Quality is the defining characteristic for high-performing drug and medical device manufacturing businesses. These operations are, of course, compliant with applicable rules. But these organizations also think beyond compliance and focus on achieving and maintaining high quality systems.
Fundamental to this shift is a manufacturer’s ability to provide regulators and executives with greater visibility into its operations and quality processes — processes that go beyond compliance and allow manufacturers to differentiate themselves in the market. Regulators recognize the importance of this concept and many of the new regulations and guidelines require that manufacturers make substantial changes to their quality systems, data management and submission processes.
In this webinar, taught by the experts from Sparta Systems, you’ll learn the six quality management success factors that are necessary to meet the evolving regulatory landscape.
Register today for the 6 Tips for Effective Quality Systems webinar to learn:
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Over the course of twenty years, Tom Middleton has conducted nearly 1,000 registration, surveillance, internal and supplier audits. Formerly an ASQ / RAB accredited ISO and Global cGMP lead compliance auditor for Underwriter’s Laboratories and Bausch + Lomb’s Surgical Division. He is currently an ASQ certified biomedical auditor.
Senior Product Manager
Mike Edwards is the product owner for TrackWise, the global leader in enterprise quality management. He has worked for Sparta for eight years and has been involved in the FDA Quality Metrics initiative for several years.