Workshop Instructor
Russel Pizzuto
Russell Pizzuto is President of PPRE Consulting, specializing in Product, Project and Regulatory Engineering.
Mr. Pizzuto has 40 year of engineering and management experience. He has developed hundreds of new products for fortune 500 companies. Mr. Pizzuto has 13 years of medical device design, manufacturing and regulatory compliance experience. As Global Director of Engineering for a major medical device manufacturer with teams in the USA, Europe, China and Mexico he delivered Class I and Class II medical device projects.
Mr. Pizzuto holds a Medical Device Certificate from the Regulatory Affairs Professionals Society (RAPS), was a member of the FDA’s Hospital Bed Safety Work Group and is an expert witness for Hospital Bed Safety litigation. Mr. Pizzuto has most recently focused on remediating Design Control and Risk Management Systems for clients under FDA legal action.
Russell Pizzuto is President of PPRE Consulting, specializing in Product, Project and Regulatory Engineering.
Mr. Pizzuto has 40 year of engineering and management experience. He has developed hundreds of new products for fortune 500 companies. Mr. Pizzuto has 13 years of medical device design, manufacturing and regulatory compliance experience. As Global Director of Engineering for a major medical device manufacturer with teams in the USA, Europe, China and Mexico he delivered Class I and Class II medical device projects.
Mr. Pizzuto holds a Medical Device Certificate from the Regulatory Affairs Professionals Society (RAPS), was a member of the FDA’s Hospital Bed Safety Work Group and is an expert witness for Hospital Bed Safety litigation. Mr. Pizzuto has most recently focused on remediating Design Control and Risk Management Systems for clients under FDA legal action.
For additional information on the workshop agenda and logistics, please call 410-501-5777 or email: info@FDAMap.com
