(1) registration requirements to establish the eligibility of a pharmacy to participate in the program;
(2) a formulary that includes all eligible prescription drugs approved by the federal Food and Drug Administration;
(3) standards and procedures for: (a) verifying whether a pharmacy or pharmacist participating in the program is licensed and in good standing with the board; (b) handling of a donated eligible prescription drug, including: (i) acceptance; (ii) identification, including redundant criteria for verification; (iii) documentation, under 21 U.S.C. Sec. 360eee-1, of transaction information, history, and statements; (iv) safe storage; (v) security; (vi) inspection; (vii) transfer; and (viii) dispensing; (c) a pharmacist or licensed pharmacy technician working in or consulting with a participating eligible donor; (d) disposition of a donated prescription drug that is a controlled substance; (e) record keeping regarding: (i) the eligible donor that donated each prescription drug; (ii) the identification and evaluation of a donated prescription drug by a pharmacist or licensed pharmacy technician; and (iii) the dispensing or disposition of a prescription drug; (f) determining the status of a medically indigent individual; (g) labeling requirements to: (i) ensure compliance with patient privacy laws relating to: (A) an individual who receives an eligible prescription drug; and (B) patient information that may appear on a donated prescription drug; (ii) clearly identify an eligible prescription drug dispensed under the program; and (iii) communicate necessary information regarding the manufacturer's recommended expiration date or the beyond use date; and (h) ensuring compliance with the requirements of this part;
(a) verifying whether a pharmacy or pharmacist participating in the program is licensed and in good standing with the board;
(b) handling of a donated eligible prescription drug, including: (i) acceptance; (ii) identification, including redundant criteria for verification; (iii) documentation, under 21 U.S.C. Sec. 360eee-1, of transaction information, history, and statements; (iv) safe storage; (v) security; (vi) inspection; (vii) transfer; and (viii) dispensing;
(i) acceptance;
(ii) identification, including redundant criteria for verification;
(iii) documentation, under 21 U.S.C. Sec. 360eee-1, of transaction information, history, and statements;
(iv) safe storage;
(v) security;
(vi) inspection;
(vii) transfer; and
(viii) dispensing;
(c) a pharmacist or licensed pharmacy technician working in or consulting with a participating eligible donor;
(d) disposition of a donated prescription drug that is a controlled substance;
(e) record keeping regarding: (i) the eligible donor that donated each prescription drug; (ii) the identification and evaluation of a donated prescription drug by a pharmacist or licensed pharmacy technician; and (iii) the dispensing or disposition of a prescription drug;
(i) the eligible donor that donated each prescription drug;
(ii) the identification and evaluation of a donated prescription drug by a pharmacist or licensed pharmacy technician; and
(iii) the dispensing or disposition of a prescription drug;
(f) determining the status of a medically indigent individual;
(g) labeling requirements to: (i) ensure compliance with patient privacy laws relating to: (A) an individual who receives an eligible prescription drug; and (B) patient information that may appear on a donated prescription drug; (ii) clearly identify an eligible prescription drug dispensed under the program; and (iii) communicate necessary information regarding the manufacturer's recommended expiration date or the beyond use date; and
(i) ensure compliance with patient privacy laws relating to: (A) an individual who receives an eligible prescription drug; and (B) patient information that may appear on a donated prescription drug;
(A) an individual who receives an eligible prescription drug; and
(B) patient information that may appear on a donated prescription drug;
(ii) clearly identify an eligible prescription drug dispensed under the program; and
(iii) communicate necessary information regarding the manufacturer's recommended expiration date or the beyond use date; and
(h) ensuring compliance with the requirements of this part;
(4) a process for seeking input from: (a) the Department of Health, created in Section 26-1-4, to establish program standards and procedures for assisted living facilities and nursing care facilities; and (b) the Division of Substance Abuse and Mental Health, created in Section 62A-15-103, to establish program standards and procedures for mental health and substance abuse clients; and
(a) the Department of Health, created in Section 26-1-4, to establish program standards and procedures for assisted living facilities and nursing care facilities; and
(b) the Division of Substance Abuse and Mental Health, created in Section 62A-15-103, to establish program standards and procedures for mental health and substance abuse clients; and
(5) the creation of a special training program that a pharmacist and a licensed pharmacy technician at an eligible pharmacy must complete before participating in the program.