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Title
Batch Production Record and Device History Record Review and Quality Assessment
URL
http://www.globalcompliancetrainings.com/index.php?route=product/product&product_id=48
Description
Written procedures are to be established and followed for a time efficient and clear evidence of the quality related elements during the review and approval for release, including packaging and labeling, 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 proceLabeling requirements Safety Data Sheets (SDS) format - 16 sections
Length
Coupon
(optional)