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Implementation of the Combat Methamphetamine Epidemic Act of 2005;
Notice of Transfers Following Importation or Exportation
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FR Doc 07-1718 [Federal Register: April 9, 2007 (Volume 72, Number 67)]
[Rules and Regulations] [Page 17401-17409] From the Federal Register Online
via GPO Access [wais.access.gpo.gov] [DOCID:fr09ap07-11]
DEPARTMENT OF JUSTICE
Drug Enforcement Administration
21 CFR Parts 1300 and 1313
[Docket No. DEA-292I] RIN 1117-AB06
Implementation of the Combat Methamphetamine Epidemic Act of 2005;
Notice of Transfers Following Importation or Exportation
AGENCY: Drug Enforcement Administration (DEA), Justice.
ACTION: Interim Final Rule with Request for Comment.
SUMMARY: This regulation implements section 716 of the Combat
Methamphetamine Epidemic Act (CMEA) of 2005 (21
U.S.C. 971 as amended), which
was enacted on March 9, 2006. DEA is amending its regulations to require
additional reporting for import, export, and international transactions
involving all List I and List II chemicals. This rule implements section 716
of the CMEA which extends current reporting requirements for importations,
exportations, and international transactions involving List I and List II
chemicals.
DATES: This rule is effective May 9, 2007. Written comments must be
postmarked, and electronic comments must be sent, on or before May 9, 2007.
ADDRESSES: To ensure proper handling of comments, please reference "Docket No. DEA-292'' on all written and electronic correspondence. Written
comments being sent via regular mail should be sent to the Deputy Assistant
Administrator, Office of Diversion Control, Drug Enforcement Administration,
Washington, DC 20537, Attention: DEA Federal Register Representative/ODL.
Written comments sent via express mail should be sent to DEA Headquarters,
Attention: DEA Federal Register Representative/ODL, 2401 Jefferson-Davis
Highway, Alexandria, VA 22301. Comments may be directly sent to DEA
electronically by sending an electronic message to dea.diversion.policy@usdoj.gov.
[[Page 17402]]
Comments may also be sent electronically through http://www.regulations.gov
using the electronic comment form provided on that site. An electronic copy of
this document is also available at the http://www.regulations.gov Web site.
DEA will accept attachments to electronic comments in Microsoft Word,
WordPerfect, Adobe PDF, or Excel file formats only. DEA will not accept any
file formats other than those specifically listed here.
FOR FURTHER INFORMATION CONTACT: Mark W. Caverly, Chief, Liaison and
Policy Section, Office of Diversion Control, Drug Enforcement Administration,
Washington, DC 20537 at (202) 307-7297.
SUPPLEMENTARY INFORMATION:
DEA's Legal Authority
DEA implements the Comprehensive Drug Abuse Prevention and Control Act of
1970, often referred to as the Controlled Substances Act (CSA) and Controlled
Substances Import and Export Act (21
U.S.C. 801 et seq.), as amended. DEA
publishes the implementing regulations for this statute in Title 21 of the
Code of Federal Regulations (CFR), Parts 1300 to end. These regulations are
designed to ensure that there is a sufficient supply of controlled substances
for legitimate medical purposes and to deter the diversion of controlled
substances to illegal purposes. The CSA mandates that DEA establish a closed
system of control for manufacturing, distributing, and dispensing controlled
substances. Any person who manufactures, distributes, dispenses, imports,
exports, or conducts research or chemical analysis with controlled substances
must register with DEA (unless exempt) and comply with the applicable
requirements for the activity. The CSA as amended also requires DEA to
regulate the manufacture and distribution of chemicals that may be used to
manufacture controlled substances. Listed chemicals that are classified as
List I chemicals are important to the manufacture of controlled substances.
Those classified as List II chemicals may be used to manufacture controlled
substances.
On March 9, 2006, the President signed the CMEA of 2005, which is Title VII
of the USA PATRIOT Improvement and Reauthorization Act of 2005 (Pub. L.
109-177). DEA is promulgating this rule as an interim final rule rather than a
proposed rule because the changes being made merely codify statutory
provisions. Much of the statute is self- implementing; the changes discussed
in this rule became effective on March 9, 2006. An agency may find good cause
to exempt a rule from certain provisions of the Administrative Procedure Act (APA)
(5 U.S.C. 553), including Notice of Proposed Rulemaking and the opportunity
for public comment, if it is determined to be unnecessary, impracticable, or
contrary to the public interest. The requirements of the CMEA of 2005 included
in this rulemaking were set out in such detail as to be self-implementing.
Therefore the changes in this rulemaking provide conforming amendments to make
the language of the regulations consistent with that of the law. DEA has no
authority to revise the changes and is simply implementing, and making its
regulations conform to, the statute.
