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Integration of Agile and Regulatory Methodologies

Webinaire à la demande | 32 minutes

Join us in watching this part two of a four-course series

Next-Generation Software Development for Digital Health A Siemens Industry Software Master Class Series

Through this four-course series, we explore how to architect complex software solutions, balance agile with regulatory constraints, and showcase how low-code development catalyzes devops. Attendees will learn how to reconcile the speed of modern software development with current regulatory frameworks in digital health applications. The end goal is to paint a picture of how companies, big and small, can transform their software offering by getting away from the monolithic status quo.

About our Digital Health Series

The lifesaving gifts of today’s medical solutions are predicated on software in every aspect of the value chain. With all evidence pointing towards a future being exponentially software-driven, it is important for developers of medical device solutions to not only understand but adopt the latest and greatest approaches. The speed of adoption in this realm translates to better outcomes for patients and their families. This series will build off our previous master classes on Intelligent Design Control as well as parts of Design Excellence. As a leading global provider and developer of software, Siemens has expertise in sharing how it enables transformation with not only its customers but also in regard to its own journey.

In this webinar you will learn: agile software development doesn't naturally lend itself to design control and regulated environments. In this session we cover traceability of standards, integrating risk management, and delve into how agile teams can show data in a hierarchical sense as opposed to just what's inherently an agile perspective. What are these complexities and how can design control help manage it?

About our master class host:

Larry Sampson

With 20-years of operational experience in Medical Device, Larry Sampson knows firsthand how to balance device development agility and regulatory considerations. As a Sr. Director of Medical Device Processes at Siemens, Larry spends his days educating medical device manufacturers on best practices in all aspects of their product lifecycles. Outside the 9-5, Larry enjoys the great outdoors of Colorado with his family.

Larry Sampson, Senior Director of Medical Device Processes
Siemens Digital Industry Software