Authors


Gretchen R. Peck

Latest:

Tablet Relaxation and Physiocomechanical Stability of Lactose, Microcrystalline Cellulose, and Dibasic Calcuim Phosphate

The authors discuss the physiocomechanical characteristics of three commonly used pharmaceutical excipients and describe the effects of variables on their physiocomechanical stability.


Mary K. Gemoules

Latest:

Tablet Relaxation and Physiocomechanical Stability of Lactose, Microcrystalline Cellulose, and Dibasic Calcuim Phosphate

The authors discuss the physiocomechanical characteristics of three commonly used pharmaceutical excipients and describe the effects of variables on their physiocomechanical stability.


Debra M. Besserman

Latest:

Tablet Relaxation and Physiocomechanical Stability of Lactose, Microcrystalline Cellulose, and Dibasic Calcuim Phosphate

The authors discuss the physiocomechanical characteristics of three commonly used pharmaceutical excipients and describe the effects of variables on their physiocomechanical stability.


William B. Bierce

Latest:

Truth in Outsourcing

Contract service providers and clients alike must be realistic and forthcoming about their expectations to accomplish a truthful outsourcing partnership.


Jack Cole

Latest:

A Comprehensive Approach to Pharmaceutical Engineering Training

A training program at Rutgers University combines the disciplines of engineering and pharmaceutics to provide a thorough educational experience in drug manufacturing.


Richard J. Davis

Latest:

Investigation of Out-of-Specification Results

The authors summarize the results of the September 2000 PhRMA workshop discussions about conducting out-of-specification investigations.


Sol Motola, PhD

Latest:

Investigation of Out-of-Specification Results

The authors summarize the results of the September 2000 PhRMA workshop discussions about conducting out-of-specification investigations.


Alex M. Hoinowski

Latest:

Investigation of Out-of-Specification Results

The authors summarize the results of the September 2000 PhRMA workshop discussions about conducting out-of-specification investigations.


David J. Wirtanen

Latest:

Novel Acrylate Adhesives for Transdermal Drug Delivery

The authors discuss the solubility and adhesive performances of adhesives that incorporate monomers such as hydroxyethyl acrylate or pyrrolidonoethyl acrylate.


Heather B. Hayes

Latest:

Reaping the Benefits of E-Procurement

Implementing an e-procurement solution requires executive sponsorship, up-front analysis of current processes, integration with back-end systems, and change mangement.


C.J. Matice, PhD

Latest:

The Role of Computational Fluid Dynamics in the Pharmaceutical Industry

Computational fluid dynamics can be a valuable tool for analyzing the efficiencies and performances of process equipment, which can lead to potential cost savings.


T.J. Fry, PhD

Latest:

The Role of Computational Fluid Dynamics in the Pharmaceutical Industry

Computational fluid dynamics can be a valuable tool for analyzing the efficiencies and performances of process equipment, which can lead to potential cost savings.


Karen M. Alsante, PhD

Latest:

Available Guidance and Best Practices for Conducting Forced Degradation Studies

Participants at a Pharmaceutical Research and Manufacturers of America workshop share their views about the acceptable analytical practices of conducting forced degradation studies.


Kevin L. Facchine, PhD

Latest:

Available Guidance and Best Practices for Conducting Forced Degradation Studies

Participants at a Pharmaceutical Research and Manufacturers of America workshop share their views about the acceptable analytical practices of conducting forced degradation studies.


June F. Mullaney, PhD

Latest:

Available Guidance and Best Practices for Conducting Forced Degradation Studies

Participants at a Pharmaceutical Research and Manufacturers of America workshop share their views about the acceptable analytical practices of conducting forced degradation studies.


Michael G. Motto, PhD

Latest:

Available Guidance and Best Practices for Conducting Forced Degradation Studies

Participants at a Pharmaceutical Research and Manufacturers of America workshop share their views about the acceptable analytical practices of conducting forced degradation studies.


Todd D. Hatajik

Latest:

Available Guidance and Best Practices for Conducting Forced Degradation Studies

Participants at a Pharmaceutical Research and Manufacturers of America workshop share their views about the acceptable analytical practices of conducting forced degradation studies.


