National Voluntary Laboratory Accreditation Program; Operating Procedures, 78814-78815 [2011-32256]
Download as PDF
78814
Federal Register / Vol. 76, No. 244 / Tuesday, December 20, 2011 / Rules and Regulations
Cook, MN, Cook Muni, Takeoff Minimums
and Obstacle DP, Amdt 1
Ely, MN, Ely Muni, Takeoff Minimums and
Obstacle DP, Amdt 3
Aurora, MO, Jerry Sumners Sr Aurora Muni,
GPS RWY 36, Orig, CANCELLED
Aurora, MO, Jerry Sumners Sr Aurora Muni,
RNAV (GPS) RWY 18, Orig
Aurora, MO, Jerry Sumners Sr Aurora Muni,
RNAV (GPS) RWY 36, Orig
Branson West, MO, Branson West MuniEmerson Field, RNAV (GPS) RWY 3, Orig
Branson West, MO, Branson West MuniEmerson Field, RNAV (GPS) RWY 21, Orig
Farmington, MO, Farmington Rgnl, VOR/
DME–A, Orig-B
Jackson, MS, Hawkins Field, ILS OR LOC
RWY 16, Amdt 5A
West Yellowstone, MT, Yellowstone, Takeoff
Minimums and Obstacle DP, Amdt 2
West Yellowstone, MT, Yellowstone, TARGY
ONE Graphic DP
Hickory, NC, Hickory Rgnl, HICKORY
THREE Graphic DP
Northwood, ND, Northwood Muni-Vince
Field, Takeoff Minimums and Obstacle DP,
Orig
Zelienople, PA, Zelienople Muni, RNAV
(GPS) RWY 17, Orig-A
Hohenwald, TN, John A. Baker Fld, NDB
RWY 2, Orig-B
Hohenwald, TN, John A. Baker Fld, RNAV
(GPS) RWY 2, Amdt 1
Seymour, TX, Seymour Muni, Takeoff
Minimums and Obstacle DP, Orig
Norfolk, VA, Chesapeake Rgnl, Takeoff
Minimums and Obstacle DP, Amdt 3
La Crosse, WI, La Crosse Muni, ILS OR LOC
RWY 18, Amdt 20
Rescinded: On December 12, 2011 (76 FR
77112), the FAA published an Amendment
in Docket No. 30815, Amdt No. 3454 to Part
97 of the Federal Aviation Regulations under
section 97.33. The following four entries,
effective December 15, 2011, are hereby
rescinded in their entirety:
Rota Island-North Mariana Island, CQ, Rota
Intl, GPS RWY 9, Orig-C, CANCELLED
Rota Island-North Mariana Island, CQ, Rota
Intl, GPS RWY 27, Orig-C, CANCELLED
Rota Island-North Mariana Island, CQ, Rota
Intl, RNAV (GPS) RWY 9, Orig
Rota Island-North Mariana Island, CQ, Rota
Intl, RNAV (GPS) RWY 27, Orig
[FR Doc. 2011–32506 Filed 12–19–11; 8:45 am]
BILLING CODE 4910–13–P
DEPARTMENT OF COMMERCE
National Institute of Standards and
Technology
15 CFR Part 285
pmangrum on DSK3VPTVN1PROD with RULES
[Docket No 110125063–1687–02]
RIN 0693–AB61
National Voluntary Laboratory
Accreditation Program; Operating
Procedures
National Institute of Standards
and Technology (NIST), Commerce.
AGENCY:
VerDate Mar<15>2010
15:31 Dec 19, 2011
Jkt 226001
ACTION:
Description and Explanation of Change
Final rule.
The Director of the National
Institute of Standards and Technology
(NIST), United States Department of
Commerce, is issuing a final rule
amending the regulations pertaining to
the National Voluntary Laboratory
Accreditation Program (NVLAP).
Regulations concerning the
establishment of laboratory
accreditation programs (LAPs) within
NVLAP are being amended to clarify the
original intent of this section and to
improve the readability and
understanding of the agency’s
regulations.
SUMMARY:
This rule is effective on
December 20, 2011.
ADDRESSES: David F. Alderman, Acting
Chief, National Voluntary Laboratory
Accreditation Program, National
Institute of Standards and Technology,
100 Bureau Drive, Stop 2140,
Gaithersburg, MD 20899–2140.
