCN
1E001 and requires a license to all destinations, worldwide, continues
to require a license to all destinations even if such technology is
applicable to a product controlled at a lower level, such as a vaccine
or immunotoxin controlled under ECCN 1C991 that requires a license only
to embargoed destinations and countries of concern for chemical and
biological weapons proliferation reasons (Country Group D:3 in
Supplement No. 1 to Part 740 of the EAR).
C. Reduction in the Scope of the Chemical and Biological Weapons
Proliferation (CB) License Requirements Applicable to St. Kitts and
Nevis
This rule removes the license requirements for exports and
reexports to St. Kitts and Nevis of items that require a license for
export or reexport only to countries of concern for CB reasons (i.e.,
ECCN 1C991.d items to countries listed in Country Group D:3 in
Supplement No. 1 to Part 740 of the EAR). Specifically, this rule
amends the Commerce Country Chart (Supplement No. 1 to Part 738 of the
EAR) by removing the ``X'' that indicated a license requirement for St.
Kitts and Nevis under CB Column 3. This change is being made because
St. Kitts and Nevis is not listed in Country Group D:3. As a result of
this change, there is now a one-to-one correspondence between the
countries included in Country Group D:3 and the countries for which a
license requirement is indicated under CB Column 3 of the Commerce
Country Chart. This change also eliminates the discrepancy that
existed, prior to the publication of this rule, with respect to the
country scope of the CB license requirements described in Section
742.2(a)(3) of the EAR.
D. Revisions to the EAR Based on the Addition of New States Parties to
the Chemical Weapons Convention (CWC)
This rule revises Supplement No. 2 to Part 745 of the EAR (titled
``States Parties to the Convention on the Prohibition of the
Development, Production, Stockpiling, and Use of Chemical Weapons and
on Their Destruction'') by adding Antigua and Barbuda, Bhutan,
Cambodia, the Democratic Republic of the Congo, Djibouti, Grenada,
Haiti, Honduras, Liberia, and Vanuatu, which recently became States
Parties to the CWC. As a result of this change, the license
requirements and policies that apply to exports and reexports of items
controlled for CW reasons to each of these seven countries now conform
with those applicable to other CWC States Parties, as described in
Section 742.18 of the EAR.
Although the Export Administration Act expired on August 20, 2001,
the President, through Executive Order 13222 of August 17, 2001, 3 CFR,
2001 Comp., p. 783 (2002), as extended by the Notice of August 2, 2005,
70 FR 45273 (August 5, 2005), has continued the Export Administration
Regulations in
[[Page 33618]]
effect under the International Emergency Economic Powers Act.
Expansion of Foreign Policy-Based Export Controls
This rule imposes new export controls for foreign policy reasons.
As required by section 6 of the Export Administration Act of 1979, as
amended (the Act), a report on the imposition of these controls was
delivered to the Congress on June 1, 2006. Although the Act expired on
August 20, 2001, Executive Order 13222 of August 17, 2001, 3 CFR, 2001
Comp., p. 783 (2002), as extended by the Notice of August 2, 2005, 70
FR 45273 (August 5, 2005), has continued the Export Administration
Regulations in effect under the International Emergency Economic Powers
Act.
Saving Clause
Shipments of items removed from eligibility for export or reexport
under a license exception or without a license (i.e., under the
designator ``NLR'') as a result of this regulatory action that were on
dock for loading, on lighter, laden aboard an exporting carrier, or en
route aboard a carrier to a port of export, on July 12, 2006, pursuant
to actual orders for export or reexport to a foreign destination, may
proceed to that destination under the previously applicable license
exception or without a license (NLR) so long as they are exported or
reexported before July 27, 2006. Any such items not actually exported
or reexported before midnight, on July 27, 2006, require a license in
accordance with this regulation.
``Deemed'' exports of ``technology'' and ``source code'' removed
from eligibility for export under a license exception or without a
license (under the designator ``NLR'') as a result of this regulatory
action may continue to be made under the previously available license
exception or without a license (NLR) before July 27, 2006. Beginning at
midnight on July 27, 2006, such ``technology'' and ``source code'' may
no longer be released, without a license, to a foreign national subject
to the ``deemed'' export controls in the EAR when a license would be
required to the home country of the foreign national in accordance with
this regulation.
