Online Exclusives

Articles

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Knowledge Briefs

  1. Weigh and Dispense
    July 2014

  2. Refrigeration Systems and Energy Efficiency
    February 2014

  3. How to Determine Rouge Limits to Initiate Derouging and Passivation
    January 2014

  4. Sustainable Pharmaceutical Packaging
    June 2013

  5. Understanding Dissolved Ozone and Its Use in Pharmaceutical Water Systems
    May 2013

  6. Electric Motor Asset Management
    March 2013

  7. Packaging Equipment: Blow/Fill/Seal (B/F/S) Technology
    June 2012

  8. Environmental and Financial Benefits of Single-Use Technology
    May 2012

  9. Using OEE for Packaging Line Improvement
    October 2011

  10. Ozone Sanitized Pharmaceutical Water Systems: Tank Venting Concerns
    June 2010

  11. Packaging Equipment - Theroformers
    March 2010

  12. Method for Implementing Disposables into a Bioprocess Facility
    March 2010

  13. Applied Risk Management in Commissioning and Qualification
    January 2010

  14. Forecasting for Clinical Trials
    November 2009

  15. Best Practices in the Sponsor-Provider Partnership to Optimize the Clinical Trials Development Process
    November 2009

  16. Clinical Supply Chain Logistics of Small Molecules vs. Biologics – A Provider’s Perspective
    November 2009

  17. Packaging Material Selection: Things to Consider
    October 2009

  18. Recent Evolution of Clinical Trial-Related Regulatory Environment in Belgium
    October 2009

  19. Containment Hierarchy of Controls
    October 2009

  20. Technology Solutions for Challenges in Cold Chain
    October 2009

  21. Removal of Use By Dates from Clinical Trial Materials
    June 2009

  22. Dry Powder Sampling
    May 2009

  23. Regulatory Framework - PIC/S and ICH
    April 2009

  24. Regulatory Framework - EMEA
    April 2009

  25. Regulatory Framework - US FDA
    April 2009

  26. Packaging Equipment - Slat Fillers
    January 2009

  27. Reducing the Cost of Manufacturing
    December 2008

  28. Risk Based Approaches to Cross-Contamination
    October 2008

  29. Commissioning and Qualification of Biopharmaceutical Facilities
    June 2008

  30. Biotech Basics
    June 2008

  31. Quality by Design
    June 2008

 

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