Articles | Volume 7, issue 1
https://doi.org/10.5194/pb-7-1-2020
https://doi.org/10.5194/pb-7-1-2020
Short communication
 | 
11 Mar 2020
Short communication |  | 11 Mar 2020

Group size experiences with enhanced pre- and postnatal development studies in the long-tailed macaque (Macaca fascicularis)

C. Marc Luetjens, Antje Fuchs, Ann Baker, and Gerhard F. Weinbauer

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Cited articles

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ICH M3(R2): Guidance on nonclinical safety studies for the conduct of human clinical trials and marketing authorization for pharmaceuticals, available at: https://database.ich.org/sites/default/files/M3_R2_Guideline.pdf (last access: 3 March 2020), 2009. 
ICH S6(R1): Preclinical safety evaluation of biotechnology-derived pharmaceuticals, available at: https://database.ich.org/sites/default/files/S6_R1_Guideline_0.pdf (last access: 3 March 2020), 2011. 
Jarvis, P., Srivastav, S., Vogelwedde, E., Stewart, J., Mitchard, T., and Weinbauer, G. F.: The cynomolgus monkey as a model for developmental toxicity studies: variability of pregnancy losses, statistical power estimates and group size considerations, Birth Defects Res. B, 89, 175–187, 2010.  
Krejsa, M., Neradilek, M. B., Polissar, N. L., Cox, N., Clark, D., Cowan, L., Bussiere, J., and Lebrec, H.: An inter-laboratory retrospective analysis of immunotoxicological endpoints in non-human primates: Flow cytometry immunophenotyping, J. Immunotoxicol., 10, 361–372, 2013. 
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