Rulemaking Requirements
1. This rule has been determined to be not significant for purposes
of Executive Order 12866.
2. Notwithstanding any other provision of law, no person is
required to respond to, nor shall any person be subject to a penalty
for failure to comply with, a collection of information subject to the
requirements of the Paperwork Reduction Act of 1995 (44 U.S.C. 3501 et
seq.) (PRA), unless that collection of information displays a currently
valid Office of Management and Budget (OMB) Control Number. This rule
contains a collection of information subject to the requirements of the
PRA. This collection has been approved by OMB under Control Number
0694-0088 (Multi-Purpose Application), which carries a burden hour
estimate of 58 minutes to prepare and submit form BIS-748. Send
comments regarding this burden estimate or any other aspect of this
collection of information, including suggestions for reducing the
burden, to David Rostker, Office of Management and Budget (OMB), and to
the Regulatory Policy Division, Bureau of Industry and Security,
Department of Commerce, as indicated in the ADDRESSES section of this
rule.
3. This rule does not contain policies with federalism implications
as that term is defined in Executive Order 13132.
4. The provisions of the Administrative Procedure Act (5 U.S.C.
553) requiring notice of proposed rulemaking, the opportunity for
public participation, and a delay in effective date, are inapplicable
because this regulation involves a military and foreign affairs
function of the United States (Sec. 5 U.S.C. 553(a)(1)). Further, no
other law requires that a notice of proposed rulemaking and an
opportunity for public comment be given for this final rule. Because a
notice of proposed rulemaking and an opportunity for public comment are
not required to be given for this rule under 5 U.S.C. 553 or by any
other law, the analytical requirements of the Regulatory Flexibility
Act (5 U.S.C. 601 et seq.) are not applicable.
Therefore, this regulation is issued in final form. Although there
is no formal comment period, public comments on this regulation are
welcome on a continuing basis.
List of Subjects
15 CFR Part 738
Administrative practice and procedure, Exports, Foreign trade.
15 CFR Part 742
Exports, Foreign trade.
15 CFR Part 745
Administrative practice and procedure, Chemicals, Exports, Foreign
trade, Reporting and recordkeeping requirements.
15 CFR Part 774
Exports, Foreign trade, Reporting and recordkeeping requirements.
0
Accordingly, Parts 738, 742, 745, and 774 of the Export Administration
Regulations (15 CFR parts 730-799) are amended as follows:
PART 738--[AMENDED]
0
1. The authority citation for 15 CFR part 738 continues to read as
follows:
Authority: 50 U.S.C. app. 2401 et seq.; 50 U.S.C. 1701 et seq.;
10 U.S.C. 7420; 10 U.S.C. 7430(e); 18 U.S.C. 2510 et seq.; 22 U.S.C.
287c; 22 U.S.C. 3201 et seq.; 22 U.S.C. 6004; 30 U.S.C. 185(s),
185(u); 42 U.S.C. 2139a; 42 U.S.C. 6212; 43 U.S.C. 1354; 46 U.S.C.
app. 466c; 50 U.S.C. app. 5; sec. 901-911, Pub. L. 106-387; sec.
221, Pub. L. 107-56; E.O. 13026, 61 FR 58767, 3 CFR, 1996 Comp., p.
228; E.O. 13222, 66 FR 44025, 3 CFR, 2001 Comp., p. 783; Notice of
August 2, 2005, 70 FR 45273 (August 5, 2005).
0
2. Supplement No. 1 to part 738 is amended by revising the entry for
``St. Kitts and Nevis'' to read as follows:
Supplement No. 1 to Part 738--Commerce Country Chart
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weapons nonproliferation security -------------- stability convention --------------------------------------------
Countries --------------------------------------------------------------- --------------------------------
CB 1 CB 2 CB 3 NP 1 NP 2 NS 1 NS 2 MT 1 RS 1 RS 2 FC 1 CC 1 CC 2 CC 3 AT 1 AT 2
------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------
* * * * * * *
St. Kitts and Nevis................... X X ....... X ....... X X X X X X X ....... X ....... .......
