Manufacturer of the Year Continues to Build on Experience, Quality, and Success
ISO 13485 Certified and FDA registered Medical Product Developer and Contract Manufacturer focuses on Excellence and Innovation


VALLEY FORGE, PA, December 09, 2009 /24-7PressRelease/ -- Inteprod LLC, a medical device developer and contract manufacturer, announced 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.

In addition to the recent ISO 13485 Certification, Inteprod is now registered with the FDA as a Contract Manufacturer and continues to develop new services for the benefit and success of their clients. Inteprod has added a Biosafety laboratory and now offers Assay Development services to their Diagnostic clients in the Medical, Food Safety, and Pathogen Detection industries. These services include molecular and microbiology studies and analyses.

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 and new Assay Development service validate our commitment to high quality standards and are a reflection of Inteprod's commitment to continually exceed customer expectations."

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Press Release Contact Information:

Lori Pegon
Inteprod LLC
Marketing & Communications
970-200 Rittenhouse Rd
Eagleville, PA
USA 19403
Voice: 610-650-9002
Fax: 610-650-9003
Website: Visit Our Website