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Experience:
Our experts possess an average of 20+ years of industry experience
specializing in FDA GLP, cGMP, and Quality System Regulation. Areas of expertise
include: coordinating and conducting aseptic processing training courses,
cleaning validation, GMP and technical training documentation, equipment and
process change management, drawing control, validation master plans, safety
incident monitoring, equipment engineering standards, NDA reviews, and trending
process data, to name a few.
Click
on the CVs button on the left to view the complete curriculum
vitae.
| John M. Lindsay, President
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27-years
Industry Experience
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Master’s
Degree in Microbiology
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Past
Chair of the National Registry of Microbiologists
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Coordinator
of Parenteral Drug Association 2-week Aseptic Processing Training Course
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Author
of various Articles/Book Chapters on Environmental Control and Cleaning
Validation
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Recipient
of Pharmaceutical Awards/Recognition Citations
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Taught
Training Courses on Facility Design, Sanitization Methods, Airflow
Visualization Testing, Media Fills, Good Documentation Practices, Good
Aseptic Techniques, Basic Microbiology |
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