* * * * * * *
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[[Page 33619]]
PART 742--[AMENDED]
0
3. The authority citation for 15 CFR part 742 is revised to read as
follows:
Authority: 50 U.S.C. app. 2401 et seq.; 50 U.S.C. 1701 et seq.;
18 U.S.C. 2510 et seq.; 22 U.S.C. 3201 et seq.; 42 U.S.C. 2139a;
sec. 901-911, Pub. L. 106-387; sec. 221, Pub. L. 107-56; sec. 1503,
Pub. L. 108-11, 117 Stat. 559; E.O. 12058, 43 FR 20947, 3 CFR, 1978
Comp., p. 179; E.O. 12851, 58 FR 33181, 3 CFR, 1993 Comp., p. 608;
E.O. 12938, 59 FR 59099, 3 CFR, 1994 Comp., p. 950; E.O. 13026, 61
FR 58767, 3 CFR, 1996 Comp., p. 228; E.O. 13222, 66 FR 44025, 3 CFR,
2001 Comp., p. 783; Presidential Determination 2003-23 of May 7,
2003, 68 FR 26459, May 16, 2003; Notice of August 2, 2005, 70 FR
45273 (August 5, 2005); Notice of October 25, 2005, 70 FR 62027
(October 27, 2005).
Sec. 742.2 [Amended]
0
4. Section 742.2 is amended by revising the phrase ``ECCNs 1C351,
1C352, 1C353 and 1C354'' in paragraph (a)(1)(i) to read ``ECCNs 1C351,
1C352, 1C353, 1C354 and 1C360''.
PART 745--[AMENDED]
0
5. The authority citation for 15 CFR part 745 is revised to read as
follows:
Authority: 50 U.S.C. 1701 et seq.; E.O. 12938, 59 FR 59099, 3
CFR, 1994 Comp., p. 950; Notice of October 25, 2005, 70 FR 62027
(October 27, 2005).
Supplement No. 2 to Part 745--[Amended]
0
6. Supplement No. 2 to Part 745 is amended by revising the undesignated
center heading ``List of States Parties as of August 1, 2005'' to read
``List of States Parties as of March 25, 2006'' and by adding, in
alphabetical order, the countries ``Antigua and Barbuda'', ``Bhutan'',
``Cambodia'', ``Congo (Democratic Republic of the)'', ``Djibouti'',
``Grenada'', ``Haiti'', ``Honduras'', ``Liberia'', and ``Vanuatu''.
PART 774--[AMENDED]
0
7. The authority citation for 15 CFR Part 774 continues to read as
follows:
Authority: 50 U.S.C. app. 2401 et seq.; 50 U.S.C. 1701 et seq.;
10 U.S.C. 7420; 10 U.S.C. 7430(e); 18 U.S.C. 2510 et seq.; 22 U.S.C.
287c; 22 U.S.C. 3201 et seq.; 22 U.S.C. 6004; 30 U.S.C. 185(s),
185(u); 42 U.S.C. 2139a; 42 U.S.C. 6212; 43 U.S.C. 1354; 46 U.S.C.
app. 466c; 50 U.S.C. app. 5; sec. 901-911, Pub. L. 106-387; sec.
221, Pub. L. 107-56; E.O. 13026, 61 FR 58767, 3 CFR, 1996 Comp., p.
228; E.O. 13222, 66 FR 44025, 3 CFR, 2001 Comp., p. 783; Notice of
August 2, 2005, 70 FR 45273 (August 5, 2005).
Supplement No. 1 to Part 774--[Amended]
0
8. In Supplement No. 1 to Part 774 (the Commerce Control List),
Category 1--Materials, Chemicals, ``Microorganisms''& ``Toxins,'' ECCN
1C351 is amended by revising the List of Items Controlled to read as
follows:
1C351 Human and zoonotic pathogens and ``toxins'', as follows (see
List of Items Controlled).
* * * * *
List of Items Controlled
Unit: $ value.
Related Controls: (1) Certain forms of ricin and saxitoxin in
1C351.d.5 and d.6 are CWC Schedule 1 chemicals (see Sec. 742.18 of
the EAR). The U.S. Government must provide advance notification and
annual reports to the OPCW of all exports of Schedule 1 chemicals.
See Sec. 745.1 of the EAR for notification procedures. See 22 CFR
part 121, Category XIV and Sec. 121.7 for additional CWC Schedule 1
chemicals controlled by the Department of State. (2) All vaccines
and ``immunotoxins'' are excluded from the scope of this entry.
