Evolution of the Quality Management System

An efficient and effective Quality Management System is the cornerstone for organizations in the regulated industries. Such a QMS signals to the regulatory authorities such as the FDA and others, that there are no lacunae in the completeness, accuracy, and consistency of an organization’s QMS.

It is not to satisfy the regulatory bodies alone that a robust QMS is necessary: it also gives the organization’s personnel the ability to meet quality requirements with consistency and accuracy. Accuracy of outcomes and quality of work are the results of such an assurance.

It is to help organizations in the regulated industries understand and get their QMS right, in the prescribed manner, that GlobalCompliancePanel, a leading provider of professional training for all the areas of regulatory compliance, is organizing a long, six-hour webinar, on Jan 21, 2020.

GlobalCompliancePanel brings Susanne Manz, a well-known and highly accomplished leader in the medical device industry with emphasis on quality, compliance, and Six Sigma, as the Director of this web seminar. To register for this highly valuable learning, please log on to GlobalCompliancePanel

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The regulatory guidelines state that the organization should “…establish and maintain a quality system that is appropriate for the specific medical device(s) designed and manufactured”. This makes it imperative for organizations to understand the exact requirements relevant to them and tailor them to their precise needs.
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