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Iso 13485 2016 Medical Devices Services In Usa California

2 services found
ISO 13485 Medical Device Manufacturing System Quality Management Certification from NSAI

ISO 13485 Medical Device Manufacturing System Quality Management Certification from NSAI

by:NSAI Inc.   based inNashua, NEW HAMPSHIRE (USA)
ISO 13485 is a necessary certification for medical device manufacturers. It proves that you have a quality manufacturing process and the management standards in place to maintain high quality. ISO 13485 certification is the first step towards achieving compliance with European, Canadian and other regulatory requirements for medical device ...
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Medical Device Development Phases

Medical Device Development Phases

by:NOVO Engineering   based inVista, CALIFORNIA (USA)
NOVO specializes in medical device development services for Class I, II, and III FDA-regulated devices. The scope of our ISO 13485:2016-certified quality management system (QMS) covers a five-phase product development process (PDP) from concept through manufacturing transfer, including support ...
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