Certain medical products and diagnostic and food testing kits that
contain biological toxins controlled under paragraph (d) of this
entry, with the exception of toxins controlled for CW reasons under
d.5 and d.6, are excluded from the scope of this entry. Vaccines,
``immunotoxins'', certain medical products, and diagnostic and food
testing kits excluded from the scope of this entry are controlled
under ECCN 1C991. (3) For the purposes of this entry, only saxitoxin
is controlled under paragraph d.6; other members of the paralytic
shellfish poison family (e.g. neosaxitoxin) are classified as EAR99.
(4) Clostridium perfringens strains, other than the epsilon toxin-
producing strains of Clostridium perfringens described in c.14, are
excluded from the scope of this entry, since they may be used as
positive control cultures for food testing and quality control. (5)
The Animal and Plant Health Inspection Service (APHIS), U.S.
Department of Agriculture, and the Centers for Disease Control and
Prevention (CDC), U.S. Department of Health and Human Services,
maintain controls on the possession, use, and transfer within the
United States of certain items controlled by this ECCN (for APHIS,
see 7 CFR 331.3(c), 9 CFR 121.3(c), and 9 CFR 121.4(c); for CDC, see
42 CFR 73.3(c) and 42 CFR 73.4(c)).
Related Definitions: (1) For the purposes of this entry
``immunotoxin'' is defined as an antibody-toxin conjugate intended
to destroy specific target cells (e.g., tumor cells) that bear
antigens homologous to the antibody. (2) For the purposes of this
entry ``subunit'' is defined as a portion of the ``toxin''.
Items:
a. Viruses, as follows:
a.1. Chikungunya virus;
a.2. Congo-Crimean haemorrhagic fever virus (a.k.a. Crimean-
Congo haemorrhagic fever virus);
a.3. Dengue fever virus;
a.4. Eastern equine encephalitis virus;
a.5. Ebola virus;
a.6. Hantaan virus;
a.7. Japanese encephalitis virus;
a.8. Junin virus;
a.9. Lassa fever virus;
a.10. Lymphocytic choriomeningitis virus;
a.11. Machupo virus;
a.12. Marburg virus;
a.13. Monkey pox virus;
a.14. Rift Valley fever virus;
a.15. Tick-borne encephalitis virus (Russian Spring-Summer
encephalitis virus);
a.16. Variola virus;
a.17. Venezuelan equine encephalitis virus;
a.18. Western equine encephalitis virus;
a.19. White pox;
a.20. Yellow fever virus;
a.21. Kyasanur Forest virus;
a.22. Louping ill virus;
a.23. Murray Valley encephalitis virus;
a.24. Omsk haemorrhagic fever virus;
a.25. Oropouche virus;
a.26. Powassan virus;
a.27. Rocio virus;
a.28. St. Louis encephalitis virus;
a.29. Hendra virus (Equine morbillivirus);
a.30. South American haemorrhagic fever (Sabia, Flexal,
Guanarito);
a.31. Pulmonary and renal syndrome-haemorrhagic fever viruses
(Seoul, Dobrava, Puumala, Sin Nombre); or
a.32. Nipah virus.
b. Rickettsiae, as follows:
b.1. Bartonella quintana (Rochalimea quintana, Rickettsia
quintana);
b.2. Coxiella burnetii;
b.3. Rickettsia prowasecki (a.k.a. Rickettsia prowazekii); or
b.4. Rickettsia rickettsii.
c. Bacteria, as follows:
c.1. Bacillus anthracis;
c.2. Brucella abortus;
c.3. Brucella melitensis;
c.4. Brucella suis;
c.5. Burkholderia mallei (Pseudomonas mallei);
c.6. Burkholderia pseudomallei (Pseudomonas pseudomallei);
c.7. Chlamydia psittaci;
c.8. Clostridium botulinum;
c.9. Francisella tularensis;
c.10. Salmonella typhi;
c.11. Shigella dysenteriae;
c.12. Vibrio cholerae;
c.13. Yersinia pestis;
c.14. Clostridium perfringens, epsilon toxin producing types; or
c.15. Enterohaemorrhagic Escherichia coli, serotype O157 and
other verotoxin producing serotypes.
