Zobrazeno 1 - 10
of 240
pro vyhledávání: '"C.L. Galli"'
Autor:
C.L. Galli
Publikováno v:
Toxicology Letters. 368:S9
Publikováno v:
Toxicology Letters. 368:S102
Publikováno v:
Toxicology Letters. 368:S149
Akademický článek
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Autor:
Christophe Rousselle, U. Bernauer, L. Bodin, Q. Chaudhry, P.J. Coenraads, M. Dusinska, J. Ezendam, E. Gaffet, C.L. Galli, B. Granum, E. Panteri, V. Rogiers, Ch. Rousselle, M. Stepnik, T. Vanhaecke, S. Wijnhoven, A. Koutsodimou, A. Simonnard, W. Uter
Publikováno v:
Regulatory Toxicology and Pharmacology
Regulatory Toxicology and Pharmacology, Elsevier, 2018, 99, pp.129-130. ⟨10.1016/j.yrtph.2018.09.006⟩
Regulatory Toxicology and Pharmacology, Elsevier, 2018, 99, pp.129-130. ⟨10.1016/j.yrtph.2018.09.006⟩
Based on the data provided in the dossier, the SCCS considers Phenylene Bis-Diphenyltriazine, S86, safe for use as a UV-filter in sunscreen products at a concentration up to 5%. Because of the insoluble nature of S86 and as no data were provided on s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::48bd0775d5baeb2b927ec400a611d04e
https://hal.archives-ouvertes.fr/hal-01947582
https://hal.archives-ouvertes.fr/hal-01947582
Autor:
Vera Rogiers, U. Bernauer, L. Bodin, Q. Chaudhry, P.J. Coenraads, M. Dusinska, E. Ezendam, C.L. Galli, B. Granum, E. Panteri, V. Rogiers, Ch. Rousselle, M. Stepnik, T. Vanhaecke, S. Wijnhoven
Publikováno v:
Regulatory Toxicology and Pharmacology
Regulatory Toxicology and Pharmacology, Elsevier, 2017, 88, pp.328-329. ⟨10.1016/j.yrtph.2017.04.013⟩
Regulatory Toxicology and Pharmacology, Elsevier, 2017, 88, pp.328-329. ⟨10.1016/j.yrtph.2017.04.013⟩
• The SCCS considers the use of the Polyaminopropyl Biguanide not safe up to maximal concentration of 0.3% as preservative.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5eb1c61fca6d8e3627c70d9d9159d768
https://doi.org/10.1016/j.yrtph.2017.04.013
https://doi.org/10.1016/j.yrtph.2017.04.013
Autor:
Ulrike Bernauer, U. Bernauer, L. Bodin, Q. Chaudhry, P.J. Coenraads, M. Dusinska, E. Ezendam, C.L. Galli, B. Granum, E. Panteri, V. Rogiers, Ch. Rousselle, M. Stepnik, T. Vanhaecke, S. Wijnhoven
Publikováno v:
Regulatory Toxicology and Pharmacology
Regulatory Toxicology and Pharmacology, Elsevier, 2017, 88, pp.330-331. ⟨10.1016/j.yrtph.2017.04.014⟩
Regulatory Toxicology and Pharmacology, Elsevier, 2017, 88, pp.330-331. ⟨10.1016/j.yrtph.2017.04.014⟩
International audience
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::86ae8b9291ae0346ab02d5d04fff8fbd
https://hal.archives-ouvertes.fr/hal-01650477
https://hal.archives-ouvertes.fr/hal-01650477
Publikováno v:
Toxicology Letters. 258:S264-S265
Publikováno v:
Toxicology Letters. 238:S369-S370
Autor:
D.C. Dorman, G.J. Harry, R.A. Smith, Hugh A. Tilson, I.L. Campbell, Arie Bruinink, D. Ray, C.L. Galli, W. Classen, Melvin L. Billingsley
Publikováno v:
Environmental Health Perspectives
Risk assessment is a process often divided into the following steps: a) hazard identification, b) dose-response assessment, c) exposure assessment, and d) risk characterization. Regulatory toxicity studies usually are aimed at providing data for the