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Regulatory Toxicology and Pharmacology : RTP|January 17, 2023
The use of recovery animals in nonclinical safety assessment studies with monoclonal antibodies: further 3Rs opportunities remainHelen Prior, Laura Andrews, Annick Cauvin, et al.Regulatory Toxicology and Pharmacology : RTP|January 2, 2023
Re-evaluating the need for chronic toxicity studies with therapeutic monoclonal antibodies, using a weight of evidence approachHsiao-Tzu Chien, Helen Prior, Laura Andrews, et al.Journal of Pharmacological and Toxicological Methods|May 14, 2013
A multi-site comparison of in vivo safety pharmacology studies conducted to support ICH S7A & B regulatory submissionsLorna Ewart, Aileen Milne, Debbie Adkins, et al.Regulatory Toxicology and Pharmacology : RTP|April 13, 2026
Minimizing use of nonhuman primates to inform risk to fertility and of adverse pregnancy outcomes with pharmaceuticalsChristopher J Bowman, Ann Baker, Diann L Blanset, et al.Regulatory Toxicology and Pharmacology : RTP|March 4, 2020
Opportunities for use of one species for longer-term toxicology testing during drug development: A cross-industry evaluationHelen Prior, Paul Baldrick, Sonja Beken, et al.Journal of Pharmacological and Toxicological Methods|June 23, 2020
INSPIRE: A European training network to foster research and training in cardiovascular safety pharmacologyPieter-Jan D Guns, Brian D Guth, Stefan Braam, et al.Pageof 3