Combat Methamphetamine Epidemic Act of 2005
The portion of the CMEA being implemented in this rulemaking addresses the
importation, exportation, and international transactions of all List I and
List II chemicals. Section 716 of the CMEA (21
U.S.C. 971 as amended) closes a
loophole in the current regulatory system for imports, exports, and
international transactions of listed chemicals used in the illicit manufacture
of controlled substances. Prior to enactment of the CMEA, a company that
wanted to import or export any List I or List II chemical was required to
either: (1) Notify the Department of Justice 15 days in advance of the import
or export; or (2) be a company that previously imported or exported a listed
chemical and that was proposing to import from or export the chemicals to a
customer with whom the company had previously dealt. (See 21 U.S.C. 971(a),
(b))
A problem can arise, however, when the sale that the importer or exporter
originally planned falls through. When this happens, the importer or exporter
must quickly find a new buyer for the chemicals on what is called the "spot
market''--a wholesale market. Sellers are often under presure to find a buyer
in a short amount of time, meaning that they may be tempted to entertain bids
from companies without a strong record of preventing diversion. More
importantly, DEA is not made aware of, and has no opportunity to review, such
transactions in advance in order to suspend them if there is a danger of
diversion to the clandestine manufacture of a controlled substance.
Section 716 of the CMEA extends the current reporting requirements--as well
as the current exemption for regular importers and regular customers--to
post-import and post-export transactions of List I and List II chemicals.
Importers, exporters, brokers, and traders are now required to notify DEA,
before the transaction is to take place, of certain information regarding
their downstream customers. If the person to whom the chemical is being
transferred is not a regular customer, the importer, exporter, broker, or
trader must notify DEA no later than 15 days before the transaction is to take
place; upon receipt, DEA will have 15 days to review the notification.
Specifically, the United States importer or exporter must provide the name and
address of each person to whom the listed chemicals will be transferred, and
the name and quantity of the listed chemicals to be transferred, including
package information. This person is referred to as the "transferee'' of the
United States importer or exporter. The spot market reporting requirements
also apply, to a limited extent, to United States brokers and traders that
arrange international transactions (i.e., transactions between customers in
two foreign countries).
For a United States exporter, the transferee is the foreign importer. Thus,
this aspect of the new requirement does not represent a change for United
States exporters, who have previously notified DEA of information on their
purchasers. For a United States broker or trader, the transferee is the
foreign customer purchasing the listed chemicals. Again, this requirement is
not a change for brokers and traders, who have previously notified DEA of
information on their purchasers. The requirement is, however, a change for
United States importers. For a United States importer, the "transferee'' is
the person to whom the importer transfers the listed chemicals--the downstream
customer. Until the CMEA, importers were required to provide information
regarding their suppliers, but not regarding the parties purchasing the
chemicals in the United States. Under the CMEA, importers will have to list
both the foreign supplier and each United States customer for the imported
chemical.
The provision of customer information by the importer provides DEA with an
opportunity to evaluate the transaction. DEA will have 15 days from the time
the customer information is submitted to review the transaction and determine
whether it may be diverted to the clandestine manufacture of a controlled
substance. If DEA determines that the transaction does not pose an
unacceptable risk of diversion, DEA will take no action. The importer will
thus be granted regular importer status for transactions involving the
specific chemical to be imported to the specific
[[Page 17403]]
customer. The transferee--the downstream customer--will be granted regular
customer status for imports of the specified chemical by the specified
importer. DEA must review each import transaction based not only on the
chemical to be imported, but also on the transferee to whom the chemical will
be transferred.
If, after submission of the initial DEA Form 486, Import/Export
Declaration, the importer, exporter, broker, or trader will not be
transferring the listed chemical to the person initially named on the DEA Form
486, or if the importer or exporter will be transferring a greater quantity
than originally indicated on the DEA Form 486, then the importer, exporter,
broker, or trader must file an amended DEA Form 486 reporting the change. This
is a new requirement for both United States importers and exporters, as well
as brokers and traders. This amendment must provide the name of the new
prospective customer and/or the greater quantity of the listed chemical to be
transferred. The requirement to notify DEA of a change in the transferee or an
increase in the quantity of the chemical to be transferred applies to amended
DEA Forms 486 in the same manner that it applies to original submissions.
Thus, if an importer, exporter, broker, or trader is required to file an
initial advance notice with DEA 15 days before the transaction is to take
place, and the originally planned sale falls through, the importer, exporter,
broker, or trader is required to file a second advance notice with DEA,
identifying the new proposed purchaser. DEA will again have 15 days to review
the new transaction and determine whether it may be diverted to the
clandestine manufacture of a controlled substance. In the case of a
transaction reported by a broker or trader, DEA cannot suspend the
transaction, but could alert authorities in the foreign country involved in
the transaction of the risk of diversion. In addition, even if an importer or
exporter did not have to file an initial notification--either because he is a
regular importer selling to a regular customer, or an exporter selling to a
regular customer--if the newly arranged spot market sale is to a new customer
(i.e., not a "regular customer''), the importer or exporter must file an
advance notice 15 days prior to transferring the chemical to the new customer.
As is the case under existing law, a suspension can be appealed through an
administrative hearing. (See 21 U.S.C.
