Description

The FDA has proposed changes to its current good manufacturing practice (cGMP) requirements for medical devices. What will this mean for manufacturers? Find out from Exponent’s Ryan Siskey, M.S., in the presentation, “Revisiting Risk Management for Medical Devices – cGMP requirements and ISO 13485.” 

This webinar will discuss the impacts on risk management practices for medical device manufacturers per ISO 13845, including supplier selection, staff training on risk management procedures, developing procedures that incorporate ISO 13485, and tracking, trending, and reporting on risk management activities.

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Connect with Mr. Siskey: https://hubs.li/Q02H-z5z0