Oregon Chapter 438
Chapter 438 — Clinical and Environmental LaboratoriesDownload Full 2005 Oregon Revised Statutes (coming soon!)
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Chapter 438 —
Clinical and Environmental Laboratories
2007 EDITION
CLINICAL AND ENVIRONMENTAL LABORATORIES
PUBLIC HEALTH AND SAFETY
CLINICAL LABORATORIES
(Generally)
438.010 Definitions
for ORS 438.010 to 438.510
438.030 Policy
438.040 Laboratory
license; out-of-state laboratory permit; qualifications of director
438.050 Application;
exceptions
438.055 Exemption
438.060 Permit
for health screen testing; exception
438.070 Personnel;
rules
(Clinical Laboratory License)
438.110 Standards
for issuance and renewal of laboratory license
438.120 Standards
for licensing specialties; exceptions
438.130 License
application; fees; expiration and renewal
438.140 License
content; display; nontransferability; voidability; special permit when director
changes
438.150 Temporary
permit; fees; health screen testing permit; conditions and limitations; rules
438.160 Refusal
to issue or renew license; suspension or revocation of license or permit
(Clinical Laboratory Director)
438.210 Qualifications
of laboratory director
438.220 Special
qualifications for laboratory director at chiropractic college
(Inspection and Evaluation)
438.310 Inspection
of laboratory premises; owner to submit reports and findings on communicable
disease; information confidential
438.320 Laboratory
evaluation system; rules; quality control systems
(Miscellaneous)
438.420 Communicable
disease reports to be from licensed laboratory
438.430 Examination,
specimens; reports and results
438.435 Testing
for substance of abuse; rules; fees
438.440 Disposition
of fees
438.450 Rules
438.510 Prohibited
acts
ENVIRONMENTAL LABORATORIES
438.605 Definitions
for ORS 438.605 to 438.620, 448.280 and 448.285
438.610 Standards
for accreditation; rules
438.615 Environmental
laboratory accreditation program; rules
438.620 Accreditation
fees; disposition of fees
PENALTIES
438.990 Penalties
CLINICAL LABORATORIES
(Generally)
438.010
Definitions for ORS 438.010 to 438.510. As used in ORS 438.010 to 438.510, unless the context requires otherwise:
(1) “Clinical laboratory” or “laboratory”
means a facility where the microbiological, serological, chemical,
hematological, immunohematological, immunological, toxicological,
cytogenetical, exfoliative cytological, histological, pathological or other examinations
are performed on materials derived from the human body, for the purpose of
diagnosis, prevention of disease or treatment of patients by physicians,
dentists and other persons who are authorized by license to diagnose or treat
humans.
(2) “Clinical laboratory specialty” or “laboratory
specialty” means the examination of materials derived from the human body for
the purpose of diagnosis and treatment of patients or assessment of health,
employing one of the following sciences: Serology, microbiology, chemistry,
hematology, immunohematology, immunology, toxicology, cytogenetics, exfoliative
cytology, histology or pathology.
(3) “Clinician” means a nurse practitioner
licensed and certified by the Oregon State Board of Nursing, or a physician
assistant licensed by the Oregon Medical Board.
(4) “Custody chain” means the handling of
specimens in a way that supports legal testimony to prove that the sample
integrity and identification of the sample have not been violated, as well as
the documentation describing those procedures from specimen collection to the
final report.
(5) “Dentist” means a person licensed to
practice dentistry by the Oregon Board of Dentistry.
(6) “Department” means the Department of
Human Services.
(7) “Director of clinical laboratory” or “director”
means the person who plans, organizes, directs and participates in any or all
of the technical operations of a clinical laboratory, including but not limited
to reviewing laboratory procedures and their results, training and supervising
laboratory personnel, and evaluating the technical competency of such
personnel.
(8) “Health screen testing” means tests
performed for the purpose of identifying health risks, providing health
information and referring the person being tested to medical care.
