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Regulatory acceptance and use of the Extended One Generation Reproductive Toxicity Study within Europe.
Schiffelers, Marie-Jeanne W A; Blaauboer, Bas J; Bakker, Wieger E; Hendriksen, Coenraad F M; Krul, Cyrille.
Afiliación
  • Schiffelers MJ; Utrecht University School of Governance, Bijlhouwerstraat 6, 3511 ZC Utrecht, The Netherlands. Electronic address: m.j.w.a.schiffelers@uu.nl.
  • Blaauboer BJ; Utrecht University, Institute for Risk Assessment Sciences (IRAS), P.O. Box 80.178, 3508 TD Utrecht, The Netherlands.
  • Bakker WE; Utrecht University School of Governance, Bijlhouwerstraat 6, 3511 ZC Utrecht, The Netherlands.
  • Hendriksen CF; Utrecht University, Faculty of Veterinary Medicine, Department Animals in Science and Society, P.O. Box 80.163, 3508 TD Utrecht, The Netherlands; Institute for Translational Vaccinology (Intravacc), P.O. Box 450, 3720 AL Bilthoven, The Netherlands.
  • Krul C; TNO, P.O. Box 360, 3700 AJ Zeist, The Netherlands; University of Applied Sciences Utrecht, Life Sciences & Chemistry, F.C. Dondersstraat 65, 3572 JE Utrecht, The Netherlands.
Regul Toxicol Pharmacol ; 71(1): 114-24, 2015 Feb.
Article en En | MEDLINE | ID: mdl-25445002
ABSTRACT
The two-generation study (OECD TG 416) is the standard requirement within REACH to test reproductive toxicity effects of chemicals with production volumes >100 tonnes. This test is criticized in terms of scientific relevance and animal welfare. The Extended One Generation Reproductive Toxicity Study (EOGRTS), incorporated into the OECD test guidelines in 2011 (OECD TG 443) has the potential to replace TG 416, while using only one generation of rats and being more informative. However, its regulatory acceptance proved challenging. This article reconstructs the process of regulatory acceptance and use of the EOGRTS and describes drivers and barriers influencing the process. The findings derive from literature research and expert interviews. A distinction is made between three sub-stages; The stage of Formal Incorporation of the EOGRTS into OECD test guidelines was stimulated by retrospective analyses on the value of the second generation (F2), strong EOGRTS advocates, animal welfare concern and changing US and EU chemicals legislation; the stage of Actual Regulatory Acceptance within REACH was challenged by legal factors and ongoing scientific disputes, while the stage of Use by Industry is influenced by uncertainty of registrants about regulatory acceptance, high costs, the risk of false positives and the manageability of the EOGRTS.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Reproducción / Industria Química / Guías como Asunto / Pruebas de Toxicidad / Regulación Gubernamental Tipo de estudio: Guideline / Prognostic_studies / Qualitative_research País/Región como asunto: Europa Idioma: En Revista: Regul Toxicol Pharmacol Año: 2015 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Reproducción / Industria Química / Guías como Asunto / Pruebas de Toxicidad / Regulación Gubernamental Tipo de estudio: Guideline / Prognostic_studies / Qualitative_research País/Región como asunto: Europa Idioma: En Revista: Regul Toxicol Pharmacol Año: 2015 Tipo del documento: Article
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