971(c)(2))
If, however, the new proposed purchaser qualifies as a "regular customer''
under existing law, the importer or exporter is not required to file a second
advance notice 15 days prior to the transfer of the listed chemical. Rather,
notice must be filed on or before the date of the transfer. Note that the
second notice may occur after importation or exportation. (Brokers and traders
are required to report all regulated international transactions.) If DEA
determines that a listed chemical shipment handled by a regular importer or a
regular customer (including a regular customer who is substituted for the
original customer listed on the original advance notification) may be diverted
to the clandestine manufacture of a controlled substance, DEA may disqualify
the regular importer or regular customer status of such importer or customer
and may suspend the shipment. If the importer or customer (including a new
proposed customer) is not a regular importer or customer, then DEA may suspend
the shipment, since there would be no regular importer or regular customer
status to disqualify. The procedures are set forth in the new regulatory text
at 21 CFR 1313.16(d). Similarly, in the case of an export of a listed chemical
that may be diverted to the clandestine manufacture of a controlled substance,
DEA may disqualify the regular customer status of the transferee and suspend
the shipment. See 21 CFR 1313.26(d).
Finally, within 30 days after the importation, exportation, or
international transaction is completed, the importer, exporter, broker, or
trader must send DEA a return declaration containing information regarding the
transaction, including the name of the transferee, date the import or export
and any subsequent transfer occurred, the name of the chemical transferred,
the actual quantity transferred, the container, and any other information that
DEA may specify. This is a new requirement for United States importers,
exporters, brokers, and traders. For importers, a single return declaration
may include the information for both the importation and distribution. If the
importer has not distributed all chemicals imported by the end of the initial
30-day period, the importer must file supplemental return declarations no
later than 30 days from the date of any further distribution, until the
distribution or other disposition of all chemicals imported under the import
notification or any update are accounted for. In addition, if an importer,
exporter, broker, or trader files a DEA Form 486, but the transfer covered
fails to take place (e.g., the import or export is canceled prior to
shipment), the person must file an amended DEA Form 486 to notify DEA of the
cancellation. These additional filings will ensure that DEA has an accurate
record of importations, exportations, and international transactions.
Summary of Changes Made by This Interim Final Rule
The table below provides a comparison of the previous requirements
regarding imports, exports, and international transactions with the new
requirements of the CMEA:
Table 1.--Comparison of Previous and New Requirements
Requirement
|
Previous rule
|
New rule
|
Notify DEA prior to import/export/international transactions
|
Yes
|
Yes
|
Identify source of imports/international transactions
|
Yes
|
Yes
|
Identify transferees of exports/international transactions
|
Yes
|
Yes
|
Identify transferees (downstream customers) of imports
|
No
|
Yes
|
Notify DEA of change in transferees of exports and international
transactions prior to transaction
|
No
|
Yes
|
Notify DEA of change in transferees (downstream customers) of
imports prior to transaction
|
No
|
Yes
|
Notify DEA of increase in chemical quantity transferred for
exports and international transactions prior to transaction
|
No
|
Yes
|
Notify DEA of increase in chemical quantity transferred for
import transactions prior to transaction
|
No
|
Yes
|
File return declaration when imports/exports and international
transactions are distributed
|
No
|
Yes
|
File subsequent return declaration if entire quantity of import
not distributed within 30 days of importation
|
No
|
Yes
|
[[Page 17404]]
Specific Changes Made by This Interim Final Rule
In this interim final rule, DEA is incorporating the provisions of section
716 of the CMEA into Title 21 of the Code of Federal Regulations. Specific
changes are discussed below.
Certain definitions relating to listed chemicals in section 1300.02 are
being revised or amended. The definition of "established business
relationship'' is being revised to remove language regarding foreign
customers; this definition is now a general definition relating to any
business relationship, either import or export. Further, parts of this
definition are moved to new Section 1313.05, requirements of an established
business relationship. The definition of "established record as an importer''
is being revised by moving certain information into new Section 1313.08.
Finally, the definition of "regular customer'' is being revised to update the
cross reference.
As noted previously, Section 1313.05 is added to specify requirements of an
established business relationship. Information in this section was previously
found in the definition of "established business relationship.''
As noted previously, Section 1313.08 is added to specify requirements for
establishing a record as an importer. Information in this section was
previously found in the definition of "established record as an importer.''
Section 1313.15(a) is being amended to update the cross reference accordingly.
Section
1313.12, requirement of authorization to import, is amended by
revising paragraph (c) to add the requirement that, to qualify for a waiver of
the 15 day advance notice, not only does the importer have to be known to DEA
as a regular importer, but also that the customer must meet the requirements
in Section 1313.05 to be regarded as a regular customer. The effect of this
new requirement is that, effective May 9, 2007, all persons previously granted
regular importer status will be required to provide advance notification of
imports with information regarding transferees, even for customers that they
did business with in the past. This advance notification will provide DEA the
opportunity to review and approve the customer as a regular customer (see the
new definition in Section 1300.02 and the requirements in new Section
1313.05). If the 15-day notification period elapses without DEA taking action,
then that importer is granted regular importer status for all imports of that
particular chemical intended for the specified customer.