(9) “High complexity laboratory” means a
facility that performs testing classified as highly complex in the specialties
of microbiology, chemistry, hematology, diagnostic immunology,
immunohematology, clinical cytogenetics, cytology, histopathology, oral
pathology, pathology, radiobioassay and histocompatibility and that may also
perform moderate complexity tests and waived tests.
(10) “High complexity test” means a
procedure performed on materials derived from the human body that meet the
criteria for this category of testing in the specialties of microbiology,
chemistry, hematology, immunohematology, diagnostic immunology, clinical
cytogenetics, cytology, histopathology, oral pathology, pathology,
radiobioassay and histocompatibility as established by the department.
(11) “Laboratory evaluation system” means
a system of testing clinical laboratory methods, procedures and proficiency by
periodic performance and reporting on test specimens submitted for examination.
(12) “Moderate complexity laboratory”
means a facility that performs testing classified as moderately complex in the
specialties of microbiology, hematology, chemistry, immunohematology or
diagnostic immunology and may also perform any waived test.
(13) “Moderate complexity test” means a
procedure performed on materials derived from the human body that meet the
criteria for this category of testing in the specialties of microbiology,
hematology, chemistry, immunohematology or diagnostic immunology as established
by the department.
(14) “Operator of a substances of abuse
on-site screening facility” or “operator” means the person who plans,
organizes, directs and participates in any or all of the technical and
administrative operations of a substances of abuse on-site screening facility.
(15) “Owner of a clinical laboratory”
means the person who owns the clinical laboratory, or a county or municipality
operating a clinical laboratory or the owner of any institution operating a
clinical laboratory.
(16) “Physician” means a person licensed
to practice medicine by the Oregon Medical Board.
(17) “Physician performed microscopy
procedure” means a test personally performed by a physician or other clinician
during a patient’s visit on a specimen obtained during the examination of the
patient.
(18) “Physician performed microscopy
procedures” means a limited group of tests that are performed only by a
physician or clinician.
(19) “Specimen” means materials derived
from a human being or body.
(20) “Substances of abuse” means ethanol
and controlled substances, except those used as allowed by law and as defined
in ORS chapter 475 or as used in ORS 689.005.
(21) “Substances of abuse on-site
screening facility” or “on-site facility” means a location where on-site tests
are performed on specimens for the purpose of screening for the detection of
substances of abuse.
(22) “Substances of abuse on-site
screening test” or “on-site test” means a substances of abuse test that is
easily portable and can meet the requirements of the federal Food and Drug Administration
for commercial distribution or an alcohol screening test that meets the
requirements of the conforming products list found in the United States
Department of Transportation National Highway Traffic Safety Administration
Docket No. 94-004 and meets the standards of the United States Department of
Transportation Alcohol Testing Procedure, 49 C.F.R. part 40, in effect on
October 23, 1999.
(23) “Waived test” means a procedure
performed on materials derived from the human body that meet the criteria for
this category of testing as established by the department. [1969 c.685 §2; 1989
c.776 §1; 1993 c.109 §3; 1997 c.355 §1; 1999 c.739 §1; 2001 c.104 §168; 2001
c.900 §255]
438.030
Policy. It shall be the
declarative purpose of ORS 438.010 to 438.510 to ensure the quality of medical
laboratory work in order to protect the health and welfare of the people of the
State of
438.040
Laboratory license; out-of-state laboratory permit; qualifications of director. It is unlawful:
(1) For any owner or director of a
clinical laboratory to operate or maintain a clinical laboratory without a
license issued under ORS 438.110 or without a temporary permit issued under ORS
438.150 or to perform or permit the performance of any laboratory specialty for
which the laboratory is not licensed except as specified under ORS 438.050,
unless the laboratory has been issued a valid certificate from the federal
government under the Clinical Laboratory Improvement Amendments of 1988 (P.L.
100-578, 42 U.S.C. 201 and 263a).
(2) For an out-of-state laboratory to
perform health screen testing in
(3) For any person to serve in the
capacity of director of a clinical laboratory without being qualified as a
clinical laboratory director under ORS 438.210. [1969 c.685 §3; 1999 c.341 §1;
2005 c.22 §298]
438.050
Application; exceptions. (1)
ORS 438.010 to 438.510 apply to all clinical laboratories and laboratory
personnel within the State of
(a) Clinical laboratories operated by the
United States Government.
