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Total Product Life Cycle Seminar 2017

Hilton Garden Inn Philadelphia Center City

Thursday, May 25, 2017

 

 

This workshop style training course is supported by comprehensive knowledge of U.S. FDA laws and regulations and 30 year of extensive experience working within in the U.S. FDA regulated industries. In these 2 days, the following essential topics will be covered: • Total Product Life Cycle and Your Medical Device • An Overview of U.S. FDA Medical Device Regulation • Regulations for Design and Product Development • Premarket Notification - 510(k) and Premarket Approval (PMA) • Regulations for Production & Process Control • Readiness for FDA Facility Inspection

 

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