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Australia OGTR - DIR 124 - Invitation to comment on commercial release of genetically modified cotton


Australia
March 14, 2014

DIR 124 - Commercial release of cotton genetically modified for insect resistance and herbicide tolerance

DIR 124 - Invitation to comment on commercial release of genetically modified (GM) cotton
19 March 2014

DIR 124 - Invitation to Comment on a Consultation Risk Assessment and Risk Management Plan (RARMP) for Commercial Release of Cotton Genetically Modified for Insect Resistance and Herbicide Tolerance - Comments close on 14 May 2014 - posted 19 March 2014 (PDF 30 KB)

DIR 124 - Questions & Answers (PDF 16 KB)

DIR 124 - Consultation Risk Assessment and Risk Management Plan (RARMP) Summary (PDF 95 KB)

DIR 124 – Full Consultation Risk Assessment and Risk Management Plan (RARMP) for Commercial Release of Cotton Genetically Modified for Insect Resistance and Herbicide Tolerance (PDF 603 KB)

DIR 124 – Licence Application Summary (PDF 45 KB)

Australia’s gene technology regulatory system is designed to protect the health and safety of people and the environment by identifying risks posed by, or as a result of, gene technology and managing those risks.

The Gene Technology Regulator is currently assessing licence application DIR 124 from Monsanto Australia Ltd for a commercial release of two types of GM cotton. Bollgard® III cotton has been genetically modified for insect resistance and Bollgard® III x Roundup Ready Flex® cotton has been genetically modified both for insect resistance and for tolerance to the herbicide glyphosate.

Subject to any State government requirements imposed for marketing reasons, the proposed commercial release of the GM cotton plants would be Australia wide. Products from the GM cotton plants are proposed to be used in the same way as those from non-GM and other commercially approved GM cotton.

A consultation Risk Assessment and Risk Management Plan (RARMP) has been prepared, which concludes that the proposed release would pose negligible risk to human health and safety or to the environment. Draft licence conditions are proposed to ensure there is ongoing oversight of the release.

The Regulator welcomes written submissions in order to finalise the RARMP, which will then inform the decision on whether or not to issue a licence. The consultation RARMP and related documents can be obtained from the OGTR website under ‘What’s New’ or by contacting the Office. Please quote application DIR 124 in any correspondence.

Submissions should be received by close of business on 14 May 2014.

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
OGTR Website
 

Reference material

 



More news from: OGTR (Office of the Gene Technology Regulator)


Website: http://www.ogtr.gov.au

Published: March 19, 2014

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