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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 

27-years Industry Experience           

Masterís Degree in Microbiology

Past Chair of the National Registry of Microbiologists

Coordinator of Parenteral Drug Association 2-week Aseptic Processing Training Course

Author of various Articles/Book Chapters on Environmental Control and Cleaning Validation

Recipient of Pharmaceutical Awards/Recognition Citations

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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Last modified: April 6, 2014