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Monday, December 07, 2009

Manufacturer of the Year Continues to Build on Experience, Quality, and Success

Posted to Announcement by Ms. Lori K. Pegon of Inteprod LLC at 4:34 PM

ISO 13485 Certified and FDA registered Medical Product Developer and Contract Manufacturer focuses on Excellence and Innovation.

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.

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Thursday, August 06, 2009

Inteprod Achieves Significant Milestone with ISO 13485 Certification

Posted to Milestone by Ms. Lori K. Pegon of Inteprod LLC at 4:26 PM

Inteprod Achieves Significant Milestone with ISO 13485 Certification

Manufacturer of the Year Continues to Build on Experience, Quality, and Success

Eagleville, PA, July 31, 2009 – 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.

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.”