Pharmaceutical Technology, Mar 1, 2010 - Pharmaceutical Technology

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Pharmaceutical Technology, Mar 1, 2010
Featured Content
Trends in Bioprocessing
By Michelle Hoffman
The second annual Pharmaceutical Technology Bioprocessing Survey offers a snapshot of the industry following 2009's megamergers.
Industrialized Production of Human iPSC-Derived Cardiomyocytes for Use in Drug Discovery and Toxicity Testing
By Blake Anson , Emile Nuwaysir , Brad Swanson , Wen Bo Wang
The authors describe an industrialized process for the manufacture of iPSC-derived human cardiomyocytes. This article is part of a special issue on Bioprocessing and Sterile Manufacturing.
A Detail View of Single-Use Equipment Opportunities
By Thomas Paust , Detelv Szarafinksi , Christian Manzke , Thorsten Peuker , Maik W. Jornitz
The authors propose increased use of single-use technologies in biopharmaceutical manufacturing to achieve operational excellence without compromising product quality.
Disposable Technologies for Fill-Finish of Clinical-Trial Materials
By Tony Pidgeon
The author examines the use and advantages of disposable technologies in the fill–finish of sterile pharmaceutical products and how these technologies can reduce costs and time in producing clinical-trial materials.
Cost Advantages of Single-Use Technologies
By Niels Guldager
Single-use technologies can help simplify equipment and facility design, thus bringing cost advantages. But how are these cost advantages realized and what criteria can be used to assess their impact? This article is part of a special issue on Bioprocessing and Sterile Manufacturing.
Integrated Microfluidic LC-MS
By Maggie Bynum , Tomasz Baginski , Kevin Killeen , Rodney Keck
The authors describe a new microfluidic-based workflow that integrates and automates glycan cleaveage, purification, and chromatographic separation onto a microfluidic liquid chromatography–mass spectrometry chip for MS detection.
Gamma Irradiation in the Pharmaceutical Manufacturing Environment
By Betty Howard
The author reviews the benefits, challenges, and considerations to be made when selecting a gamma-irradiation sterilization method.
The Myth Called "Sterility"
By James P. Agalloco , James E. Akers
The authors propose a process-centric approach for carrying out aseptic-processing and suggest further dialogue. This articles contains bonus online-exclusive material.
An Overview of Rapid Microbial-Detection Methods
By Erik Greb
Pharmaceutical Technology talked to drugmakers, equipment vendors, and service providers to learn more about the advantages and disadvantages of rapid microbial-detection methods.
Surface Plasmon Resonance as an Analytical Tool for Bioprocessing
By Michelle Hoffman
A Q&A with GE Healthcare

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Survey
FDASIA was signed into law two years ago. Where has the most progress been made in implementation?
Reducing drug shortages
Breakthrough designations
Protecting the supply chain
Expedited reviews of drug submissions
More stakeholder involvement
Reducing drug shortages
70%
Breakthrough designations
4%
Protecting the supply chain
17%
Expedited reviews of drug submissions
2%
More stakeholder involvement
7%
View Results
Eric Langerr Outsourcing Outlook Eric LangerTargeting Different Off-Shore Destinations
Cynthia Challener, PhD Ingredients Insider Cynthia ChallenerAsymmetric Synthesis Continues to Advance
Jill Wechsler Regulatory Watch Jill Wechsler Data Integrity Key to GMP Compliance
Sean Milmo European Regulatory WatchSean MilmoExtending the Scope of Pharmacovigilance Comes at a Price
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