Provides a validated QMS solution to accommodate increased regulatory requirements
Somersworth, NH (October 11, 2019) – J-Pac Medical, a leading medical device outsourcing partner announced that it has adopted an electronic Quality Management System that seamlessly integrates all of its quality and regulatory compliance processes. The suite of validated, FDA/ISO compliant electronic business processes is designed to comply with strict regulatory requirements and enable industry best practices.
“Implementing an electronic Quality Management System takes our compliance system to the next level in order to better serve our medical device customers,” said Jeff Barrett, President and CEO. “The new system will allow us to maintain regulatory compliance while we continue to grow. Our customers are increasingly outsourcing more medical device assembly and packaging while regulatory requirements continue to become more burdensome. The new system gives customers peace of mind and allows us to scale our business while ensuring compliance to FDA and ISO regulations.”
About J-Pac Medical
J-Pac is an ISO 13485:2016 certified supplier of assembled, packaged and sterilized medical and diagnostic devices. J-Pac is a manufacturing solution for both large and small medical device and diagnostic companies that need a one-stop manufacturing partner for single-use medical devices, biotextile products, and point-of-care diagnostic consumables.
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