                                 CODE OF VIRGINIA

DEFINITIONS (§ 54.1-3401)

As used in this chapter, unless the context requires a different meaning:
		&#8220;Administer&#8221; means the direct application of a controlled
substance, whether by injection, inhalation, ingestion, or any other means, to
the body of a patient or research subject by (i) a practitioner or by his
authorized agent and under his direction or (ii) the patient or research subject
at the direction and in the presence of the practitioner.
		&#8220;Advertisement&#8221; means all representations disseminated in any
manner or by any means, other than by labeling, for the purpose of inducing, or
which are likely to induce, directly or indirectly, the purchase of drugs or
devices.
		&#8220;Agent&#8221; means an authorized person who acts on behalf of or at the
direction of a manufacturer, distributor, or dispenser. &#8220;Agent&#8221; does
not include a common or contract carrier, public warehouseman, or employee of
the carrier or warehouseman.
		&#8220;Anabolic steroid&#8221; means any drug or hormonal substance,
chemically and pharmacologically related to testosterone, other than estrogens,
progestins, corticosteroids, and dehydroepiandrosterone.
		&#8220;Animal&#8221; means any nonhuman animate being endowed with the power
of voluntary action.
		&#8220;Automated drug dispensing system&#8221; means a mechanical or
electronic system that performs operations or activities, other than compounding
or administration, relating to pharmacy services, including the storage,
dispensing, or distribution of drugs and the collection, control, and
maintenance of all transaction information, to provide security and
accountability for such drugs.
		&#8220;Biological product&#8221; means a virus, therapeutic serum, toxin,
antitoxin, vaccine, blood, blood component or derivative, allergenic product,
protein other than a chemically synthesized polypeptide, or analogous product,
or arsphenamine or any derivative of arsphenamine or any other trivalent organic
arsenic compound, applicable to the prevention, treatment, or cure of a disease
or condition of human beings.
		&#8220;Biosimilar&#8221; means a biological product that is highly similar to
a specific reference biological product, notwithstanding minor differences in
clinically inactive compounds, such that there are no clinically meaningful
differences between the reference biological product and the biological product
that has been licensed as a biosimilar pursuant to 42 U.S.C. § 262(k) in terms
of safety, purity, and potency of the product.
		&#8220;Board&#8221; means the Board of Pharmacy.
		&#8220;Bulk drug substance&#8221; means any substance that is represented for
use, and that, when used in the compounding, manufacturing, processing, or
packaging of a drug, becomes an active ingredient or a finished dosage form of
the drug; however, &#8220;bulk drug substance&#8221; does not include
intermediates that are used in the synthesis of such substances.
		&#8220;Change of ownership&#8221; of an existing entity permitted, registered,
or licensed by the Board means (i) the sale or transfer of all or substantially
all of the assets of the entity or of any corporation that owns or controls the
entity; (ii) the creation of a partnership by a sole proprietor, the dissolution
of a partnership, or a change in partnership composition; (iii) the acquisition
or disposal of 50 percent or more of the outstanding shares of voting stock of a
corporation owning the entity or of the parent corporation of a wholly owned
subsidiary owning the entity, except that this shall not apply to any
corporation the voting stock of which is actively traded on any securities
exchange or in any over-the-counter market; (iv) the merger of a corporation
owning the entity or of the parent corporation of a wholly owned subsidiary
owning the entity with another business or corporation; or (v) the expiration or
forfeiture of a corporation&#8217;s charter.
		&#8220;Co-licensed partner&#8221; means a person who, with at least one other
person, has the right to engage in the manufacturing or marketing of a
prescription drug, consistent with state and federal law.
		&#8220;Compounding&#8221; means the combining of two or more ingredients to
fabricate such ingredients into a single preparation and includes the mixing,
assembling, packaging, or labeling of a drug or device (i) by a pharmacist, or
within a permitted pharmacy, pursuant to a valid prescription issued for a
medicinal or therapeutic purpose in the context of a bona fide
practitioner-patient-pharmacist relationship, or in expectation of receiving a
valid prescription based on observed historical patterns of prescribing and
dispensing; (ii) by a practitioner of medicine, osteopathy, podiatry, dentistry,
or veterinary medicine as an incident to his administering or dispensing, if
authorized to dispense, a controlled substance in the course of his professional
practice; or (iii) for the purpose of, or as incident to, research, teaching, or
chemical analysis and not for sale or for dispensing. The mixing, diluting, or
reconstituting of a manufacturer&#8217;s product drugs for the purpose of
administration to a patient, when performed by a practitioner of medicine or
osteopathy licensed under Chapter 29 (§ 54.1-2900 et seq.), a person supervised
by such practitioner pursuant to subdivision A 6 or 19 of § 54.1-2901, or a
person supervised by such practitioner or a licensed advanced practice
registered nurse or physician assistant pursuant to subdivision A 4 of §
54.1-2901 shall not be considered compounding.
