Batch Production Records Web-based Seminars
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From GlobalCompliancePanel
Master Production Record Requirements - Webinar By GlobalCompliancePanel
This program will address the 21CFR and Eudralex Volume 4 requirements and interpretation, as well as FDA Guidance regarding the creation, review and approval, and control of Master Production Records.
The material will enable attendees to establish a consistent approach to the design of MPR, including cover page content, instructions, processing requirements and limits, and signature
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Requirements of the Master Production Record - Webinar By GlobalCompliancePanel
...the process and requirements for issuance and handling of Batch Production Records (BPR), and clearly describe the difference between the master and the batch production record.
Why should you attend: All the requirements for the master production record (MPR) are based on relevant US and EU regulations. Failure to recognize and implement those requirements can have devastating effects on
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