Third Party Testing for Certain Children's Products; Notice of Requirements for Accreditation of Third Party Conformity Assessment Bodies To Assess Conformity With Part 1508, Part 1509, and/or Part 1511 of Title 16, Code of Federal Regulations, 62965-62967 [E8-25096]
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sroberts on PROD1PC70 with NOTICES
Federal Register / Vol. 73, No. 205 / Wednesday, October 22, 2008 / Notices
most stringent receiving water
requirements identified in a permit.
Response: NMFS has reassessed its
position in the conservation plan.
NMFS acknowledges that a lack of
sewage treatment in a growing urban
area would have negative impacts.
Further, NMFS acknowledges that
wastewater treatment needs can be
tailored to meet a permit’s requirements;
therefore, this prohibition was removed.
Comment 25: One commenter noted
that Type I and II habitat management
measures place severe restrictions on
any work that would be associated with
placing and maintaining undersea
electrical cables. The commenter said it
is not aware that previous cable circuit
installation and subsequent operation
have negative impacts on the beluga
whale population.
Response: NMFS has no evidence that
electrical cable operation or
maintenance has had negative impacts
on beluga whales. Any cable installation
must go through the Corps of Engineers
permitting process, as required by law.
The goal of the conservation plan is not
to restrict development or prohibit
maintenance for undersea electrical
cables, but rather to protect beluga
habitat and allow the population to
recover and expand to its historic range.
Projects in Type I habitat area (which
has been redefined in the conservation
plan) should not adversely affect the
beluga habitat.
Comment 26: One commenter says
that NMFS must continue to study
belugas to help future preservation and
knowledge efforts, and must not delay
actions ensuring the belugas’ survival.
Response: With the continued annual
decline at 1.5 percent since harvest was
regulated in 1999, we agree that
conservation actions need to occur
immediately. The conservation plan
develops a strategy based on: (1)
improving our knowledge about the
biology of these belugas and the factors
that are limiting their population
growth; (2) stopping direct losses to the
population; (3) protecting valuable
habitat; and (4) evaluating the
effectiveness of these strategies and the
success of the conservations actions in
restoring the Cook Inlet stock to its OSP.
NMFS pursued a scientifically-based
conservation plan while using a
precautionary approach to management.
As monitoring and studies provide
additional scientific information,
management can be adjusted
accordingly. This section was clarified
in the final conservation plan.
Comment 27: One commenter is
concerned that NMFS plans to re-assess
this stock for possible listing under
ESA, and asserts that it is inappropriate
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for NMFS to abandon the current comanagement agreement and
conservation measures.
Response: Although NMFS is listing
Cook Inlet beluga whales as an
endangered species, NMFS will
continue to co-manage Cook Inlet
belugas with the Cook Inlet hunters and
make use of conservation measures
under the MMPA while a recovery plan
under the ESA is being prepared.
Comment 28: NMFS should not
manage or authorize fishing operations
that are likely to have an impact on
beluga whales. The commenter adds
that the draft conservation plan is
unclear as to NMFS’ role in Federal and
State fisheries.
Response: The conservation plan has
been clarified to differentiate between
managing Federal fisheries and
providing input to State fisheries.
Dated: October 16, 2008.
James W. Balsiger,
Acting Assistant Administrator for Fisheries,
National Marine Fisheries Service.
[FR Doc. E8–25101 Filed 10–17–08; 11:15
am]
BILLING CODE 3510–22–S
CONSUMER PRODUCT SAFETY
COMMISSION
Third Party Testing for Certain
Children’s Products; Notice of
Requirements for Accreditation of
Third Party Conformity Assessment
Bodies To Assess Conformity With
Part 1508, Part 1509, and/or Part 1511
of Title 16, Code of Federal
Regulations
Consumer Product Safety
Commission.
ACTION: Notice of Requirements for
Accreditation of Third Party Conformity
Assessment Bodies To Assess
Conformity With Part 1508, Part 1509,
and/or Part 1511 of Title 16, Code of
Federal Regulations.
