Dosage Forms

Apr 01, 2017
Pharmaceutical Technology
A venture between GEA and Siemens aims to familiarize more pharmaceutical companies with more modern control and continuous processing.
Mar 02, 2017
Pharmaceutical Technology
Effective solutions for overcoming the high molecular weight, hydrophilicity, and instability of large biomolecules have yet to be identified.
Jan 09, 2017
PTSM: Pharmaceutical Technology Sourcing and Management
By Pharmaceutical Technology Editors
Catalent announces a development agreement with JOT to evaluate softgel options for a resveratrol drug candidate.
Dec 07, 2016
PTSM: Pharmaceutical Technology Sourcing and Management
Principles of dissolution testing, including method development and testing apparatus, are reviewed.
Nov 02, 2016
Pharmaceutical Technology
A dissolution method should have adequate discriminatory power to detect formulation changes that affect the dissolution rate of a drug product.
Nov 02, 2016
Pharmaceutical Technology
This article will clarify reasonable expectations for the responsibilities of topical product formulation developers and for excipient suppliers regarding the information and samples for experiments needed for QbD.
Oct 02, 2016
Pharmaceutical Technology
Understanding the components of a reference marketed pMDI is needed to develop a generic pMDI.
Oct 02, 2016
Pharmaceutical Technology
This article will equip the excipient vendor with an understanding of QbD from the perspective of the topical pharmaceutical product manufacturer.
Sep 01, 2016
Pharmaceutical Technology
The authors review the regulatory changes associated with the use of dimethyl sulfoxide in finished pharmaceutical dosage forms.
Sep 01, 2016
Pharmaceutical Technology
By Pharmaceutical Technology Editors
Analytics and science-based approaches are shedding more light on these complex dosage forms, promising to improve process control and product design.
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