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• Improving Quality by Focusing on Human Error
• FDA / GMP Update for 2006-07
  

• NEW! Risk Assessment and Risk Management in the Phamaceutical Industry: Clear and Simple (2006)
• GMP in Practice: Regulatory Expectations for the Pharmaceutical Industry (2002 - Third Edition)
• Documentation Systems: Clear and Simple (1997)
• Quality and GMP Auditing: Clear and Simple (1997)
• Training for the Healthcare Manufacturing Industries: Tools and Techniques to Improve Performance (1993)

Articles by James L. Vesper

• Training and the FDA Draft Guidance on Quality Systems (co-author Thomas Reeves; reprinted from BioPharm Magazine, May 2006)
• Challenges in Providing e-Learning Solutions in the Regulated Pharmaceutical Industry (Portable Document Format ) 
• What Are GMPs Anyway? (reprinted from BioProcess International, February 2003)
• Writing Procedures That Contribute to Performance (reprinted from BioPharm Magazine, August 2001)
• Performance: The Goal of Training (reprinted from BioPharm Magazine, February 2001)
• Defining Your GMP Program with a Training Procedure (reprinted from BioPharm Magazine, November 2000)