In progress

Click on the tabs for more information about the status of each phase in the review process. For more information about how each phase is conducted, please read about the reconsideration process.


Work Plan

Click on the tabs for more information about the status of each phase in the review process. For more information about how each phase is conducted, please read about the reconsideration process.

Neonicotinoids Timeframe calculation pursuant to Regulation 78B of the Agricultural and Veterinary Chemicals Code Regulations 1995
A + B + 2E + 3C + J + D + X = 42 months

A = 13 months (Environment – level 1)
B = 13 months (Health – level 1)
C = 3 months (Finalisation – type 1)
D = 4 months
E = 0 months
J = 3 months (consultation with jurisdictional coordinator)
X = 0 months (in any other case)
1. Nomination Completed

1. Nomination

Phase status: Completed

Neonicotinoid (acetamiprid, clothianidin, dinotefuran, imidacloprid, thiacloprid, thiamethoxam) active constituents, product registrations and label approvals were nominated for review following identification of new environmental risks in 2019. As a result of the limited use pattern (in companion animals) and formulation (as oral tablets), the registered products and approved active constituent containing nitenpyram are considered to be outside the scope of this review.

2. Prioritisation Completed

2. Prioritisation

Phase status: Completed

3. Scoping and work plan Completed

3. Scoping and work plan

Phase status: Completed

The scope of the review includes reconsideration of neonicotinoid active constituents, chemical products and labels through assessments related to environment and worker safety.

The review scope document is available in the publication archive tab.

The work plan was first published on 19 November 2019.

4. Notice of reconsideration Completed

4. Notice of reconsideration

Phase status: Completed

The s 32 notice of reconsideration for active constituents, chemical products and labels for neonicotinoids was published in the Gazette on 19 November 2019.

The s 32 notice of reconsideration was given to holders and chemical coordinators of the states and territories upon commencement of the review on 19 November 2019.

An s 33 notice was sent to a holder on 6 April 2023 to request additional data.

5. Assessment In Progress

5. Assessment

Phase status: In Progress

When the component risk assessments have been completed, the proposed regulatory decisions will be drafted.

6. Proposed regulatory decision Forecasted

6. Proposed regulatory decision

Phase status: Forecasted

Publication of the proposed regulatory decisions for individual neonicotinoid actives are expected between August 2024 and June 2025.

7. Consultation Forecasted

7. Consultation

Phase status: Forecasted

The legislated timeframe for consultation following publication of the proposed regulatory decision is 3 months.

8. Final regulatory decision Forecasted

8. Final regulatory decision

Phase status: Forecasted

Following the close of the public consultation period on the proposed regulatory decision and consideration of submissions received, the final regulatory decision will be published.

Publication of the final regulatory decisions for all the neonicotinoids is forecast for November 2025.

9. Implementation Forecasted

9. Implementation

Phase status: Forecasted

The implementation period will begin on the date the final regulatory decision is made.

Publication Archive
Type Title Publication date
Gazette Notice of Reconsideration 19 November 2019