Webinar Description :
FDA has been utilizing information based on inspections conducted by third parties and other regulators in different circumstances pursuant to MDUFMA 2002. This webinar is intended to help you get familiar with FDA's implementation of statutory requirements for setting risk-based FDA inspectional priorities. In particular, it deals with FDA's accepting voluntary ISO 13485 audit report submission requirements. This webinar is further intended to better understand FDA's medical device quality compliance program.
Live Session for one participant
Price: $225.00
Corporate Live Session 4 to 10 participants in single location.
Price:$885.00
Recorded Session Access recorded sessions only for one participant unlimited viewing for 6 months.
Price: $275.00
FDA has been utilizing information based on inspections conducted by third parties and other regulators in different circumstances pursuant to MDUFMA 2002. This webinar is intended to help you get familiar with FDA's implementation of statutory requirements for setting risk-based FDA inspectional priorities. In particular, it deals with FDA's accepting voluntary ISO 13485 audit report submission requirements. This webinar is further intended to better understand FDA's medical device quality compliance program.
Live Session for one participant
Price: $225.00
Corporate Live Session 4 to 10 participants in single location.
Price:$885.00
Recorded Session Access recorded sessions only for one participant unlimited viewing for 6 months.
Price: $275.00
