A rationale for determining, testing, and controlling specific impurities in pharmaceuticals that possess potential for genotoxicity

Lutz Müller(Roche (Switzerland)), Larry P. Yotti(University of Vermont), Sheila M. Galloway(United States Military Academy), Betsy Fritschel(Johnson & Johnson (United States)), Ganapathy Mohan(Sanofi (United States)), John D. Mackinnon(GlaxoSmithKline (United Kingdom)), Charles Humfrey(AstraZeneca (United Kingdom)), Robert J. Mauthe(Pfizer (United States)), Chris Beels(GlaxoSmithKline (United Kingdom)), Christopher M. Riley(University of Strathclyde), Daniel Ness(Eli Lilly (United States)), Gopi Vudathala, Marta M. Andino(Pfizer (United States)), Alfons G. M. De Knaep(Janssen (Belgium)), David De Antonis(Pfizer (United States)), Dean Ellison(United States Military Academy), Rebecca D. Frank, Mark D. Smith, Joseph J. DeGeorge(United States Military Academy), Jane A. Fagerland(Abbott Fund), Michael R. O’Donovan, Nirdosh K. Jagota, Ernie Harpur(Sanofi (United States)), Alexander S. Jacks
Regulatory Toxicology and Pharmacology
January 19, 2006
Cited by 461


Related Papers