North Olmsted, OH, September 22, 2011 --(PR.com
)-- IQS, a leader of enterprise quality and compliance management software is proud to announce that a major medical device manufacturing company will implement IQS’ integrated quality management system.
They will implement IQS’ full product offering including; Customer Complaints, Non-Conformance, Corrective Action, Preventive Maintenance, Document Control, Gage Calibration, Employee Training and Skills Management.
They manufacture critical silicone rubber components that go into lifesaving medical devices, state of the art laboratory and surgical equipment, and medication management systems.
Their engineers can optimize key features of your medical product that will get you to market faster and more cost-effectively. Their multi-class clean room facility provides you with confidence and peace of mind, knowing that your critical medical silicone components are in good hands.
One of the key objectives was the ability of the IQS system to integrate with their AS 400 based ERP system, in order to support their need to maintain Device History Records or DHR’s. Implementation will start with the Illinois plant later this month.
IQS helps customers reduce risk and improve visibility among key aspects of business processes and performance. The IQS software model provides an enterprise-wide framework to manage compliance with multiple regulations, quality standards and compliance mandates. IQS’ integrated data hub allows increased visibility into total business process within organizations to provide actionable insight into performance and risk related metrics. Leading companies across multiple industries are using IQS today to manage and improve key business processes assuring higher levels of quality compliance and risk management. IQS is headquartered in Cleveland, OH and can be reached at www.iqs.com.