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Therapeutic Innovation & Regulatory Science
|
September 21, 2018
FDA Analysis of Atorvastatin Products Refutes Report of Methyl Ester Impurities
Janet Woodcock, Mansoor A Khan
International Journal of Pharmaceutics
|
February 13, 2002
Optimization and characterization of controlled release multi-particulate beads formulated with a customized cellulose acetate butyrate dispersion
Siva Vaithiyalingam, Mansoor A Khan
AAPS Pharmscitech
|
August 15, 2003
Response surface methodology for the optimization of ubiquinone self-nanoemulsified drug delivery system
Sami Nazzal, Mansoor A Khan
Journal of Pharmaceutical Sciences
|
September 24, 2009
Quality-by-Design (QbD): an integrated process analytical technology (PAT) approach for real-time monitoring and mapping the state of a pharmaceutical coprecipitation process
Huiquan Wu, Mansoor A Khan
International Journal of Pharmaceutics
|
September 3, 2013
Hunter screening design to understand the product variability of solid dispersion formulation of a peptide antibiotic
Ziyaur Rahman, Mansoor A Khan
Journal of Pharmaceutical Sciences
|
March 5, 2011
Quality-by-design: an integrated process analytical technology approach to determine the nucleation and growth mechanisms during a dynamic pharmaceutical coprecipitation process
Huiquan Wu, Mansoor A Khan
International Journal of Pharmaceutics
|
March 28, 2006
Controlled release of a self-emulsifying formulation from a tablet dosage form: stability assessment and optimization of some processing parameters
Sami Nazzal, Mansoor A Khan
International Journal of Pharmaceutics
|
March 11, 2004
Evaluation of cytotoxicity of oils used in coenzyme Q10 Self-emulsifying Drug Delivery Systems (SEDDS)
Anitha Palamakula, Mansoor A Khan
International Journal of Pharmaceutics
|
November 13, 2013
Challenges of pediatric formulations: a FDA science perspective
Abhay Gupta, Mansoor A Khan
Journal of Pharmaceutical Sciences
|
January 1, 2009
Quality-by-design (QbD): an integrated approach for evaluation of powder blending process kinetics and determination of powder blending end-point
Huiquan Wu, Mansoor A Khan
Page
of 24
Search research articles
Search
Showing results (1-10 of 237) with videos related to
Sort By:
Page
of 24
Therapeutic Innovation & Regulatory Science
|
September 21, 2018
FDA Analysis of Atorvastatin Products Refutes Report of Methyl Ester Impurities
Janet Woodcock, Mansoor A Khan
International Journal of Pharmaceutics
|
February 13, 2002
Optimization and characterization of controlled release multi-particulate beads formulated with a customized cellulose acetate butyrate dispersion
Siva Vaithiyalingam, Mansoor A Khan
AAPS Pharmscitech
|
August 15, 2003
Response surface methodology for the optimization of ubiquinone self-nanoemulsified drug delivery system
Sami Nazzal, Mansoor A Khan
Journal of Pharmaceutical Sciences
|
September 24, 2009
Quality-by-Design (QbD): an integrated process analytical technology (PAT) approach for real-time monitoring and mapping the state of a pharmaceutical coprecipitation process
Huiquan Wu, Mansoor A Khan
International Journal of Pharmaceutics
|
September 3, 2013
Hunter screening design to understand the product variability of solid dispersion formulation of a peptide antibiotic
Ziyaur Rahman, Mansoor A Khan
Journal of Pharmaceutical Sciences
|
March 5, 2011
Quality-by-design: an integrated process analytical technology approach to determine the nucleation and growth mechanisms during a dynamic pharmaceutical coprecipitation process
Huiquan Wu, Mansoor A Khan
International Journal of Pharmaceutics
|
March 28, 2006
Controlled release of a self-emulsifying formulation from a tablet dosage form: stability assessment and optimization of some processing parameters
Sami Nazzal, Mansoor A Khan
International Journal of Pharmaceutics
|
March 11, 2004
Evaluation of cytotoxicity of oils used in coenzyme Q10 Self-emulsifying Drug Delivery Systems (SEDDS)
Anitha Palamakula, Mansoor A Khan
International Journal of Pharmaceutics
|
November 13, 2013
Challenges of pediatric formulations: a FDA science perspective
Abhay Gupta, Mansoor A Khan
Journal of Pharmaceutical Sciences
|
January 1, 2009
Quality-by-design (QbD): an integrated approach for evaluation of powder blending process kinetics and determination of powder blending end-point
Huiquan Wu, Mansoor A Khan
Page
of 24