环境风险评估

Integrated Life-Cycle and Risk Assessment for Industrial Processes and Products Pub Date : 2003-11-24 DOI:10.1201/9780203488171.CH4

M. Schuhmacher, M. Mari, Michael P. Tsang, G. Sonnemann

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引用次数: 0

摘要

新药物在开发过程中对其生物降解性和初始生态毒性进行了研究。注册时，根据相关法规的要求，根据长期环境影响和先进的环境命运数据，制定最先进的全面环境风险评估。虽然不是监管要求，但罗氏也调查旧的药物物质，通常以更简单的规模，以评估其环境风险。

本文章由计算机程序翻译，如有差异，请以英文原文为准。

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Environmental Risk Assessment

New pharmaceutical substances are investigated for biodegradability and initial ecotoxicity during their development. For registration, a full state-of-the-art environmental risk assessment is developed based on chronic environmental effects and advanced environmental fate data, as required by the pertinent regulations. While not a regulatory requirement, Roche also investigates older pharmaceutical substances, normally at a simpler scale, in order to assess their environmental risks.

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Integrated Life-Cycle and Risk Assessment for Industrial Processes and Products

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