Section
1313.13, contents of import declaration, is amended by requiring
the importer to provide information regarding the person or persons to whom
the importer intends to transfer the chemical. Section 1313.16 is added to
specify requirements regarding transfers after importation, Section 1313.26 is
added to specify requirements regarding transfers after exportation, and
Section 1313.32 is amended to specify requirements for brokers and traders
regarding international transactions. These requirements specify what the U.S.
importer, the U.S. exporter, or the U.S. broker or trader must do if an
originally planned sale falls through and the importer or exporter arranges a
subsequent spot market sale, as explained earlier in the preamble. For brokers
and traders, the situation is somewhat more complicated because the broker or
trader does not control the sale. If a transaction is not completed, the
broker or trader could be asked to find another buyer for the chemical or the
broker or trader may not be involved in arranging the subsequent sale. If the
broker or trader arranges a subsequent sale to replace the previously arranged
transaction, this transaction is a new transaction and must be reported as
such; a return declaration must be filed when the transaction is completed.
Sections 1313.17(a), 1313.27(a), and 1313.35(a) are added to specify the
requirement that within 30 days of the completion of a transaction, the
importer, exporter, broker, or trader must send DEA a return declaration
containing information regarding the transaction, including the name of the
transferee, date the import, export, or international transaction and any
subsequent transfer occurred, the name of the chemical transferred, the actual
quantity transferred, the container, and any other information that DEA may
specify.
Sections 1313.17(b), 1313.27(b), and 1313.35(b) are added to specify the
requirement that if an importation, exportation, or international transaction
reported on a DEA Form 486 fails to be completed, the importer, exporter,
broker, or trader must file an amendment to the Form 486 to notify DEA.
Revision of DEA Form 486: Import/Export Declaration for Precursor and
Essential Chemicals
To comply with the changes made to the Controlled Substances Act by the
Combat Methamphetamine Epidemic Act of 2005, DEA is revising the existing DEA
Form 486, Import/Export Declaration. DEA notes that this form has not been
revised or amended since its inception in 1989. Thus, this form has not kept
pace with subsequent legislation including the Domestic Chemical Diversion
Control Act of 1993, the Comprehensive Methamphetamine Control Act of 1996,
and the Methamphetamine Anti- Proliferation Act of 2000. Therefore, some of
the changes DEA is making to this form are not directly related to the CMEA.
However, these changes are necessary for ease of use and clarity of the form.
Changes being made include the following:
- Changing the title of the form to: "Import/Export Declaration for List I
and List II Chemicals'' to more accurately characterize the use of the form.
- Adding a check box for "international transaction'' in addition to
existing fields for "import'' and "export.''
- Adding fields for DEA registration number and company identifier, if
applicable.
- Adding a field for the foreign permit number, if applicable.
- Adding check boxes for the type of submission of the form: "original,'' "amended,'' and
"withdrawn.''
- Adding fields for the actual date and quantity imported.
- Adding fields for reporting by importers of the person to whom the listed
chemical will be transferred, the downstream customer, per requirements of the
CMEA.
- Adding fields regarding return declaration by importers and exporters.
- Removing the certification by the Customs District Director; this
certification is now the responsibility of the importer or exporter as part of
the return declaration.
- Eliminating a number of fields, including: gross weight of chemicals
imported/exported; intermediate carriers; address of intermediate consignees.
- Reorganizing layout for clarity.
Implementation of This Rule
Effective May 9, 2007, all United States importers and exporters of List I
and List II chemicals must use the revised DEA Form 486 to notify DEA of their
imports and exports. This revised form will be available on the Diversion
Control Program Web site, http://www.deadiversion.usdoj.gov .
Effective May 9, 2007, all persons previously granted regular importer
status will no longer hold that status. Every import of a List I and List II
chemical must be reported to DEA not later than 15 days prior to the proposed
importation. This report must include
[[Page 17405]]
the name of the person to whom the chemical is proposed to be transferred
and the amount of the chemical proposed to be transferred. DEA will evaluate
each proposed importation based not only on the chemical to be imported but on
the transferee information supplied by the importer as well. This process will
allow for the establishment of regular customer status by transferees of
United States importers, and for establishment of regular importer status by
importers importing a specific listed chemical intended for sale to a specific
customer.
Effective May 9, 2007, all persons importing and exporting List I and List
II chemicals must provide the above discussed return declarations to DEA.
Note Regarding Importation of the List I Chemicals Ephedrine,
Pseudoephedrine, and Phenylpropanolamine
This rulemaking addresses all List I and List II chemicals. While
ephedrine, pseudoephedrine, and phenylpropanolamine are List I chemicals and
are covered by these regulations, other provisions of section 721 of the CMEA
require the reporting of certain information regarding the foreign chain of
distribution of these three List I chemicals. Other provisions of the CMEA
require that these three List I chemicals be imported only if there is a
medical, scientific, or other legitimate purpose for these chemicals. DEA is
addressing these provisions in a separate rulemaking. Persons importing
ephedrine, pseudoephedrine, and phenylpropanolamine are required to comply
with the provisions of this rule until such time as the rulemaking regarding
provision of information about the foreign chain of distribution is
promulgated. At that time, persons importing these three List I chemicals will
then be subject to those additional requirements.
Further, since the CMEA requires that these three List I chemicals be
imported only if there is a medical, scientific, or other legitimate purpose
for these chemicals, DEA must establish import quotas for ephedrine,
pseudoephedrine, and phenylpropanolamine. DEA is addressing these provisions
in separate rulemakings.
