Using Lean Strategy to Improve Efficiency in Pharmaceutical QC Labs
Using Lean Strategy to Improve Efficiency in Pharmaceutical QC Labs Read More »
Tunnell’s Kip Wolf explains how firms that create and manage electronic documents can improve compliance.
Mar. 2018 – Julia O’Neill discusses current practices for specification-setting in the pharmaceutical industry.
Tunnell Managing Consultant, Kip Wolf, discusses observations of CGMP violations involving data integrity.
Cheating In The Lab: 3 Data Integrity Pitfalls to Avoid in Laboratory Operations Read More »
Tunnell Managing Consultant, Kip Wolf, discusses the challenges to M&A integration and maintaining business continuity, transferring appropriate knowledge, and transferring information assets.
Information Management Strategies to Improve Data Integrity During M&As Read More »
“Minimum viable product” may work well for software, but pharma needs to get it right the first time, and develop a culture of quality, tied to metrics, and encouraging change where the work actually takes place. This article in Innovation Excellence quotes Tunnell’s Al Riles and Bob Johnson on defining the four components of a quality culture.
Quality Culture: Getting it Right the First Time Read More »