20 CSR 2220-2.012
Technology Assisted Prescription/
Medication Order Verification (Intern Pharmacists and
Pharmacy Technicians)
PURPOSE: This rule establishes requirements for pharmacy
technicians/intern pharmacists performing technology assisted
prescription/medication order verification under the supervision
of a pharmacist.
(1) Definitions.
(A) “Authorized intern pharmacist”—An individual who
holds a current and active Missouri intern pharmacist license
and has completed employer-approved training in technology
assisted verification using the pharmacy’s approved technology
assisted verification system.
(B) “Authorized pharmacy technician”—A currently registered
Missouri pharmacy technician who—
1. Holds an active pharmacy technician certification issued
by a certification entity accredited by the National Commission
for Certifying Agencies;
2. Has completed employer-approved training in technology
assisted verification using the pharmacy’s approved technology
assisted verification system; and
3. Has assisted in the practice of pharmacy as a registered/
licensed pharmacy technician in the state of Missouri or
another U.S. state or territory for a minimum of one (1) year.
(C) “Technology Assisted Verification” (TAV)—The process
of verification of the final prescription or medication order
and affixed label by an authorized pharmacy technician or
authorized intern pharmacist using a technology assisted
verification system that complies with this rule.
(D) “Technology Assisted Verification System” (TAVS)—An
electronic system that utilizes barcode technology or another
electronic process/method to electronically verify the final
medication prescription or medication order has been properly
dispensed and to electronically verify the prescription/medication
order has been properly labeled for the correct patient.
(2) Pharmacy Technicians/Intern Pharmacists. A Missourilicensed pharmacist may allow an authorized pharmacy
technician or authorized intern pharmacist to verify the final
prescription/medication order using a TAVS if—
(A) The medication is a non-controlled substance and
will be dispensed in the original manufacturer’s unopened
unit of use package, or the non-controlled medication has
been repackaged in compliance with 20 CSR 2220-2.130 and
previously verified by a pharmacist;
(B) The authorized pharmacy technician or intern pharmacist
is under the supervision of a Missouri-licensed pharmacist
who is physically present within the dispensing area and able
to provide immediate assistance. A current list of pharmacy
technicians/intern pharmacists authorized to perform TAV
must be maintained at the pharmacy along with proof of the
required training and competency assessment;
(C) The authorized pharmacy technician/intern pharmacist
is competent to perform the duties assigned and has completed
a documented initial and annual assessment of competency
using the pharmacy’s approved TAVS. A pharmacist may
not simultaneously supervise a total of more than two (2)
pharmacy technicians or intern pharmacists performing TAV
as authorized by this rule. The pharmacist-in-charge may
petition the board to increase the number of supervised
technicians/intern pharmacists for good cause;
(D) A pharmacist verifies the accuracy of prescription/
medication order data entry prior to dispensing and completes
a prospective drug utilization review. The identity of the
verifying pharmacist must be recorded in the pharmacy’s
records as required by 20 CSR 2220-2.080;
(E) The TAVS is used to verify the proper prescription label has
been affixed to the correct manufacturer unit of use package
AND INSURANCE
or repacked container for the correct patient. The identity of
the authorized pharmacy technician or intern pharmacist
performing the TAV and the supervising pharmacist must be
documented in the pharmacy’s records; and
(F) No manual manipulation of the prescription/medication
order occurs after the TAV occurs. For purposes of this rule,
manual intervention does not include preparing a finished
prescription/medication order for mailing, delivery, or storage.
(3) Technology Requirements. Technology assisted verification
systems must be maintained in good working order, and
must verify prescriptions/medication orders and the affixed
labels with one hundred percent (100%) accuracy. Use of the
TAVS must be terminated and the root cause identified and
corrected if a verification error is detected. Only a pharmacist
shall be authorized to initiate the operation of a TAVS or
override any technology generated errors, warnings, alerts,
or exceptions related to TAVS functioning or medication
verification/accuracy.
(A) The TAVS must be implemented and validated by a
pharmacist prior to initial use to confirm the technology’s
accuracy and correctness. At a minimum, the TAVS must
complete
one
thousand
(1,000)
consecutive
product
verifications during the initial validation process with a one
hundred percent (100%) accuracy rate. A pharmacist must audit
one hundred percent (100%) of product verifications completed
during the initial validation process before dispensing and
confirm accuracy. The required pharmacist audit may not be
delegated to an intern pharmacist or a pharmacy technician.
(B) A pharmacist must conduct daily random quality testing
on a sample size of prescriptions verified by the TAVS. The
required sample size shall not be less than two percent (2%) of
prescriptions/medication orders verified via the TAVS on the last
day of system operation. Use of the TAVS must be terminated
and the root cause identified and corrected if quality testing
results show less than one hundred percent (100%) accuracy.
(C) A TAVS must be revalidated by a pharmacist in accordance
with the pharmacy’s policies and procedures.
(D) The required revalidation process must include a
sampling of prescriptions/medication order verifications by
the TAVS using a sample size that is sufficient to confirm
the technology is properly and accurately functioning. A
pharmacist must audit and verify one hundred percent (100%)
accuracy of the sampled verifications prior to further use of the
TAVS. The required pharmacist audit may not be delegated to
an intern pharmacist or a pharmacy technician.
(E) Proof of compliance with validation, revalidation, and
testing requirements must be documented and maintained in
the pharmacy’s records, including but not limited to the name,
initials, or identification code(s) of the pharmacist performing
the required validation/testing and validation/testing date(s)
and results.
(5) Quality Assurance. Pharmacies using TAV as authorized by
this rule must maintain an ongoing and documented quality
assurance system that monitors the performance of the TAVS
and the TAV process to ensure proper and accurate functioning.
The quality assurance system must include procedures for
reporting dispensing errors, system malfunctions, or other
compliance concerns. Notification of any dispensing error
involving a TAV that reaches the patient must be submitted
to the board electronically or in writing within ten (10)
days of discovery. The required notification must include the
date of the incident, patient name, the technician or intern
pharmacist who performed the TAV, a description of the
error, the applicable prescription/medication order number or
unique identifier, and the supervising pharmacist of record.
(6) Policies and Procedures. Pharmacies using TAV must
maintain current, written policies and procedures governing
all aspects of technology assisted verification activities,
including but not limited to—
(A) Staff training and competency assessments;
(B) Operation of the required quality assurance system,
including reporting, investigating, and addressing errors,
system malfunctions, and other quality assurance issues;
(C) Testing, validation, and revalidation of the TAVS to ensure
proper functioning; and
(D) System maintenance, including any routine or
preventative maintenance.
(7) Recordkeeping. Records required by this rule must be
maintained by the pharmacy electronically or in writing for a
minimum of two (2) years. Records must be made available for
inspection or copying and produced to the board or the board’s
authorized designee upon request.
(8) Applicability. Compliance with this rule is not required
if a pharmacist physically verifies the final prescription/
medication order and the affixed label before dispensing.
Final prescription/medication order verification for a Class R
Remote Dispensing Site pharmacy must comply with 20 CSR
2220-2.680.
AUTHORITY: sections 338.140 and 338.210, RSMo Supp. 2021, and
sections 338.240, 338.280, and 338.400, RSMo 2016.* Original rule
filed Feb. 9, 2022, effective Aug. 30, 2022.
*Original authority: 338.140, RSMo 1939, amended 1981, 1989, 1997, 2011, 2019;
338.210, RSMo 1951, amended 2001, 2011, 2020; 338.240, RSMo 1951, amended 2011;
338.280, RSMo 1951, amended 1971, 1981; and 338.400, RSMo 2011.