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Safety and quality are non-negotiables in the medical devices industry. Regulatory requirements are increasingly stringent throughout every step of a product’s life cycle, including service and delivery. Increasingly, organizations in the industry are expected to demonstrate their quality management processes and ensure best practice in everything they do.
ISO 13485, Medical devices – Quality management systems – Requirements for regulatory purposes, is an internationally agreed standard that sets out the requirements for a quality management system specific to the medical devices industry.
Sam brings an accomplished 20+ year career to QMS, working in the Electronics Manufacturing, Engineering Services, Information Technology, and Telecommunications industries. His extensive background includes leadership positions in General Management, Sales, Marketing, Operations, Quality Management, and Engineering.