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Did Not Advance

Kentucky legislature establishes terminal distributor permits and broadens drug safety oversight in Jimmie's Law

Original title: AN ACT relating to pharmaceutical drug safety and declaring an emergency.

Last action · March 4, 2026: to Licensing, Occupations, & Administrative Regulations (H)Sponsors: Vanessa Grossl and 2 others

Introduced
Committee
Floor Vote
Passed
Law

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What This Bill Proposed

Kentucky enacts Jimmie's Law to strengthen pharmaceutical drug safety by requiring s of prescription drugs to obtain a board permit starting January 1, 2027, establishing strict and adverse event reporting rules, and declaring an emergency for immediate implementation upon passage.

Why it matters

The measure introduces mandatory state permitting for s and new reporting duties for adverse events, altering operational compliance for entities handling prescription drugs within Kentucky and establishing criminal penalties for unauthorized drug transfers.

Background
  • The Kentucky General Assembly regularly updates pharmaceutical regulations under KRS Chapter 315 to ensure drug safety and oversee practitioners and pharmacies. context

Who It Would Have Affected

Groups the bill's text would have affected, as described in the record. Being affected is not a position for or against it.

Directly affected

Terminal distributors of prescription drugs

Entities possessing, holding, or procuring prescription drugs must obtain a separate permit for each location starting January 1, 2027, and comply with board inspection and safety rules.

Directly affected

Pharmacies and Pharmacists

Pharmacies face new reporting timelines for serious adverse events, stricter compounding guidelines under USP standards, and restrictions on drug purchasing sources.

Directly affected

Kentucky Board of Pharmacy

The board receives expanded regulatory and inspection authority over terminal distributors, new reporting requirements to professional licensing boards, and mandates to submit annual reports to the Legislative Research Commission.

Key Facts

You don't have to trust us. Each fact below is taken straight from the official document - click any one to see the exact passage, highlighted in the original.

Frequently Asked Questions

What must pharmacies do if they become aware of a serious adverse event?
Pharmacies or s that become aware of a serious adverse event associated with a drug product must report it to the board within five business days.
Who is exempt from obtaining a terminal distributor permit?
Exemptions include licensed practitioners prescribing in their usual course of practice without possessing or dispensing drugs, persons possessing specific emergency or school medications like asthma or overdose reversal drugs, and facilities owned and operated by federal agencies such as the Department of Defense or Department of Veterans Affairs.

What else do you want to know?

News Coverage

No news coverage found yet. Articles are indexed twice daily.

Where This Stands

This bill did not become law - Died at adjournment · in House committee.

Procedural history

2 actions
  1. Mar 4, 2026HouseCommittee
    to Licensing, Occupations, & Administrative Regulations (H)
  2. Feb 25, 2026HouseIntroduced
    introduced in House to Committee on Committees (H)

Version history

Only one version on file - nothing to compare yet. As later stages (committee substitute, engrossed, enrolled) are captured, the redline appears here.

View official text →

Lobbying Activity

No state lobbying filings in our records match this bill. Federal lobbying reports (LDA) cover Congress, so they are not listed on state bills.

Full breakdown

Who this bill affects and the strongest case for and against it, written only from the bill’s own text.

Sponsors

Discoveries

1 pattern noticed across the record

Patterns POLISCOPE noticed across the record. These are observations to investigate, not conclusions.

policy shift99% confidence

Mandatory Terminal Distributor Permitting

Kentucky is extending formal permit requirements to terminal distributors of prescription drugs with an enforcement deadline of January 1, 2027.

Connected Entities

Interim Joint Committee on Health Services, Legislative Research Commission, Franklin Circuit Court and 8 more
OrganizationInterim Joint Committee on Health Services“Committee receiving reports on audits and inspections”Map →
OrganizationLegislative Research Commission“Recipient of annual inspection and investigation reports”Map →
locationFranklin Circuit Court“Court for appeals of final board orders”Map →
PersonKim Moser“Cosponsor of the bill”Map →
OrganizationGeneral Assembly“Legislative body enacting the measure”Map →
PersonVanessa Grossl“Primary sponsor of the bill”Map →
OrganizationNational Association of Boards of Pharmacy“Provider of Digital Pharmacy Accreditation Program”Map →
OrganizationCabinet for Health and Family Services“State cabinet involved in health and sanitation standards”Map →
OrganizationKentucky Board of Pharmacy“Board tasked with issuing permits and regulating pharmacies and distributors”Map →
PersonRobert Duvall“Cosponsor of the bill”Map →
OrganizationUnited States Food and Drug Administration“Federal agency approving drugs and facilities”Map →

Sources

Open source document

apps.legislature.ky.gov

Analysis Score

0–100
  • Significance20
    Lowered because this bill did not pass (its text scored 85)
  • Controversy25
    Intensity of disagreement among stakeholders
  • Entertainment5
    Compellingness for a non-policy-wonk reader
  • Buzz30
    Current news / social attention level

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