FOR FURTHER INFORMATION CONTACT:
David F. Alderman, Acting Chief,
National Voluntary Laboratory
Accreditation Program, National
Institute of Standards and Technology,
100 Bureau Drive, Stop 2140,
Gaithersburg, MD 20899–2140;
telephone number: (301) 975–4019;
email address:
david.alderman@nist.gov; NVLAP Web
site: www.nist.gov/nvlap.
SUPPLEMENTARY INFORMATION:
DATES:
Background
Title 15 Part 285 of the Code of
Federal Regulations sets out procedures
and general requirements under which
the National Voluntary Laboratory
Accreditation Program (NVLAP)
operates as an unbiased third party to
accredit both testing and calibration
laboratories. NVLAP establishes
laboratory accreditation programs
(LAPs) in response to legislation or
requests from government agencies and
private sector entities.
The NVLAP procedures were first
published in the Federal Register on
February 25, 1976, and have been
revised several times. In 2001, major
revisions to the procedures were
published to ensure their consistency
with certain international standards and
guidance documents, and to reorganize
and simplify Part 285 for ease of use and
understanding. While the existing
regulations were accurate, the language
was complex and difficult to
understand; therefore, the procedures
were rewritten in plain English and
their subparts consolidated in order to
make the regulations more user friendly.
PO 00000
Frm 00010
Fmt 4700
Sfmt 4700
The purpose of this rule is to amend
section 285.4, Establishment of
laboratory accreditation programs
(LAPs) within NVLAP, so that it
conforms to the intent of the 2001
revisions to Part 285 of Title 15 of the
CFR and makes the regulations easier to
understand. NIST is amending the last
sentence in section 285.4 as follows:
change the third instance of the word
‘‘and’’ to ‘‘or,’’ and add the words ‘‘to
ensure open participation’’ after the
phrase ‘‘other means.’’
As a signatory to the International
Laboratory Accreditation Cooperation
(ILAC) Mutual Recognition
Arrangement (MRA), NVLAP complies
with the requirements of ISO/IEC 17011,
Conformity assessment—General
requirements for accreditation bodies
accrediting conformity assessment
bodies. The change will allow NVLAP
more flexibility in determining how to
best fulfill the requirements for
impartiality found in ISO/IEC 17011,
4.3.2, by assuring a balanced
representation of interested parties
when evaluating the need for a
requested LAP.
The original intent of the last sentence
of section 285.4 was to allow NVLAP
the flexibility to employ the most
appropriate means to ensure open
participation of stakeholders; however,
the use of the word ‘‘and’’ may be
misinterpreted to mean that a public
workshop is required for each and every
LAP request. There are numerous means
by which consultation with interested
parties may be accomplished exclusive
of a workshop, which include, but are
not limited to meeting with government
and individual industry stakeholders on
a frequent basis, attending consortia and
conferences at which regulators,
specifiers, and requesters are in
attendance, and soliciting public
comments via public notices, electronic
communications, and news articles.
Further, the use of the word ‘‘or’’ does
not preclude the use of both workshops
and other means to collect the necessary
information.
Summary of Comments
On March 29, 2011, the National
Institute of Standards and Technology
published a notice of proposed
rulemaking and request for comments in
the Federal Register (76 FR 17367)
pertaining to the proposed amendment
to section 285.4 of Part 285 of Title 15
of the CFR. The comment period closed
on April 28, 2011. No comments were
received and there is no other reason to
believe that any alteration to the
proposed rule is necessary; therefore,
E:\FR\FM\20DER1.SGM
20DER1
Federal Register / Vol. 76, No. 244 / Tuesday, December 20, 2011 / Rules and Regulations
NIST will implement the rulemaking as
proposed.
National Environmental Policy Act of
1969.
Classification
List of Subjects in 15 CFR Part 285
Executive Order 12866
Accreditation, Business and industry,
Calibration, Commerce, Conformity
assessment, Laboratories, Measurement
standards, Testing.
For the reasons set forth in the
preamble, title 15 of the Code of Federal
Regulations is amended as follows:
This rule is not a significant rule for
the purposes of Executive Order 12866.
Executive Order 12612
This rule does not contain policies
with Federalism implications sufficient
to warrant preparation of a Federalism
assessment under Executive Order
12612.
