cGMP Consulting Inc.
Kevin Linde has over 20 years of experience in the FDA regulated industries. Kevin started their career at Abbott as an Independent Contract Engineer, working with national and international pharmaceutical, biotech, and medical device clients. Some of their key achievements include implementing a DSCSA Compliant Serialization program for all US products at AbbVie, developing quality improvement plans to release three manufacturers from warning letter status, and creating risk-based validation strategies for lower-risk clients in FDA regulated industries. In 2001, Kevin founded cGMP Consulting Inc., where they currently serve as the CEO. The company provides engineering, project management, and quality systems support to FDA regulated industries, with Kevin also taking on the role of Owner and Senior Engineering Consultant. Kevin provides compliance and engineering services to clients, identifies and develops engineering talent, and acts as a mentor and expert to staff. Kevin's extensive experience and expertise in the field make him a valuable asset to their clients.
Kevin Linde attended the University of Missouri-Columbia from 1992 to 1996, where they pursued a Bachelor of Science degree in Chemical Engineering.
cGMP Consulting Inc.
Founded in 2001, cGMP Consulting Inc. has strived to help our clients adopt new technologies and ensure that changes to your processes are compliant with current Good Manufacturing Practices (cGMP). Our experienced engineering and quality assurance consultants have helped many industry leading companies identify and remediate gaps, support international pharmaceutical manufacturing, and implement cGMP requirements.