Germany | BCH-RA-DE-112108 | Risk Assessment generated by a regulatory process | Biosafety Clearing-House

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Risk Assessment generated by a regulatory process (RA)
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BCH-RA-DE-112108-2   |   PDF   |   Print   |  
last updated: 23 Nov 2020
General Information
6786-01-0090 (adv. 42010.0090); Summary of the risk assessment of a deliberate release (field trial) of genetically modified oilseed rape (Brassica napus L. ssp. oleifera) Ms8, Rf3 and Ms8 x Rf3, issued by the German Competent Authority
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22 Jul 1998
Risk assessment details
Methodology and points to consider
The execution of this field trial is not expected to have a negative impact on human or animal health, or on the environment.
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Adverse effects on human or animal health or on the environment are not expected.
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8 field sites in Germany, for details refer to the German LMO/GMO location register (https://apps2.bvl.bund.de/stareg_web/localeSwitch.do?language=en&page=/showflaechen.do?)
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PCR-based event-specific methods for Ms8 (InVigor™ canola – ACS-BNØØ5-8) and Rf3 (InVigor™ canola – ACS-BNØØ3-6) were submitted with a notification for placing on the market [under Directive 90/220/EEC].
These methods are available at: http://gmo-crl.jrc.ec.europa.eu/StatusOfDossiers.aspx
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Additional information
-   deliberate release, no placing on the market
-   field trial, not for human consumption or for feed purposes

-  There is no Summary Notification Information Format available on the Internet (WebSNIF) for B/DE/98/90
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Records referencing this document Show in search
Record type Field Record(s)
Country's Decision or any other Communication Risk assessment 1