d. ``Toxins'', as follows, and ``subunits'' thereof:
d.1. Botulinum toxins;
d.2. Clostridium perfringens toxins;
d.3. Conotoxin;
d.4. Microcystin (Cyanginosin);
d.5. Ricin;
d.6. Saxitoxin;
d.7. Shiga toxin;
d.8. Staphylococcus aureus toxins;
d.9. Tetrodotoxin;
d.10. Verotoxin;
d.11. Aflatoxins;
d.12. Abrin;
d.13. Cholera toxin;
d.14. Diacetoxyscirpenol toxin;
d.15. T-2 toxin;
d.16. HT-2 toxin;
d.17. Modeccin toxin;
d.18. Volkensin toxin; or
d.19. Viscum Album Lectin 1 (Viscumin).
[[Page 33620]]
Technical Note: Verotoxins (1C351.d.10) are Shiga-like ribosome
inactivating proteins (also see ECCN 1C360.a.3.a).
0
9. In Supplement No. 1 to Part 774 (the Commerce Control List),
Category 1--Materials, Chemicals, ``Microorganisms'' & ``Toxins,'' ECCN
1C352 is amended by revising the Related Controls paragraph in the List
of Items Controlled to read as follows:
1C352 Animal pathogens, as follows (see List of Items Controlled).
* * * * *
List of Items Controlled
Unit: * * *
Related Controls: (1) All vaccines are excluded from the scope
of this entry. See also 1C991. (2) The Animal and Plant Health
Inspection Service (APHIS), U.S. Department of Agriculture, and the
Centers for Disease Control and Prevention (CDC), U.S. Department of
Health and Human Services, maintain controls on the possession, use,
and transfer within the United States of certain items controlled by
this ECCN (for APHIS, see 7 CFR 331.3(c), 9 CFR 121.3(c), and 9 CFR
121.4(c); for CDC, see 42 CFR 73.3(c) and 42 CFR 73.4(c)).
Related Definition: * * *
Items: * * *
* * * * *
0
10. In Supplement No. 1 to Part 774 (the Commerce Control List),
Category 1--Materials, Chemicals, ``Microorganisms'' & ``Toxins,'' ECCN
1C353 is amended by revising the List of Items Controlled to read as
follows:
1C353 Genetic elements and genetically-modified organisms, as
follows (see List of Items Controlled).
* * * * *
List of Items Controlled
Unit: $ value
Related Controls: Vaccines that contain genetic elements or
genetically modified organisms identified in this entry are
controlled by ECCN 1C991. The Animal and Plant Health Inspection
Service (APHIS), U.S. Department of Agriculture, and the Centers for
Disease Control and Prevention (CDC), U.S. Department of Health and
Human Services, maintain controls on the possession, use, and
transfer within the United States of certain items controlled by
this ECCN, including (but not limited to) genetic elements,
recombinant nucleic acids, and recombinant organisms associated with
the agents or toxins in ECCN 1C360 (for APHIS, see 7 CFR 331.3(c), 9
CFR 121.3(c), and 9 CFR 121.4(c); for CDC, see 42 CFR 73.3(c) and 42
CFR 73.4(c)).
Related Definition: N/A
Items:
a. Genetic elements, as follows:
a.1. Genetic elements that contain nucleic acid sequences
associated with the pathogenicity of microorganisms controlled by
1C351.a to .c, 1C352, 1C354, or 1C360;
a.2. Genetic elements that contain nucleic acid sequences coding
for any of the ``toxins'' controlled by 1C351.d or 1C360.a.3, or
``sub-units of toxins'' thereof.
b. Genetically modified organisms, as follows:
b.1. Genetically modified organisms that contain nucleic acid
sequences associated with the pathogenicity of microorganisms
controlled by 1C351.a to .c, 1C352, 1C354, or 1C360;
b.2. Genetically modified organisms that contain nucleic acid
sequences coding for any of the ``toxins'' controlled by 1C351.d or
1C360.a.3, or ``sub-units of toxins'' thereof.
Technical Note: 1. ``Genetic elements'' include, inter alia,
chromosomes, genomes, plasmids, transposons, and vectors, whether
genetically modified or unmodified.
