Jerome P. Skelly

发表

Workshop/conference report—Quantitative bioanalytical methods validation and implementation: Best practices for chromatographic and ligand binding assays

Vinod P. Shah, C. T. Viswanathan, Jeffrey Sailstad, 2007, The AAPS Journal.

Report of the Workshop on Controlled-Release Dosage Forms: Issues and Controversies

Vinod P. Shah, Avraham Yacobi, Jerome P. Skelly, 1987, Pharmaceutical Research.

Opportunities for Integration of Pharmacokinetics, Pharmacodynamics, and Toxicokinetics in Rational Drug Development

Lewis B. Sheiner, Vinod P. Shah, C. T. Viswanathan, 1992, Pharmaceutical Research.

Analytical Methods Validation: Bioavailability, Bioequivalence and Pharmacokinetic Studies

Thomas Layloff, Vinod P. Shah, Kamal K. Midha, 1992, Pharmaceutical Research.

In vitro and in vivo testing and correlation for oral controlled/ modified release dosage forms. report of the 2nd workshop held December 1988, Washington, DC. U.S.A.

Vinod P. Shah, Avraham Yacobi, Jerome P. Skelly, 1990 .

In Vitro and in Vivo Testing and Correlation for Oral Controlled/Modified-Release Dosage Forms

J. E. Carter, Vinod P. Shah, Avraham Yacobi, 2004, Pharmaceutical Research.

In Vitro Dissolution Profile of Water-Insoluble Drug Dosage Forms in the Presence of Surfactants

Vinod P. Shah, Jerome P. Skelly, Richard L. Everett, 1989, Pharmaceutical Research.

In vitro dissolution of sparingly water-soluble drug dosage forms

Vinod P. Shah, Jerome P. Skelly, Richard L. Everett, 1995 .

Analytical Methods Validation: Bioavailability, Bioequivalence, and Pharmacokinetic Studies

Thomas Layloff, Vinod P. Shah, Kamal K. Midha, 1992 .

In Vitro Release of Hydrocortisone from Topical Preparations and Automated Procedure

Vinod P. Shah, Jerome P. Skelly, V. Shah, 2004, Pharmaceutical Research.

Analysis of in Vitro Dissolution of Whole vs. Half Controlled-Release Theophylline Tablets

Vinod P. Shah, Jerome P. Skelly, Jerome Elkins, 2004, Pharmaceutical Research.

Workshop/conference report—Quantitative bioanalytical methods validation and implementation: Best practices for chromatographic and ligand binding assays

Vinod P. Shah, C. T. Viswanathan, Jeffrey Sailstad, 2007 .

Quantitative Bioanalytical Methods Validation and Implementation: Best Practices for Chromatographic and Ligand Binding Assays

Vinod P. Shah, C. T. Viswanathan, Jeffrey Sailstad, 2007 .

SCALE-UP OF CONTROLLED-RELEASE PRODUCTS : PRELIMINARY CONSIDERATIONS

Vinod P. Shah, Jerome P. Skelly, Gordon L. Amidon, 1992 .

Analytical methods validation: Bioavailability, bioequivalence and pharmacokinetic studies

Thomas Layloff, Vinod P. Shah, Kamal K. Midha, 1992 .