Michigan Office of Administrative Hearings and Rules  
Administrative Rules Division (ARD)  
611 W. Ottawa Street  
Lansing, MI 48909  
Phone: 517-335-8658 Fax: 517-335-9512  
REQUEST FOR RULEMAKING (RFR)  
1. Department:  
Licensing and Regulatory Affairs  
2. Bureau:  
Bureau of Professional Licensing  
3. Promulgation type:  
Full Process  
4. Title of proposed rule set:  
Pharmacy Technicians  
5. Rule numbers or rule set range of numbers:  
R 338.3651 – R 338.3665  
6. Estimated time frame:  
12 months  
Name of person filling out RFR:  
Andria Ditschman  
E-mail of person filling out RFR:  
Phone number of person filling out RFR:  
517-290-3361  
Address of person filling out RFR:  
611 West Ottawa Street #rd Floor  
7. Describe the general purpose of these rules, including any problems the changes are intended  
to address.  
The purpose of the Board of Pharmacy - Pharmacy Technicians Rules is to regulate the  
prelicensure programs, examinations, licensure, licensure renewal, relicensure, continuing  
education, and delegation of activities and functions for pharmacy technicians. The proposed  
rules are intended to: address the shortage of pharmacy technicians; add a minimum examination  
passing score; clarify the licensure requirements; clarify the requirements for licensure by  
endorsement; clarify the requirements for a temporary license; review the date of program  
accreditation; add a process for rescinding approval of an examination or program; clarify the  
requirements for relicensure and add relicensure requirements for individuals licensed in another  
state; clarify the continuing education requirements; modify the process for review of continuing  
education for consistency with the pharmacist continuing education review process; delete the  
reference to American Society of Health-System Pharmacists (ASHP) when used to refer to  
continuing education; and clarify and broaden the activities and functions that may be delegated to  
a pharmacy technician’s scope of practice.  
8. Please cite the specific promulgation authority for the rules (i.e. department director,  
commission, board, etc.).  
MCL 333.16145 authorizes the Board to promulgate rules necessary or appropriate to fulfill its  
functions as prescribed in the Article 15 of the Public Health Code (Code).  
MCL 24.239  
RFR-Page 2  
A. Please list all applicable statutory references (MCLs, Executive Orders, etc.).  
MCL 333.16145, 333.16148, 333.16184, 333.16186, 333.16201, 333.16204, 333.16205,  
333.16215, 333.16287, 333.17731, 333.17739, 333.17739a, 333.17739b, and 333.17739c, and  
Executive Reorganization Order No. 1991-9, MCL 338.3501; Executive Reorganization Order No.  
1996-2, MCL 445.2001; Executive Reorganization Order No. 2003-1, MCL 445.2011; and  
Executive Reorganization Order No. 2011-4, MCL 445.2030.  
B. Are the rules mandated by any applicable constitutional or statutory provision? If so, please  
explain.  
Yes, the Department in consultation with the Board is required to promulgate rules as follows: to  
include training standards for identifying victims of human trafficking, pursuant to MCL  
333.16148; to complete continuing education (CE) hours in pain and symptom management for an  
applicant for licensure renewal, pursuant to MCL 333.16204 and MCL 333.17731; and to  
implement sections 16284 and 18285 of the Code, regarding telehealth, pursuant to MCL  
333.16287.  
9. Please describe the extent to which the rules conflict with or duplicate similar rules,  
compliance requirements, or other standards adopted at the state, regional, or federal level.  
Each state establishes its own requirements with respect to pharmacy technicians. The rules do  
not conflict with or duplicate similar rules, compliance requirements, or other standards adopted at  
the state, regional, or federal level.  
10. Is the subject matter of the rules currently contained in any guideline, handbook, manual,  
instructional bulletin, form with instructions, or operational memoranda?  
No. The subject matter of these rules is not currently contained in any guideline, handbook,  
manual, instructional bulletin, form with instructions, or operational memoranda.  
11. Are the rules listed on the department’s annual regulatory plan as rules to be processed  
for the current year?  
Yes.  
12. Will the proposed rules be promulgated under Section 44 of the Administrative Procedures  
Act, 1969 PA 306, MCL 24.244, or under the full rulemaking process?  
Full Process  
13. Please describe the extent to which the rules exceed similar regulations, compliance  
requirements, or other standards adopted at the state, regional, or federal level.  
The rules do not exceed similar regulations, compliance requirements, or other standards adopted  
at the state, regional, or federal level.  
14. Do the rules incorporate the recommendations received from the public regarding any  
complaints or comments regarding the rules? If yes, please explain.  
The Department will work with various associations, educational institutions, pharmacy related  
businesses, and lobbyists in preparing the proposed rules.  
15. If amending an existing rule set, please provide the date of the last evaluation of the rules  
and the degree, if any, to which technology, economic conditions, or other factors have changed  
the regulatory activity covered by the rules since the last evaluation.  
The rules were promulgated in 2021. There have been no technological factors, economic  
conditions, or other factors that would necessitate amendment of the rules.  
16. Are there any changes or developments since implementation that demonstrate there is no  
continued need for the rules, or any portion of the rules?  
MCL 24.239  
RFR-Page 3  
No, there are no changes or developments since implementation of the rules that demonstrate there  
is no continued need for the rules, or any portion of the rules.  
17. Is there an applicable decision record (as defined in MCL 24.203(6) and required by MCL  
24.239(2))? If so, please attach the decision record.  
Yes  
MCL 24.239  
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