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    Regulatory Services

    Quality Management System Certifications for Medical Devices

    Quality Management System Certifications can be used to monitor and continually improve the quality of your products and services.

    Medical device manufacturing is one of the most regulated sectors in which significant quality systems and product requirements must be satisfied.

    The regulatory requirements are intended to ensure that manufacturers consistently design, produce and place onto the market medical devices that are safe and fit for their intended purpose.

    We offer a wide range of proven regulatory and quality management programs that work together for full international compliance.

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