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Australian OGTR: DIR 089 - Notification of Licence Application - Limited and controlled release of white clover genetically modified to resist infection by Alfalfa mosaic virus

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Australia
August 8, 2008

DIR 089 - Limited and controlled release of white clover genetically modified to resist infection by Alfalfa mosaic virus
http://www.ogtr.gov.au/internet/ogtr/publishing.nsf/Content/dir089-3/$FILE/dir089ebnotific.pdf

NOTIFICATION OF APPLICATION

Receipt of licence application from the Victorian Department of Primary Industries for dealings involving intentional release of genetically modified white clover: DIR 089

Application

The Office of the Gene Technology Regulator (OGTR) has received a licence application (DIR 089) from the Victorian Department of Primary Industries (DPI Victoria) for an intentional release of genetically modified (GM) white clover into the Australian environment which qualifies as a limited and controlled release under section 50A of the Gene Technology Act 2000 (the Act).

DPI Victoria is seeking approval to conduct research with one white clover line that has been genetically modified to resist infection with Alfalfa mosaic virus. The release is proposed to take place at one site in the NSW shire of Greater Hume, on a maximum area of 633 m2 between March 2009 and August 2011.

The GM white clover line proposed for release in this application has been previously approved for release under DIR 047/2003, and was the subject of four earlier releases under the former voluntary system overseen by the Genetic Manipulation Advisory Committee (GMAC): PR-64, PR-64X, PR-64X2 and PR-67. No plant materials from the GM white clover would be used for human food or animal feed.

Purpose of this notification

A comprehensive Risk Assessment and Risk Management Plan (RARMP) for the application is currently being prepared. I expect this to be released for public comment and advice from a broad range of experts, agencies and authorities in October 2008. The Act specifies a 30 day minimum consultation period if no significant risks to human health and safety of the environment are identified, and a 50 day minimum consultation period if significant risks are identified.

In the interim, you can obtain a copy of the application itself by contacting my Office (see contact details below, please quote the reference number DIR 089. As the application is quite lengthy, you may prefer to view a summary of the application, which is posted on our website along with this document (under ‘What’s New’). If you would like to receive a hard copy of the application summary, please contact us and we will post it to you.

If you have questions about the application, or how you can provide comment, please contact the OGTR at:
The Office of the Gene Technology Regulator,
MDP 54, GPO Box 9848, Canberra, ACT, 2601
Telephone: 1800 181 030
Facsimile: 02 6271 4202
E-mail: ogtr@health.gov.au
Website http://www.ogtr.gov.au

DIR 089 - Licence Application Summary (PDF 75 KB)

 

 

 

 

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