		&#8220;Controlled substance&#8221; means a drug, substance, or immediate
precursor in Schedules I through VI of this chapter. &#8220;Controlled
substance&#8221; does not include distilled spirits, wine, malt beverages, or
tobacco as those terms are defined or used in Title 3.2 or Title 4.1. The term
&#8220;controlled substance&#8221; includes a controlled substance analog that
has been placed into Schedule I or II by the Board pursuant to the regulatory
authority in subsection D of § 54.1-3443.
		&#8220;Controlled substance analog&#8221; means a substance the chemical
structure of which is substantially similar to the chemical structure of a
controlled substance in Schedule I or II and either (i) which has a stimulant,
depressant, or hallucinogenic effect on the central nervous system that is
substantially similar to or greater than the stimulant, depressant, or
hallucinogenic effect on the central nervous system of a controlled substance in
Schedule I or II or (ii) with respect to a particular person, which such person
represents or intends to have a stimulant, depressant, or hallucinogenic effect
on the central nervous system that is substantially similar to or greater than
the stimulant, depressant, or hallucinogenic effect on the central nervous
system of a controlled substance in Schedule I or II. &#8220;Controlled
substance analog&#8221; does not include (a) any substance for which there is an
approved new drug application as defined under § 505 of the Federal Food, Drug,
and Cosmetic Act (21 U.S.C. § 355) or that is generally recognized as safe and
effective pursuant to §§ 501, 502, and 503 of the Federal Food, Drug, and
Cosmetic Act (21 U.S.C. §§ 351, 352, and 353) and 21 C.F.R. Part 330; (b) with
respect to a particular person, any substance for which an exemption is in
effect for investigational use for that person under § 505 of the Federal Food,
Drug, and Cosmetic Act to the extent that the conduct with respect to that
substance is pursuant to such exemption; or (c) any substance to the extent not
intended for human consumption before such an exemption takes effect with
respect to that substance.
		&#8220;DEA&#8221; means the Drug Enforcement Administration, U.S. Department
of Justice, or its successor agency.
		&#8220;Deliver&#8221; or &#8220;delivery&#8221; means the actual,
constructive, or attempted transfer of any item regulated by this chapter,
whether or not there exists an agency relationship, including delivery of a
Schedule VI prescription device to an ultimate user or consumer on behalf of a
medical equipment supplier by a manufacturer, nonresident manufacturer,
wholesale distributor, nonresident wholesale distributor, warehouser,
nonresident warehouser, third-party logistics provider, or nonresident
third-party logistics provider at the direction of a medical equipment supplier
in accordance with § 54.1-3415.1.
		&#8220;Device&#8221; means instruments, apparatus, and contrivances, including
their components, parts, and accessories, intended for use in the diagnosis,
cure, mitigation, treatment, or prevention of disease in man or animals or to
affect the structure or any function of the body of man or animals.
		&#8220;Dialysis care technician&#8221; or &#8220;dialysis patient care
technician&#8221; means an individual who is certified by an organization
approved by the Department of Health Professions pursuant to Chapter 27.01 (§
54.1-2729.1 et seq.) and who, under the supervision of a licensed physician, an
advanced practice registered nurse, a physician assistant, or a registered
nurse, assists in the care of patients undergoing renal dialysis treatments in a
Medicare-certified renal dialysis facility.
		&#8220;Dialysis solution&#8221; means either the commercially available,
unopened, sterile solutions whose purpose is to be instilled into the peritoneal
cavity during the medical procedure known as peritoneal dialysis, or
commercially available solutions whose purpose is to be used in the performance
of hemodialysis not to include any solutions administered to the patient
intravenously.
