Batch Record Review & Analytical Method Validation Training

With more than 30 years of industry experience, Judy Carmody, Ph.D., takes a unique approach to Life Sciences training that is grounded in the real-world experience she has gained as a bench chemist, a founder of a GMP CRO, a senior leader, and a consultant working in the field daily. She heads up Carmody Quality Solutions, LLC., one of the most trusted innovative Pharmaceutical and Biotech Quality and QA consulting agencies in the industry.

Scientific understanding underscores her unique approach to the GMP-related training that includes Analytical Method for Biologics, Biopharmaceuticals, and other therapeutic products. More specifically, she offers courses that cover the foundations of GMP, Root Cause Analysis and how to develop effective CAPA strategies, GMP facility compliance, implementing compliant stability programs that are clinical phase-appropriate and incorporate Quality Risk Management (QRM), and the elements of an effective product batch review process. 

A seasoned GMP veteran, Dr. Carmody earned her Ph.D. in Analytical Chemistry from Clark University in Worcester, Massachusetts. Since then, she has developed a reputation as someone that creatively integrates technologies from diverse fields to solve common client problems.

Dr. Carmody offers her training courses through the Center for Professional Innovation and Education (CfPIE). CfPIE provides technical training for Pharmaceutical, Biotech, Medical Device and Skin/Cosmetics professionals. CfPIE offers more than 350 class sessions annually across 80 course titles in multiple formats, such as classroom, on-site, and certification programs. Since its founding in 2001, CfPIE has trained more than 38,000 people in more than 6,100 companies, government agencies, and nonprofit organizations.