Regulatory Certifications
Administrative Procedure Act (5 U.S.C. 553)
The Administrative Procedure Act (APA) generally requires agencies to
publish a notice of proposed rulemaking and allow for a period of public
comment prior to implementing new rules. The APA also provides, however, that
agencies can be excepted from these requirements when "the agency for good
cause finds (and incorporates the finding and a brief statement of reasons
therefor in the rules issued) that notice and public procedure thereon are
impracticable, unnecessary, or contrary to the public interest.'' (5 U.S.C.
553(b)(B).
DEA has concluded that "good cause'' exists to promulgate this rule as an
interim final rule rather than a proposed rule because the mandates of the
CMEA were set forth in such detail as to be self- implementing. The changes
announced in this interim final rule render DEA's regulations consistent with
the new provisions of the CMEA. Since DEA is without authority to revise this
rule based on public comments, DEA finds that notice and opportunity for
comment are unnecessary and impracticable under the APA (5 U.S.C. 553(b)(B)).
DEA is cognizant of the fact that exceptions to the APA's notice and
comment procedures are to be "narrowly construed and only reluctantly
countenanced.'' American Federation of Government Employees v. Block, 655 F2d
1153, 1156 (D.C. Cir. 1981) (quoting New Jersey Department of Environmental
Protection v. EPA, 626 F2d 1038, 1045 (D.C. Cir. 1980)). Based on the detailed
requirements set forth in the CMEA which give no discretion in their
implementation, however, DEA finds that the invocation of the "good cause''
exception, and the issuance of this rule as an interim final rule, is
justified.
Regulatory Flexibility Act
The Deputy Administrator hereby certifies that this rulemaking has been
drafted in accordance with the Regulatory Flexibility Act (RFA) (5 U.S.C.
605(b)). The RFA applies to rules that are subject to notice and comment.
Because this rule is simply codifying statutory provisions, DEA has
determined, as explained above, that public notice and comment are not
necessary. Consequently, the RFA does not apply.
Executive Order 12866
The Deputy Administrator further certifies that this rulemaking has been
drafted in accordance with the principles in Executive Order 12866 Sec. 1(b).
It has been determined that this is "a significant regulatory action.''
Therefore, this action has been reviewed by the Office of Management and
Budget (OMB). As discussed above, this action is codifying statutory
provisions and involves no agency discretion. This statutory change imposes
minimal costs on United States importers, exporters, brokers, and traders;
they simply have to file a form with DEA in advance of spot market
transactions. They must also provide a return declaration after the import or
export has occurred.
Paperwork Reduction Act
As discussed previously, the DEA is revising an information collection by
revising the information collected on DEA Form 486: Import/Export Declaration
for List I and List II Chemicals [OMB information collection 1117-0023]. Those
changes have been discussed above, and are necessary for DEA to implement the
provisions of the CMEA of 2005.
The Department of Justice, DEA, has submitted the following information
collection request to the OMB for review and clearance in accordance with
review procedures of the Paperwork Reduction Act of 1995. The information
collection is published to obtain comments from the public and affected
agencies.
All comments and suggestions, or questions regarding additional
information, to include obtaining a copy of the information collection
instrument with instructions, should be directed to Mark W. Caverly, Chief,
Liaison and Policy Section, Office of Diversion Control, Drug Enforcement
Administration, Washington, DC 20537.
Written comments and suggestions from the public and affected agencies
concerning the collection of information are encouraged. Your comments on the
information collection-related aspects of this rule should address one or more
of the following four points:
(1) Evaluate whether the proposed collection of information is necessary
for the proper performance of the functions of the agency, including whether
the information will have practical utility;
(2) Evaluate the accuracy of the agency's estimate of the burden of the
proposed collection of information, including the validity of the methodology
and assumptions used;
(3) Enhance the quality, utility, and clarity of the information to be
collected; and
(4) Minimize the burden of the collection of information on those who are
to respond, including through the use of appropriate automated, electronic,
mechanical, or other technological collection techniques or other forms of
information technology, e.g., permitting electronic submission of responses.
Overview of this information collection:
[[Page 17406]]
(1) Type of Information Collection: revision of an existing
collection.
(2) Title of the Form/Collection: Import/Export Declaration for
List I and List II Chemicals.
(3) Agency form number, if any, and the applicable component of the
Department of Justice sponsoring the collection: Form Number: DEA Form
486. Office of Diversion Control, Drug Enforcement Administration, U.S.
Department of Justice.
(4) Affected public who will be asked or required to respond, as well
as a brief abstract:Primary: business or other for-profit. Other:
none. Abstract: Persons importing, exporting, and conducting
international transactions with List I and List II chemicals must notify DEA
of those transactions in advance of their occurrence, including information
regarding the person(s) to whom the chemical will be transferred and the
quantity to be transferred. For importations, persons must also provide
return declarations, confirming the date of the importation and transfer,
and the amounts of the chemical transferred. This information is used to
prevent shipments not intended for legitimate purposes.
