We are currently working on the 2020 Agenda. If you would like to get emailed a copy once it's ready please let us know HERE.
SDMD is Europe’s only international forum dedicated to medical device software design, regulatory compliance and cybersecurity. We are returning in February to continue to welcome all regulatory, security and design representatives involved in creating a software-based medical device.
The event addresses challenges around usability, software development and risk management by highlighting case studies from both big and small medical deveice manufacturers, to ensure that all attendees leave with the tools required to perfect their device software and get their products to market as soon as possible.
SDMD 2020 is Europe’s only international forum dedicated to medical device software design and compliance.
Join us in February to explore the principle challenges associated with complex and integrated systems of medical devices.
Download the full agenda on the right >>
Early confirmed speakers include:
- Jan Van Moll, Director of Quality and Regulatory, Philips
- Nancy Van Schooenderwoert, Principal Consultant, Lean Agile Partners
- Georg Heidenreich, Director of Healthcare IT Standards, Siemens
- Harsh Jain, Product Quality Engineering Manager, Google Verily Life Sciences
See the full 2020 speaker faculty, download the agenda >>