2. This ECCN does not control nucleic acid sequences associated
with the pathogenicity of enterohaemorrhagic Escherichia coli,
serotype O157 and other verotoxin producing strains, except those
nucleic acid sequences that contain coding for the verotoxin or its
sub-units.
3. ``Nucleic acid sequences associated with the pathogenicity of
any of the microorganisms controlled by 1C351.a to .c, 1C352, 1C354,
or 1C360'' means any sequence specific to the relevant controlled
microorganism that:
a. In itself or through its transcribed or translated products
represents a significant hazard to human, animal or plant health; or
b. Is known to enhance the ability of a microorganism controlled
by 1C351.a to .c, 1C352, 1C354, or 1C360, or any other organism into
which it may be inserted or otherwise integrated, to cause serious
harm to human, animal or plant health.
0
11. In Supplement No. 1 to Part 774 (the Commerce Control List),
Category 1--Materials, Chemicals, ``Microorganisms'' & ``Toxins,'' ECCN
1C354 is amended by revising the Related Controls paragraph in the List
of Items Controlled to read as follows:
1C354 Plant pathogens, as follows (see List of Items Controlled).
* * * * *
List of Items Controlled
Unit: * * *
Related Controls: (1) All vaccines are excluded from the scope
of this entry. See ECCN 1C991. (2) The Animal and Plant Health
Inspection Service (APHIS), U.S. Department of Agriculture,
maintains controls on the possession, use, and transfer within the
United States of certain items controlled by this ECCN (see 7 CFR
331.3(c), 9 CFR 121.3(c), and 9 CFR 121.4(c)).
Related Definitions: * * *
Items: * * *
* * * * *
0
12. In Supplement No. 1 to Part 774 (the Commerce Control List),
Category 1--Materials, Chemicals, ``Microorganisms'' & ``Toxins,'' a
new ECCN 1C360 is added, immediately following ECCN 1C355, to read as
follows:
1C360 Select agents and toxins not controlled under ECCN 1C351,
1C352, or 1C354.
License Requirements
Reason for Control: CB, AT
------------------------------------------------------------------------
Controls Country chart
------------------------------------------------------------------------
CB applies to entire entry................ CB Column 1
AT applies to entire entry................ AT Column 1
------------------------------------------------------------------------
License Exceptions
LVS: N/A
GBS: N/A
CIV: N/A
List of Items Controlled
Unit: $ value.
Related Controls: (1) All vaccines and ``immunotoxins'' are
excluded from the scope of this entry. Certain medical products and
diagnostic and food testing kits, which contain biological toxins
identified in paragraph (a)(3) of this entry, are excluded from the
scope of this entry. Vaccines, ``immunotoxins'', certain medical
products, and diagnostic and food testing kits excluded from the
scope of this entry are controlled under ECCN 1C991. (2) Also see
ECCNs 1C351 (AG-controlled human and zoonotic pathogens and
``toxins''), 1C352 (AG-controlled animal pathogens), and 1C354 (AG-
controlled plant pathogens). (3) The Animal and Plant Health
Inspection Service (APHIS), U.S. Department of Agriculture, and the
Centers for Disease Control and Prevention (CDC), U.S. Department of
Health and Human Services, maintain controls on the possession, use,
and transfer within the United States of items controlled by this
ECCN (for APHIS, see 7 CFR 331.3(b), 9 CFR 121.3(b), and 9 CFR
121.4(b); for CDC, see 42 CFR 73.3(b) and 42 CFR 73.4(b)).
Related Definitions: N/A.
Items:
Note: The control status of items listed in this ECCN is not
affected by the exemptions or exclusions contained in the domestic
possession, use, and transfer regulations maintained by APHIS (at 7
CFR part 331 and 9 CFR part 121) and/or CDC (at 42 CFR part 73).