(5) An estimate of the total number of respondents and the amount of time
estimated for an average respondent to respond:
|
Number of respondents
|
Number of responses
|
Average time per response
|
Total hours
|
Form 486 (export)
|
225
|
7,917
|
0.2 hour (12 minutes)
|
1,583.4 hours.
|
Form 486 (export return declaration) |
225
|
7,917
|
0.08 hour (5 minutes)
|
659.75 hours.
|
Form 486 (import)
|
216
|
2,278
|
0.25 hour (15 minutes)
|
569.5 hours.
|
Form 486 (import return declaration)*
|
216
|
2,506
|
0.08 hour (5 minutes)
|
208.8 hours.
|
Form 486 (international transaction) |
9
|
111
|
0.2 hour (12 minutes)
|
22.2 hours.
|
Form 486 (international transaction return declaration)
|
9
|
111
|
0.08 hour (5 minutes)
|
9.25 hours.
|
Quarterly reports for imports of acetone, 2-butanone, and
toluene
|
110
|
440
|
0.5 hour (30 minutes) |
220 hours.
|
Total
|
225
|
................. |
..............
|
3,272.9 hours.
|
* DEA assumes 10% of all imports will not be transferred in the
first thirty days and will necessitate submission of a subsequent return
declaration.
(6) An estimate of the total public burden (in hours) associated with the
collection: DEA estimates that this collection will take 3,272.9 hours
annually.
If additional information is required, contact: Lynn Bryant, Department
Clearance Officer, Information Management and Security Staff, Justice
Management Division, Department of Justice, Patrick Henry Building, Suite
1600, 601 D Street, NW., Washington, DC 20530.
Executive Order 12988
This regulation meets the applicable standards set forth in sections 3(a)
and 3(b)(2) of Executive Order 12988, Civil Justice Reform.
Executive Order 13132
This rulemaking does not preempt or modify any provision of State law; nor
does it impose enforcement responsibilities on any State; nor does it diminish
the power of any State to enforce its own laws. Accordingly, this rulemaking
does not have federalism implications warranting the application of Executive
Order 13132.
Unfunded Mandates Reform Act of 1995
This rule will not result in the expenditure by State, local, and tribal
governments, in the aggregate, or by the private sector, of $118,000,000 or
more in any one year, and will not significantly or uniquely affect small
governments. Therefore, no actions were deemed necessary under the provisions
of the Unfunded Mandates Reform Act of 1995.
Congressional Review Act
This rule is not a major rule as defined by Sec. 804 of the Small Business
Regulatory Enforcement Fairness Act of 1996 (Congressional Review Act). This
rule will not result in an annual effect on the economy of $100,000,000 or
more; a major increase in costs or prices; or significant adverse effects on
competition, employment, investment, productivity, innovation, or on the
ability of United States-based companies to compete with foreign-based
companies in domestic and export markets.
List of Subjects
21 CFR Part 1300
Chemicals, Drug traffic control.
21 CFR Part 1313
Administrative practice and procedure, Drug traffic control, Exports,
Imports, Reporting and recordkeeping requirements.
- For the reasons set out above, 21 CFR parts 1300 and 1313 are amended as
follows:
PART 1300--DEFINITIONS
- 1. The authority citation for part 1300 continues to read as follows:
Authority: 21
U.S.C. 802, 871(b),
951, 958(f).
- 2. Section 1300.02 is amended by revising paragraphs (b)(12), (b)(13),
and (b)(25) to read as follows:
Sec. 1300.02 Definitions related to listed chemicals.
* * * * *
(b) * * *
(12) The term established business relationship means the regulated
person has imported or exported a listed chemical at least once within the
past six months, or twice within the past twelve months from or to a foreign
manufacturer, distributor, or end user of the chemical that has an established
business with a fixed street address. A person or business that functions as a
broker or intermediary is not a customer for purposes of this definition.
[[Page 17407]]
(13) The term established record as an importer means that the regulated
person has imported a listed chemical at least once within the past six
months, or twice within the past twelve months from a foreign supplier.
* * * * *
(25) The term regular customer means a person with whom the regulated
person has an established business relationship for a specified listed
chemical or chemicals that has been reported to the Administration subject to
the criteria established in part 1313 of this chapter.
* * * * *
PART 1313--IMPORTATION AND EXPORTATION OF LIST I AND LIST II CHEMICALS
- 3. The authority citation for part 1313 continues to read as follows:
Authority: 21
U.S.C. 802, 830,
871(b), 971.
- 4. The heading of part 1313 is revised to read as set forth above.
- 5. Section 1313.05 is added to read as follows:
Sec. 1313.05 Requirements for an established business relationship.
To document that an importer or exporter has an established business
relationship with a customer, the importer or exporter must provide the
Administrator with the following information in accordance with the waiver of
15-day advance notice requirements of Sec. 1313.15 or Sec.
1313.24:
(a) The name and street address of the chemical importer or exporter and
of each regular customer;
(b) The telephone number, contact person, and where available, the
facsimile number for the chemical importer or exporter and for each regular
customer;
(c) The nature of the regular customer's business (i.e., importer,
exporter, distributor, manufacturer, etc.), and if known, the use to which
the listed chemical or chemicals will be applied;
(d) The duration of the business relationship;
(e) The frequency and number of transactions occurring during the
preceding 12-month period;
(f) The amounts and the listed chemical or chemicals involved in
regulated transactions between the chemical importer or exporter and regular
customer;
(g) The method of delivery (direct shipment or through a broker or
forwarding agent); and
(h) Other information that the chemical importer or exporter considers
relevant for determining whether a customer is a regular customer.