Regulatory Flexibility Act
The Chief Counsel for Regulation,
Department of Commerce, certified to
the Chief Counsel for Advocacy, Small
Business Administration, at the
proposed rule stage, under the
provisions of the Regulatory Flexibility
Act (5 U.S.C. 605(b)), that this rule will
not have a significant economic impact
on a substantial number of small entities
for the following reasons: (1) The
regulation is procedural and has no
impact on any entity unless that entity
chooses to participate, in which case,
the cost to the participant is the same
cost for any size participant; (2) access
to NVLAP’s accreditation system is not
conditional upon the size of a laboratory
or membership of any association or
group, nor are there undue financial
conditions to restrict participation; and
(3) the technical criteria, against which
individual laboratories are assessed, are
not changed by this rule. No comments
were received on this certification;
therefore no regulatory flexibility
analysis is required and none was
prepared.
pmangrum on DSK3VPTVN1PROD with RULES
Paperwork Reduction Act
This rule does not involve a new
collection of information subject to the
Paperwork Reduction Act (PRA). The
collection of information for NVLAP has
been approved by the Office of
Management and Budget (OMB) under
control number 0693–0003.
Notwithstanding any other provision of
the law, no person is required to
comply, nor shall any person be subject
to penalty for failure to comply with, a
collection of information, subject to the
requirements of the Paperwork
Reduction Act, unless that collection of
information displays a currently valid
OMB Control Number.
National Environmental Policy Act
This rule will not significantly affect
the quality of the human environment.
Therefore, an environmental assessment
or Environmental Impact Statement is
not required to be prepared under the
VerDate Mar<15>2010
15:31 Dec 19, 2011
Jkt 226001
PART 285—NATIONAL VOLUNTARY
LABORATORY ACCREDITATION
PROGRAM
1. The authority citation for 15 CFR
Part 285 continues to read as follows:
■
Authority: 15 U.S.C. 272 et seq.
2. Section 285.4 is amended by
revising the last sentence to read as
follows:
■
§ 285.4 Establishment of laboratory
accreditation programs (LAPs) within
NVLAP.
* * * For requests from private sector
entities and government agencies, the
Chief of NVLAP shall analyze each
request, and, after consultation with
interested parties through public
workshops or other means to ensure
open participation, shall establish the
requested LAP, if the Chief of NVLAP
determines there is need for the
requested LAP.
Dated: December 8, 2011.
Willie E. May,
Associate Director for Laboratory Programs.
[FR Doc. 2011–32256 Filed 12–19–11; 8:45 am]
BILLING CODE 3510–13–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2011–N–0003]
21 CFR Part 520
Oral Dosage Form New Animal Drugs;
Cyclosporine
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Final rule.
The Food and Drug
Administration (FDA) is amending the
animal drug regulations to reflect
approval of a new animal drug
application (NADA) filed by Novartis
Animal Health US, Inc. The NADA
provides for the veterinary prescription
use of cyclosporine oral solution, USP
(MODIFIED) for the control of feline
allergic dermatitis.
Frm 00011
Fmt 4700
This rule is effective December
20, 2011.
FOR FURTHER INFORMATION CONTACT:
Angela K.S. Clarke, Center for
Veterinary Medicine (HFV–112), Food
and Drug Administration, 7500 Standish
Pl., Rockville, MD 20855, (240) 276–
8318, email: angela.clarke@fda.hhs.gov.
SUPPLEMENTARY INFORMATION: Novartis
Animal Health US, Inc., 3200 Northline
Ave., suite 300, Greensboro, NC 27408,
filed NADA 141–329 that provides for
the use of ATOPICA for Cats
(cyclosporine oral solution, USP
(MODIFIED)) by veterinary prescription
for the control of feline allergic
dermatitis in cats at least 6 months of
age and weighing at least 3 pounds. The
NADA is approved as of August 8, 2011,
and 21 CFR 520.522 is amended to
reflect the approval.
A summary of safety and effectiveness
data and information submitted to
support approval of this application
may be seen in the Division of Dockets
Management (HFA–305), Food and Drug
Administration, 5630 Fishers Lane, rm.
1061, Rockville, MD 20852, between
9 a.m. and 4 p.m., Monday through
Friday.
The Agency has determined under 21
CFR 25.33 that this action is of a type
that does not individually or
cumulatively have a significant effect on
the human environment. Therefore,
neither an environmental assessment
nor an environmental impact statement
is required.
