Public consultation on proposed amendments to the Poisons Standard - ACMS, ACCS & Joint ACMS-ACCS, MARCH 2026
Overview
Scheduling amendments referred to expert advisory committee
This consultation is for applications and delegate initiated proposals to amend the Poisons Standard. The scheduling amendments and any submissions received will be considered at the MARCH 2026 meetings of the Advisory Committee on Medicines Scheduling (ACMS) and the Advisory Committee on Chemicals Scheduling (ACCS) and the Joint meeting of ACMS and ACCS.
The closing date for this consultation is close of business 29 January 2026. All submissions received by the deadline will be considered by the delegate before they make an interim decision.
The proposals under consultation are detailed in the public notice of March 2026.
Substances for which public comment is sought:
ACMS:
- First-generation sedating antihistamines
- Melatonin
ACCS:
- Flufenoximacil
- Oxalic Acid
Joint meeting of ACMS-ACCS:
- Methylene blue
What happens next
All public submissions will be published on the TGA website at Public submissions on scheduling matters, unless marked confidential or indicated otherwise in the submission information (see Privacy and your Personal information).
Public submissions are an important part of the process for amending the Poison Standard, and are published on the TGA website using the consultation hub. Submissions by the public may not reflect the views of the Department of Health, Disability and Ageing or TGA. Published submissions should not be taken as being endorsed by the Department or TGA.
Following consideration of public submissions received before the closing date and advice from the expert advisory committee/s, decisions on the proposed amendments are anticipated to be published as interim decisions on the TGA website: Scheduling delegate's interim decisions & invitations for further comment at a later date.
Audiences
- Anyone from any background
Interests
- Aboriginal and Torres Strait Islander health
- Advertising
- Advisory bodies and committees
- Alcohol
- Applications and Forms
- Artificial Intelligence (AI)
- Children's health
- Chronic disease
- Clinical trials
- Communicable diseases
- Compliance and enforcement
- COVID-19
- Dental health
- Drugs and substance abuse
- e-Health
- Environmental health
- Fees and payments
- Food standards
- Health insurance
- Health technology
- Hearing
- Hospitals
- Immunisation
- Import and export
- Labelling and packaging
- Learning and development
- Legislation
- Manufacturing
- Medicare
- Mental health
- Non-prescription medicines
- Organ and tissue donation
- Pharmaceutical benefits
- Pharmacovigilance
- Prescription drugs
- Preventative health
- Regulatory policy
- Rural health services
- Safety
- Scheduling/Poisons standard
- Shortages
- Tobacco
- Unique Device Identification (UDI)
- Women's health
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