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ISO 13485

Safety and quality are non-negotiable in the medical devices industry – they can literally mean the difference between life and death. With increasingly strict regulatory requirements and expectations from customers and organizations throughout the supply chain, it is critical to demonstrate best practice in quality management processes – and ISO 13485 certification can do that. By partnering with Kiwa, you can use ISO 13485 to ensure the products or services you offer in the medical devices field are in accordance with internationally accepted standards, helping you build trust with customers and meet legal requirements.

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