FDAnews Announces — Auditing for Quality Manufacturing: Five Areas of Risk for Drug and Device Manufacturers Management Report

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Drug and device manufacturers: prepare, organize and streamline manufacturing auditing processes using a risk-based approach.

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WCG FDAnews

Auditing for Quality Manufacturing:
Five Areas of Risk for Drug and Device Manufacturers
Management Report
https://www.fdanews.com/products/59566

Running 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/59566

Management Report PDF:
$397

Easy Ways to Order:
Online: https://www.fdanews.com/products/59566

About FDAnews:
FDAnews is the premier provider of domestic and international regulatory, legislative, and business news and information for executives in industries regulated by the US FDA and the European Medicines Agency. Pharmaceutical and medical device professionals rely on FDAnews' print and electronic newsletters, books and conferences to stay in compliance with international standards and the FDA's complex and ever-changing regulations

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Michelle Bultler
FDAnews
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