Kansas Administrative Code

Notice. This notice shall specifically statethenatureofthecomplaintsagainsttheperson to whom they are made and shall set forth the time and place of the hearing. (Authorized by and im- plementing K.S.A. 74-5806; effective May 1, 1982.) REQUIREMENTS 67-10-1 to 67-10-10. (Authorize…

(Authorized by K.S.A. 1975 Supp. 65-1630; effective Jan. 1, 1966; revoked, E-76-31, Aug. 11, 1975; revoked May 1, 1976.)

Application for registrations or permits; withdrawal of application. Af- ter an application for a registration or permit has been accepted, the failure of the applicant or authorized representative to respond to offi- cial correspondence regarding the application, when sent by re…

Continuing education for phar- macists. (a)(1) “Continuing education” shall mean an organized and systematic education experience beyond basic preparation that is de- signed to achieve the following: (A)(i) Increase knowledge, improve skills, or enhance the practice of pharmacy; …

(Authorized by and implementing K.S.A. 1982 Supp. 65-1631; effective May 1, 1983; revoked May 1, 1987.)

Approved schools. The following may be recognized and approved by the board: (a) Any school or college of pharmacy or department of a university accredited by the accreditation council for pharmacy education; and (b) any other school or college of pharmacy or department of a univ…

(Authorized by and implementing K.S.A. 65-1631; effective May 1, 1983; amended May 1, 1987; revoked March 22, 2002.)

Foreign graduates. (a) Each appli- cant who has graduated from a school or college of pharmacy or a pharmacy department of a universi- tylocatedoutsideoftheUnitedStatesorwhoisnot a citizen of the United States shall provide proof that the applicant has reasonable ability to commu…

(Authorized by and implementing K.S.A. 65-1631; effective Oct. 20, 2006; revoked Aug. 19, 2016.)

Foreign pharmacy graduate equivalency examination. In addition to meet- ing the requirements of K.A.R. 68-1-1f, each for- 823 Registration and Examination of Pharmacists 68-1-3a eign applicant shall meet the following require- ments for licensure under the pharmacy act of the sta…

Grades required. (a) Each success- ful applicant for licensure by examination under the pharmacy act of the state of Kansas shall: (1) pass an examination approved by the board; and (2) obtain a grade of not less than 75% on the law examination administered by the board. (b) Each…

Pharmacist-in-charge examina- tion; acknowledgment. (a) Each prospective pharmacist-in-charge shall take a pharmacy law examination administered by the board, with a passing score of at least 85%. The examination shall include the statutes and rules and regula- tions, both state …

(Authorized by and implementing K.S.A. 65-1630; effective Jan. 1, 1966; amended Jan. 1, 1967; amended, E-76-31, Aug. 11, 1975; amended May 1, 1976; amended May 1, 1978; amended May 1, 1983; revoked March 22, 2002.)

Qualifying pharmaceutical expe- rience. (a) Pharmaceutical experience that quali- fies as one year of experience shall consist of 1,740 clock-hours as a pharmacy student or registered in- tern while being supervised by a preceptor. A pre- ceptor may supervise at any time no more …

(Authorized by K.S.A. 1975 Supp. 65-1630; effective Jan. 1, 1966; revoked, E-76-31, Aug. 11, 1975; revoked May 1, 1976.)

(Authorized by K.S.A. 1975 Supp. 65-1630; effective Jan. 1, 1966; amended, E-76- 31, Aug. 11, 1975; amended May 1, 1976; revoked May 1, 1987.)

(Authorized by K.S.A. 1975 Supp. 65-1630; effective Jan. 1, 1966; revoked, E-76-31, Aug. 11, 1975; revoked May 1, 1976.)

Reinstatement after lapse. Upon failure of a pharmacist to renew a registration un- dertheprovisionsofK.S.A.65-1632forthreecon- secutive years or more, the board shall require the applicant to take a written or oral examination pri- or to reinstatement. Upon satisfactory completi…

Registered pharmacist to be on duty. It shall be the duty of the pharmacist in charge of every premise having a pharmacy reg- istration, to ensure that a registered pharmacist is on duty at all times during which the pharmacy is open. (Authorized by and implementing K.S.A. 65-163…

Fees for examination and licen- sure as a pharmacist. The following fees shall be paid to the board by each applicant for exam- ination and licensure as a pharmacist: (a) Each applicant for examination shall pay a fee of $100.00. (b) Each applicant for reciprocal licensure shall …

Fees for premises and service registrations and permits. (a) Pharmacy regis- tration fees shall be as follows: (1) Each new pharmacy registration shall be $150.00. (2) Each renewal pharmacy registration shall be $125.00. (b) Manufacturer registration fees shall be as follows: (1)…

Fees for registration as a phar- macy technician or pharmacy intern. The fol- lowing fees shall be paid to the board: (a) Each applicant for initial registration as a pharmacy technician shall pay a fee of $20.00. (b) Each registered pharmacy technician shall pay a renewal fee of…

(Authorized by and implementing K.S.A. 65-1637a; rejected, L. 1983, Ch. 356, ef- fective May 1, 1983.)

Resaleofdispensedprescription drugs. Except for prescription drugs in unit-dose systems that contain only one medication and in which the drug has not reached the patient and is still intact, prescription drugs that have been dis- pensed to the final consumer shall not be resold,…

(Authorized by K.S.A. 65-1630; im- plementing K.S.A. 2001 Supp. 65-1642; effective May 1, 1988; amended Feb. 7, 2003; revoked Jan. 4, 2019.)