(b) Clinical laboratories operated and
maintained purely for research or teaching purposes, and that involve no
patient or public health services.
(2) Nothing in ORS 438.010 to 438.510 is
intended to confer on any licensed practitioner of the healing arts any
authority the practitioner would not otherwise possess under the license. [1969
c.685 §§4,20; 1973 c.829 §54; 1979 c.193 §1; 1993 c.109 §4; 2001 c.104 §170]
438.055
Exemption. Clinical
laboratories operated by physicians or clinicians that conduct only waived
tests and physician performed microscopy procedures used exclusively for the
diagnosis and treatment of their patients shall not be subject to regulation
that is more strict than regulation imposed under the Clinical Laboratory
Improvement Amendments of 1988 (P.L. 100-578; 42 U.S.C. 201 and 263a). [1993
c.109 §12; 1999 c.341 §2]
438.060
Permit for health screen testing; exception. Notwithstanding ORS 438.050, any person performing health screen
testing must obtain a permit under ORS 438.150 (5). However, an employer
providing health screen testing to employees of the employer is exempt from the
applications of ORS 438.010, 438.130, 438.150 and this section if such employer
contracts for the testing through a licensed physician, a clinical laboratory
or a hospital, which is a permittee of the Department of Human Services as
provided in this section. [1989 c.776 §3]
438.070
Personnel; rules. The
Department of Human Services shall establish by rule the qualifications and
responsibilities of technical and clinical consultants, general and technical
supervisors and testing personnel. A person is qualified to act as a technical
or clinical consultant, a general or technical supervisor, or a testing person
in a clinical laboratory if the person meets the requirements established by
the department. Rules adopted under this section shall not be more stringent than
comparable rules adopted under the Clinical Laboratory Improvement Amendments
of 1988 (P.L. 100-578; 42 U.S.C. 201 and 263a). [1993 c.109 §2]
(Clinical
Laboratory License)
438.110
Standards for issuance and renewal of laboratory license. (1) The Department of Human Services shall
establish four levels of laboratory licenses as follows:
(a) A high complexity laboratory license;
(b) A moderate complexity laboratory
license;
(c) A physician performed microscopy
laboratory license; and
(d) A waived laboratory license.
(2) The department shall issue and renew
licenses required under ORS 438.040 for any or all clinical laboratory
specialties to the owners of clinical laboratories who demonstrate to the
satisfaction of the department that:
(a) The clinical laboratory is in
compliance with ORS 438.010 to 438.510 and the rules of the department adopted
under ORS 438.450;
(b) The laboratory is adequately equipped
to perform proficiently within the scope of its license;
(c) The clinical laboratory has facilities
for retaining and does retain complete laboratory records for an appropriate
length of time as the department by rule may require; and
(d) The clinical laboratory meets the
standards of the department for safety, sanitary conditions, plumbing, ventilation,
handling of specimens, maintenance of equipment and requirements of general
hygiene to insure protection of the public health. [1969 c.685 §5; 1971 c.650 §18;
1993 c.109 §5; 1999 c.341 §3; 2001 c.104 §171]
438.120
Standards for licensing specialties; exceptions. (1) In determining the specialties that are
authorized to be performed in a clinical laboratory, the Department of Human
Services shall consider laboratory personnel, with particular emphasis on the
qualifications of the director, laboratory equipment and any other relevant
factors affecting the ability of the laboratory to perform different laboratory
specialties.
(2) No laboratory shall be licensed to
perform examinations in the fields of surgical pathology, autopsy pathology,
exfoliative cytology, or immunohematology, except as the Department of Human
Services may establish exemptions from the requirements of this subsection in
the field of immunohematology, unless its director is a physician or dentist
specifically qualified in these fields.
