Biopharmaceutics applications in drug development

di Krishna, Rajesh., Yu, Lawrence.
Pubblicazione 2008.

Evaluation of USP apparatus 3 for dissolution testing of immediate-release products

di Yu, Lawrence X., Wang, Jin T., Hussain, Ajaz S.
Pubblicazione 2002

Batch-to-Batch Quality Consistency Evaluation of Botanical Drug Products Using Multivariate Statistical Analysis of the Chromatographic Fingerprint

di Xiong, Haoshu, Yu, Lawrence X., Qu, Haibin
Pubblicazione 2013

Impact of Osmotically Active Excipients on Bioavailability and Bioequivalence of BCS Class III Drugs

di Chen, Mei-Ling, Sadrieh, Nakissa, Yu, Lawrence
Pubblicazione 2013

Chronically Implanted Pressure Sensors: Challenges and State of the Field

di Yu, Lawrence, Kim, Brian J., Meng, Ellis
Pubblicato in Sensors (Basel) (2014)

A case of orf disease in a patient with scleroderma

di Maor, Danit, Yu, Lawrence L., Brand, Roland
Pubblicato in JAAD Case Rep (2017)

Mechanistic Approaches to Predicting Oral Drug Absorption

di Huang, Weili, Lee, Sau Lawrence, Yu, Lawrence X.
Pubblicazione 2009

Generic Development of Topical Dermatologic Products: Formulation Development, Process Development, and Testing of Topical Dermatologic Products

di Chang, Rong-Kun, Raw, Andre, Lionberger, Robert, Yu, Lawrence
Pubblicazione 2012

Generic Development of Topical Dermatologic Products, Part II: Quality by Design for Topical Semisolid Products

di Chang, Rong-Kun, Raw, Andre, Lionberger, Robert, Yu, Lawrence
Pubblicazione 2013

Erratum to: Generic Development of Topical Dermatologic Products: Formulation Development, Process Development, and Testing of Topical Dermatologic Products

di Chang, Rong-Kun, Raw, Andre, Lionberger, Robert, Yu, Lawrence
Pubblicato in AAPS J (2015)

Utility of Physiologically Based Absorption Modeling in Implementing Quality by Design in Drug Development

di Zhang, Xinyuan, Lionberger, Robert A., Davit, Barbara M., Yu, Lawrence X.
Pubblicazione 2011

Dissolution Testing for Generic Drugs: An FDA Perspective

di Anand, Om, Yu, Lawrence X., Conner, Dale P., Davit, Barbara M.
Pubblicazione 2011

Application of Quality by Design to the Process Development of Botanical Drug Products: A Case Study

di Zhang, Lei, Yan, Binjun, Gong, Xingchu, Yu, Lawrence X., Qu, Haibin
Pubblicazione 2013

International Guidelines for Bioequivalence of Systemically Available Orally Administered Generic Drug Products: A Survey of Similarities and Differences

di Davit, Barbara, Braddy, April C., Conner, Dale P., Yu, Lawrence X.
Pubblicazione 2013

Influence of drug release properties of conventional solid dosage forms on the systemic exposure of highly soluble drugs

di Yu, Lawrence X., Ellison, Christopher D., Conner, Dale P., Lesko, Larry J., Hussain, Ajaz S.
Pubblicazione 2001

Quality by Design: Concepts for ANDAs

di Lionberger, Robert A., Lee, Sau Lawrence, Lee, LaiMing, Raw, Andre, Yu, Lawrence X.
Pubblicazione 2008

A multiple biomarker assay for quality assessment of botanical drugs using a versatile microfluidic chip

di Li, Zhen-Hao, Ai, Ni, Yu, Lawrence X., Qian, Zhong-Zhi, Cheng, Yi-Yu
Pubblicato in Sci Rep (2017)

FDA’s new pharmaceutical quality initiative: Knowledge-aided assessment & structured applications

di Yu, Lawrence X., Raw, Andre, Wu, Larisa, Capacci-Daniel, Christina, Zhang, Ying, Rosencrance, Susan
Pubblicato in Int J Pharm X (2019)

Applications of Human Pharmacokinetic Prediction in First-in-Human Dose Estimation

di Zou, Peng, Yu, Yanke, Zheng, Nan, Yang, Yongsheng, Paholak, Hayley J., Yu, Lawrence X., Sun, Duxin
Pubblicazione 2012

Evaluation of a Scaling Approach for the Bioequivalence of Highly Variable Drugs

di Haidar, Sam H., Makhlouf, Fairouz, Schuirmann, Donald J., Hyslop, Terry, Davit, Barbara, Conner, Dale, Yu, Lawrence X.
Pubblicazione 2008