Evaluation of confirmatory data following the Article 12 MRL review for fludioxonil

The applicant Syngenta submitted a request to the competent national authority in France to evaluate the confirmatory data that were identified in the framework of the maximum residue level (MRL) review under Article 12 of Regulation (EC) No 396/2005 as not available. The applicant provided residue...

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Vydáno v:EFSA J
Hlavní autoři: Anastassiadou, Maria, Brancato, Alba, Carrasco Cabrera, Luis, Ferreira, Lucien, Greco, Luna, Jarrah, Samira, Kazocina, Aija, Leuschner, Renata, Magrans, Jose Oriol, Miron, Ileana, Nave, Stefanie, Pedersen, Ragnor, Reich, Hermine, Rojas, Alejandro, Sacchi, Angela, Santos, Miguel, Stanek, Alois, Theobald, Anne, Vagenende, Benedicte, Verani, Alessia
Médium: Artigo
Jazyk:Inglês
Vydáno: John Wiley and Sons Inc. 2019
Témata:
Reasoned Opinion
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC7009037/
https://ncbi.nlm.nih.gov/pubmed/32626430
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2903/j.efsa.2019.5812
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