Avoid the guesswork in preparing for a QSIT audit
The Quality System Inspection Technique (QSIT) instructs U.S. Food and Drug Administration (FDA) staff on how to assess medical device manufacturers’ compliance with quality system regulations.
The FDA uses a “top-down” approach to look at your company’s subsystems (corrective action/preventive action (CAPA), design controls, process controls, change controls, etc.). This review is to ensure that your company has sufficiently defined and documented the subsystems’ procedures. Is your documentation complete, controlled, up to date, and ready for an audit?
Northeast Scientific is a market leader in high-end peripheral vascular catheter remanufacturing. The intense regulatory scrutiny on their processes makes it important that the production and quality departments work in sync. See how they use MasterControl’s Quality Excellence software to maintain high levels of quality while getting their products back into doctors’ hands as soon as possible.
I like having the ability to take paper-based records and create digital customizations for the end users. Some of the best things about this is reducing the time spent reviewing batch records and the reduction of errors from GDP perspective.
A digitized quality management system (QMS) is essential for efficient document control tasks. But it’s also valuable in simplifying training, CAPA, supplier management, audits, and more. The same interconnectivity that improves document control also streamlines the interaction between different aspects of a QMS.
Make quality a differentiator in getting products approved and on the market. A digital quality management system like MasterControl Quality Excellence, automates your quality tasks at every phase of the product’s life cycle.
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