Genotoxic Impurities in Pharmaceutical Manufacturing: Sources, Regulations, and Mitigation-Reference-Cited by-同舟云学术

Genotoxic Impurities in Pharmaceutical Manufacturing: Sources, Regulations, and Mitigation

Published:2015-08-07 Issue:16 Volume:115 Page:8182-8229
ISSN:0009-2665
Container-title:Chemical Reviews
language:en
Short-container-title:Chem. Rev.

Author:

Szekely Gyorgy¹,Amores de Sousa Miriam C.²,Gil Marco³,Castelo Ferreira Frederico²,Heggie William³

Affiliation:

1. School of Chemical Engineering & Analytical Science, The University of Manchester, The Mill, Sackville Street, Manchester M13 9PL, United Kingdom

2. Department of Bioengineering and Institute for Bioengineering and Biosciences (iBB), Instituto Superior Técnico, Universidade de Lisboa, Avenida Rovisco Pais, 1049-001, Lisbon, Portugal

3. Hovione FarmaCiencia SA, R&D, Sete Casas, 2674-506, Loures, Portugal

Funder

Fundação para a Ciência e a Tecnologia

Publisher

American Chemical Society (ACS)

Subject

General Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/cr300095f

Reference316 articles.

1. Web of Science.http://thomsonreuters.com/products_services/science/science_products/a-z/web_of_science/, accessed April 27, 2012.

2. Approaches to Assessment, Testing Decisions, and Analytical Determination of Genotoxic Impurities in Drug Substances

3. Three new consensus QSAR models for the prediction of Ames genotoxicity

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