Pharmaceutical Technology’s Pharma Knowledge Resources Newsletter:
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PharmTech
July 2018
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In This Issue

Build your pharma development and manufacturing knowledge base with the latest whitepapers, application notes, posters, and other educational resources from bio/pharma industry suppliers.

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FEATURED WHITEPAPER

Analysis Using Counter-Rotating Twin Screw Extruder

Brian Machado, Abbe Haser, Feng Haight, Charlie Martin, Augie Zhang; Leistritz Extrusion

Various extrusion operating conditions and formulations were used to enhance the solubility and recovery of Meloxicam (MLX) in copovidone to near 100% on a counter-rotating twin screw extruder (TSE).

Quality

Three Critical Processes for Improving Quality Management in the Life Sciences

Brenda Percy; EtQ

This whitepaper explores the three most critical functions for automation in a life-science organization so you can smoothly transition to an effective quality management process while increasing effectiveness and efficiency.

How Quality Data Can Impact Company-Wide Performance

Jaseem Mahmmdla, senior product manager; Mike Edwards, senior product manager; Sparta Systems

In this paper, we examine key factors driving manufacturers toward a more holistic form of quality management, and provide a new data model that companies can use as part of their quality management systems (QMS) to more easily create meaningful business insights that help the organization as a whole.

Manufacturing

Applications in Pharmaceutical Manufacturing

Alconox, Inc.

The use of aqueous cleaning in pharmaceutical manufacturing can provide numerous benefits in terms of effectiveness, minimal surface residue, and easier cleaning validation.

A New PAT for Wet Granulation

Tim Freeman, Dr Valery Sheverev; Freeman Technology

Optimal process analytical technology (PAT) for wet granulation monitoring has significant potential to improve the efficiency of tableting operations. This whitepaper showcases the value of dynamic powder testing and a complementary new in-line PAT for real-time granulation monitoring. Together, these technologies deliver efficient endpoint detection and continuous process measurement.

Supply Chain

Regulatory Considerations for Incorporating PCID into SODF Drugs

Michael O'Neill, Chief Science Officer; TruTag Technologies, Inc.

Diverted and falsified drug products create safety risks in the supply chain. On-dose authentication methods can assign special code libraries to groups, lots, or manufacturing segments of product and can complement serialization.

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