François Sallans—2017 Member of the Year
January 2018
Special Report Serialization
January 2018
Special Report on Data Integrity
November 2017
Biotechnology Special Report
September 2017
Sustainability Special Report
March 2017
Innovative Building Design Removes Barriers, Fosters Collaboration
January 2017
YP Voices Special Report
January 2017
Quarterly Report on Quality Culture
November 2016
Defects Produced in Orbital Welding for Pharmaceutical Process Piping: Case Study and Simulation
September 2016
Biotechnology Quarterly Report
September 2016
Data Integrity Special Report
March 2016
Quality Metrics Special Report
January 2016
Quality Culture Quarterly Report
September 2015
Global Regulatory News
September 2015
Global Regulatory News: August 2015
August 2015
Pharmaceutical Engineering Facility of the Year Supplement June 2015
June 2015
Global Regulatory News
May 2015
Global Regulatory News
March 2015
Global Regulatory News
January 2015
2014 Project Management Supplement Digital Edition
December 2014
Starting Materials Selection and Life Cycle Management
November 2014
Weigh and Dispense
July 2014
Refrigeration Systems and Energy Efficiency
February 2014
How to Determine Rouge Limits to Initiate Derouging and Passivation
January 2014
Sustainable Pharmaceutical Packaging
June 2013
Understanding Dissolved Ozone and Its Use in Pharmaceutical Water Systems
May 2013
Electric Motor Asset Management
March 2013
Packaging Equipment: Blow/Fill/Seal (B/F/S) Technology
June 2012
Environmental and Financial Benefits of Single-Use Technology
May 2012
Using OEE for Packaging Line Improvement
October 2011
Ozone Sanitized Pharmaceutical Water Systems: Tank Venting Concerns
June 2010
Packaging Equipment - Theroformers
March 2010
Method for Implementing Disposables into a Bioprocess Facility
March 2010
Applied Risk Management in Commissioning and Qualification
January 2010
Forecasting for Clinical Trials
November 2009
Best Practices in the Sponsor-Provider Partnership to Optimize the Clinical Trials Development Process
November 2009
Clinical Supply Chain Logistics of Small Molecules vs. Biologics – A Provider’s Perspective
November 2009
Packaging Material Selection: Things to Consider
October 2009
Recent Evolution of Clinical Trial-Related Regulatory Environment in Belgium
October 2009
Containment Hierarchy of Controls
October 2009
Technology Solutions for Challenges in Cold Chain
October 2009
Removal of Use By Dates from Clinical Trial Materials
June 2009
Dry Powder Sampling
May 2009
Regulatory Framework - PIC/S and ICH
April 2009
Regulatory Framework - EMEA
April 2009
Regulatory Framework - US FDA
April 2009
Packaging Equipment - Slat Fillers
January 2009
Reducing the Cost of Manufacturing
December 2008
Risk Based Approaches to Cross-Contamination
October 2008
Commissioning and Qualification of Biopharmaceutical Facilities
June 2008
Biotech Basics
June 2008
Quality by Design
June 2008