A quality audit examines your company's quality management system. A quality system auditor closely guards the checklist he uses and can adapt the list to ensure it applies to your business. If you ...

How often and how much does your firm think about quality? Every auditor is, by nature, committed to quality. Every firm has final quality control steps built into its production process. However, ...

FDA has published and makes available ALL regulations required for medical device companies. Look them up by searching 21 CFR part 820. And for outside U.S., you can easily obtain ISO 13485 for a ...

The introduction of new EU pharmacovigilance legislation presents opportunities in risk-based audits, QMS, and compliance improvement across regulatory activities. Training courses support ...

The evolving, risk-based approach to audit firm quality management is consistent with a trend that has become well established in the accounting profession. Over the past 15 years or so, leaders of ...

CHICAGO, IL--(Marketwired - August 18, 2016) - In the medical device industry, the complexity of supplier-manufacturer relationships poses quality and compliance related risks that could be very ...

With the agency’s increased vigilance over device manufacturers, how can companies better position themselves to achieve and sustain compliance? One key tool is the establishment of an effective ...

This modified pharmaceutical quality management systems lead auditor training course focuses on auditing to the ISO 9001 standard and the PQG's Application Standards for suppliers to the ...

Dublin, July 28, 2025 (GLOBE NEWSWIRE) -- The "Medical Device Single Audit Programme (MDSAP) Training Course" has been added to ResearchAndMarkets.com's offering. The Medical Device Single Audit ...

This modified pharmaceutical quality management systems lead auditor training course focuses on auditing to the ISO 9001 standard and the PQG's Application Standards for suppliers to the ...