©bongkarn thanyakij via Canva.com
Batch Production Record and Device History Record Review and Quality Assessment
This Webinar is over| Date | May 5, 2014 |
| Time | 12:00 AM EDT |
| Cost | $225.00 |
|
Online
|
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.
Create your own event
Turn your passion into a business.
Turn your passion into a business.