- 6. Section 1313.08 is added to read as follows:
Sec. 1313.08 Requirements for establishing a record as an importer.
To establish a record as an importer, the regulated person must provide the
Administrator with the following information in accordance with the waiver of
the 15-day advance notice requirements of Sec.
1313.15:
(a) The name, DEA
registration number (where applicable), street address, telephone number, and,
where available, the facsimile number of the regulated person and of each
foreign supplier; and
(b) The frequency and number of transactions occurring during the
preceding 12 month period.
- 7. Section 1313.12 is amended by revising paragraph (c) to read as
follows:
Sec. 1313.12 Requirement of authorization to import.
* * * * *
(c) The 15-day advance notification requirement for listed chemical
imports may be waived for the following:
(1) Any importation that meets both of the following requirements:
(i) The regulated person has satisfied the requirements for reporting
to the Administration as a regular importer of the listed chemicals.
(ii) The importer intends to transfer the listed chemicals to a person
who is a regular customer for the chemical, as defined in Sec. 1300.02 of
this chapter.
(2) A specific listed chemical, as set forth in paragraph (f) of this
section, for which the Administrator determines that advance notification
is not necessary for effective chemical diversion control.
* * * * *
- 8. Section 1313.13 is amended by revising paragraph (c)(4) and adding
paragraph (c)(5) to read as follows:
Sec. 1313.13 Contents of import declaration.
* * * * *
(c) * * *
(4) The name, address, telephone number, telex number, and, where
available, the facsimile number of the consigner in the foreign country of
exportation; and
(5) The name, address, telephone number, and where available, the facsimile
number of the person or persons to whom the importer intends to transfer the
listed chemical and the quantity to be transferred to each transferee.
- 9. Section 1313.15 is amended by revising paragraph (a) to read as
follows:
Sec. 1313.15 Waiver of 15-day advance notice for regular importers.
(a) Each regulated person seeking designation as a "regular importer''
shall provide, by certified mail return receipt requested, to the
Administration such information as is required under Sec. 1313.08 documenting
their status as a regular importer.
* * * * *
- 10. Section 1313.16 is added to read as follows:
Sec. 1313.16 Transfers following importation.
(a) In the case of a notice under Sec. 1313.12(a) submitted by a regulated
person, if the transferee identified in the notice is not a regular customer,
the importer may not transfer the listed chemical until after the expiration
of the 15-day period beginning on the date on which the notice is submitted to
the Administration.
(b) After a notice under Sec. 1313.12(a) or (d) is submitted to the
Administration, if circumstances change and the importer will not be
transferring the listed chemical to the transferee identified in the notice,
or will be transferring a greater quantity of the chemical than specified in
the notice, the importer must update the notice to identify the most recent
prospective transferee or the most recent quantity or both (as the case may
be) and may not transfer the listed chemical until after the expiration of the
15-day period beginning on the date on which the update is submitted to the
Administration, except that the 15-day restriction does not apply if the
prospective transferee identified in the update is a regular customer. The
preceding sentence applies with respect to changing circumstances regarding a
transferee or quantity identified in an update to the same extent and in the
same manner as the sentence applies with respect to changing circumstances
regarding a transferee or quantity identified in the original notice under
Sec. 1313.12(a) or (d).
(c) In the case of a transfer of a listed chemical that is subject to a
15-day restriction, the transferee involved shall, upon the expiration of the
15-day period, be considered to qualify as a regular customer, unless the
Administration otherwise notifies the importer involved in writing.
(d) With respect to a transfer of a listed chemical with which a notice or
update referred to in Sec. 1313.12(a) or (d) is concerned:
(1) The Administration--
(i) May, in accordance with the same procedures as apply under Sec. Sec.
1313.51 through 1313.57, order the suspension
[[Page 17408]]
of the transfer of the listed chemical by the importer involved, except for
a transfer to a regular customer, on the ground that the chemical may be
diverted to the clandestine manufacture of a controlled substance (without
regard to the form of the chemical that may be diverted, including the
diversion of a finished drug product to be manufactured from bulk chemicals to
be transferred), subject to the Administration ordering the suspension before
the expiration of the 15- day period with respect to the importation (in any
case in which such a period applies); and
(ii) May, for purposes of this paragraph (d), disqualify a regular customer
on that ground.
(2) From and after the time when the Administration provides written notice
of the order under paragraph (d)(1)(i) of this section (including a statement
of the legal and factual basis for the order) to the importer, the importer
may not carry out the transfer.
(e) For purposes of this section:
(1) The term transfer, with respect to a listed chemical, includes the sale
of the chemical.
(2) The term transferee means a person to whom an importer transfers a
listed chemical.
- 11. Section 1313.17 is added to read as follows:
Sec. 1313.17 Return declaration or amendment to Form 486 for imports.
(a) Within 30 days after a transaction is completed, the importer must send
to the Administration a return declaration containing particulars of the
transaction, including the date, quantity, chemical, container, name of
transferees, and any other information as the Administration may specify. A
single return declaration may include the particulars of both the importation
and distribution. If the importer has not distributed all chemicals imported
by the end of the initial 30-day period, the importer must file supplemental
return declarations no later than 30 days from the date of any further
distribution, until the distribution or other disposition of all chemicals
imported under the import notification or any update are accounted for.
