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Follow on Google News | Inteprod Achieves ISO 13485:2003 RecertificationConsistent Record of Zero Findings Underscores Medical Contract Manufacturer’s Commitment to Quality, Reliability, and Excellence
By: Inteprod LLC Inteprod achieved ISO 13485 recertification and move verification following two separate audits by accredited certification body, BSI Group. Both audits resulted in zero findings, and further confirmed Inteprod’s unwavering commitment to quality, reliability, and excellence in medical product manufacturing. ISO 13485:2003 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 and manufacture of safe and effective medical devices. “Achieving and maintaining a consistent record of zero findings is no small feat”, stated Suzanne Smethers, Inteprod’s President. “The auditor’s objective is to find nonconformance( The scope of Inteprod’s recertification and move verification include the contract design, development, and manufacture of electromechanical medical devices, medical diagnostics, and consumables. End
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