(3) The list of waived tests, physician
performed microscopy procedures and moderate and high complexity tests shall be
established by the department. [1969 c.685 §6; 1993 c.109 §6; 1999 c.341 §4]
438.130
License application; fees; expiration and renewal. (1) The application for a license for a
clinical laboratory shall be made on forms provided by the Department of Human
Services and shall be executed by the owner or one of the owners or by an
officer of the firm or corporation owning the clinical laboratory, or in the
case of a county or municipality, by the public official responsible for
operation of the laboratory, or in the case of an institution, by the
administrator of the institution. The application shall contain the names of
the owner, the director or directors of the clinical laboratory, the location
and physical description of the clinical laboratory, the laboratory specialties
for which a license is requested and such other information as the department
may require.
(2)(a) The application shall be
accompanied by an annual or biennial license fee to be established by the
department. The fee shall be based on test volume, test complexity, the number
of specialties performed and private laboratory accreditation. For each level
of laboratory testing, the fee shall be not more than 100 percent of the
corresponding fee charged by the federal laboratory certification program known
as the Clinical Laboratory Improvement Amendments of 1988 (P.L. 100-578, 42
U.S.C. 201 and 263a) in effect on July 1, 1999. The fee for substance of abuse
screening laboratories not certified under the Clinical Laboratory Improvement
Amendments of 1988 shall be comparable to the clinical laboratory fee
established under this section.
(b) The department may establish prorated
fees for licenses issued for a year or less and when there is a change in the
laboratory’s owner, director or address. A prorated license fee shall be issued
to a laboratory accredited by an organization recognized by the department.
(3) Unless sooner voided, suspended or
revoked, all licenses issued under this section expire on June 30 of the
one-year or two-year cycle following the date of issuance or on such date as
may be specified by department rule. Licenses issued under this section shall be
renewable in the manner prescribed by the department.
(4) Subject to prior approval of the
Oregon Department of Administrative Services and a report to the Emergency
Board prior to adopting the fees and charges, the fees and charges established
under this section shall not exceed the cost of administering the regulatory
program of the Department of Human Services pertaining to the purpose for which
the fee or charge is established, as authorized by the Legislative Assembly
within the department’s budget, as the budget may be modified by the Emergency
Board. [1969 c.685 §7; 1977 c.284 §3; 1979 c.696 §2; 1989 c.776 §5; 1991 c.703 §6;
1993 c.109 §7; 1999 c.341 §§5,6; 2007 c.768 §4]
438.140
License content; display; nontransferability; voidability; special permit when
director changes. (1) A
license issued to the owner of a clinical laboratory shall show on its face the
names of the owners and directors, the location of the laboratory and the
clinical laboratory specialties authorized under the license. The license shall
be displayed at all times in a prominent place in the laboratory.
(2) A license issued to the owner of a
clinical laboratory is not transferable. The license of the laboratory is
voided 30 days after a change in its director if it has only one director or if
all directors change or a change in the ownership or in the location of the
laboratory. In case of death of a director, immediate notification to the
Director of Human Services or a designee who shall be empowered to issue a
special temporary permit of 30 days’ duration issued to a designated substitute
director is required. If a license is voided or a special temporary permit is
issued under this section, a new license application, accompanied by the
nonrefundable license fee prescribed in ORS 438.130, shall be filed with the
Department of Human Services. [1969 c.685 §8]
438.150
Temporary permit; fees; health screen testing permit; conditions and
limitations; rules. (1) In
addition to the license of a clinical laboratory required by ORS 438.040, the
Department of Human Services may issue a temporary permit valid for a period,
to be determined by the department, from the date of issuance in any or all
clinical laboratory specialties upon payment of the respective required fees as
described in ORS 438.130 (2).
(2) In issuing the temporary permit, the
department may require that:
(a) Plans for compliance with applicable
laws and rules be submitted with the application for the temporary permit;
(b) During the period in which the
temporary permit is in effect periodic reports be submitted on the progress of
the plans for compliance; and
(c) Special temporary provisions specified
by the department upon application of the temporary permit be maintained for
the protection of the public.
