High-Throughput In Vivo Genotoxicity Testing: An Automated Readout System for the Somatic Mutation and Recombination Test (SMART)

Author:

Lombardot Benoit,Oh Chun-Taek,Kwak Jihoon,Genovesio Auguste,Kang Myungjoo,Hansen Michael Adsett Edberg,Han Sung-Jun

Publisher

Public Library of Science (PLoS)

Subject

Multidisciplinary

Reference30 articles.

1. Technical Guidance Document in Support of Commission Directive 93/67/EEC on Risk Assessment for New Notified Substances and Commission Regulation (EC) No 1488/94 on Risk Assessment for Existing Substances,1996

2. Regulation (EC) No 1907/2006 of the European Parliament and of the Council of 18 December 2006 Concerning the Registration, Evaluation, Authorisation and Restriction of Chemicals (REACH), Establishing a European Chemicals Agency, Amending Directive 1999/45/EC and Repealing Council Regulation (EEC) No 793/93 and Commission Regulation (EC) No 1488/94 as well as Council Directive 76/769/EEC and Commission Directives 91/155/EEC, 93/67/EEC, 93/105/EC and 2000/21/EC,2006

3. The International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use (ICH), Guidance on Genotoxicity Testing and Data Interpretation for Pharmaceuticals Intended for Human Use S2 (R1). 2012, Current Ste 2 version dated June. http://www.ich.org.

4. Can the pharmaceutical industry reduce attrition rates?;I Kola;Nature Reviews Drug Discovery,2004

5. Genotoxicity testing, a regulatory requirement for drug discovery and development: Impact of ICH guidelines;GB Jena;Indian Journal of Pharmacology,2002

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