[Federal Register Volume 71, Number 112 (Monday, June 12, 2006)]
[Rules and Regulations]
[Pages 33614-33622]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: E6-8995]


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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: [email protected]. 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 [email protected], 
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
------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------
                                          Chemical & biological         Nuclear          National      Missile tech      Regional        Firearms          Crime control         Anti-terrorism
                                                 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   .......  .......
 
                                                                                          * * * * * * *
------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------


[[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