		&#8220;Dispense&#8221; means to deliver a drug to an ultimate user or research
subject by or pursuant to the lawful order of a practitioner, including the
prescribing and administering, packaging, labeling, or compounding necessary to
prepare the substance for that delivery. However, &#8220;dispensing&#8221; does
not include the transportation of drugs mixed, diluted, or reconstituted in
accordance with this chapter to other sites operated by such practitioner or
that practitioner&#8217;s medical practice for the purpose of administration of
such drugs to patients of the practitioner or that practitioner&#8217;s medical
practice at such other sites. For practitioners of medicine or osteopathy,
&#8220;dispense&#8221; includes only the provision of drugs by a practitioner to
patients to take with them away from the practitioner&#8217;s place of practice.
		&#8220;Dispenser&#8221; means a practitioner who dispenses.
		&#8220;Distribute&#8221; means to deliver other than by administering or
dispensing a controlled substance.
		&#8220;Distributor&#8221; means a person who distributes.
		&#8220;Drug&#8221; means (i) articles or substances recognized in the official
United States Pharmacopoeia National Formulary or official Homeopathic
Pharmacopoeia of the United States, or any supplement to any of them; (ii)
articles or substances intended for use in the diagnosis, cure, mitigation,
treatment, or prevention of disease in man or animals; (iii) articles or
substances, other than food, intended to affect the structure or any function of
the body of man or animals; (iv) articles or substances intended for use as a
component of any article specified in clause (i), (ii), or (iii); or (v) a
biological product. &#8220;Drug&#8221; does not include devices or their
components, parts, or accessories.
		&#8220;Drug product&#8221; means a specific drug in dosage form from a known
source of manufacture, whether by brand or therapeutically equivalent drug
product name.
		&#8220;Electronic prescription&#8221; means a written prescription that is
generated on an electronic application and is transmitted to a pharmacy as an
electronic data file; Schedules II through V prescriptions shall be transmitted
in accordance with 21 C.F.R. Part 1300.
		&#8220;Facsimile (FAX) prescription&#8221; means a written prescription or
order that is transmitted by an electronic device over telephone lines that
sends the exact image to the receiving pharmacy in hard copy form.
		&#8220;FDA&#8221; means the U.S. Food and Drug Administration.
		&#8220;Immediate precursor&#8221; means a substance which the Board of
Pharmacy has found to be and by regulation designates as being the principal
compound commonly used or produced primarily for use, and which is an immediate
chemical intermediary used or likely to be used in the manufacture of a
controlled substance, the control of which is necessary to prevent, curtail, or
limit manufacture.
		&#8220;Interchangeable&#8221; means a biosimilar that meets safety standards
for determining interchangeability pursuant to 42 U.S.C. § 262(k)(4).
		&#8220;Label&#8221; means a display of written, printed, or graphic matter
upon the immediate container of any article. A requirement made by or under
authority of this chapter that any word, statement, or other information appear
on the label shall not be considered to be complied with unless such word,
statement, or other information also appears on the outside container or
wrapper, if any, of the retail package of such article or is easily legible
through the outside container or wrapper.
		&#8220;Labeling&#8221; means all labels and other written, printed, or graphic
matter on an article or any of its containers or wrappers, or accompanying such
article.
		&#8220;Manufacture&#8221; means the production, preparation, propagation,
conversion, or processing of any item regulated by this chapter, either directly
or indirectly by extraction from substances of natural origin, or independently
by means of chemical synthesis, or by a combination of extraction and chemical
synthesis, and includes any packaging or repackaging of the substance or
labeling or relabeling of its container. &#8220;Manufacture&#8221; does not
include compounding.
		&#8220;Manufacturer&#8221; means every person who manufactures, a
manufacturer&#8217;s co-licensed partner, or a repackager.
		&#8220;Marijuana&#8221; means any part of a plant of the genus Cannabis
whether growing or not, its seeds, or its resin; and every compound,
manufacture, salt, derivative, mixture, or preparation of such plant, its seeds,
its resin, or any extract containing one or more cannabinoids.
&#8220;Marijuana&#8221; does not include (i) the mature stalks of such plant,
fiber produced from such stalk, or oil or cake made from the seeds of such
plant, unless such stalks, fiber, oil, or cake is combined with other parts of
plants of the genus Cannabis; (ii) industrial hemp, as defined in § 3.2-4112,
that is possessed by a person registered pursuant to subsection A of § 3.2-4115
or his agent; (iii) industrial hemp, as defined in § 3.2-4112, that is
possessed by a person who holds a hemp producer license issued by the U.S.
