Inteprod Achieves Significant Milestone with ISO 13485 Certification

Aug. 4, 2009 - PRLog -- Eagleville, PA – Inteprod LLC, a medical device developer and contract manufacturer, announced today that it has received an ISO 13485 Certificate of Registration issued by KEMA Quality B.V.  This certification is a major milestone in Inteprod’s 5 year history and confirms Inteprod’s steadfast commitment to continual improvement, risk management, compliance with statutory and regulatory requirements, and complete customer satisfaction.

ISO 13485 is an internationally recognized standardization system which defines the standards for the design, development, production, and distribution of medical devices.  It ensures conformity with specified quality controls in the development of safe and effective medical devices.  

According to Inteprod’s President and Founder, Rick T. Smethers, “Inteprod continually strives to be the leader in the contract development and manufacture of medical products.  This certification is a tribute to Inteprod’s continued focus on exceeding customer expectations, and validates our commitment to high quality standards.”

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About Inteprod: Inteprod is an innovative and highly experienced full-service supplier of comprehensive design, development, and contract manufacturing solutions for products in the medical device, medical diagnostics, and food safety diagnostics industries. Focused on and committed to the medical and food safety industries, Inteprod is a strategic partner and resource for major Medical OEMs and emerging Biotechnology and Life Science companies. Inteprod’s deep expertise and capabilities in developing and manufacturing medical products include: hand-held devices, point of care diagnostics, bedside diagnostics, LOC technology, patient monitoring, analytical instruments, and minimally invasive surgical instruments.

To learn more about Inteprod, please visit www.inteprod.com or contact Lori Pegon at (610)650-9002, or lp@inteprod.com.