(3) If at any time the department
determines that the clinical laboratory can no longer operate in a manner that
protects the public health and safety or that the requirements imposed under
subsection (2) of this section are not being maintained, the department shall
cancel the temporary permit.
(4) One renewal of the temporary permit
may be granted if deemed to be in the best interest of public health by the
department. The fee for renewal is the respective required fee as described in
ORS 438.130 (2).
(5) The department may issue permits for
health screen testing.
(6) The department by rule shall specify:
(a) Appropriate quality assurance
procedures;
(b) Personnel qualifications;
(c) Standards for counseling and referral
of persons being tested;
(d) Tests a health testing service may
conduct;
(e) The procedure for applying for a
permit; and
(f) The procedure for reporting to the
department the location of all health screening facilities.
(7) The department by rule may specify the
maximum length of time a health screen testing service may remain in one
location. [1969 c.685 §9; 1989 c.776 §2; 2007 c.71 §122]
438.160
Refusal to issue or renew license; suspension or revocation of license or
permit. Subject to ORS
chapter 183, the Department of Human Services may refuse to issue or renew the
license, or may suspend or revoke the license or health screen testing permit,
of a clinical laboratory if it finds that the owner or director has:
(1) Intentionally made false statements on
an application for a clinical laboratory license or any other documents
required by the department, or made any misrepresentation in seeking to obtain
or retain a license.
(2) Demonstrated incompetence as defined
pursuant to regulations promulgated after public hearing.
(3) Intentionally falsified any report.
(4) Referred a specimen for examination to
a nonlicensed or an unlicensed clinical laboratory in this state unless the
laboratory is exempt from the application of ORS 438.010 to 438.510.
(5) Misrepresented the scope of laboratory
service offered by the clinical laboratory or the clinical laboratory
specialties authorized by the license.
(6) Rendered a report on clinical
laboratory work actually performed in another clinical laboratory without
designating the name and address of the clinical laboratory in which the test
was performed.
(7) Knowingly had professional connection
with or permitted the use of the name of the licensed clinical laboratory or
its director by a clinical laboratory that is required to but has not obtained
a license.
(8) Failed to perform or cause to be
performed within the time specified analysis of test samples as authorized by
ORS 438.320, or failed to report on the results of such analysis within the
specified time.
(9) Failed to permit within a reasonable
time the entry or inspection authorized by ORS 438.310.
(10) Failed to continue to meet
requirements of ORS 438.110 and 438.120.
(11) Violated any provision of ORS 438.010
to 438.510. [1969 c.685 §10; 1993 c.109 §13; 1999 c.341 §8; 2001 c.104 §172]
(Clinical
Laboratory Director)
438.210
Qualifications of laboratory director. A person is qualified to act as a laboratory director of a clinical
laboratory if:
(1) The person is a pathologist certified
in clinical or anatomical pathology by a national organization or organizations
recognized by the Department of Human Services, or is a physician who possesses
qualifications equivalent to those required for such certification;
(2) The person is a physician who
possesses special qualifications that enable the person to perform as a
laboratory director, or is directing a laboratory on January 1, 1970;
(3) The person has an earned degree of
Doctor of Science or Doctor of Philosophy, or an acceptable degree as
determined by the department, from an accredited college or university, with a
major in the chemical, physical, or biological sciences and possesses special
qualifications as described in the administrative rules of the department that
enable the person to perform as a laboratory director;
(4) The person is a member of a group of
five or more physicians who operate on November 4, 1993, a laboratory
performing work only on their patients and is the member designated by the
group to be the director; or
(5) The person was responsible for the
direction of a clinical laboratory for at least 12 months within the five years
preceding January 1, 1970, and has had at least two years of pertinent clinical
laboratory experience, as determined by the department. [1969 c.685 §12; 1993
c.109 §8; 2007 c.71 §123]
438.220
Special qualifications for laboratory director at chiropractic college. Notwithstanding ORS 438.210, a person is
qualified to act as the laboratory director of the clinical laboratory at any
accredited chiropractic college in this state for the benefit of chiropractic
patients if that person is a chiropractic physician licensed by the State Board
of Chiropractic Examiners, and possesses special qualifications, as determined
by the State Board of Chiropractic Examiners, that enable that person to
perform as a laboratory director. [1979 c.303 §2]
(Inspection
and Evaluation)
438.310
Inspection of laboratory premises; owner to submit reports and findings on
communicable disease; information confidential. (1) The Department of Human Services or its
authorized representative may:
(a) At reasonable times enter the premises
of a clinical laboratory licensed or subject to being licensed under ORS
438.010 to 438.510 to inspect the facilities, methods, procedures, materials,
staff, equipment, laboratory results and records of the clinical laboratory.