Department of Agriculture pursuant to 7 C.F.R. Part 990; (iv) a hemp product, as
defined in § 3.2-4112; (v) an industrial hemp extract, as defined in §
3.2-5145.1; or (vi) any substance containing a tetrahydrocannabinol isomer,
ester, ether, salt, or salts of such isomer, ester, or ether that has been
placed by the Board of Pharmacy into one of the schedules set forth in the Drug
Control Act (§ 54.1-3400 et seq.) pursuant to § 54.1-3443.
		&#8220;Medical equipment supplier&#8221; means any person, as defined in §
1-230, engaged in the delivery to the ultimate consumer, pursuant to the lawful
order of a practitioner, of hypodermic syringes and needles, medicinal oxygen,
Schedule VI controlled devices, those Schedule VI controlled substances with no
medicinal properties that are used for the operation and cleaning of medical
equipment, solutions for peritoneal dialysis, and sterile water or saline for
irrigation.
		&#8220;Narcotic drug&#8221; means any of the following, whether produced
directly or indirectly by extraction from substances of vegetable origin, or
independently by means of chemical synthesis, or by a combination of extraction
and chemical synthesis: (i) opium, opiates, and any salt, compound, derivative,
or preparation of opium or opiates; (ii) any salt, compound, isomer, derivative,
or preparation thereof which is chemically equivalent or identical with any of
the substances referred to in clause (i), but not including the isoquinoline
alkaloids of opium; (iii) opium poppy and poppy straw; or (iv) coca leaves and
any salt, compound, derivative, or preparation of coca leaves, and any salt,
compound, isomer, derivative, or preparation thereof which is chemically
equivalent or identical with any of these substances, but not including
decocainized coca leaves or extraction of coca leaves which do not contain
cocaine or ecgonine.
		&#8220;New drug&#8221; means (i) any drug, except a new animal drug or an
animal feed bearing or containing a new animal drug, the composition of which is
such that such drug is not generally recognized, among experts qualified by
scientific training and experience to evaluate the safety and effectiveness of
drugs, as safe and effective for use under the conditions prescribed,
recommended, or suggested in the labeling, except that such a drug not so
recognized shall not be deemed to be a &#8220;new drug&#8221; if at any time
prior to the enactment of this chapter it was subject to the Food and Drugs Act
of June 30, 1906, as amended, and if at such time its labeling contained the
same representations concerning the conditions of its use, or (ii) any drug,
except a new animal drug or an animal feed bearing or containing a new animal
drug, the composition of which is such that such drug, as a result of
investigations to determine its safety and effectiveness for use under such
conditions, has become so recognized, but which has not, otherwise than in such
investigations, been used to a material extent or for a material time under such
conditions.
		&#8220;Nuclear medicine technologist&#8221; means an individual who holds a
current certification with the American Registry of Radiological Technologists
or the Nuclear Medicine Technology Certification Board.
		&#8220;Official compendium&#8221; means the official United States
Pharmacopoeia National Formulary, official Homeopathic Pharmacopoeia of the
United States, or any supplement to any of them.
		&#8220;Official written order&#8221; means an order written on a form provided
for that purpose by the U.S. Drug Enforcement Administration, under any laws of
the United States making provision therefor, if such order forms are authorized
and required by federal law, and if no such order form is provided then on an
official form provided for that purpose by the Board of Pharmacy.
		&#8220;Opiate&#8221; means any substance having an addiction-forming or
addiction-sustaining liability similar to morphine or being capable of
conversion into a drug having such addiction-forming or addiction-sustaining
liability. &#8220;Opiate&#8221; does not include, unless specifically designated
as controlled under Article 4 (§ 54.1-3437 et seq.), the dextrorotatory isomer
of 3-methoxy-n-methylmorphinan and its salts (dextromethorphan).
&#8220;Opiate&#8221; does include its racemic and levorotatory forms.
		&#8220;Opium poppy&#8221; means the plant of the species Papaver somniferum
L., except the seeds thereof.
		&#8220;Original package&#8221; means the unbroken container or wrapping in
which any drug or medicine is enclosed together with label and labeling, put up
by or for the manufacturer, wholesaler, or distributor for use in the delivery
or display of such article.
		&#8220;Outsourcing facility&#8221; means a facility that is engaged in the
compounding of sterile drugs and is currently registered as an outsourcing
facility with the U.S. Secretary of Health and Human Services and that complies
with all applicable requirements of federal and state law, including the Federal
Food, Drug, and Cosmetic Act, 21 U.S.C. § 301 et seq.
		&#8220;Person&#8221; means both the plural and singular, as the case demands,
and includes an individual, partnership, corporation, association, governmental
agency, trust, or other institution or entity.
