Permitted Daily Exposure for Diisopropyl Ether as a Residual Solvent in Pharmaceuticals
Author:
Affiliation:
1. Department of Physiology and Pharmacology Vittorio Erspamer, University of Rome Sapienza, Rome, Italy
2. Agenzia Italiana del Farmaco (AIFA), Rome, Italy
Publisher
The Korean Society of Toxicology
Subject
Health, Toxicology and Mutagenesis,Toxicology
Link
http://pdf.medrang.co.kr/TR/2018/034/TR034-02-04.pdf
Reference49 articles.
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2. Harrington, PJ (2011). Pharmaceutical Process Chemistry for Synthesis: Rethinking the Routes to Scale-Up. Hoboken, NJ, USA: John Wiley & Sons
3. Sittig, M (2013). Pharmaceutical Manufacturing Encyclopedia. Norwich, NY, USA: William Andrew Publishing
4. Klimisch, HJ, Andreae, M, and Tillmann, U (1997). A systematic approach for evaluating the quality of experimental toxicological and ecotoxicological data. Regul Toxicol Pharmacol. 25, 1-5.
5. A Systematic Approach for Evaluating the Quality of Experimental Toxicological and Ecotoxicological Data
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