Nevada
AB186
AB186 - Revises provisions governing pharmacists. (BDR 54-344)
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EXEMPT
(Reprinted with amendments adopted on April 21, 2025)
FIRST REPRINT
A.B. 186
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*AB186_R1*
ASSEMBLY BILL NO. 186–ASSEMBLYMEMBER ORENTLICHER
PREFILED FEBRUARY 3, 2025
____________
Referred to Committee on Commerce and Labor
SUMMARY—Revises
provisions
governing
pharmacists.
(BDR 54-344)
FISCAL NOTE: Effect on Local Government: No.
Effect on the State: Yes.
~
EXPLANATION – Matter in bolded italics is new; matter between brackets [omitted material] is material to be omitted.
AN ACT relating to pharmacy; authorizing a registered pharmacist
to prescribe drugs and devices to treat certain health
conditions and dispense a refill without the authorization
of a practitioner, other than a pharmacist, under certain
circumstances; authorizing a registered pharmacist to
administer drugs; authorizing a registered pharmacist to
engage in certain activity relating to laboratories and
laboratory testing; and providing other matters properly
relating thereto.
Legislative Counsel’s Digest:
Existing law authorizes, under certain conditions, a pharmacist to dispense a
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self-administered hormonal contraceptive without a prescription and prescribe and
2
dispense a drug for the medication-assisted treatment of opioid use disorder. (NRS
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639.28078, 639.28079) Section 1 of this bill authorizes a registered pharmacist to
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prescribe and dispense drugs and devices for the treatment of health conditions that:
5
(1) have been previously diagnosed; (2) are self-limiting; or (3) are acute conditions
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diagnosed after the performance of certain tests. Section 1 additionally authorizes a
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registered pharmacist to dispense a one-time refill of a prescription without the
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authorization of a practitioner, other than a pharmacist, if the drug was previously
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prescribed to the patient and losing access to the drug would threaten the health of
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the patient. Section 1 additionally prohibits a registered pharmacist from taking
11
such action with regard to: (1) drugs and devices not approved by the United States
12
Food and Drug Administration; (2) controlled substances that are not opioids,
13
except in certain clinical settings; and (3) controlled substances that are an opioid
14
except in accordance with the protocols for prescribing and dispensing a drug for
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medication-assisted treatment. (NRS 639.28079) Section 1 also authorizes the State
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Board of Pharmacy to adopt regulations establishing: (1) the scope of the ability of
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a registered pharmacist to prescribe drugs and devices and dispense refills without
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the authorization of another type of practitioner; (2) the standard of care required of
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a registered pharmacist who engages in such activities; and (3) the requirements for
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adequate liability insurance for registered pharmacists who engage in such
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activities. Section 2 of this bill provides that prescribing and dispensing drugs and
22
devices and dispensing refills pursuant to section 1 constitutes the practice of
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pharmacy. Sections 3, 10-13 and 15 of this bill make additional changes necessary
24
to authorize a registered pharmacist to prescribe and dispense drugs and devices
25
and dispense refills without the authorization of another type of practitioner
26
pursuant to section 1. The Board would be authorized to suspend or revoke the
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registration of a pharmacist who prescribes or dispenses a drug or device or
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dispenses a refill without the authorization of another type of practitioner and fails
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to comply with the provisions of section 1 or the regulations adopted pursuant
30
thereto. (NRS 639.210)
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Existing law includes within the practice of pharmacy the performance or
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supervision of activities associated with manufacturing, compounding, labeling,
33
dispensing and distributing a drug. (NRS 629.0124) Section 2 additionally includes
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the performance or supervision of activities associated with administering a drug,
35
thereby authorizing a registered pharmacist to perform or supervise such activities.
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Sections 14, 16 and 17 of this bill accordingly provide general authorization for a
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registered pharmacist to possess and administer controlled substances and
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dangerous drugs.
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Existing law requires the Board to adopt regulations governing the
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manipulation of a person for the collection of specimens by a registered pharmacist
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that: (1) require the pharmacist to use only a fingerstick or oral or nasal swab to
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collect the specimens; and (2) set forth the procedures and requirements the
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pharmacist is required to follow when manipulating a person for the collection of a
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specimen. (NRS 639.0747) Section 4 of this bill removes the requirement that a
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pharmacist use only a fingerstick or oral or nasal swab to collect a specimen,
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thereby authorizing a pharmacist to collect a specimen using any method available
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for the collection of the specimen.
