Quality assurance is the cornerstone of our success. Each of our manufacturing sites is registered to both ISO 13485 and ISO 9001 and complies with Directive 98/79/EC, on in Vitro Diagnostic Medical Devices. We promote continuous improvement across the group, and all staff are encouraged to contribute to this programme.
At all times, we aim to ensure compliance with all relevant statutory, regulatory and legal requirements.
The overriding quality policy is driven by the need to consistently measure, satisfy, and maximise customer satisfaction with the products and services provided by us.
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