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Throughout the world, medical device manufacturers and their suppliers are required to satisfy the highest quality assurance regulations and standards such as ISO 13485. Established by the International Organization for Standardization (ISO), ISO 13485 is the global regulatory standard for organizations that design and manufacture medical products, devices and components. Conformance with this important standard is confirmed through a complex auditing and certification process. While meeting the many requirements contained in the standard is challenging, an ISO 13485 audit checklist can simplify the process.

Holen Sie sich heute noch Insiderinformationen zu den relevantesten Themen in Bezug auf ISO 13485, und erfahren Sie, wie Sie die Komplexitäten der FDA- und ISO-Compliance umgehen und bewältigen.

Erfahren Sie, wie Sie mit MasterControl ISO 13485 Ihren Qualitätsprozess verwalten und gleichzeitig Risiken mindern, die Markteinführung beschleunigen und Ihren ROI verbessern können.

ISO 13485 Audit Checklist . Throughout the world, medical device manufacturers and their suppliers are required to satisfy the highest quality assurance regulations ...


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