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ZEISS technology for the medical industry

30 de julio de 2021

ZEISS technology for the medical industry

Zeiss has a long relationship with the Medical Industry and continues to accompany it from the production and control of the different parts that are manufactured by traditional extractive processes as well as additives through 3D Printing.

From AMS in Argentina we offer the local market alternatives for 3D Scanning, Quality Control and 3D Printing of Polymers and Metal with different technologies, ensuring Industrial Additive Manufacturing Processes with certified quality in line with the requirements of your application.

Quality and ComplianceWith its high regulatory requirements and a large number of products that have a direct impact on people's quality of life, medical technology in the industry depends on reliable quality assurance systems.

Zeiss offers tailored software and hardware solutions that support industry standards and work as a cohesive system to give manufacturers the certainty they need to achieve the productivity they desire.

ZEISS Medical | Solutions for the Medical industry

To meet the regulatory demands of medical technology authorities, manufacturers must go beyond the usual quality assurance requirements. Not only must industry-specific workflows be configured correctly, they must also be able to document and validate that these workflows are consistently followed. To this end, QA hardware and software must work hand in hand and provide appropriate functionality.

ZEISS offers a complete, connected portfolio of hardware solutions including optical and tactile coordinate measurement machines (CMMs), 3D scanners, microscopes, as well as X-ray and CT solutions. Our customers benefit from class-leading resolution, accuracy, measurement speed and powerful automation features. However, the key to regulatory compliance lies in ZEISS software that seamlessly adapts to the hardware and helps manufacturers comply with the required step-by-step processes.

ZEISS software solutions include:• Compliance with the requirements of DIN EN ISO 13485 and FDA 21 CFR Part 11 • Secure user management • Integration of audit trail and version management. • Automated creation of certificates and manufacturer test certificates. • Continuous validation • Document version control and protection against modifications. • Detailed authorization concepts including electronic signatures • Disaster recovery • Enterprise-wide online performance indicators and key performance indicators

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ZEISS technology for the medical industry | AMS