Claudia Stark

发表

Nonclinical Safety and Toxicology.

T. Steger-Hartmann, Claudia Stark, 2016, Handbook of experimental pharmacology.

Science‐Based Approach to Harmonize Contraception Recommendations in Clinical Trials and Pharmaceutical Labels

K. Turner, C. Bowman, K. Thompson, 2022, Clinical pharmacology and therapeutics.

Regulatory acceptability of the minipig in the development of pharmaceuticals, chemicals and other products.

J. W. van der Laan, Claudia Stark, P. Mcanulty, 2010, Journal of pharmacological and toxicological methods.

A European pharmaceutical company initiative challenging the regulatory requirement for acute toxicity studies in pharmaceutical drug development.

Sally Robinson, Kathryn Chapman, David Dreher, 2008, Regulatory toxicology and pharmacology : RTP.

Challenging the regulatory requirement for conventional acute toxicity studies in pharmaceutical drug development

David Dreher, Kathryn L Chapman, S. Robinson, 2007 .

Vehicle Systems and Excipients Used in Minipig Drug Development Studies

M. Festag, I. B. Bøgh, S. Milano, 2016, Toxicologic pathology.

A global pharmaceutical company initiative: an evidence-based approach to define the upper limit of body weight loss in short term toxicity studies.

Fiona Sewell, Sally Robinson, Kathryn Chapman, 2013, Regulatory toxicology and pharmacology : RTP.

Optimising the design of preliminary toxicity studies for pharmaceutical safety testing in the dog.

Robert Combes, David Smith, Barry Phillips, 2005, Regulatory toxicology and pharmacology : RTP.

A European pharmaceutical company initiative challenging the regulatory requirement for acute toxicity studies in pharmaceutical drug development.

David Dreher, Kathryn L Chapman, M. Festag, 2008, Regulatory toxicology and pharmacology : RTP.

Vehicle Systems and Excipients Used in Minipig Drug Development Studies

M. Festag, I. B. Bøgh, S. Milano, 2016, Toxicologic pathology.