The QT9 QMS platform offers smart workflow tools to help with automated compliance workflows, comprehensive task and approval ...
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 ...
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, ...
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 ...
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 ...
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 ...
Dual certifications streamline global design transfers and regulatory compliance. TAIPEI, Nov. 21, 2025 /PRNewswire/ -- IEI Integration Corp. ("IEI"), a global provider of medical and industrial ...
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 ...
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