a. Human and zoonotic pathogens and toxins, as follows:
a.1. Viruses, as follows:
a.1.a. Central European tick-borne encephalitis viruses, as
follows:
a.1.a.1. Absettarov;
a.1.a.2. Hanzalova;
a.1.a.3. Hypr;
a.1.a.4. Kumlinge;
a.1.b. Cercopithecine herpesvirus 1 (Herpes B virus);
a.1.c. Reconstructed replication competent forms of the 1918
pandemic influenza virus containing any portion of the coding
regions of all eight gene segments;
a.2. Fungi, as follows:
a.2.a. Coccidioides immitis;
a.2.b. Coccidioides posadasii;
a.3. Toxins, as follows:
[[Page 33621]]
a.3.a. Shiga-like ribosome inactivating proteins not controlled
under ECCN 1C351.d.10;
a.3.b. [Reserved];
b. Animal pathogens, as follows:
b.1. Viruses, as follows:
b.1.a. Akabane virus;
b.1.b. Bovine spongiform encephalopathy agent;
b.1.c. Camel pox virus;
b.1.d. Malignant catarrhal fever virus;
b.1.e. Menangle virus;
b.2. Mycoplasma, as follows:
b.2.a. Mycoplasma capricolum;
b.2.b. Mycoplasma F38;
b.3. Rickettsia, as follows:
b.3.a. Erhlichia ruminantium (a.k.a. Cowdria ruminantium);
b.3.b. [Reserved];
c. Plant pathogens, as follows:
c.1. Bacteria, as follows:
c.1.a. Candidatus Liberobacter africanus (a.k.a. Liberobacter
africanus);
c.1.b. Candidatus Liberobacter asiaticus (a.k.a. Liberobacter
asiaticus);
c.1.c. Xylella fastidiosa pv. citrus variegated chlorosis (CVC);
c.2. Fungi, as follows:
c.2.a. Peronosclerospora philippinensis;
c.2.b. Sclerophthora rayssiae var. zeae;
c.2.c. Synchytrium endobioticum.
0
13. In Supplement No. 1 to Part 774 (the Commerce Control List),
Category 1--Materials, Chemicals, ``Microorganisms'' & ``Toxins,'' ECCN
1C991 is amended by revising the List of Items Controlled to read as
follows:
1C991 Vaccines, immunotoxins, medical products, diagnostic and food
testing kits, as follows (see List of Items controlled).
* * * * *
List of Items Controlled
Unit: $ value
Related Controls: (1) Medical products containing ricin or
saxitoxin, as follows, are controlled for CW reasons under ECCN
1C351:
(a) Ricinus Communis Agglutinin II
(RCAII ), also known as ricin D, or Ricinus Communis
Lectin III (RCLIII );
(b) Ricinus Communis Lectin IV (RCLIV ),
also known as ricin E; or
(c) Saxitoxin identified by C.A.S. 35523-89-8.
(2) The export of a ``medical product'' that is an
``Investigational New Drug'' (IND), as defined in 21 CFR 312.3, is
subject to certain U.S. Food and Drug Administration (FDA)
requirements that are independent of the export requirements
specified in this ECCN or elsewhere in the EAR. These FDA
requirements are described in 21 CFR 312.110 and must be satisfied
in addition to any requirements specified in the EAR.
(3) Also see 21 CFR 314.410 for FDA requirements concerning
exports of new drugs and new drug substances.
Related Definitions: For the purpose of this entry,
``immunotoxin'' is defined as an antibody-toxin conjugate intended
to destroy specific target cells (e.g., tumor cells) that bear
antigens homologous to the antibody. For the purpose of this entry,
``medical products'' are: (1) pharmaceutical formulations designed
for testing and human administration in the treatment of medical
conditions, (2) prepackaged for distribution as clinical or medical
products, and (3) approved by the U.S. Food and Drug Administration
either to be marketed as clinical or medical products or for use as
an ``Investigational New Drug'' (IND) (see 21 CFR part 312). For the
purpose of this entry, ``diagnostic and food testing kits'' are
specifically developed, packaged and marketed for diagnostic or
public health purposes. Biological toxins in any other
configuration, including bulk shipments, or for any other end-uses
are controlled by ECCN 1C351 or ECCN 1C360. For the purpose of this
entry, ``vaccine'' is defined as a medicinal (or veterinary) product
in a pharmaceutical formulation, approved by the U.S. Food and Drug
Administration or the U.S. Department of Agriculture to be marketed
as a medical (or veterinary) product or for use in clinical trials,
that is intended to stimulate a protective immunological response in
humans or animals in order to prevent disease in those to whom or to
which it is administered.