		&#8220;Pharmacist-in-charge&#8221; means the person who, being licensed as a
pharmacist, signs the application for a pharmacy permit and assumes full legal
responsibility for the operation of the relevant pharmacy in a manner complying
with the laws and regulations for the practice of pharmacy and the sale and
dispensing of controlled substances; the &#8220;pharmacist-in-charge&#8221;
shall personally supervise the pharmacy and the pharmacy&#8217;s personnel as
required by § 54.1-3432.
		&#8220;Poppy straw&#8221; means all parts, except the seeds, of the opium
poppy, after mowing.
		&#8220;Practitioner&#8221; means a physician, dentist, licensed advanced
practice registered nurse pursuant to § 54.1-2957.01, licensed physician
assistant pursuant to § 54.1-2952.1, pharmacist pursuant to § 54.1-3300,
TPA-certified optometrist pursuant to Article 5 (§ 54.1-3222 et seq.) of
Chapter 32, veterinarian, scientific investigator, or other person licensed,
registered, or otherwise permitted to distribute, dispense, prescribe and
administer, or conduct research with respect to a controlled substance in the
course of professional practice or research in the Commonwealth.
		&#8220;Prescriber&#8221; means a practitioner who is authorized pursuant to
§§ 54.1-3303 and 54.1-3408 to issue a prescription.
		&#8220;Prescription&#8221; means an order for drugs or medical supplies,
written or signed or transmitted by word of mouth, telephone, telegraph, or
other means of communication to a pharmacist by a duly licensed physician,
dentist, veterinarian, or other practitioner authorized by law to prescribe and
administer such drugs or medical supplies.
		&#8220;Prescription drug&#8221; means any drug required by federal law or
regulation to be dispensed only pursuant to a prescription, including finished
dosage forms and active ingredients subject to § 503(b) of the Federal Food,
Drug, and Cosmetic Act (21 U.S.C. § 353(b)).
		&#8220;Production&#8221; or &#8220;produce&#8221; includes the manufacture,
planting, cultivation, growing, or harvesting of a controlled substance or
marijuana.
		&#8220;Proprietary medicine&#8221; means a completely compounded
nonprescription drug in its unbroken, original package which does not contain
any controlled substance or marijuana as defined in this chapter and is not in
itself poisonous, and which is sold, offered, promoted, or advertised directly
to the general public by or under the authority of the manufacturer or primary
distributor, under a trademark, trade name, or other trade symbol privately
owned, and the labeling of which conforms to the requirements of this chapter
and applicable federal law. However, &#8220;proprietary medicine&#8221; does not
include a drug that is only advertised or promoted professionally to licensed
practitioners, a narcotic or drug containing a narcotic, a drug that may be
dispensed only upon prescription or the label of which bears substantially the
statement &#8220;Warning may be habit-forming,&#8221; or a drug intended for
injection.
		&#8220;Radiopharmaceutical&#8221; means any drug that exhibits spontaneous
disintegration of unstable nuclei with the emission of nuclear particles or
photons and includes any non-radioactive reagent kit or radionuclide generator
that is intended to be used in the preparation of any such substance, but does
not include drugs such as carbon-containing compounds or potassium-containing
salts that include trace quantities of naturally occurring radionuclides.
&#8220;Radiopharmaceutical&#8221; also includes any biological product that is
labeled with a radionuclide or intended solely to be labeled with a
radionuclide.
		&#8220;Reference biological product&#8221; means the single biological product
licensed pursuant to 42 U.S.C. § 262(a) against which a biological product is
evaluated in an application submitted to the U.S. Food and Drug Administration
for licensure of biological products as biosimilar or interchangeable pursuant
to 42 U.S.C. § 262(k).
		&#8220;Remote dispensing system&#8221; means a profile-driven automated drug
dispensing system that performs operations or activities relative to the
storage, packaging, labeling, or dispensing of medications employing
bidirectional audio-visual technology to facilitate pharmacist communication
with a patient, authorized agent of the patient, or person licensed to
administer drugs, and collects, controls, and maintains all information online.
Drugs intended to be administered by the patient or a person not licensed to
administer drugs must fully comply with the labeling requirements in §§
54.1-3410 and 54.1-3463 and Board regulations. Directions for use may only be
abbreviated when drugs are administered exclusively by persons licensed to
administer drugs.