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Existing law authorizes a registered pharmacist or a registered intern
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pharmacist to: (1) perform a home blood glucose test; and (2) order and perform
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laboratory tests that are necessary for therapy that uses a drug approved by the
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United States Food and Drug Administration for preventing the acquisition of
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human immunodeficiency virus. (NRS 639.2808, 639.28085) Section 5 of this bill
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additionally authorizes a registered pharmacist to: (1) order laboratory tests that are
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necessary for any drug therapy or that otherwise facilitate the care of a patient
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within the authorized scope of practice of the pharmacist; and (2) perform certain
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other laboratory tests determined by the Federal Government to be simple
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laboratory examinations and procedures that have an insignificant risk of an
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erroneous result. (42 U.S.C. 263a(d)(3); 42 C.F.R. Part 493, Subpart A) Section 5
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also authorizes the State Board of Pharmacy to adopt regulations to authorize
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registered intern pharmacists to order and perform such laboratory tests. Section 2
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provides that ordering and performing such laboratory tests constitutes the practice
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of pharmacy. Sections 2 and 6 of this bill remove duplicative provisions from
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existing law. Sections 8, 9 and 18-24 of this bill make conforming changes so that
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requirements for insurance coverage of certain services performed by registered
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pharmacists are not changed by this bill.
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Existing law requires the State Board of Health to adopt regulations for the
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certification and licensure of laboratory directors. (NRS 652.125) Existing
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regulations define an exempt laboratory to be a laboratory that: (1) conducts only
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certain microscopy tests and tests determined by the Federal Government to be
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simple laboratory examinations and procedures that have an insignificant risk of an
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erroneous result; and (2) does not perform only tests for human immunodeficiency
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virus. (42 U.S.C. 493.19; 42 C.F.R. Part 493, Subpart A; NAC 652.072) Section 7
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of this bill requires regulations of the Board to authorize a registered pharmacist to
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serve as the laboratory director of an exempt laboratory.
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THE PEOPLE OF THE STATE OF NEVADA, REPRESENTED IN
SENATE AND ASSEMBLY, DO ENACT AS FOLLOWS:
Section 1. Chapter 639 of NRS is hereby amended by adding
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thereto a new section to read as follows:
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1. Subject to the limitations set forth in subsection 2, a
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registered pharmacist may, in accordance with any requirements
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prescribed pursuant to subsection 3:
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(a) Prescribe drugs or devices that are used for the treatment
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of health conditions, other than opioid use disorder, that:
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(1) Have been previously diagnosed;
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(2) Are self-limiting; or
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(3) Are acute conditions diagnosed after performing a test
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that is classified as a waived test pursuant to 42 C.F.R. Part 493,
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Subpart A; and
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(b) Dispense a one-time refill of an existing prescription
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without authorization from a practitioner, other than a
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pharmacist, if, in the professional judgment of the pharmacist, the
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health of the patient will be harmed without the patient continuing
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to have access to the prescribed drug.
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2. A registered pharmacist shall not take any action described
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in subsection 1 with regard to a:
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(a) Drug or device that is not approved by the United States
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Food and Drug Administration.
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(b) Controlled substance that is not an opioid, except if the
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registered pharmacist is prescribing such a controlled substance
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in:
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(1) An inpatient medical facility in accordance with the
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policies of the facility;
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(2) An outpatient medical facility or clinic, only if the
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registered pharmacist is acting within a multidisciplinary team;
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(3) A program for hospice care or palliative care; or
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(4) A program for treatment for substance use disorder.
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(c) Controlled substance that is an opioid.
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3. The Board may adopt regulations:
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(a) Requiring a registered pharmacist who takes the actions
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authorized by this section to be covered by adequate liability
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insurance, as determined by the Board;
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(b) Establishing the scope of the ability for a registered
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pharmacist to prescribe drugs and devices and dispense refills as
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authorized by subsection 1; and
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(c) Establishing the standard of care required of a registered
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pharmacist who prescribes drugs and devices and dispenses refills
2
as authorized by subsection 1.
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4. As used in this section:
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(a) “Medical facility” has the meaning ascribed to it in
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NRS 449.0151.
