Software Design for Medical Devices

Are you struggling to find the right balance between complying with regulations and fostering progress in the development of medical device software?

The medical device industry is constantly changing and evolving, especially in recent years with adjustments to regulations and the implementation of new standards.

With representatives from the BIGGEST and most innovative medical device companies in the world, as well as major regulatory bodies, at the 6th Annual Software Design for Medical Devices Europe conference will provide you with answers to all your technical and regulatory questions.

Join us to discuss the hottest topics in the industry:

• Overcoming your regulatory challenges - with a keynote address from the MHRA on the new EU medical device regulation proposal
• Driving innovation in production development while maintaining regulatory compliance - with case studies from Philips and GEHealthcare
• Effectively implementing agile development methodologies - with hands-on training from a certified Agile Coach
• Maintaining compliance in a changing regulatory landscape – with insight from Siemens Healthcare
• Applying Human Factors and Usability methodologies to minimize use-related hazards and optimize
device design – with help fromRoche Diagnostics Now in its 6th year running, SDMD Europe has proved itself as the leader in the field. 2016’s event will continue to serve as a platform to exchange best practices, ideas and help drive innovative solutions for medical devices.

Price: SPECIAL OFFER FOR ALL MEDICAL DEVICE MANUFACTURERS: 2-for-1 passes valid for the 2 day conference are available until 18th December : EUR 3,299 to EUR 400 EUR 2,199 Standard Price For Medical Device Professionals: EUR 3,699 to EUR 2,599 Conference Only - Standard Price For Solution Providers and Consultants: EUR 2,899

Speakers: Shoebar Associates, Brian Shoemaker, Principal Consultant Lean-Agile Partners, Nancy Van Schooenderwoert, President and Managing Partner MHRA, Rob Higgins, Head of Regulatory Affairs (Devices) Siemens Healthcare, GmbH Siemens Healthcare, Georg Heidenreich, Director of Healthcare IT Standards Miracor Medical Systems, Martin Haidacher, Project Manager Software Development and Data Analysis Quantum MDx, Jonathan Salmon, Manager of Research Convidien Hagai Livni, Global Head of Software Validation, Convidien Philips Healthcare, Holger Mikolon, Senior Software Architect Roche Diagnostics, Urs Suter, Usability Engineer Novartis, Andrew Smart, Human Factors Engineer Drägerwerk AG and Co, Bob Hunt, Senior Program Manager NayaMed, Olivier Blandin, Head of Operations Elekta, Rostyslav Dorozoh, Software Project Engineer Philips Healthcare, Sven Grand, Software Quality GE Healthcare, Holger Most, Regulatory Affairs Leader Biotronik, Heidi Manijeh Mehrzad, Principal Human Factors Specialist Systelab Technologies, Celestina Bianco, Quality Assurance and Regulatory Affairs Director Systelab Technologies. Albert Ferre, Project Manager of Software DevelopmentEvent Promotion by @evvnt - http://bit.ly/septPROMOTE