AGENCY:
Introduction: The Consumer Product
Safety Act (‘‘CPSA’’), at section
14(a)(3)(B)(ii) as added by section
102(a)(2) of the Consumer Product
Safety Improvement Act of 2008
(‘‘CPSIA’’), Public Law 110–314, directs
the U.S. Consumer Product Safety
Commission (‘‘CPSC’’ or ‘‘Commission’’)
to publish this notice of requirements
for accreditation of third party
conformity assessment bodies (‘‘third
party laboratories’’) to test children’s
products for conformity with the
Commission’s regulations for full-size
baby cribs at 16 CFR part 1508, for nonfull-size baby cribs at 16 CFR part 1509,
and/or for pacifiers at 16 CFR part
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62965
1511.1 2 Each manufacturer (including
the importer) or private labeler of cribs
and/or pacifiers subject to those
regulations must have products
manufactured more than 90 days after
the Federal Register publication date of
this notice tested by a laboratory
accredited to do so and must issue a
certificate of compliance with the
applicable regulations based on that
testing.3 4
The Commission is also recognizing
limited circumstances in which testing
performed by a laboratory on or after
May 16, 2008, 90 days prior to the date
of enactment of CPSIA (August 14,
2008), but prior to Commission
acceptance of the laboratory’s
preexisting accreditation, provided that
accreditation is accepted not later than
December 26, 2008, may form the basis
for the certificate of compliance with
the crib and/or pacifier regulations
required of the manufacturer or private
labeler.
This notice provides the criteria and
process for Commission acceptance of
accreditation of ‘‘third party’’
laboratories for testing to the regulations
for cribs and/or pacifiers (laboratories
that are not owned, managed, or
controlled by a manufacturer or private
labeler of a children’s product to be
tested by the laboratory for certification
purposes), ‘‘firewalled’’ laboratories
(those that are owned, managed, or
controlled by a manufacturer or private
labeler of a children’s product to be
tested by the laboratory for certification
purposes and that seek accreditation
under the additional statutory criteria
for ‘‘firewalled’’ laboratories), and
laboratories owned or controlled in
whole or in part by a government.
The requirements of this notice are
effective upon its publication in the
Federal Register and are exempted by
CPSIA from the notice and comment
rulemaking requirements of the
Administrative Procedure Act, 5 U.S.C.
553.5
1 Section 102 of CPSIA also required the
Commission to publish requirements for
accreditation of laboratories for testing to the lead
paint ban at 16 CFR part 1303. Those requirements
were published in the Federal Register on
September 22, 2008. 73 FR 54564–6.
2 Children’s products are those designed or
intended for use primarily by children 12 years old
and younger.
3 Section 14(a)(2) of the CPSA as added by
§ 102(a)(2) of CPSIA requires that certification be
based on testing of sufficient samples of the
product, or samples that are identical in all material
respects to the product.
4 Of course, irrespective of certification, the
children’s product in question must comply with
applicable CPSC requirements. See, e.g., CPSA
§ 14(h) as added by CPSIA § 102(b).
5 CPSA section 14(a)(3)(G) as added by section
102(a)(2) of CPSIA exempts publication of this
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Baseline accreditation of each
category of laboratory to the
International Organization for
Standardization (‘‘ISO’’) Standard ISO/
IEC 17025:2005—General Requirements
for the Competence of Testing and
Calibration Laboratories—is required.
The accreditation must be by an
accreditation body that is a signatory to
the International Laboratory
Accreditation Cooperation—Mutual
Recognition Arrangement (‘‘ILAC–
MRA’’) and the scope of the
accreditation must include testing for
compliance with the crib regulations of
16 CFR part 1508 and/or part 1509 and/
or the pacifier regulations of part 1511.6
A laboratory owned or controlled by a
manufacturer or private labeler of
products to be tested by the laboratory
is subject to additional requirements
intended to assure that the Commission
is immediately and confidentially
notified of any attempt by the
manufacturer, private labeler or other
interested party to hide or exert undue
influence over the laboratory’s test
results. A governmental laboratory may
be accredited subject to additional
requirements concerning independence
of its relationship with the host
government and freedom of
manufacturers in the host country to
elect to use accredited non-government
laboratories for certification testing
without suffering disadvantage.
The Commission has established an
electronic accreditation registration and
listing system that can be accessed via
its Web site.
Although the accreditation
requirements in this notice for testing to
the crib and/or pacifier regulations are
effective upon their publication in the
Federal Register, the Commission
solicits comments on the accreditation
procedures as they apply to that testing
and on the accreditation approach in
general, since the Commission must
publish additional testing laboratory
accreditation procedures over the
coming months.
