Publications
- Commissioning for Regulated and Non-Regulated Industries (ISA March/April 2011)
- A Comparison of the FDA's Draft Process Validation Guidance and ASTM E2500 (Pharmaceutical Engineering May/June 2009)
- Case Study: Parenteral Facility Upgrade Project with Fill Line Install (Pharmaceutical Engineering July/August 2008)
- Commissioning, Qualification, and Verification: A Review Solving the Terminology Conundrum (Pharmaceutical Engineering July/August 2008)
- Commissioning and Qualification: A New ASTM Standard - GMP Regulations (Pharmaceutical Engineering Nov/Dec 2007)
- Biotech CIP Cycle Development: Case Study Examples Utilizing QRM (Pharmaceutical Engineering Sep/Oct 2006)
- Biotech CIP Cycle Development (Pharmaceutical Engineering Sep/Oct 2004)
- Integrating Commissioning and Qualification (The Great Lakers Press Winter 2001)
- Tame the Paper Monster (World Pharmaceutical Frontiers)