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(b) “Program of hospice care” means a program of hospice
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care described in NRS 449.196.
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(c) “Self-limiting” means that a health condition generally
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persists for a limited period of time.
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Sec. 2. NRS 639.0124 is hereby amended to read as follows:
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639.0124 1. “Practice of pharmacy” includes, but is not
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limited to, the:
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(a) Performance or supervision of activities associated with
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manufacturing,
compounding,
labeling,
dispensing
,
[and]
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distributing [of] and administering a drug, including the receipt,
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handling and storage of prescriptions and other confidential
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information relating to patients.
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(b) Interpretation and evaluation of prescriptions or orders for
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medicine.
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(c) Participation in drug evaluation and drug research.
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(d) Advising of the therapeutic value, reaction, drug interaction,
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hazard and use of a drug.
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(e) Selection of the source, storage and distribution of a drug.
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(f) Maintenance of proper documentation of the source, storage
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and distribution of a drug.
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(g) Interpretation of clinical data contained in a person’s record
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of medication.
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(h) Development of written guidelines and protocols in
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collaboration with a practitioner which authorize collaborative drug
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therapy management. The written guidelines and protocols must
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comply with NRS 639.2629.
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(i) Implementation
and
modification
of
drug
therapy,
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administering drugs and ordering and performing tests in
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accordance with a collaborative practice agreement.
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(j) Prescribing, dispensing and administering of drugs for
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preventing the acquisition of human immunodeficiency virus and
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[ordering and] conducting laboratory tests necessary for therapy that
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uses such drugs pursuant to the protocol prescribed pursuant to
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NRS 639.28085.
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(k) Dispensing a self-administered hormonal contraceptive
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pursuant to NRS 639.28078.
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(l) Assessing a patient and prescribing and dispensing a drug for
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medication-assisted treatment in accordance with NRS 639.28079.
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(m) Ordering and performing laboratory tests in accordance
1
with NRS 639.2808.
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(n) Prescribing and dispensing drugs and devices and
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dispensing refills without the authorization of a practitioner, other
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than a pharmacist, in accordance with section 1 of this act.
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2. The term does not include the changing of a prescription by
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a pharmacist or practitioner without the consent of the prescribing
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practitioner, except as otherwise provided in NRS 639.2583,
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639.28078 and 639.28085.
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Sec. 3. NRS 639.0125 is hereby amended to read as follows:
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639.0125 “Practitioner” means:
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1. A physician, dentist, veterinarian or podiatric physician who
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holds a license to practice his or her profession in this State;
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2. A hospital, pharmacy or other institution licensed, registered
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or otherwise permitted to distribute, dispense, conduct research with
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respect to or administer drugs in the course of professional practice
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or research in this State;
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3. An advanced practice registered nurse who has been
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authorized to prescribe controlled substances, poisons, dangerous
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drugs and devices;
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4. A physician assistant who:
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(a) Holds a license issued by the Board of Medical Examiners;
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and
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(b) Is authorized by the Board to possess, administer, prescribe
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or dispense controlled substances, poisons, dangerous drugs or
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devices under the supervision of a physician as required by chapter
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630 of NRS;
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5. A physician assistant who:
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(a) Holds a license issued by the State Board of Osteopathic
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Medicine; and
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(b) Is authorized by the Board to possess, administer, prescribe
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or dispense controlled substances, poisons, dangerous drugs or
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devices under the supervision of an osteopathic physician as
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required by chapter 633 of NRS;
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6. An optometrist who is certified by the Nevada State Board
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of Optometry to prescribe and administer pharmaceutical agents
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pursuant to NRS 636.288, when the optometrist prescribes or
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administers pharmaceutical agents within the scope of his or her
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certification;
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7. A dental hygienist who:
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(a) Holds a valid license to practice dental hygiene in this State;
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(b) Is authorized to prescribe and dispense the dangerous drugs
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and devices listed in NRS 631.3105 in accordance with the
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provisions of that section and the regulations adopted pursuant
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thereto; and
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(c) Holds a certificate issued pursuant to NRS 639.1374 by the
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State Board of Pharmacy authorizing him or her to so prescribe;
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8. A pharmacist who [is] :
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(a) Is registered pursuant to NRS 639.28079 to prescribe and
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dispense drugs for medication-assisted treatment; or
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(b) Prescribes drugs or devices or dispenses refills
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