DATES: Effective Date: The requirements
for accreditation of laboratories for
testing to the crib and/or pacifier
notice from the rulemaking requirements of the
Administrative Procedure Act, 5 U.S.C. 553, and
from the Regulatory Flexibility Act, 5 U.S.C. 601–
612.
6 A description of the history and content of the
ILAC–MRA approach and of the requirements of the
ISO 17025:2005 laboratory accreditation standard is
provided in the CPSC staff briefing memorandum
Third Party Conformity Assessment Body
Accreditation Requirements for Testing Compliance
with 16 CFR Part 1508, Part 1509, and Part 1511
(Cribs and Pacifiers) as Required by the Consumer
Product Safety Improvement Act of 2008, October
2008, available on the CPSC Web site at https://
cpsc.gov/library/foia/foia09/brief/tpacp.pdf.
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17:50 Oct 21, 2008
Jkt 217001
regulations are effective upon
publication of this notice in the Federal
Register, that is October 22, 2008.
Request for Comments: Please provide
comments in response to this notice by
November 21, 2008. Comments on this
notice should be captioned ‘‘Laboratory
Accreditation Process for Crib and
Pacifier Testing.’’ Comments should be
submitted to the Office of the Secretary
by e-mail at cpscos@cpsc.gov, or mailed
or delivered, preferably in five copies, to
the Office of the Secretary, Consumer
Product Safety Commission, 4330 East
West Highway, Bethesda, Maryland
20814. Comments may also be filed by
facsimile to (301) 504–0127.
FOR FURTHER INFORMATION CONTACT:
Robert ‘‘Jay’’ Howell, Acting Assistant
Executive Director for Hazard
Identification and Reduction, U.S.
Consumer Product Safety Commission,
4330 East West Highway, Bethesda,
Maryland 20814; e-mail
rhowell@cpsc.gov.
I. Accreditation Requirements
A. Baseline Third Party Laboratory
Accreditation Requirements
For a third party laboratory to be
accredited to test children’s products for
conformity with the Commission’s crib
and/or pacifier regulations, it must be
accredited by an ILAC–MRA signatory
accrediting body and the accreditation
must be registered with, and accepted
by, the Commission. A listing of ILAC–
MRA signatory accrediting bodies is
available on the Internet at https://
ilac.org/membersbycategory.html. The
accreditation must be to ISO Standard
ISO/IEC 17025:2005—General
Requirements for the Competence of
Testing and Calibration Laboratories
and the scope of the accreditation must
expressly include testing to the
regulations of 16 CFR part 1508, 1509,
and/or 1511 as applicable to the
product(s) to be tested.7 A true copy of
the accreditation and scope documents
demonstrating compliance with these
requirements must be registered with
the Commission electronically. The
additional requirements for
accreditation of firewalled and
governmental laboratories are described
below in sections I.B and I.C.
The Commission will maintain on its
Web site an up-to-date listing of
laboratories whose accreditations it has
accepted and the scope of each
7 A laboratory may seek Commission acceptance
of accreditation to test only full-size cribs, only
non-full-size cribs, or only pacifiers, or some
combination thereof. However, required
manufacturer certifications may only be based on
testing by a laboratory accredited to test the specific
product in question.
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accreditation. Subject to the limited
provisions for acceptance of
‘‘retrospective’’ testing performed by
other than firewalled laboratories noted
in Section III. below, once the
Commission adds a laboratory to that
list, the laboratory may commence
testing of children’s products to support
certification by the manufacturer or
private labeler of compliance with the
crib and/or pacifier regulations, as
applicable.
B. Additional Accreditation
Requirements for Firewalled
Laboratories
In addition to the baseline
accreditation requirements in section
I.A, firewalled laboratories seeking
accredited status must submit to the
Commission for review copies of their
training documents showing how
employees are trained to notify the
Commission immediately and
confidentially of any attempt by the
manufacturer, private labeler or other
interested party to hide or exert undue
influence over the laboratory’s test
results. This additional requirement
applies to any laboratory in which a
manufacturer or private labeler of a
children’s product to be tested by the
laboratory owns a ten percent or more
interest. While the Commission is not
addressing common parentage of a lab
and a children’s product manufacturer
at this time, it will be vigilant to see if
this issue needs to be dealt with in the
future.
