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The FDA's Digital Health Regulatory Journey
Join us in watching this part three of a four-course series
FDA's Digital Health Regulatory Journey
Through this four-course series, we will explore how to architect complex software solutions, balance agile with regulatory constraints, and showcase how low-code development catalyzes dev-ops. 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:
Join us for an interview with Bakul Patel, FDA Director of Digital Health to discuss the FDA's digital health regulatory journey. Bakul speaks about the FDA’s digital health journey, their stance on digital transformation, what logical next steps look like in your digital transformation journey and constraints that the FDA is working on to lower the barrier of entry into digital transformation.
Meet our presenter:
Senior Director of Medical Device Processes, Siemens Digital Industries Software
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.
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