This rule does not meet the definition
of ‘‘rule’’ in 5 U.S.C. 804(3)(A) because
it is a rule of ‘‘particular applicability.’’
Therefore, it is not subject to the
congressional review requirements in 5
U.S.C. 801–808.
DATES:
List of Subjects in 21 CFR Part 520
Animal drugs.
Therefore, under the Federal Food,
Drug, and Cosmetic Act and under
authority delegated to the Commissioner
of Food and Drugs and redelegated to
the Center for Veterinary Medicine, 21
CFR part 520 is amended as follows:
PART 520—ORAL DOSAGE FORM
NEW ANIMAL DRUGS
1. The authority citation for 21 CFR
part 520 continues to read as follows:
■
SUMMARY:
PO 00000
78815
Sfmt 4700
Authority: 21 U.S.C. 360b.
2. In § 520.522, revise paragraphs (a)
and (d) to read as follows:
■
§ 520.522
Cyclosporine.
(a) Specifications—(1) Each
cyclosporine capsule, USP (MODIFIED)
contains 10, 25, 50, or 100 milligrams
(mg) cyclosporine.
E:\FR\FM\20DER1.SGM
20DER1
Agencies
[Federal Register Volume 76, Number 244 (Tuesday, December 20, 2011)]
[Rules and Regulations]
[Pages 78814-78815]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2011-32256]
=======================================================================
-----------------------------------------------------------------------
DEPARTMENT OF COMMERCE
National Institute of Standards and Technology
15 CFR Part 285
[Docket No 110125063-1687-02]
RIN 0693-AB61
National Voluntary Laboratory Accreditation Program; Operating
Procedures
AGENCY: National Institute of Standards and Technology (NIST),
Commerce.
ACTION: Final rule.
-----------------------------------------------------------------------
SUMMARY: The Director of the National Institute of Standards and
Technology (NIST), United States Department of Commerce, is issuing a
final rule amending the regulations pertaining to the National
Voluntary Laboratory Accreditation Program (NVLAP). Regulations
concerning the establishment of laboratory accreditation programs
(LAPs) within NVLAP are being amended to clarify the original intent of
this section and to improve the readability and understanding of the
agency's regulations.
DATES: This rule is effective on December 20, 2011.
ADDRESSES: David F. Alderman, Acting Chief, National Voluntary
Laboratory Accreditation Program, National Institute of Standards and
Technology, 100 Bureau Drive, Stop 2140, Gaithersburg, MD 20899-2140.
FOR FURTHER INFORMATION CONTACT: David F. Alderman, Acting Chief,
National Voluntary Laboratory Accreditation Program, National Institute
of Standards and Technology, 100 Bureau Drive, Stop 2140, Gaithersburg,
MD 20899-2140; telephone number: (301) 975-4019; email address:
david.alderman@nist.gov; NVLAP Web site: www.nist.gov/nvlap.
SUPPLEMENTARY INFORMATION:
Background
Title 15 Part 285 of the Code of Federal Regulations sets out
procedures and general requirements under which the National Voluntary
Laboratory Accreditation Program (NVLAP) operates as an unbiased third
party to accredit both testing and calibration laboratories. NVLAP
establishes laboratory accreditation programs (LAPs) in response to
legislation or requests from government agencies and private sector
entities.
The NVLAP procedures were first published in the Federal Register
on February 25, 1976, and have been revised several times. In 2001,
major revisions to the procedures were published to ensure their
consistency with certain international standards and guidance
documents, and to reorganize and simplify Part 285 for ease of use and
understanding. While the existing regulations were accurate, the
language was complex and difficult to understand; therefore, the
procedures were rewritten in plain English and their subparts
consolidated in order to make the regulations more user friendly.
Description and Explanation of Change
The purpose of this rule is to amend section 285.4, Establishment
of laboratory accreditation programs (LAPs) within NVLAP, so that it
conforms to the intent of the 2001 revisions to Part 285 of Title 15 of
the CFR and makes the regulations easier to understand. NIST is
amending the last sentence in section 285.4 as follows: change the
third instance of the word ``and'' to ``or,'' and add the words ``to
ensure open participation'' after the phrase ``other means.''