The Commission must formally
accept, by order, the accreditation
application of a laboratory before the
laboratory can become an accredited
firewalled laboratory.
C. Additional Accreditation
Requirements for Governmental
Laboratories
In addition to the baseline
accreditation requirements of section
I.A, CPSIA permits accreditation of a
laboratory owned or controlled in whole
or in part by a government if:
• To the extent practicable,
manufacturers or private labelers
located in any nation are permitted to
choose laboratories that are not owned
or controlled by the government of that
nation;
• The laboratory’s testing results are
not subject to undue influence by any
other person, including another
governmental entity;
• The laboratory is not accorded more
favorable treatment than other
laboratories in the same nation who
have been accredited;
• The laboratory’s testing results are
accorded no greater weight by other
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sroberts on PROD1PC70 with NOTICES
governmental authorities than those of
other accredited laboratories; and
• The laboratory does not exercise
undue influence over other
governmental authorities on matters
affecting its operations or on decisions
by other governmental authorities
controlling distribution of products
based on outcomes of the laboratory’s
conformity assessments.
The Commission will accept the
accreditation of a governmental
laboratory if it meets the baseline
accreditation requirements of section
I.A and meets the conditions stated
here. To obtain this assurance, CPSC
staff will engage the governmental
entities relevant to the accreditation
request.
II. How Does a Laboratory Apply for
Acceptance of Its Accreditation?
The Commission has established an
electronic accreditation acceptance and
registration system accessed via the
Commission’s Internet site at https://
www.cpsc.gov/businfo/labaccred.html.
The applicant provides basic identifying
information concerning its location, the
type of accreditation it is seeking, and
electronic copies of its ILAC–MRA
accreditation certificate and scope
statement and firewalled laboratory
training document(s), if relevant.
Commission staff reviews that
submission for accuracy and
completeness. In the case of baseline
third party laboratory accreditation and
accreditation of governmental
laboratories, when that review and any
necessary discussions with the
applicant are satisfactorily completed,
the laboratory in question is added to
the CPSC listing of accredited
laboratories at https://www.cpsc.gov/
businfo/labaccred.html. In the case of a
firewalled laboratory seeking accredited
status, when the review is complete, the
staff transmits its recommendation on
accreditation to the Commission for
consideration.8 If the Commission
accepts a staff recommendation to
accredit a firewalled laboratory, that
laboratory will then be added to the
CPSC list of accredited laboratories. In
each case, the Commission will
electronically notify the laboratory of
acceptance of its accreditation.
Subject to the limited provisions for
acceptance of ‘‘retrospective’’ testing
performed by other than accredited
firewalled laboratories noted in Section
III. below, once the Commission adds a
laboratory to the list, the laboratory may
8A
laboratory that may ultimately seek
acceptance as a firewalled laboratory could initially
request acceptance as a third party laboratory
accredited for testing of children’s products other
than those of its owners.
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17:50 Oct 21, 2008
Jkt 217001
then commence testing of children’s
products to support certification of
compliance with the crib and/or pacifier
regulations, as applicable, by the
manufacturer or private labeler.
III. Limited Acceptance of Children’s
Product Certifications Based on Third
Party Laboratory Testing Prior to
Commission Acceptance of
Accreditation
The Commission will accept a
certificate of compliance with the crib
and/or pacifier requirements based on
testing performed by an accredited third
party or governmental laboratory on or
after May 16, 2008 (90 days prior to
August 14, 2008, the date on which
CPSIA was enacted) and thus prior to
the Commission’s acceptance of the
laboratory’s accreditation if:
• The laboratory was ISO/IEC 17025
accredited by an ILAC–MRA member at
the time of the test;
• The accreditation scope in effect for
the laboratory at that time expressly
included testing to 16 CFR part 1508, or
part 1509, or part 1511, as applicable;
• The laboratory’s accreditation
application is accepted by the
Commission under the procedures of
this notice not later than December 26,
2008; and
• The laboratory’s accreditation and
inclusion of the crib and/or pacifier
requirements in its scope remains in
effect through the effective date for
mandatory third party testing and
manufacturer/private labeler
certification for cribs and pacifiers.
