Auditing for Quality Manufacturing:
Five Areas of Risk for Drug and Device Manufacturers
Management Report
https://www.fdanews.com/products/59566Running a quality manufacturing operation requires constant vigilance for drug and device manufacturers.
Is the company conducting effective manufacturing audits?
When one does, one can identify and correct issues before they impact operations. Run the processes and the business smoothly.
Auditing for Quality Manufacturing: Five Areas of Risk for Drug and Device Manufacturers will help reader prepare, organize and streamline the audit approach so one can identify quality issues to establish a more robust operation that stands up to regulatory scrutiny. This management report points to five important areas of focus in auditing to ensure quality:
Data integrity
Quality culture
Aging facilities
Investigating manufacturing problems
Risk management
By using risk-based approaches to manufacturing audits drug and device manufacturers will identify and mitigate quality issues before they impact business operations.
Management Report:
Auditing for Quality Manufacturing:
Five Areas of Risk for Drug and Device Manufacturers
Management Report
https://www.fdanews.com/products/59566Management Report PDF:
$397
Easy Ways to Order:
Online: https://www.fdanews.com/products/59566
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