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Harry Yang

Showing results (1-10 of 53) with videos related to

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PDA Journal of Pharmaceutical Science and Technology|April 10, 2013
Establishing acceptable limits of residual DNAHarry Yang
PDA Journal of Pharmaceutical Science and Technology|October 3, 2013
Setting Specifications of Correlated Quality Attributes through Multivariate Statistical ModellingHarry Yang
PDA Journal of Pharmaceutical Science and Technology|February 7, 2013
How Many Batches Are Needed for Process Validation under the New FDA Guidance?Harry Yang
Biologicals : Journal of the International Association of Biological Standardization|September 29, 2012
Statistical evaluations of viral clearance studies for biological productsNa Li, Harry Yang
Journal of Biopharmaceutical Statistics|December 2, 2014
Guest editors' note: special issue on recent developments in statistical approaches for chemistry and manufacturing control (CMC) and quality-by-design(QbD)Yi Tsong, Harry Yang
PDA Journal of Pharmaceutical Science and Technology|January 23, 2016
A Bayesian Approach to Residual Host Cell DNA Safety AssessmentHarry Yang, Jianchun Zhang
Journal of Biopharmaceutical Statistics|February 5, 2019
A fast and reliable test for parallelism in bioassaySteven Novick, Harry Yang
PDA Journal of Pharmaceutical Science and Technology|December 15, 2015
A Generalized Pivotal Quantity Approach to Analytical Method Validation Based on Total ErrorHarry Yang, Jianchun Zhang
PDA Journal of Pharmaceutical Science and Technology|April 19, 2017
Evaluation of Different Estimation Methods for Accuracy and Precision in Biological Assay ValidationBinbing Yu, Harry Yang
PDA Journal of Pharmaceutical Science and Technology|November 23, 2013
A Risk-based Approach to Setting Sterile Filtration Bioburden LimitsHarry Yang, Na Li, Stephen Chang
Pageof 6

Showing results (1-10 of 53) with videos related to

Sort By:
Pageof 6
PDA Journal of Pharmaceutical Science and Technology|April 10, 2013
Establishing acceptable limits of residual DNAHarry Yang
PDA Journal of Pharmaceutical Science and Technology|October 3, 2013
Setting Specifications of Correlated Quality Attributes through Multivariate Statistical ModellingHarry Yang
PDA Journal of Pharmaceutical Science and Technology|February 7, 2013
How Many Batches Are Needed for Process Validation under the New FDA Guidance?Harry Yang
Biologicals : Journal of the International Association of Biological Standardization|September 29, 2012
Statistical evaluations of viral clearance studies for biological productsNa Li, Harry Yang
Journal of Biopharmaceutical Statistics|December 2, 2014
Guest editors' note: special issue on recent developments in statistical approaches for chemistry and manufacturing control (CMC) and quality-by-design(QbD)Yi Tsong, Harry Yang
PDA Journal of Pharmaceutical Science and Technology|January 23, 2016
A Bayesian Approach to Residual Host Cell DNA Safety AssessmentHarry Yang, Jianchun Zhang
Journal of Biopharmaceutical Statistics|February 5, 2019
A fast and reliable test for parallelism in bioassaySteven Novick, Harry Yang
PDA Journal of Pharmaceutical Science and Technology|December 15, 2015
A Generalized Pivotal Quantity Approach to Analytical Method Validation Based on Total ErrorHarry Yang, Jianchun Zhang
PDA Journal of Pharmaceutical Science and Technology|April 19, 2017
Evaluation of Different Estimation Methods for Accuracy and Precision in Biological Assay ValidationBinbing Yu, Harry Yang
PDA Journal of Pharmaceutical Science and Technology|November 23, 2013
A Risk-based Approach to Setting Sterile Filtration Bioburden LimitsHarry Yang, Na Li, Stephen Chang
Pageof 6