Navnit H. Shah

Latest:

Effect of Formulation and Process Variables on Matrix Erosion and Drug Release from a Multiunit Erosion Matrix of a Poorly Soluble Drug

By optimizing formulation and process varibles, pellets can be prepared that can release a poorly soluble drug for 12-24 h following zero-order kinetics.


Wantanee Phuapradit, PhD

Latest:

Effect of Formulation and Process Variables on Matrix Erosion and Drug Release from a Multiunit Erosion Matrix of a Poorly Soluble Drug

By optimizing formulation and process varibles, pellets can be prepared that can release a poorly soluble drug for 12-24 h following zero-order kinetics.


A. Waseem Malick, PhD

Latest:

Effect of Formulation and Process Variables on Matrix Erosion and Drug Release from a Multiunit Erosion Matrix of a Poorly Soluble Drug

By optimizing formulation and process varibles, pellets can be prepared that can release a poorly soluble drug for 12-24 h following zero-order kinetics.


Linda Gerspach

Latest:

Oral Low Molecular Weight Heparin Absorption From Solution and Solid Dosage Forms in Rat, Dog, and Monkey Models

The delivery agent-mediated transport of low moleular weight heparin across Caco-2 cells is accomplished without opening the junctions or adversely affecting the structural integrity of the cell monolayer.


Timothy D.J. Halls

Latest:

Systematic Troubleshooting for LC/MS/MS

Meeting the challenges of large-scale LC/MS/MS such as elminating carr-over and matrix effects can increase sensitivity and improve turnaround times.


Catherina O’Shaughnessy

Latest:

Oral Low Molecular Weight Heparin Absorption From Solution and Solid Dosage Forms in Rat, Dog, and Monkey Models

The delivery agent-mediated transport of low moleular weight heparin across Caco-2 cells is accomplished without opening the junctions or adversely affecting the structural integrity of the cell monolayer.


Rajesh Agarwal

Latest:

Oral Low Molecular Weight Heparin Absorption From Solution and Solid Dosage Forms in Rat, Dog, and Monkey Models

The delivery agent-mediated transport of low moleular weight heparin across Caco-2 cells is accomplished without opening the junctions or adversely affecting the structural integrity of the cell monolayer.


Connie Rosado-Gray

Latest:

Oral Low Molecular Weight Heparin Absorption From Solution and Solid Dosage Forms in Rat, Dog, and Monkey Models

The delivery agent-mediated transport of low moleular weight heparin across Caco-2 cells is accomplished without opening the junctions or adversely affecting the structural integrity of the cell monolayer.


Theresa Rivera-Schaub

Latest:

Oral Low Molecular Weight Heparin Absorption From Solution and Solid Dosage Forms in Rat, Dog, and Monkey Models

The delivery agent-mediated transport of low moleular weight heparin across Caco-2 cells is accomplished without opening the junctions or adversely affecting the structural integrity of the cell monolayer.


Robert A. Baughman

Latest:

Oral Low Molecular Weight Heparin Absorption From Solution and Solid Dosage Forms in Rat, Dog, and Monkey Models

The delivery agent-mediated transport of low moleular weight heparin across Caco-2 cells is accomplished without opening the junctions or adversely affecting the structural integrity of the cell monolayer.


Pam Anderson

Latest:

Validation Changes to the USP Assay Method for Ibuprofen Tablets

This study investigated the effectiveness of the direct extraction of tablets and shaking time on the disintegration of tablets, solubilization, and recovery of ibuprofen from tablets of various formulations, strengths, and spiked placebo.


Lynn Massad

Latest:

Validation Changes to the USP Assay Method for Ibuprofen Tablets

This study investigated the effectiveness of the direct extraction of tablets and shaking time on the disintegration of tablets, solubilization, and recovery of ibuprofen from tablets of various formulations, strengths, and spiked placebo.


Philip Burns

Latest:

Validation Changes to the USP Assay Method for Ibuprofen Tablets

This study investigated the effectiveness of the direct extraction of tablets and shaking time on the disintegration of tablets, solubilization, and recovery of ibuprofen from tablets of various formulations, strengths, and spiked placebo.