Testing performed by a firewalled
laboratory prior to Commission
acceptance of its accreditation cannot be
used as the basis for certification by a
manufacturer or private labeler with a
10 percent or greater ownership interest
in the laboratory pursuant to CPSA
section 14(a)(3)(B)(ii) of compliance
with the crib and/or pacifier regulations.
Dated: October 15, 2008.
Todd A. Stevenson,
Secretary, Consumer Product Safety
Commission.
[FR Doc. E8–25096 Filed 10–21–08; 8:45 am]
BILLING CODE 6355–01–P
DEPARTMENT OF EDUCATION
Submission for OMB Review;
Comment Request
Department of Education.
SUMMARY: The IC Clearance Official,
Regulatory Information Management
Services, Office of Management invites
comments on the submission for OMB
review as required by the Paperwork
Reduction Act of 1995.
AGENCY:
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62967
Interested persons are invited to
submit comments on or before
November 21, 2008.
ADDRESSES: Written comments should
be addressed to the Office of
Information and Regulatory Affairs,
Attention: Education Desk Officer,
Office of Management and Budget, 725
17th Street, NW., Room 10222,
Washington, DC 20503. Commenters are
encouraged to submit responses
electronically by e-mail to
oira_submission@omb.eop.gov or via fax
to (202) 395–6974. Commenters should
include the following subject line in
their response ‘‘Comment: [insert OMB
number], [insert abbreviated collection
name, e.g., ‘‘Upward Bound
Evaluation’’]. Persons submitting
comments electronically should not
submit paper copies.
SUPPLEMENTARY INFORMATION: Section
3506 of the Paperwork Reduction Act of
1995 (44 U.S.C. Chapter 35) requires
that the Office of Management and
Budget (OMB) provide interested
Federal agencies and the public an early
opportunity to comment on information
collection requests. OMB may amend or
waive the requirement for public
consultation to the extent that public
participation in the approval process
would defeat the purpose of the
information collection, violate State or
Federal law, or substantially interfere
with any agency’s ability to perform its
statutory obligations. The IC Clearance
Official, Regulatory Information
Management Services, Office of
Management, publishes that notice
containing proposed information
collection requests prior to submission
of these requests to OMB. Each
proposed information collection,
grouped by office, contains the
following: (1) Type of review requested,
e.g. new, revision, extension, existing or
reinstatement; (2) Title; (3) Summary of
the collection; (4) Description of the
need for, and proposed use of, the
information; (5) Respondents and
frequency of collection; and (6)
Reporting and/or Recordkeeping
burden. OMB invites public comment.
DATES:
Dated: October 16, 2008.
Sheila Carey,
Acting Director, Information Collection
Clearance Division, Regulatory Information
Management Services, Office of Management.
Office of Special Education and
Rehabilitative Services
Type of Review: Revision.
Title: IDEA Part B State Performance
Plan (SPP) and Annual Performance
Report (APR).
Frequency: Annually.
E:\FR\FM\22OCN1.SGM
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Agencies
[Federal Register Volume 73, Number 205 (Wednesday, October 22, 2008)]
[Notices]
[Pages 62965-62967]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E8-25096]
=======================================================================
-----------------------------------------------------------------------
CONSUMER PRODUCT SAFETY COMMISSION
Third Party Testing for Certain Children's Products; Notice of
Requirements for Accreditation of Third Party Conformity Assessment
Bodies To Assess Conformity With Part 1508, Part 1509, and/or Part 1511
of Title 16, Code of Federal Regulations
AGENCY: Consumer Product Safety Commission.
ACTION: Notice of Requirements for Accreditation of Third Party
Conformity Assessment Bodies To Assess Conformity With Part 1508, Part
1509, and/or Part 1511 of Title 16, Code of Federal Regulations.