Definitions. As used in this article of the board’s regulations, each of the following terms shall have the meaning specified in this regulation: (a) “Active ingredients” means chemicals, sub- stances, or other components intended for use in the diagnosis, cure, mitigation, treat…

Nonsterile preparations. (a) This regulation shall apply to the following: (1) Nonsterile preparations that are compound- ed in Kansas; and (2) nonsterile preparations that are shipped or delivered into Kansas by a pharmacy and are to be administered to a patient in Kansas. (b) “…

(Authorized by K.S.A. 65-1630; imple- menting K.S.A. 65-1634; effective May 1, 1978; amended Dec. 15, 2017; amended Nov. 29, 2019.)

(Authorized by K.S.A. 65-1630; im- plementing K.S.A. 1998 Supp. 65-1643; effective June 15, 1992; amended March 20, 1995; amend- ed July 30, 1999; revoked Jan. 3, 2020.)

Definitions. As used in this article of the board’s regulations and the pharmacy prac- tice act, each of the following terms shall have the meaning specified in this regulation: (a) “Blood” means whole blood collected from a single donor and processed either for transfusion or fo…

(Authorized by and implementing K.S.A. 1998 Supp. 65-1655 and 65-1643; effective June 15, 1992; amended July 23, 1999; revoked Jan. 3, 2020.)

Minimum required information for registration. (a) Each wholesale distributor, virtual wholesale distributor, third-party logistics provider, or outsourcing facility shall provide the board with the following minimum information as part of the registration requirements described …

Personnel. (a) Each wholesale dis- tributor registrant, virtual wholesale distributor registrant, third-party logistics registrant, or out- sourcing facility registrant shall require each per- son employed in any wholesale distribution, virtu- al wholesale distribution, third-par…

Violations and penalties. Any license or registration granted under this article may be suspended or revoked by the board for willful and serious violation of these regulations. (Authorized by and implementing K.S.A. 1991 Supp. 65-1655; effective June 15, 1992.)

Wholesale distributors; mini- mum requirements for the storage and han- dling of prescription-only drugs and devices and for the establishment and maintenance of prescription-only drug and device dis- tribution records. Each wholesale distributor registrant shall meet the followi…

Third-party logistics provid- ers; minimum requirements for operation and maintenance of records. Each third-party logistics provider registrant shall meet the follow- ing minimum requirements for operation and the maintenance of records: (a) Facilities. Each facility at which a …

Outsourcing facilities; mini- mum requirements for operation and main- tenance of records. Each registrant who is the owner of an outsourcing facility shall meet the fol- lowing minimum requirements for operation and the maintenance of records: (a) Facilities. Each outsourcing fa…

Wholesale distributors transac- tion. (a) Notwithstanding any other provision of these regulations under article 14, a wholesale dis- tributor, duly registered with the board, may sell or deliver to a layperson responsible for the control of an animal, a prescription-only drug to…

Nonprescription wholesale dis- tributors. “Nonprescription wholesale distribu- tor” shall mean any person, partnership, corpo- ration, or business firm registered in this state and engaging in the distribution of drugs that are not prescription-only drugs to persons or entities o…

Nonprescription wholesale dis- tributor registration required. A nonprescrip- tion wholesale distributor may engage in the dis- tribution of nonprescription drugs to persons or entities, other than a consumer or patient in Kan- sas, if both of the following conditions are met: (a…

Minimum requirements for storage. All drugs shall be stored at appropriate temperatures and under appropriate conditions in accordance with any requirements in the labeling or packaging of the drugs, or with any require- ments in the United States pharmacopeia: the na- 871 Utiliz…

(Authorized by and implement- ing K.S.A. 2007 Supp. 65-1667; effective Dec. 1, 2006; amended April 10, 2009; revoked Feb. 13, 2015.)

(Authorized by and implementing K.S.A. 2005 Supp. 65-1667; effective Dec. 1, 2006; revoked Feb. 13, 2015.)

(Authorized by and implementing K.S.A. 2005 Supp. 65-1665 and K.S.A. 2005 Supp. 65-1667; effective Dec. 1, 2006; revoked Feb. 13, 2015.) 68-16-6, 68-16-7, 68-16-8, and

(Authorized by and implementing K.S.A. 2005 Supp. 65-1667; effective Dec. 1, 2006; revoked Feb. 13, 2015.) UNUSED MEDICATIONS

Transferring unused medica- tions. (a) Each administrator or operator of an adult care home, pharmacist-in-charge of a mail service pharmacy, and administrator of a medical care facility who wants to become a donating enti- ty, as defined in L. 2008, ch. 9, sec. 2 and amend- ment…

Accepting unused medications. (a) Each qualifying center or clinic that elects to participate in the unused medications program shall submit to the board written notification of intent to participate on a form approved by the board. (b) Each qualifying center or clinic shall main…

Recall of unused medications. (a) If an unused medication is recalled and the qualifying center or clinic does not have the lot number on the label to differentiate between the recalled medications and the nonrecalled med- ications, all of the unused medications shall be destroye…

Minimum program require- ments. Each pharmacy’s continuous quality im- provement program shall meet the following min- imum requirements: (a) Meet at least once each quarter of each cal- endar year; (b) have the pharmacy’s pharmacist-in-charge in attendance at each meeting; and (…

Cessation of operations. (a) When any pharmacy ceases operations at the lo- cation for which the registration was received, the pharmacist-in-charge shall meet the following re- quirements: (1) Within five days after ceasing operations at that location, submit to the board, on a …