Solid/Semi-Solid Dosage

Jan 02, 2017
Pharmaceutical Technology
Moisture uptake during the end-to-end manufacturing process and supply chain can affect product quality. Simulation tools based on mechanistic models help define storage and handling requirements for oral solid-dosage drugs.
Dec 07, 2016
PTSM: Pharmaceutical Technology Sourcing and Management
Principles of dissolution testing, including method development and testing apparatus, are reviewed.
Dec 05, 2016
By Pharmaceutical Technology Editors
FDA and BARDA awarded a contract to Continuus Pharmaceuticals to develop an end-to-end continuous manufacturing process for solid-dosage drugs.
Dec 02, 2016
Pharmaceutical Technology
Hot-melt coating was used to develop taste-masked orally disintegrating granules of acetaminophen and caffeine.
Nov 28, 2016
PTSM: Pharmaceutical Technology Sourcing and Management
By Pharmaceutical Technology Editors
Catalent adds two softgel facilities and packaging capabilities with acquisition of Canada-based Accucaps.
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
Shear-sensitive ingredients in a tableting formulation experience different conditions in a batch tumble blender than they would in a continuous paddle blender.
Nov 02, 2016
Pharmaceutical Technology
A lifecycle approach can be used to develop GMP-compliant cleaning procedures for continuous manufacturing of solid-dosage pharmaceuticals.
Oct 02, 2016
Pharmaceutical Technology
Excipients play a crucial role in the manufacturing of solid-dosage forms and the performance of the finished drug product.
Oct 02, 2016
Pharmaceutical Technology
Designing loss-in-weight feeders for accurate and consistent refill is crucial to a continuous solid-dosage process.
native1_300x100
lorem ipsum