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Regulatory Update #115

3 December - 17 December 2010

Registration model for oral equine electrolyte products

The APVMA has published a model for certain low-risk oral electrolytes for horses in exercise.  This model will allow such products to be registered with reduced cost and without technical evaluation.

Report on adverse experiences for 2009 published

The APVMA has released its 2009 report containing information on reports we have received about adverse experiences with veterinary medicines and agricultural chemicals.

New community questions on how endocrine disrupting chemicals and pesticides in drinking water are managed

The APVMA has published two new community questions:

State and territory contact details now available for management of use issues

Contact details have been published for the state and territory agencies that are responsible for managing the use of pesticides and veterinary medicines.

Amendment to the standard for the active constituent fenitrothion

The APVMA invites comment on a proposed change to nomenclature and limits of toxicological significant impurities (section 5.2) for the standard for fenitrothion until 7 February 2011.

New proposed standard for the active constituent N,N-Bis-(3-aminopropyl)-dodecylamine

The APVMA invites comment on the proposed standard for N,N-Bis-(3-aminopropyl)-dodecylamine until 7 February 2011.

Proposed variation to the registration of pyroxsulam and cloquintocet-mexyl in the product Crusader Herbicide

The APVMA invites comment on the trade implications of proposed variations to the registration of pyroxsulam and cloquintocet-mexyl in the product Crusader Herbicide until 4 January 2010.

Proposed variation to the registration of flupropanate in the product Tussock Herbicide

The APVMA invites comment on the trade implications of proposed variations to the registration of flupropanate in the product Tussock Herbicide until 4 January 2010.

New standard for the active constituent foramsulfuron

The APVMA has published a new standard for the active constituent foramsulfuron.

Call for Good Manufacturing Practice (GMP) Auditors

Are you an experienced auditor wanting to utilise your skills in a regulatory capacity?

Do you have high level experience in the production, regulation or quality control of veterinary chemicals or pharmaceuticals?

If this sounds like you, find out more about applying to become an APVMA-authorised GMP Auditor.

MRL Standards and ESI & WHP documents updated

The Maximum Residue Limits Standards and Export Slaughter Intervals and Chemical Withholding Periods documents have been updated for December 2010.

Reminder - open for public consultation

The APVMA is currently seeking comment on:

Applications

Read the latest Advice Summaries and Application Summaries.

Last updated on 17 February, 2011