Batch Production Record and Device History Record Review and Quality Assessment

MessageThis Webinar is over
Date May 5, 2014
Time 12:00 AM EDT
Cost $225.00
To determine compliance of the intermediates (FDA definition) and/or finished product with established specifications before a batch can be released for distribution BPRs, DHRs and laboratory control records for critical process steps are to be reviewed and approved by the quality unit(s) before a finished product batch is released for distribution.


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