Peter is an Independent Pharmaceutical Water Systems Consultant working with several companies. He has 25 years of experience in the Pharmaceutical area which includes 10 years with Pharmaceutical Water Systems.
Peter’s experience includes being a member of GMP Teams to Design / Construct / Start Up /Commission and Qualify new or expanded pharmaceutical facilities. These were GMP Production spaces, Manufacturing Equipment, Utilities and their Control Systems. Among the assignments were Parenterals, Biologics, OSD and their Pharmaceutical production rooms and equipment. The utilities and facilities Validation documentation were included and lead to the completion of Validation and initial production batches.
Peter completed his Bachelor’s Degree and his Master of Environmental Management Degree from Drexel University. He is an active ISPE member that participates in current and new technology publications and forums assuring current knowledge of industry practices in GMP Manufacturing, Clean Utilities, Quality and FDA guidance. He has been a contributing author on all the ISPE Communities of Practice Publications for GMP Pharmaceutical Water, Steam and Compressed Gasses where he worked with Industry Experts.
All Pharmaceutical products and R & D require USP and FDA Pharmaceutical Grades of Water. It is used as an ingredient, cleaning manufacturing equipment, a key ingredient for Quality tests and sold in containers. If a company cannot meet,...
All Pharmaceutical products and R&D require USP and FDA Pharmaceutical Grades of Water. The Water is used as an ingredient, cleaning manufacturing equipment and a key ingredient for Quality testing. If a company cannot meet, maintain and demonstrate the...