Mike Magee joins CCE as Lead Auditor

CCE is pleased to announce that Mike Magee, R.Ph., ASQ CPGP, owner of Kenformete Solutions, LLC, has joined our team as Lead Auditor, 503B Accreditation & GMP Compliance. He is also heading up CCE's 503B accreditation program, which is currently in its beta site phase.

Mike is a quality and compliance executive with more than 30 years of leadership experience spanning pharmaceutical, biopharmaceutical, medical device, and 503B outsourcing operations. His extensive background includes quality systems, regulatory compliance, risk management, auditing, and GMP implementation.

He has already been instrumental in helping CCE develop its hybrid checklist and risk-based auditing methodology, which combines traditional compliance verification with modern quality risk management principles. This approach reflects CCE's commitment to providing rigorous, practical, and patient-focused accreditation services for 503A and, now, 503B facilities.

Mike holds the American Society for Quality's Certified Pharmaceutical GMP Professional (ASQ CPGP) credential, demonstrating advanced knowledge of pharmaceutical quality systems and current good manufacturing practices. His expertise will be particularly valuable as CCE expands its accreditation programs and incorporates proven quality management concepts that can strengthen compliance and operational excellence across the compounding industry.