(b) Require the owner or director to
submit reports on the operations and procedures of the laboratory.
(c) Require the owner or director to
submit initial laboratory findings indicative of communicable disease as
defined by law or by rule. Each report shall include the name of the person
from whom the specimen was obtained, if the name was reported to the
laboratory, and the name and address of the physician for whom such examination
or test was made. Such reports shall not be construed as constituting a
diagnosis nor shall any laboratory making such report be held liable under the
laws of this state for having violated a trust or confidential relationship.
(2) The Director of Human Services or a
designee, the department, or any employee thereof, shall not disclose
information contained in reports on communicable diseases submitted to the
department under subsection (1) of this section except as such information is
made available to employees of the department and to local health officers for
purposes of administering the public health laws of this state. However,
information contained in such reports may be used in compiling statistical and
other data in which persons are not identified by name or otherwise.
(3) The department shall by rule set
standards for the recognition of private laboratory accrediting organizations
whose standards meet or exceed federal standards. A laboratory that is
accredited by a private laboratory accrediting organization recognized by the
department under this section may submit proof of such accreditation to the
department. Upon receipt of such proof, the department shall issue a license
pursuant to ORS 438.130. [1969 c.685 §13; 1993 c.109 §9; 2001 c.104 §173]
438.320
Laboratory evaluation system; rules; quality control systems. (1) The Department of Human Services shall
institute a laboratory evaluation system, as defined in ORS 438.010, and shall
make such rules as are necessary to insure quality control of laboratory work.
(2) As part of this system, the department
may require each laboratory to:
(a) Participate in on-site inspection and
testing;
(b) Analyze test samples submitted by the
department prior to, during or subsequent to the inspection; and
(c) Contract with, at the laboratory’s own
expense, a department-approved source of test samples for such test samples to
be submitted periodically to the laboratory and to be returned to that source
for grading after testing. The test results shall be made available to the department.
(3) The procedures under subsection (2) of
this section shall be referred to as external quality control. The samples are
to be tested by regularly assigned personnel using routine methods. The test
samples shall be confined to the specialty of the laboratory as indicated on
the license. A specified time shall be allowed for such testing and reporting
of the results and shall be the time required under conditions of normal
operation.
(4) In addition to external quality
control, each clinical laboratory shall establish an internal laboratory
quality control system pursuant to rules of the department including but not
necessarily limited to the testing of reference or control sera and other
biological samples, verifying concurrent calibration standards and control
charts recordings, and reporting on its control system as required by the
department. [1969 c.685 §14; 1983 c.740 §154; 1993 c.109 §10]
438.410 [Formerly 433.310; repealed by 1971 c.650 §51]
(Miscellaneous)
438.420
Communicable disease reports to be from licensed laboratory. When the control or release of a case
contact or carrier of a communicable disease is dependent on laboratory
findings, the health officer may require such findings to be obtained by a
clinical laboratory licensed by the Department of Human Services. [Formerly
433.325]
438.430
Examination, specimens; reports and results. (1) Except as otherwise provided in ORS 438.010 to 438.510, a clinical
laboratory shall examine specimens only at the request of a physician, dentist,
or other person authorized by law to use the findings of laboratory
examinations.
(2) A person may not report the result of
any test, examination, or analysis of a specimen submitted for evidence of
human disease except to:
(a) The patient; and
(b) A physician, dentist, their agents, or
other person authorized by law to employ the results thereof in the conduct of
a practice or in the fulfillment of official duties.
