Vantage ALM Custom Configures Polarion to Help Medical Device Company Launch Complex Robotics Device

Overview

When a medical device company needed a custom-configured instance of Polarion to accommodate the complex design and development of a new surgical device, they turned to their trusted partners at Vantage ALM.  

Challenge

A global orthopedics medical device company had been partnering with Vantage MedTech to solve their design and development challenges for more than a decade. Shortly after they began work on their most recent project, a robotics surgical device, the client realized they needed their own instance of the product lifecycle management (Vantage ALM) software tool, Polarion. The project was highly complex, requiring a more customized Polarion configuration that could support more users, additional work items and multi-layered sub-systems.

Solution

Based on detailed input from the client, Vantage ALM configured a Polarion instance with custom-built plugins and scripts that could accommodate hundreds of users, complex traceability reporting, robust testing functionality and more.

With the platform built to the medical device company’s specifications, the team moved the existing data from the Sterling server and test cases from a third-party platform onto the client’s instance of Polarion to serve as one centralized Vantage ALM system. The Vantage ALM team then trained 180 users on the new platform to ensure consistent use of the tool. As additional needs arose, Vantage ALM further customized and configured the tool to meet the evolving demands of the highly complex project.

Today, Vantage ALM offers ongoing support as needed—from answering basic questions and troubleshooting to setting up accounts, importing documents and more.

Result

By migrating the customer onto their own instance of Polarion configured for their use, Vantage ALM helped the medical device company work more efficiently with greater control and flexibility to accommodate their evolving complexities. In under two years, the customer designed, developed and submitted the highly complex surgical robotics device for FDA approval.

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