Meron Medical, LLC Announces Successful Transition to ISO 13485:2016

Warminster, Pennsylvania – October 31, 2018 – Meron Medical, LLC announces successful transition to ISO 13485:2016.

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. With greater attention on the organization's ability to meet applicable customer and regulatory requirements, ISO 13485:2016 focuses on the entire supply chain of the medical device industry, with added emphasis on risk management. Increasingly, organizationSteve s in the industry are expected to demonstrate their quality management processes and ensure best practice in everything they do.

The heightened areas of focus of the new standard fit well with the continuous improvement, and cultural-based business strategies at Meron Medical, and will provide excellent opportunities for the company to separate itself even further from competitors in its space.

Meron Medical, LLC provides high precision grinding services for projects ranging from R&D through commercialization for the medical device industry. The company draws on more than 60 years of industry experience from its parent company, M&S Centerless Grinding, Inc, and is considered a leader in difficult-to-grind guidewire and hypo-tube applications.

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