-----------------------------------------------------------------------
Introduction: The Consumer Product Safety Act (``CPSA''), at
section 14(a)(3)(B)(ii) as added by section 102(a)(2) of the Consumer
Product Safety Improvement Act of 2008 (``CPSIA''), Public Law 110-314,
directs the U.S. Consumer Product Safety Commission (``CPSC'' or
``Commission'') to publish this notice of requirements for
accreditation of third party conformity assessment bodies (``third
party laboratories'') to test children's products for conformity with
the Commission's regulations for full-size baby cribs at 16 CFR part
1508, for non-full-size baby cribs at 16 CFR part 1509, and/or for
pacifiers at 16 CFR part 1511.1 2 Each manufacturer
(including the importer) or private labeler of cribs and/or pacifiers
subject to those regulations must have products manufactured more than
90 days after the Federal Register publication date of this notice
tested by a laboratory accredited to do so and must issue a certificate
of compliance with the applicable regulations based on that
testing.3 4
---------------------------------------------------------------------------
\1\ Section 102 of CPSIA also required the Commission to publish
requirements for accreditation of laboratories for testing to the
lead paint ban at 16 CFR part 1303. Those requirements were
published in the Federal Register on September 22, 2008. 73 FR
54564-6.
\2\ Children's products are those designed or intended for use
primarily by children 12 years old and younger.
\3\ Section 14(a)(2) of the CPSA as added by Sec. 102(a)(2) of
CPSIA requires that certification be based on testing of sufficient
samples of the product, or samples that are identical in all
material respects to the product.
\4\ Of course, irrespective of certification, the children's
product in question must comply with applicable CPSC requirements.
See, e.g., CPSA Sec. 14(h) as added by CPSIA Sec. 102(b).
---------------------------------------------------------------------------
The Commission is also recognizing limited circumstances in which
testing performed by a laboratory on or after May 16, 2008, 90 days
prior to the date of enactment of CPSIA (August 14, 2008), but prior to
Commission acceptance of the laboratory's preexisting accreditation,
provided that accreditation is accepted not later than December 26,
2008, may form the basis for the certificate of compliance with the
crib and/or pacifier regulations required of the manufacturer or
private labeler.
This notice provides the criteria and process for Commission
acceptance of accreditation of ``third party'' laboratories for testing
to the regulations for cribs and/or pacifiers (laboratories that are
not owned, managed, or controlled by a manufacturer or private labeler
of a children's product to be tested by the laboratory for
certification purposes), ``firewalled'' laboratories (those that are
owned, managed, or controlled by a manufacturer or private labeler of a
children's product to be tested by the laboratory for certification
purposes and that seek accreditation under the additional statutory
criteria for ``firewalled'' laboratories), and laboratories owned or
controlled in whole or in part by a government.
The requirements of this notice are effective upon its publication
in the Federal Register and are exempted by CPSIA from the notice and
comment rulemaking requirements of the Administrative Procedure Act, 5
U.S.C. 553.\5\
---------------------------------------------------------------------------
\5\ CPSA section 14(a)(3)(G) as added by section 102(a)(2) of
CPSIA exempts publication of this notice from the rulemaking
requirements of the Administrative Procedure Act, 5 U.S.C. 553, and
from the Regulatory Flexibility Act, 5 U.S.C. 601-612.
---------------------------------------------------------------------------
[[Page 62966]]
Baseline accreditation of each category of laboratory to the
International Organization for Standardization (``ISO'') Standard ISO/
IEC 17025:2005--General Requirements for the Competence of Testing and
Calibration Laboratories--is required. The accreditation must be by an
accreditation body that is a signatory to the International Laboratory
Accreditation Cooperation--Mutual Recognition Arrangement (``ILAC-
MRA'') and the scope of the accreditation must include testing for
compliance with the crib regulations of 16 CFR part 1508 and/or part
1509 and/or the pacifier regulations of part 1511.\6\ A laboratory
owned or controlled by a manufacturer or private labeler of products to
be tested by the laboratory is subject to additional requirements
intended to assure that the Commission is immediately and
confidentially notified of any attempt by the manufacturer, private
labeler or other interested party to hide or exert undue influence over
the laboratory's test results. A governmental laboratory may be
accredited subject to additional requirements concerning independence
of its relationship with the host government and freedom of
manufacturers in the host country to elect to use accredited non-
government laboratories for certification testing without suffering
disadvantage.
