Title 5
Businesses and Professions

Chapter 19.1
Pharmacies

R.I. Gen. Laws § 5-19.1-38

§ 5-19.1-38. Pharmacy technicians — Scope of practice — Pharmacy technician dispensing process validation within institutional pharmacies.

(a) In accordance with this chapter and adopted by the state board of pharmacy, a pharmacy technician or pharmacy intern may perform technology-assisted dispensing process validation for medications prepared for distribution by another pharmacy technician or intern within an institutional pharmacy.

(b) Definitions. For purposes of this section, the following words and terms shall have the following meanings:

(1) “Automated storage and distribution devices” means a mechanical device that delivers drugs other than by administration, and uses automated data processing technology to:

(i) Provide effective storage and security of drugs contained in the device;

(ii) Limit access to authorized individuals;

(iii) Record the identity of all personnel who access the drugs stored within the device;

(iv) Provide documentation of storage and removal of contents;

(v) Provide ongoing documentation that monitors proper delivery of drugs to ensure patient safety; and

(vi) Comply with all relevant statutes, rules, and regulations.

(2) “Controlled substance” means a drug or substance, or an immediate precursor of such drug or substance, so designated under or pursuant to the provisions of chapter 28 of title 21.

(3) “Dispensing process validation” means the physical verification that ensures the drug, drug dosage, and drug form selected is the correct drug, drug dosage, and drug form for the purpose for which it was selected. When applicable, dispensing process validation is subject to, and occurs after, licensed pharmacist drug utilization review and clinical conflict resolution.

(4) “Institutional pharmacy” means any pharmacy that is located within or off-site, and contracted with, any hospital, clinic, or dispensary in which drugs are compounded or dispensed to its patients or patients of another licensed in-patient healthcare facility with whom it has a contract.

(5) “Supervision” means oversight and control by a licensed pharmacist who is responsible for work performed by pharmacy technicians and pharmacy interns.

(6) “Technology” means an electronic system designed to achieve accuracy in drug product identity verification including, but not limited to, barcode scanning and radio frequency identification (RFID).

(c)(1) With regard to activities authorized, acting in compliance with this section, a licensed pharmacist may delegate, and a pharmacy technician or pharmacy intern may perform under the supervision of the pharmacist, technology-assisted dispensing process validation of medications prepared for distribution by another pharmacy technician or pharmacy intern when such medication will be administered to the patient by a licensed healthcare professional, including:

(i) Patient-specific medication orders;

(ii) Automated storage and distribution devices stock;

(iii) Repackaged medication from bulk to unit-of-use doses; and

(iv) Emergency kits.

(2) Acting in compliance with this section, a licensed pharmacist shall not delegate dispensing process validation for:

(i) Controlled substances; or

(ii) Compounded products (whether sterile or non-sterile) unless the compounded products have been previously verified by a licensed pharmacist (e.g., previously batched compounded product).

(3) In delegating activities under this section, a licensed pharmacist shall use reasonable professional judgment and shall ensure that authorized activities do not require the exercise of discretion or clinical judgment by the pharmacy technician or pharmacy intern.

(d)(1) With regard to quality and control, the institutional pharmacy where activities authorized in this section are conducted shall:

(i) Document a pharmacy technician or pharmacy intern dispensing process validation policy and procedure;

(ii) Maintain an institutional pharmacy-specific training program including a record of pharmacy technicians and/or pharmacy interns trained; and

(iii) Maintain a continuous quality assessment system to periodically verify the accuracy of the pharmacy technician or pharmacy intern dispensing process validation, including:

(A) Recording any errors which reach the patient;

(B) Recording any quality related events; and

(C) Specific limits of acceptable quality related event levels before reassessment.

(2) No pharmacy technician or pharmacy intern shall engage in authorized activities without documentation of training.

(e) The pharmacist-in-charge is responsible for ensuring that delegation of technology-assisted dispensing process validation of medications by a licensed pharmacist under this section does not lead to medication errors.

(f) With regards to rules and regulations, the board of pharmacy shall make, adopt, amend, and repeal such rules and regulations as may be deemed necessary by the board from time to time for the proper administration and enforcement of this section. Such rules and regulations shall be promulgated in accordance with the procedures specified in chapter 35 of title 42 (“administrative procedures”).

History of Section.
P.L. 2025, ch. 320, § 1, effective June 30, 2025; P.L. 2025, ch. 322, § 1, effective June 30, 2025.