Items:
a. Vaccines against items controlled by ECCN 1C351, 1C352,
1C353, 1C354, or 1C360;
b. Immunotoxins containing items controlled by 1C351.d or
1C360.a.3;
c. Medical products containing botulinum toxins controlled by
ECCN 1C351.d.1 or conotoxins controlled by ECCN 1C351.d.3;
d. Medical products containing any of the following items:
d.1. Items controlled by ECCN 1C351.d (except botulinum toxins
controlled by ECCN 1C351.d.1, conotoxins controlled by ECCN
1C351.d.3, and items controlled for CW reasons under 1C351.d.5 or
.d.6);
d.2. Items controlled by ECCN 1C360.a.3;
e. Diagnostic and food testing kits containing any of the
following items:
e.1. Items controlled by ECCN 1C351.d (except items controlled
for CW reasons under ECCN 1C351.d.5 or .d.6);
e.2. Items controlled by ECCN 1C360.a.3.
0
14. In Supplement No. 1 to Part 774 (the Commerce Control List),
Category 1--Materials, Chemicals, ``Microorganisms''& ``Toxins,'' ECCN
1E001 is amended by revising the License Requirements section of the
ECCN to read as follows:
1E001 ``Technology'' according to the General Technology Note for
the ``development'' or ``production'' of items controlled by
1A001.b, 1A001.c, 1A002, 1A003, 1A004, 1A005, 1A101, 1B, or 1C
(except 1C355, 1C980 to 1C984, 1C988, 1C990, 1C991, 1C992, and
1C995).
License Requirements
Reason for Control: NS, MT, NP, CB, AT
------------------------------------------------------------------------
Control(s) Country chart
------------------------------------------------------------------------
NS applies to ``technology'' for items NS Column 1.
controlled by 1A001.b and .c, 1A002,
1A003, 1A005, 1B001 to 1B003, 1B018,
1C001 to 1C011, or 1C018.
NS applies to ``technology'' for items NS Column 2.
controlled by 1A004 MT applies to
``technology'' for items MT Column 1
controlled by 1A101, 1B001, 1B101,
1B102, 1B115 to 1B119, 1C001, 1C007,
1C011, 1C101, 1C102, 1C107, 1C111,
1C116, 1C117, or 1C118 for MT reasons.
NP applies to ``technology'' for items NP Column 1.
controlled by 1A002, 1B001, 1B101,
1B201, 1B225 to 1B233, 1C002, 1C010,
1C116, 1C202, 1C210, 1C216, 1C225 to
1C240 for NP reasons.
CB applies to ``technology'' for items CB Column 1.
controlled by 1C351, 1C352, 1C353,
1C354, or 1C360.
CB applies to ``technology'' for CB Column 2.
materials controlled by 1C350 and for
chemical detection systems and
dedicated detectors therefor, in
1A004.c, that also have the technical
characteristics described in 2B351.a.
AT applies to entire entry.............. AT Column 1.
------------------------------------------------------------------------
License Requirements Note: See Sec. 743.1 of the EAR for
reporting requirements for exports under License Exceptions.
* * * * *
0
15. In Supplement No. 1 to Part 774 (the Commerce Control List),
Category 1--Materials, Chemicals, ``Microorganisms'' & ``Toxins,'' ECCN
1E351 is amended by revising the ECCN heading and the License
Requirements section of the ECCN to read as follows:
1E351 ``Technology'' according to the ``General Technology Note''
for the disposal of chemicals or microbiological materials
controlled by 1C350, 1C351, 1C352, 1C353, 1C354, or 1C360.
License Requirements
Reason for Control: CB, AT
[[Page 33622]]
------------------------------------------------------------------------
Control(s) Country chart
------------------------------------------------------------------------
CB applies to ``technology'' for the CB Column 1.
disposal of items controlled by 1C351,
1C352, 1C353, 1C354, or 1C360.
CB applies to ``technology'' for the CB Column 2.
disposal of items controlled by 1C350.
AT applies to entire entry.............. AT Column 1.
------------------------------------------------------------------------
* * * * *
Dated: June 5, 2006.
Matthew S. Borman,
Deputy Assistant Secretary for Export Administration.
[FR Doc. E6-8995 Filed 6-9-06; 8:45 am]
BILLING CODE 3510-33-P