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21 CFR Part 111 - Master Manufacturing Records and Batch Production Records
Event Details
Time: January 12, 2022 from 10am to 1pm
Location: online
Street: Compliance Online
City/Town: Online
Website or Map: https://www.complianceonline.…
Phone: 8887172436
Event Type: webinar
Organized By: Complianceonline
Latest Activity: Jan 3, 2022
Event Description
The single most critical document in an FDA inspection is the master manufacturing record and associated batch production record. While the 21 CFR Part 111 regulations have a checklist of elements the documents must contain, it can be difficult to translate that into a working document. This training will review the basic principles of what an MMR & BPR must contain and give you tools to create an “FDA Acceptable” document.
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