Ximedica

Diagnostics

In vitro diagnostic platforms are evolving rapidly around nucleic acid testing, multiplexed formats, automation and demand for point-of-care technology. While platform value is often dominated by reagents, a full grasp of system (hardware, software and consumables) architecture and performance is critical to market success.

We fully understand the development process needed to deliver market-leading medical diagnostic systems.

Ximedica offers customized solutions for biotechnology devices throughout the design process. Our technical expertise and passion for human-centric design lead the industry in speed-to-market efficiency. FDA Registered and ISO 13485:2012 Certified, our competence and expertise helps us to streamline development and cut costs along the way.

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At Ximedica, our people define who we are.

More About Our People

Morris Chow

Morris Chow

Director of Asian Operations, Hong Kong

Jennet Toyjaynova

Jennet Toyjaynova

Research & Development Engineer

Chelsea Saniel

Chelsea Saniel

Program Manager

Kelly Ashfield

Kelly Ashfield

Director of Program Management

Anna Passernig

Anna Passernig

Mechanical Engineer

Maria Tavares

Maria Tavares

Documentation Control Coordinator