Michigan Office of Administrative Hearings and Rules
611 West Ottawa Street; 2nd Floor, Ottawa Building
Lansing, MI 48933
Phone: (517) 335-8658 FAX: (517) 335-9512
REQUEST FOR RULEMAKING (RFR)
Under the Administrative Procedures Act (APA), 1969 PA 306, the agency that has the statutory authority
to promulgate rules must electronically file a RFR with the Michigan Office of Administrative Hearings
and Rules (MOAHR) before initiating any changes or additions to the rules. Submit copy to the MOAHR
1. Agency Information
Agency name: Michigan Department of Health and Human Services
Division/Bureau/Office: Policy and Innovation Division
Name, title, phone number, and e-mail of person Jared Welehodsky, Department Analyst, 517-
completing this form:
284-4761, welehodskyj@michigan.gov
2. Rule Set Information
Title of proposed rule set: Nonopioid Directive
Rule number(s) or range of numbers: R 333.1001 through R 333.1004
Included in agency’s annual regulatory plan as rule to be processed in current year? No
3. Estimated timetable for completion, or statutory deadline, if applicable:
One year
4. Describe the general purpose of these rules, including any problem(s) the changes are intended to
address:
Legislative mandate for rule promulgation to develop procedures for recording, disclosure, or
distribution of data relating to a nonopioid directive form or the transmission of a nonopioid
directive form that complies with state and federal confidentiality and consent laws, rules, and
regulations.
5. Cite the specific rule promulgation authority (i.e. agency director, commission, board, etc.,
listing all applicable statutory references. If the rule(s) are mandated by any applicable
constitutional or statutory provision, please explain.
By authority conferred on the Department of Health and Human Services by sections 2226, 2233,
and 9145 of the public health code, 1978 PA 368, MCL 333.2226, 333.2233, and 333.9145.
6. Describe the extent to which the rule(s) conflict with, duplicate, or exceed similar regulations,
compliance requirements, or other standards adopted at the state, regional, or federal level.
Include applicable public act and statutory references.
The proposed rules will follow the current legislative mandate to promulgate rules to address the
creation of a Nonopioid Directive. There are no known conflicts, duplications, or anything that
exceeds current regulations, compliance requirements or other standards.
7. Is the subject matter of the rule(s) currently contained in any guideline, manual, handbook,
instructional bulletin, form with instructions, or operational memo?
There are no current guidelines, manuals, handbooks, instructional bulletins, forms, or memos
that address the subject matter of these proposed rules.
8. Explain whether the rule(s) will be promulgated under Sections 44 or 48 of the APA or the full
Revised: April 22, 2019
MCL 24.239