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Lawrence X Yu

Showing results (21-30 of 75) with videos related to

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International Journal of Pharmaceutics|January 17, 2004
Feasibility studies of utilizing disk intrinsic dissolution rate to classify drugsLawrence X Yu, Alan S Carlin, Gordon L Amidon, et al.
International Journal of Pharmaceutics|July 28, 2022
Profiling the process development of Wurster coating for modified release capsule products in approved drug product applicationsZhouxi Wang, Xiang Yu, Larisa Wu, et al.
The AAPS Journal|May 10, 2008
Quality by design: concepts for ANDAsRobert A Lionberger, Sau Lawrence Lee, Laiming Lee, et al.
International Journal of Pharmaceutics|December 29, 2016
Building parity between brand and generic peptide products: Regulatory and scientific considerations for quality of synthetic peptidesLarisa C Wu, Fu Chen, Sau L Lee, et al.
International Journal of Pharmaceutics: X|September 14, 2019
FDA's new pharmaceutical quality initiative: Knowledge-aided assessment & structured applicationsLawrence X Yu, Andre Raw, Larisa Wu, et al.
Pharmaceutical Research|April 15, 2011
The BCS, BDDCS, and regulatory guidancesMei-Ling Chen, Gordon L Amidon, Leslie Z Benet, et al.
Pharmaceutical Research|January 27, 2012
Use of partial AUC to demonstrate bioequivalence of Zolpidem Tartrate Extended Release formulationsRobert A Lionberger, Andre S Raw, Stephanie H Kim, et al.
Molecular Pharmaceutics|December 5, 2006
A provisional biopharmaceutical classification of the top 200 oral drug products in the United States, Great Britain, Spain, and JapanToshihide Takagi, Chandrasekharan Ramachandran, Marival Bermejo, et al.
Scientific Reports|September 27, 2017
A multiple biomarker assay for quality assessment of botanical drugs using a versatile microfluidic chipZhen-Hao Li, Ni Ai, Lawrence X Yu, et al.
Pharmaceutical Research|April 14, 2011
Using partial area for evaluation of bioavailability and bioequivalenceMei-Ling Chen, Barbara Davit, Robert Lionberger, et al.
Pageof 8

Showing results (21-30 of 75) with videos related to

Sort By:
Pageof 8
International Journal of Pharmaceutics|January 17, 2004
Feasibility studies of utilizing disk intrinsic dissolution rate to classify drugsLawrence X Yu, Alan S Carlin, Gordon L Amidon, et al.
International Journal of Pharmaceutics|July 28, 2022
Profiling the process development of Wurster coating for modified release capsule products in approved drug product applicationsZhouxi Wang, Xiang Yu, Larisa Wu, et al.
The AAPS Journal|May 10, 2008
Quality by design: concepts for ANDAsRobert A Lionberger, Sau Lawrence Lee, Laiming Lee, et al.
International Journal of Pharmaceutics|December 29, 2016
Building parity between brand and generic peptide products: Regulatory and scientific considerations for quality of synthetic peptidesLarisa C Wu, Fu Chen, Sau L Lee, et al.
International Journal of Pharmaceutics: X|September 14, 2019
FDA's new pharmaceutical quality initiative: Knowledge-aided assessment & structured applicationsLawrence X Yu, Andre Raw, Larisa Wu, et al.
Pharmaceutical Research|April 15, 2011
The BCS, BDDCS, and regulatory guidancesMei-Ling Chen, Gordon L Amidon, Leslie Z Benet, et al.
Pharmaceutical Research|January 27, 2012
Use of partial AUC to demonstrate bioequivalence of Zolpidem Tartrate Extended Release formulationsRobert A Lionberger, Andre S Raw, Stephanie H Kim, et al.
Molecular Pharmaceutics|December 5, 2006
A provisional biopharmaceutical classification of the top 200 oral drug products in the United States, Great Britain, Spain, and JapanToshihide Takagi, Chandrasekharan Ramachandran, Marival Bermejo, et al.
Scientific Reports|September 27, 2017
A multiple biomarker assay for quality assessment of botanical drugs using a versatile microfluidic chipZhen-Hao Li, Ni Ai, Lawrence X Yu, et al.
Pharmaceutical Research|April 14, 2011
Using partial area for evaluation of bioavailability and bioequivalenceMei-Ling Chen, Barbara Davit, Robert Lionberger, et al.
Pageof 8