Pharmaceutical Technology
October 10, 2016
Features
40
10
The authors describe some cases of container closure design flaws and actions taken by FDA to mitigate safety risks and increase patient acceptability.
October 02, 2016
Peer-Reviewed Research
40
10
This article will equip the excipient vendor with an understanding of QbD from the perspective of the topical pharmaceutical product manufacturer.
October 02, 2016
Troubleshooting
40
10
Designing loss-in-weight feeders for accurate and consistent refill is crucial to a continuous solid-dosage process.
October 02, 2016
Packaging Forum
40
10
Primary packaging and manufacturing technologies minimize product/package interaction, protect quality, support safe travel through the supply chain, and enhance performance at point of use.
October 02, 2016
Regulatory Watch
40
10
Efforts to accelerate drug development will alter fee structure and require ready production sites.
October 02, 2016
Ask the Expert
40
10
Susan Schniepp, distinguished fellow at Regulatory Compliance Associates, discusses the assessment of risk in the processing of intravenous injectable drugs.
October 02, 2016
Outsourcing Outlook
40
10
This key bioprocessing segment is expecting continued growth
October 02, 2016
From The Editor
40
10
The editors seek drug development experts to contribute technical articles for 2017.
October 02, 2016
Cover Story
40
10
Excipients play a crucial role in the manufacturing of solid-dosage forms and the performance of the finished drug product.
October 02, 2016
Features
40
10
A number of organizations have analyzed and estimated the size of pharma’s counterfeit and diversion problem.
October 02, 2016
Features
40
10
As criminals duplicate the latest overt security technologies, pharmaceutical manufacturers are evaluating covert and layered approaches to fight counterfeiting, theft, and illegal product diversion.
October 02, 2016
API Synthesis & Manufacturing
40
10
Researchers develop catalysts that mediate complex transformations under conditions appropriate for commercial manufacture.
October 02, 2016
Regulatory Watch
40
10
Regulators are tightening up on post-marketing monitoring of biological medicines to detect deficiencies caused by manufacturing problems, particularly those stemming from post-authorization changes in the manufacturing process.
October 02, 2016
Product Spotlight
40
10
The CELLdisc from Greiner Bio-One is a multilayer cell culture vessel that offers a growth area of up to one square meter for adherent mammalian cells.
October 02, 2016
Product Spotlight
40
10
The Double Planetary Mixers from Ross, Charles & Son are offered in 4-, 5-, 10-, and 25-gallon models for pilot-scale production of highly-filled pastes, dough-like materials, shear-sensitive gels, granulations, and powder blends.
October 02, 2016
Product Spotlight
40
10
The Print & Check Flex Machine from Antares Vision is a flexible high-capacity serialization unit created for track and trace.
October 02, 2016
Formulation
40
10
Understanding the components of a reference marketed pMDI is needed to develop a generic pMDI.
October 02, 2016
Product Spotlight
40
10
The aCOLade 2 Manual Colony Counter from Synbiosis includes automatic count recording.
October 02, 2016
Issue PDF
40
10
Click the title above to open the Pharmaceutical Technology October 2016 issue in an interactive PDF format.
August 01, 2016
Features
40
10
Multiple methods are required for detecting and removing protein impurities.