Evaluation of confirmatory data following the Article 12 MRL review for napropamide. [PDF]
The applicant UPL Europe Ltd submitted a request to the competent national authority in Slovenia to evaluate the confirmatory data that were identified for napropamide in the framework of the maximum residue levels (MRLs) review under Article 12 of Regulation (EC) No 396/2005 as not available.
European Food Safety Authority (EFSA) +21 more
europepmc +4 more sources
Evaluation of confirmatory data following the Article 12 MRL review for tebufenpyrad. [PDF]
The applicant Belchim Crop Protection submitted a request to the competent national authority in Germany to evaluate the confirmatory data that were identified for tebufenpyrad in the framework of the maximum residue level (MRL) review under Article 12 of Regulation (EC) No 396/2005 as not available.
European Food Safety Authority (EFSA) +22 more
europepmc +4 more sources
Evaluation of confirmatory data following the Article 12 MRL review for diquat. [PDF]
The applicant Syngenta Crop Protection AG submitted a request to the competent national authority in Sweden to evaluate the confirmatory data that were identified for diquat in the framework of the MRL review under Article 12 of Regulation (EC) No 396/2005 as not available.
European Food Safety Authority (EFSA) +20 more
europepmc +4 more sources
Evaluation of confirmatory data following the Article 12 MRL review for paclobutrazol. [PDF]
The applicant Proplan Plant Protection Company submitted a request to the competent national authority in Austria (originally the United Kingdom) to evaluate the confirmatory data that were identified for paclobutrazol in the framework of the MRL review under Article 12 of Regulation (EC) No 396/2005 as not available.
European Food Safety Authority (EFSA) +22 more
europepmc +4 more sources
Evaluation of confirmatory data following the Article 12 MRL review for aclonifen. [PDF]
The applicant Bayer Crop Science submitted a request to the competent national authority in the Netherlands to evaluate the confirmatory data that were identified for aclonifen in the framework of the maximum residue level (MRL) review under Article 12 of Regulation (EC) No 396/2005 as not available.
European Food Safety Authority (EFSA) +20 more
europepmc +5 more sources
Evaluation of confirmatory data following the Article 12 MRL review for spinetoram. [PDF]
Abstract The applicant Corteva Agriscience International Sàrl submitted a request to the competent national authority in Croatia to evaluate the confirmatory data that were identified in the framework of the MRL review under Article 12 of Regulation (EC) No 396/2005. The applicant submitted, a confirmatory analytical method for high oil content and dry
European Food Safety Authority (EFSA) +21 more
europepmc +3 more sources
Evaluation of confirmatory data following the Article 12 MRL review for thiabendazole. [PDF]
The applicant Syngenta Crop Protection AG submitted a request to the competent national authority in Spain to evaluate the confirmatory data that were identified for in the framework of the maximum residue level (MRL) review under Article 12 of Regulation (EC) No 396/2005 as not available.
European Food Safety Authority (EFSA) +21 more
europepmc +4 more sources
Targeted review of maximum residue levels (MRLs) for fenarimol
In accordance with Article 43 of Regulation (EC) 396/2005, EFSA received a request from the European Commission to review the existing maximum residue levels (MRLs) for the non-approved active substance fenarimol in view of the possible lowering of the MRLs. EFSA investigated the origin of the current EU MRLs.
European Food Safety Authority (EFSA) +30 more
openaire +3 more sources
Setting of an import tolerance for glyphosate in soyabeans
In accordance with Article 6 of Regulation (EC) No 396/2005, the applicant Corteva submitted a request to the competent national authority in Germany to set an import tolerance for the active substance glyphosate in genetically modified (GM) soyabeans ...
EFSA (European Food Safety Authority)
doaj +1 more source
Targeted review of maximum residue levels (MRLs) for fenpropathrin
In accordance with Article 43 of Regulation (EC) 396/2005, EFSA received a request from the European Commission to review the existing maximum residue levels (MRLs) for the non-approved active substance fenpropathrin in view of the possible lowering of the MRLs. EFSA investigated the origin of the current EU MRLs.
European Food Safety Authority (EFSA) +31 more
openaire +3 more sources