---------------------------------------------------------------------------
\6\ A description of the history and content of the ILAC-MRA
approach and of the requirements of the ISO 17025:2005 laboratory
accreditation standard is provided in the CPSC staff briefing
memorandum Third Party Conformity Assessment Body Accreditation
Requirements for Testing Compliance with 16 CFR Part 1508, Part
1509, and Part 1511 (Cribs and Pacifiers) as Required by the
Consumer Product Safety Improvement Act of 2008, October 2008,
available on the CPSC Web site at https://cpsc.gov/library/foia/
foia09/brief/tpacp.pdf.
---------------------------------------------------------------------------
The Commission has established an electronic accreditation
registration and listing system that can be accessed via its Web site.
Although the accreditation requirements in this notice for testing
to the crib and/or pacifier regulations are effective upon their
publication in the Federal Register, the Commission solicits comments
on the accreditation procedures as they apply to that testing and on
the accreditation approach in general, since the Commission must
publish additional testing laboratory accreditation procedures over the
coming months.
DATES: Effective Date: The requirements for accreditation of
laboratories for testing to the crib and/or pacifier regulations are
effective upon publication of this notice in the Federal Register, that
is October 22, 2008.
Request for Comments: Please provide comments in response to this
notice by November 21, 2008. Comments on this notice should be
captioned ``Laboratory Accreditation Process for Crib and Pacifier
Testing.'' Comments should be submitted to the Office of the Secretary
by e-mail at cpscos@cpsc.gov, or mailed or delivered, preferably in
five copies, to the Office of the Secretary, Consumer Product Safety
Commission, 4330 East West Highway, Bethesda, Maryland 20814. Comments
may also be filed by facsimile to (301) 504-0127.
FOR FURTHER INFORMATION CONTACT: Robert ``Jay'' Howell, Acting
Assistant Executive Director for Hazard Identification and Reduction,
U.S. Consumer Product Safety Commission, 4330 East West Highway,
Bethesda, Maryland 20814; e-mail rhowell@cpsc.gov.
I. Accreditation Requirements
A. Baseline Third Party Laboratory Accreditation Requirements
For a third party laboratory to be accredited to test children's
products for conformity with the Commission's crib and/or pacifier
regulations, it must be accredited by an ILAC-MRA signatory accrediting
body and the accreditation must be registered with, and accepted by,
the Commission. A listing of ILAC-MRA signatory accrediting bodies is
available on the Internet at https://ilac.org/membersbycategory.html.
The accreditation must be to ISO Standard ISO/IEC 17025:2005--General
Requirements for the Competence of Testing and Calibration Laboratories
and the scope of the accreditation must expressly include testing to
the regulations of 16 CFR part 1508, 1509, and/or 1511 as applicable to
the product(s) to be tested.\7\ A true copy of the accreditation and
scope documents demonstrating compliance with these requirements must
be registered with the Commission electronically. The additional
requirements for accreditation of firewalled and governmental
laboratories are described below in sections I.B and I.C.
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\7\ A laboratory may seek Commission acceptance of accreditation
to test only full-size cribs, only non-full-size cribs, or only
pacifiers, or some combination thereof. However, required
manufacturer certifications may only be based on testing by a
laboratory accredited to test the specific product in question.
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The Commission will maintain on its Web site an up-to-date listing
of laboratories whose accreditations it has accepted and the scope of
each accreditation. Subject to the limited provisions for acceptance of
``retrospective'' testing performed by other than firewalled
laboratories noted in Section III. below, once the Commission adds a
laboratory to that list, the laboratory may commence testing of
children's products to support certification by the manufacturer or
private labeler of compliance with the crib and/or pacifier
regulations, as applicable.
B. Additional Accreditation Requirements for Firewalled Laboratories
In addition to the baseline accreditation requirements in section
I.A, firewalled laboratories seeking accredited status must submit to
the Commission for review copies of their training documents showing
how employees are trained to notify the Commission immediately and
confidentially of any attempt by the manufacturer, private labeler or
other interested party to hide or exert undue influence over the
laboratory's test results. This additional requirement applies to any
laboratory in which a manufacturer or private labeler of a children's
product to be tested by the laboratory owns a ten percent or more
interest. While the Commission is not addressing common parentage of a
lab and a children's product manufacturer at this time, it will be
vigilant to see if this issue needs to be dealt with in the future.
The Commission must formally accept, by order, the accreditation
application of a laboratory before the laboratory can become an
accredited firewalled laboratory.
