Latest Quality Management Release for ISO 9000 & ISO 13485
(PRWEB) November 24, 2015 -- Glenn Kohner, Vintara’s CEO, stated, “Whether you are an ISO 9000 or ISO 13485 medical device manufacturer, measurement creates accountability. You get results by tracking ownership of data and completion of activities. Measurement is essential in quantifying performance gaps and providing insights into root causes of inadequate performance. Our latest release continues Vintara’s tradition of premier QMS software enabling companies to quantify and measure activity enterprise-wide. Our customers make informed business decisions and reduce costs while improving both company performance and customer satisfaction. You get results by tracking ownership of data and completion of activities. QMS software has evolved from an individual’s toolkit into an enterprise solution focused on increasing access to resources and overall participation across the organization requirements.”
Release Highlights
New Release highlights are as follows:
• Double Signature Validation
• Time-stamp accuracy to the second for approved documents
• Automated timely review of documents
• Cross-browser navigational compatibility across ALL browsers eliminating data loading and compatibility issues
• Templates in place and available for the newest ISO standards scheduled for implementation in September 2018
• Document change log
• Coordination with Outlook for meeting notices
Quality managers can expect to see features in several QMS centers including:
• Document Management
• Design Control
• Training Management
• Supplier Management
• Audit Management
• Equipment Calibration
• Phone, I-pad compatibility
• Auto-archiving in all Centers
STEVE ANDERSON, VINTARA, http://www.vintara.com, +1 925-386-0435, [email protected]
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