Device Master Record & Device History Record 2011 is a webinar that covers topics such as:
- Key Definitions
- The FDA`s QSR
- Quality System Record (QSR)
- Design History File (DHF)
- Device History Record (DHR)
- Device Master Record (DMR)
Device Master Record & Device History Record brings together attendees involved in design, project management, purchasing, production, servicing, installation, record keeping activities for medical device manufacturing and document control.