C. Additional Accreditation Requirements for Governmental Laboratories
In addition to the baseline accreditation requirements of section
I.A, CPSIA permits accreditation of a laboratory owned or controlled in
whole or in part by a government if:
To the extent practicable, manufacturers or private
labelers located in any nation are permitted to choose laboratories
that are not owned or controlled by the government of that nation;
The laboratory's testing results are not subject to undue
influence by any other person, including another governmental entity;
The laboratory is not accorded more favorable treatment
than other laboratories in the same nation who have been accredited;
The laboratory's testing results are accorded no greater
weight by other
[[Page 62967]]
governmental authorities than those of other accredited laboratories;
and
The laboratory does not exercise undue influence over
other governmental authorities on matters affecting its operations or
on decisions by other governmental authorities controlling distribution
of products based on outcomes of the laboratory's conformity
assessments.
The Commission will accept the accreditation of a governmental
laboratory if it meets the baseline accreditation requirements of
section I.A and meets the conditions stated here. To obtain this
assurance, CPSC staff will engage the governmental entities relevant to
the accreditation request.
II. How Does a Laboratory Apply for Acceptance of Its Accreditation?
The Commission has established an electronic accreditation
acceptance and registration system accessed via the Commission's
Internet site at https://www.cpsc.gov/businfo/labaccred.html. The
applicant provides basic identifying information concerning its
location, the type of accreditation it is seeking, and electronic
copies of its ILAC-MRA accreditation certificate and scope statement
and firewalled laboratory training document(s), if relevant. Commission
staff reviews that submission for accuracy and completeness. In the
case of baseline third party laboratory accreditation and accreditation
of governmental laboratories, when that review and any necessary
discussions with the applicant are satisfactorily completed, the
laboratory in question is added to the CPSC listing of accredited
laboratories at https://www.cpsc.gov/businfo/labaccred.html. In the case
of a firewalled laboratory seeking accredited status, when the review
is complete, the staff transmits its recommendation on accreditation to
the Commission for consideration.\8\ If the Commission accepts a staff
recommendation to accredit a firewalled laboratory, that laboratory
will then be added to the CPSC list of accredited laboratories. In each
case, the Commission will electronically notify the laboratory of
acceptance of its accreditation.
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\8\ A laboratory that may ultimately seek acceptance as a
firewalled laboratory could initially request acceptance as a third
party laboratory accredited for testing of children's products other
than those of its owners.
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Subject to the limited provisions for acceptance of
``retrospective'' testing performed by other than accredited firewalled
laboratories noted in Section III. below, once the Commission adds a
laboratory to the list, the laboratory may then commence testing of
children's products to support certification of compliance with the
crib and/or pacifier regulations, as applicable, by the manufacturer or
private labeler.
III. Limited Acceptance of Children's Product Certifications Based on
Third Party Laboratory Testing Prior to Commission Acceptance of
Accreditation
The Commission will accept a certificate of compliance with the
crib and/or pacifier requirements based on testing performed by an
accredited third party or governmental laboratory on or after May 16,
2008 (90 days prior to August 14, 2008, the date on which CPSIA was
enacted) and thus prior to the Commission's acceptance of the
laboratory's accreditation if:
The laboratory was ISO/IEC 17025 accredited by an ILAC-MRA
member at the time of the test;
The accreditation scope in effect for the laboratory at
that time expressly included testing to 16 CFR part 1508, or part 1509,
or part 1511, as applicable;
The laboratory's accreditation application is accepted by
the Commission under the procedures of this notice not later than
December 26, 2008; and
The laboratory's accreditation and inclusion of the crib
and/or pacifier requirements in its scope remains in effect through the
effective date for mandatory third party testing and manufacturer/
private labeler certification for cribs and pacifiers.
Testing performed by a firewalled laboratory prior to Commission
acceptance of its accreditation cannot be used as the basis for
certification by a manufacturer or private labeler with a 10 percent or
greater ownership interest in the laboratory pursuant to CPSA section
14(a)(3)(B)(ii) of compliance with the crib and/or pacifier
regulations.
Dated: October 15, 2008.
Todd A. Stevenson,
Secretary, Consumer Product Safety Commission.
[FR Doc. E8-25096 Filed 10-21-08; 8:45 am]
BILLING CODE 6355-01-P