Evaluating the lifetime cumulative dose as a basis for carcinogenic potency of nitrosamines – a key tenet underpinning less-than-lifetime approaches for establishing acceptable intake limits
Susan P. Felter(Procter & Gamble (United States)), Joel P. Bercu(Gilead Sciences (United States)), Matthew Schmitz(Takeda (United States)), Alisa Vespa(Health Canada), David J. Ponting, Robert Thomas, Andreas Zeller(Roche (Switzerland)), Timothy J. McGovern(Center for Drug Evaluation and Research), Bodo Haas(Federal Institute for Drugs and Medical Devices), Anthony M Lynch(Age UK), Ashley M Mudd(Procter & Gamble (United States)), Raechel Puglisi(Health and Environmental Sciences Institute), Yi Yan Yang(Institute of Bioengineering and Nanotechnology), Roland Froetschl(Federal Institute for Drugs and Medical Devices), Angela White(GlaxoSmithKline (United Kingdom))
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