(3) Not sooner than seven days after
receiving a request from a patient for the results of any test, examination or
analysis of a specimen submitted by the patient, a clinical laboratory shall
provide the results in writing to the patient. [1969 c.685 §21; 2001 c.104 §174;
2003 c.376 §1]
438.435
Testing for substance of abuse; rules; fees. (1) In addition to duties which a clinical laboratory may perform
under ORS 438.010 to 438.510, a laboratory is authorized to perform appropriate
tests, examinations or analyses on materials derived from the human body for
the purpose of detecting substances of abuse in the body. All laboratories
performing the tests, examinations or analyses must be licensed under the
provisions of ORS 438.010 to 438.510 and must employ qualified technical
personnel to perform the tests, examinations and analyses.
(2) In order to perform such tests,
examinations or analyses, the laboratory may examine specimens submitted by
persons other than those described in ORS 438.430 (1) and shall report the
result of any test, examination or analysis to the person who submitted the
specimen. When the substance of abuse test is for nonmedical employment or
pre-employment purposes, and a written request is provided, the test result
shall be reported to the person from whom the specimen was originally obtained.
(3) When the specimen of a person tested
for substances of abuse is submitted to the laboratory and the test result is
positive, the laboratory shall perform a confirming test which has been
designated by rule of the Department of Human Services as the best available
technology for use to determine whether or not the substance of abuse
identified by the first test is present in the specimen prior to reporting the
test results.
(4) The department by rule shall set
standards for special category laboratories that engage only in the initial
testing for substances of abuse in the body, including registration procedures
for such laboratories and personnel.
(5) The operator of a substances of abuse
on-site screening facility may use substances of abuse on-site screening tests
if the test results are not for use in diagnosing or preventing disease and are
not for use by physicians, dentists or other licensed health care professionals
in treating humans. Any entity using the test shall pay a yearly filing fee,
not to exceed $50, and file a registration form as provided by rule of the
department that:
(a) States the current name and address of
the entity, the telephone number of the entity, if any, and the name of a
contact individual at each on-site facility operated by the entity; and
(b) Certifies that:
(A) The tests are being administered
according to the federal Food and Drug Administration package insert that
accompanies the test;
(B) The tests are being administered
according to the instructions of the manufacturer;
(C) Custody chain procedures are being
followed;
(D) Operators of the substances of abuse
on-site screening facility are trained in the use of the substances of abuse
on-site screening tests by the manufacturer; and
(E) If the substances of abuse on-site
screening facility obtains a positive test result on a specimen and the entity
indicates that the test result is to be used to deny or deprive any person of
employment or any benefit, or may otherwise result in adverse employment
action, the same specimen shall be submitted to a clinical laboratory licensed
under ORS 438.110 and 438.150 or an equivalent out-of-state facility and the
presence of a substance of abuse confirmed prior to release of the on-site test
result.
(6) The department by rule shall set
reasonable standards for the screening by correctional agencies of inmates
within state and local correctional facilities and offenders on parole,
probation or post-prison supervision for substances of abuse. The standards
shall include, but not be limited to, the establishment of written procedures
and protocols, the qualifications and training of individuals who perform
screening tests, the approval of specific technologies and the minimum
requirements for record keeping, quality control and confirmation of positive
screening results.
(7) If an initial test by a special
category laboratory under subsection (4) of this section or a special category
screening under subsection (6) of this section shows a result indicating the
presence of a substance of abuse in the body, a confirmatory test shall be
conducted in a licensed clinical laboratory if the results are to be used to
deprive or deny any person of any employment or benefit. If a screening test of
an inmate of a state or local correctional facility is positive for a substance
of abuse, the inmate may be held in a secure facility pending the outcome of
the confirmatory test. If the confirmatory test is positive, the inmate may be
held in a secure facility pending the outcome of any hearing to determine what
action will be taken.
