Online Exclusives

Articles

  1. François Sallans—2017 Member of the Year
    January 2018

  2. Special Report Serialization
    January 2018

  3. Special Report on Data Integrity
    November 2017

  4. Biotechnology Special Report
    September 2017

  5. Continuous Manufacturing Special Report
    May 2017

  6. Sustainability Special Report
    March 2017

  7. Innovative Building Design Removes Barriers, Fosters Collaboration
    January 2017

  8. YP Voices Special Report
    January 2017

  9. Quarterly Report on Quality Culture
    November 2016

  10. Defects Produced in Orbital Welding for Pharmaceutical Process Piping: Case Study and Simulation
    September 2016

  11. Biotechnology Quarterly Report
    September 2016

  12. Supply Chain Manufacturing Special Report
    July 2016

  13. Sirabian Wet Granulation
    May 2016

  14. Facility of the Future Special Report
    May 2016

  15. Data Integrity Special Report
    March 2016

  16. Quality Metrics Special Report
    January 2016

  17. Quality Culture Quarterly Report
    September 2015

  18. Global Regulatory News
    September 2015

  19. Global Regulatory News: August 2015
    August 2015

  20. Pharmaceutical Engineering Facility of the Year Supplement June 2015
    June 2015

  21. Global Regulatory News
    May 2015

  22. Global Regulatory News
    March 2015

  23. Global Regulatory News
    January 2015

  24. 2014 Project Management Supplement Digital Edition
    December 2014

  25. Scientific and Regulatory Considerations for Implementing Mathematical Models in the Quality by Design (QbD) Framework
    November 2014

  26. Starting Materials Selection and Life Cycle Management
    November 2014

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