As a signatory to the International Laboratory Accreditation
Cooperation (ILAC) Mutual Recognition Arrangement (MRA), NVLAP complies
with the requirements of ISO/IEC 17011, Conformity assessment--General
requirements for accreditation bodies accrediting conformity assessment
bodies. The change will allow NVLAP more flexibility in determining how
to best fulfill the requirements for impartiality found in ISO/IEC
17011, 4.3.2, by assuring a balanced representation of interested
parties when evaluating the need for a requested LAP.
The original intent of the last sentence of section 285.4 was to
allow NVLAP the flexibility to employ the most appropriate means to
ensure open participation of stakeholders; however, the use of the word
``and'' may be misinterpreted to mean that a public workshop is
required for each and every LAP request. There are numerous means by
which consultation with interested parties may be accomplished
exclusive of a workshop, which include, but are not limited to meeting
with government and individual industry stakeholders on a frequent
basis, attending consortia and conferences at which regulators,
specifiers, and requesters are in attendance, and soliciting public
comments via public notices, electronic communications, and news
articles. Further, the use of the word ``or'' does not preclude the use
of both workshops and other means to collect the necessary information.
Summary of Comments
On March 29, 2011, the National Institute of Standards and
Technology published a notice of proposed rulemaking and request for
comments in the Federal Register (76 FR 17367) pertaining to the
proposed amendment to section 285.4 of Part 285 of Title 15 of the CFR.
The comment period closed on April 28, 2011. No comments were received
and there is no other reason to believe that any alteration to the
proposed rule is necessary; therefore,
[[Page 78815]]
NIST will implement the rulemaking as proposed.
Classification
Executive Order 12866
This rule is not a significant rule for the purposes of Executive
Order 12866.
Executive Order 12612
This rule does not contain policies with Federalism implications
sufficient to warrant preparation of a Federalism assessment under
Executive Order 12612.
Regulatory Flexibility Act
The Chief Counsel for Regulation, Department of Commerce, certified
to the Chief Counsel for Advocacy, Small Business Administration, at
the proposed rule stage, under the provisions of the Regulatory
Flexibility Act (5 U.S.C. 605(b)), that this rule will not have a
significant economic impact on a substantial number of small entities
for the following reasons: (1) The regulation is procedural and has no
impact on any entity unless that entity chooses to participate, in
which case, the cost to the participant is the same cost for any size
participant; (2) access to NVLAP's accreditation system is not
conditional upon the size of a laboratory or membership of any
association or group, nor are there undue financial conditions to
restrict participation; and (3) the technical criteria, against which
individual laboratories are assessed, are not changed by this rule. No
comments were received on this certification; therefore no regulatory
flexibility analysis is required and none was prepared.
Paperwork Reduction Act
This rule does not involve a new collection of information subject
to the Paperwork Reduction Act (PRA). The collection of information for
NVLAP has been approved by the Office of Management and Budget (OMB)
under control number 0693-0003. Notwithstanding any other provision of
the law, no person is required to comply, nor shall any person be
subject to penalty for failure to comply with, a collection of
information, subject to the requirements of the Paperwork Reduction
Act, unless that collection of information displays a currently valid
OMB Control Number.
National Environmental Policy Act
This rule will not significantly affect the quality of the human
environment. Therefore, an environmental assessment or Environmental
Impact Statement is not required to be prepared under the National
Environmental Policy Act of 1969.
List of Subjects in 15 CFR Part 285
Accreditation, Business and industry, Calibration, Commerce,
Conformity assessment, Laboratories, Measurement standards, Testing.
For the reasons set forth in the preamble, title 15 of the Code of
Federal Regulations is amended as follows:
PART 285--NATIONAL VOLUNTARY LABORATORY ACCREDITATION PROGRAM
0
1. The authority citation for 15 CFR Part 285 continues to read as
follows:
Authority: 15 U.S.C. 272 et seq.
0
2. Section 285.4 is amended by revising the last sentence to read as
follows:
Sec. 285.4 Establishment of laboratory accreditation programs (LAPs)
within NVLAP.
* * * For requests from private sector entities and government
agencies, the Chief of NVLAP shall analyze each request, and, after
consultation with interested parties through public workshops or other
means to ensure open participation, shall establish the requested LAP,
if the Chief of NVLAP determines there is need for the requested LAP.
Dated: December 8, 2011.
Willie E. May,
Associate Director for Laboratory Programs.
[FR Doc. 2011-32256 Filed 12-19-11; 8:45 am]
BILLING CODE 3510-13-P