Innovation and collaborative, synchronized program management for new programs
Medical device products are undergoing dramatic changes to compete in an ever-changing and rapidly expanding market. One of the key enabling factors is the software embedded within these products. Sophisticated product-intelligence software driving this advanced functionality is highly complex and challenging as devices are only becoming smarter.
Disruptive behavior is forcing med-tech companies to innovate, or be left behind. Software engineering has never been more interdependent on electrical and electronic hardware systems and mechanical systems.
Medical device products are undergoing dramatic changes to compete in an ever-changing and rapidly expanding market. One of the key enabling factors is the software embedded within these products. Sophisticated product-intelligence software driving this advanced functionality is highly complex and challenging as devices are only becoming smarter.
Disruptive behavior is forcing med-tech companies to innovate, or be left behind. Software engineering has never been more interdependent on electrical and electronic hardware systems and mechanical systems.
The need to manage sophisticated smart products in the medical device industry requires integrated software engineering solutions. Our systems-driven approach to medical device product development marries systems engineering with an integrated approach to software engineering and product engineering.
Technologies such as model based engineering (MBE) enable the Digital Twin concept that allows for quicker product evaluations, robust functionality, and operational assessments which help to reduce development time and costs, all while ensuring the end product meets consumer need.
Explore the key areas of this solution.
Provide a common source of materials information across your medical device organization, whether a basic or advanced BOM, in order to exceed market demand for more innovative and varied product offerings.
Utilize out of the box integration with popular tools for a fast start and wide range of project templates. Free, open API's help your medical device organization build personalized apps and extensions.
Accelerate functional safety compliance for ISO26262, Automotive SPICE, and CMMI standard.
Comprehensive, automated history of all artifacts facilitates proof of compliance - Integrate risk management processes leveraging the ISO 14971 template.
Equip medical device development organizations with a single, cohesive product ecosystem, directly linking of ALM and PLM data and processes.
Create, view and edit device requirements with familiar applications thanks to our integrated engineering lifecycle solution which enables a start integrated and stay integrated development process.
Achieve agility while protecting quality and compliance regulations at your medical device organization, all whole maintaining lean yet complaint approval processes.
Improve decision-making and project execution with detailed analytics and real-time status reports created specifically for the medical device industry.
Release devices frequently and without compromising the consistency, integrity, or regulatory compliance of any product.
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