(8) If any test for substances of abuse is
performed outside this state the results of which are to be used to deprive or
deny any person any employment or any benefit, the person desiring to use the
test shall have the burden to show that the testing procedure used meets or
exceeds the testing standards of this state. [1987 c.669 §2; 1991 c.808 §1;
1997 c.355 §2; 1999 c.739 §2; 2001 c.104 §175]
438.440
Disposition of fees. All
moneys received by the Department of Human Services under ORS 438.010 to
438.510 and 438.990 shall be credited to the Public Health Account and shall be
used for payment of the expenses of the department in administering the
provisions of ORS 438.010 to 438.510 and 438.990. [1969 c.685 §16]
438.450
Rules. The Department of
Human Services shall make such rules as are necessary for carrying out ORS
438.010 to 438.510 in accordance with ORS 183.330. [Formerly 433.335; 2001
c.104 §176]
438.510
Prohibited acts. It is
unlawful for the owner of a clinical laboratory or the director of a clinical
laboratory to:
(1) Operate or maintain a clinical
laboratory unless the laboratory is under personal supervision of a director
who is qualified to supervise the laboratory.
(2) Violate any provision of ORS 438.010
to 438.510. [1969 c.685 §11; 1987 c.669 §3; 2001 c.104 §177]
ENVIRONMENTAL
LABORATORIES
438.605
Definitions for ORS 438.605 to 438.620, 448.280 and 448.285. As used in ORS 438.605 to 438.620, 448.280
and 448.285:
(1) “Accrediting authority” means the
official accrediting authority for the
(2) “Department” means the Department of
Human Services.
(3) “Environmental laboratory” means a
fixed location or mobile facility that performs chemical, physical,
radiological, microbiological or biological testing of environmental samples or
the collection of environmental samples.
(4) “Environmental testing” means
laboratory analysis of any matter, pollutant, contaminant or hazardous
substance subject to regulation pursuant to:
(a) Rules adopted or enforced by the
Department of Human Services, the Department of Environmental Quality or the
State Department of Agriculture; or
(b) A federal environmental statute or
regulation administered or enforced by the United States Environmental
Protection Agency. [1999 c.1063 §1]
438.610
Standards for accreditation; rules. (1) The Department of Human Services, in concurrence with the
accrediting authority, may adopt by rule standards for any laboratory seeking
accreditation and performing environmental testing for a fee or for determining
compliance with environmental statutes, rules or regulations.
(2) In developing standards under
subsection (1) of this section, the department shall cooperate with and may
seek advice from the United States Environmental Protection Agency and any
other state or federal agency that may have adopted rules or regulations for
environmental monitoring.
(3) The standards adopted under this
section may address testing and sampling procedures or methods, record keeping,
disposal or retention of testing materials or samples, or any other practice
related to work performed by an environmental laboratory. [1999 c.1063 §2]
438.615
Environmental laboratory accreditation program; rules. The Department of Human Services, in
concurrence with the accrediting authority, shall establish by rule and
implement an environmental laboratory accreditation program. The standards for
accreditation may be equivalent to, but may not exceed, standards adopted by
national accreditation programs. [1999 c.1063 §3]
438.620
Accreditation fees; disposition of fees. (1) In conjunction with the environmental laboratory accreditation
program established under ORS 438.615, the Department of Human Services may
establish and collect a fee for laboratory accreditation under the program. A
fee imposed under this section shall not exceed the cost of administering the
program.
(2) Prior to imposing the fee under
subsection (1) of this section, the Department of Human Services shall obtain
the approval of the Oregon Department of Administrative Services and report to
the appropriate legislative committee.
(3) All moneys collected by the Department
of Human Services under this section shall be deposited in a dedicated account
of the department. Such moneys are continuously appropriated to the Department
of Human Services to pay the costs of the Department of Human Services, the
State Department of Agriculture and the Department of Environmental Quality in
administering the environmental laboratory accreditation program established
under ORS 438.615. [1999 c.1063 §4]
PENALTIES
438.990
Penalties. Violation of any
provision of ORS 438.040 or 438.510 is a Class A misdemeanor. Each day of
continuing violation shall be considered a separate offense. [1969 c.685 §22;
1977 c.582 §45]
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CHAPTER 439
[Reserved for expansion]