Is MGM-16 Legal in Iowa? (2026)

Instrument

Duty to recommend changes in schedules, temporary amendments to schedules

Source

https://www.legis.iowa.gov/docs/code/124.201.pdf

Retrieved

2026-10-29

Fingerprint

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1. The board shall administer the regulatory provisions of this chapter. Annually, within
thirty days after the convening of each regular session of the general assembly, the board
shall recommend to the general assembly any deletions from, or revisions in the schedules
of substances, enumerated in section 124.204, 124.206, 124.208, 124.210, or 124.212, which
it deems necessary or advisable.
In making a recommendation to the general assembly
regarding a substance, the board shall consider the following:

a. The actual or relative potential for abuse;
b. The scientific evidence of its pharmacological effect, if known;
c. State of current scientific knowledge regarding the substance;
d. The history and current pattern of abuse;
e. The scope, duration, and significance of abuse;
f. The risk to the public health;
g. The potential of the substance to produce psychic or physiological dependence liability;

and

h. Whether the substance is an immediate precursor of a substance already controlled

under this subchapter.

2. After considering the factors described in subsection 1, the board shall make a
recommendation to the general assembly, specifying the change which should be made in
existing schedules, if it finds that the potential for abuse or lack thereof of the substance is
not properly reflected by the existing schedules.

3.

If the board designates a substance as an immediate precursor, substances which are
precursors of the controlled precursor shall not be subject to control solely because they
are precursors of the controlled precursor. Such designations shall be made pursuant to the
procedures of chapter 17A.

4.

If any new substance is designated as a controlled substance under federal law and
notice of the designation is given to the board, the board shall similarly designate as controlled
the new substance under this chapter after the expiration of thirty days from publication in
the federal register of a final order designating a new substance as a controlled substance,
unless within that thirty-day period the board objects to the new designation. In that case the
board shall publish the reasons for objection and afford all interested parties an opportunity
to be heard. At the conclusion of the hearing the board shall announce its decision. Upon
publication of objection to a new substance being designated as a controlled substance under
this chapter by the board, control under this chapter is stayed until the board publishes its
decision. If a substance is designated as controlled by the board under this subsection the
control shall be considered a temporary amendment to the schedules of controlled substances
in this chapter. If the board so designates a substance as controlled, which is considered
a temporary amendment to the schedules of controlled substances in this chapter, and if
the general assembly does not amend this chapter to enact the temporary amendment and
make the enactment effective within two years from the date the temporary amendment
first became effective, the temporary amendment is repealed by operation of law two years
from the effective date of the temporary amendment. A temporary amendment repealed by
operation of law is subject to section 4.13 relating to the construction of statutes and the
application of a general savings provision.