“Back to the Basics: Validation 101: An Overview of Installation Qualification, Operational Qualification, and Performance Qualification”, Journal of Validation Technology ‘97.
“Technology Transfers in the Pharmaceutical Industry”, Journal of cGMP Compliance ‘98.
“Equipment Cleaning Validations for Transdermal”, Journal of Validation Technology ’98.
“Transdermal Process Validation”, 3rd Edition of Pharmaceutical Process Validation ‘03.
“Prerequisites for Successful Validations”, Journal of Validation Technology ‘03.
“Case Study: Cubic Equipment Qualification”, Journal of Validation Technology ‘05.
“Engineering Runs: An Insider’s Perspective”, Journal of Validation Technology ‘06.
“Ensuring Completeness in Technology Transfers”, Institute of International Research Technology Transfer Conference, Atlanta, GA., Spring 1999.
“Ensuring Completeness in Technology Transfers”, Japanese Pharmaceutical Symposium, Tokyo, Japan, Summer 1999.
“Protocol Basics”, Compliance in Life Science Manufacturing Conference, Jersey City, NJ, Spring 2004.
“Case Study: Cubic Equipment Qualification”, Annual Validation Week conference, Philadelphia, PA, Fall 2004.
“Challenging a System’s Performance as Part of the Validation Process: Optimizing Testing for Validation”, Annual Validation Week conference, Philadelphia, PA, Fall 2007.
“IQ/OQPQ” presentation for Center for Professional Advancement (CfPA) Client, Summer 2019
“IQ/OQPQ” presentation for CfPA Client, Winter 2019
“IQ/OQPQ for Process Validations” presentation for CfPA, Spring and Fall 2020
“IQ/OQPQ for Laboratories” presentation for CfPA, Summer 2020
“IQ/OQPQ for Process Validations” presentation for CfPA in Spring 2021, 2022, 2023, and 2024