(b) If an importation for which a Form 486 has been filed fails to take
place, the importer must file an amended Form 486 notifying the Administration
that the importation did not occur.
- 12. Section 1313.26 is added to read as follows:
Sec. 1313.26 Transfers following exportation.
(a) In the case of a notice under Sec. 1313.21(a) submitted by a regulated
person, if the transferee identified in the notice, i.e., the foreign
importer, is not a regular customer, the regulated person may not transfer the
listed chemical until after the expiration of the 15- day period beginning on
the date on which the notice is submitted to the Administration.
(b) After a notice under Sec. 1313.21(a) is submitted to the
Administration, if circumstances change and the exporter will not be
transferring the listed chemical to the transferee identified in the notice,
or will be transferring a greater quantity of the chemical than specified in
the notice, the exporter must update the notice to identify the most recent
prospective transferee or the most recent quantity or both (as the case may
be) and may not transfer the listed chemical until after the expiration of the
15-day period beginning on the date on which the update is submitted to the
Administration, except that the 15-day restriction does not apply if the
prospective transferee identified in the update is a regular customer. The
preceding sentence applies with respect to changing circumstances regarding a
transferee or quantity identified in an update to the same extent and in the
same manner as the sentence applies with respect to changing circumstances
regarding a transferee or quantity identified in the original notice under
paragraph (a) of this section.
(c) In the case of a transfer of a listed chemical that is subject to a
15-day restriction, the transferee involved shall, upon the expiration of the
15-day period, be considered to qualify as a regular customer, unless the
Administration otherwise notifies the exporter involved in writing.
(d) With respect to a transfer of a listed chemical with which a notice or
update referred to in Sec. 1313.21(a) is concerned:
(1) The Administration--
(i) May, in accordance with the same procedures as apply under Sec. Sec.
1313.51 through 1313.57, order the suspension of the transfer of the listed
chemical by the exporter involved, except for a transfer to a regular
customer, on the ground that the chemical may be diverted to the clandestine
manufacture of a controlled substance (without regard to the form of the
chemical that may be diverted, including the diversion of a finished drug
product to be manufactured from bulk chemicals to be transferred), subject to
the Administration ordering the suspension before the expiration of the 15-day
period with respect to the exportation (in any case in which such a period
applies); and
(ii) May, for purposes of this paragraph (d), disqualify a regular customer
on that ground.
(2) From and after the time when the Administration provides written notice
of the order under paragraph (d)(1)(i) of this section (including a statement
of the legal and factual basis for the order) to the exporter, the exporter
may not carry out the transfer.
(e) For purposes of this section:
(1) The term transfer, with respect to a listed chemical, includes the sale
of the chemical.
(2) The term transferee means a person to whom an exporter transfers a
listed chemical.
- 13. Section 1313.27 is added to read as follows:
Sec. 1313.27 Return declaration or amendment to Form 486 for exports.
(a) Within 30 days after a transaction is completed, the exporter must send
to the Administration a return declaration containing particulars of the
transaction, including the date, quantity, chemical, container, name of
transferees, and any other information as the Administration may specify.
(b) If an exportation for which a Form 486 has been filed fails to take
place, the exporter must file an amended Form 486 notifying the Administration
that the exportation did not occur.
- 14. Section 1313.32 is amended by adding paragraphs (d) and (e) to read
as follows:
Sec. 1313.32 Requirement of authorization for international transactions.
* * * * *
(d) After a notice under paragraph (a) of this section is
submitted to the Administration, if circumstances change and the broker or
trader will not be transferring the listed chemical to the transferee
identified in the notice, or will be transferring a greater quantity of the
chemical than specified in the notice, the broker or trader must update the
notice to identify the most recent prospective transferee or the most recent
quantity or both (as the case may be). The preceding sentence applies with
respect to changing circumstances regarding a transferee or quantity
identified in an update to the same extent and in the same manner as the
sentence applies with respect to changing circumstances regarding a transferee
or quantity identified in the original notice under paragraph (a) of this
section.
(e) For purposes of this section:
(1) The term transfer, with respect to a listed chemical, includes the sale
of the chemical.
[[Page 17409]]
(2) The term transferee means a person to whom an exporter transfers a
listed chemical.
- 15. Section 1313.35 is added to read as follows:
Sec. 1313.35 Return declaration or amendment to Form 486 for international
transactions.
(a) Within 30 days after a transaction is completed, the broker or trader
must send to the Administration a return declaration containing particulars of
the transaction, including the date, quantity, chemical, container, name of
transferees, and any other information as the Administration may specify.
(b) If a transaction for which a Form 486 has been filed fails to take
place, the broker or trader must file an amended Form 486 notifying the
Administration that the transaction did not occur.
Dated: March 30, 2007.
Michele M. Leonhart,
Deputy Administrator.
[FR Doc. 07-1718 Filed 4-6-07; 8:45 am]
BILLING CODE 4410-09-P
NOTICE: This is an
unofficial version. An official version of these publications may be obtained
directly from the Government Printing Office (GPO).
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