		&#8220;Sale&#8221; includes barter, exchange, or gift, or offer therefor, and
each such transaction made by any person, whether as an individual, proprietor,
agent, servant, or employee.
		&#8220;Tetrahydrocannabinol&#8221; means any naturally occurring or synthetic
tetrahydrocannabinol, including its salts, isomers, and salts of isomers
whenever the existence of such salts, isomers, and salts of isomers is possible
within the specific chemical designation and any preparation, mixture, or
substance containing, or mixed or infused with, any detectable amount of
tetrahydrocannabinol. For the purposes of this definition, &#8220;isomer&#8221;
means the optical, position, and geometric isomers.
		&#8220;Therapeutically equivalent drug products&#8221; means drug products
that contain the same active ingredients and are identical in strength or
concentration, dosage form, and route of administration and that are classified
as being therapeutically equivalent by the U.S. Food and Drug Administration
pursuant to the definition of &#8220;therapeutically equivalent drug
products&#8221; set forth in the most recent edition of the Approved Drug
Products with Therapeutic Equivalence Evaluations, otherwise known as the
&#8220;Orange Book.&#8221;
		&#8220;Third-party logistics provider&#8221; means a person that provides or
coordinates warehousing of or other logistics services for a drug or device in
interstate commerce on behalf of a manufacturer, wholesale distributor, or
dispenser of the drug or device but does not take ownership of the product or
have responsibility for directing the sale or disposition of the product.
		&#8220;Total tetrahydrocannabinol&#8221; means the sum, after the application
of any necessary conversion factor, of the percentage by weight of
tetrahydrocannabinol and the percentage by weight of tetrahydrocannabinolic
acid.
		&#8220;USP-NF&#8221; means the current edition of the United States
Pharmacopeia-National Formulary.
		&#8220;Warehouser&#8221; means any person, other than a wholesale distributor,
manufacturer, or third-party logistics provider, engaged in the business of (i)
selling or otherwise distributing prescription drugs or devices to any person
who is not the ultimate user or consumer and (ii) delivering Schedule VI
prescription devices to the ultimate user or consumer pursuant to §
54.1-3415.1. No person shall be subject to any state or local tax by reason of
this definition.
		&#8220;Wholesale distribution&#8221; means (i) distribution of prescription
drugs to persons other than consumers or patients and (ii) delivery of Schedule
VI prescription devices to the ultimate user or consumer pursuant to §
54.1-3415.1, subject to the exemptions set forth in the federal Drug Supply
Chain Security Act.
		&#8220;Wholesale distributor&#8221; means any person other than a
manufacturer, a manufacturer&#8217;s co-licensed partner, a third-party
logistics provider, or a repackager that engages in wholesale distribution.
		The words &#8220;drugs&#8221; and &#8220;devices&#8221; as used in Chapter 33
(§ 54.1-3300 et seq.) and in this chapter do not include surgical or dental
instruments, physical therapy equipment, X-ray apparatus, or glasses or lenses
for the eyes.
		The terms &#8220;pharmacist,&#8221; &#8220;pharmacy,&#8221; and
&#8220;practice of pharmacy&#8221; as used in this chapter have the same
meanings as provided in Chapter 33 (§ 54.1-3300 et seq.) unless the context
requires a different meaning.

HISTORY: Code 1950, §§ 54-399, 54-487; 1952, c. 451; 1958, c. 551, §
54-524.2; 1966, c. 193; 1968, c. 582; 1970, c. 650; 1971, Ex. Sess., c. 94;
1972, c. 798; 1975, c. 425; 1976, c. 14; 1977, c. 193; 1978, c. 833; 1979, c.
435; 1980, c. 150; 1988, c. 765; 1991, cc. 519, 524; 1992, cc. 737, 793; 1996,
cc. 37, 152, 158, 407, 408; 1997, cc. 20, 677, 806; 1998, c. 470; 1999, cc. 661,
750; 2000, cc. 861, 878, 935; 2003, cc. 509, 639, 995; 2005, cc. 475, 839; 2006,
c. 346; 2012, c. 213; 2013, cc. 412, 504, 544, 765; 2014, cc. 674, 719; 2015,
cc. 158, 180, 300; 2016, cc. 221, 495; 2017, cc. 115, 429; 2018, cc. 241, 242,
689, 690; 2019, cc. 653, 654; 2020, cc. 831, 1285, 1286; 2021, Sp. Sess. I, c.
110; 2023, cc. 183, 744, 794; 2024, cc. 63, 513; 2025, c. 341.