Integrating Expertise from Software Development, Quality Assurance, Regulatory Affairs, and Product Teams to Drive Innovation in Alignment with Global Regulatory Guidelines, AI and ML Enabled Software, Cybersecurity, and Agile Methodologies
The European market is capturing 30% of the global medical device field driven by rapid advances in innovative software, AI, and ML. But as medical device developers are met with tedious submission processes, ever-changing software patches, and red tape at every turn, it has never been more important to break out of cross-functional silos and stay two steps ahead of compliance guidelines.

Dedicated to unravelling a matrix of multi-layered European and global regulations, mitigating vulnerabilities in security, and managing updates to legacy devices, the 3rd Medical Device Software Development Summit Europe is uniting medical device giants and innovative start-ups to share case studies and best practices in advancing and maintaining compliance of innovative software.

We will be shining the spotlight on:

Working strategies shown through examples of documentation for AI enabled medical device software
Implementing automation tools to establish feedback loops throughout the software development process
Implementing rigorous data validation and

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Integrating Expertise from Software Development, Quality Assurance, Regulatory Affairs, and Product Teams to Drive Innovation in Alignment with Global Regulatory Guidelines, AI and ML Enabled Software, Cybersecurity, and Agile Methodologies
The European market is capturing 30% of the global medical device field driven by rapid advances in innovative software, AI, and ML. But as medical device developers are met with tedious submission processes, ever-changing software patches, and red tape at every turn, it has never been more important to break out of cross-functional silos and stay two steps ahead of compliance guidelines.

Dedicated to unravelling a matrix of multi-layered European and global regulations, mitigating vulnerabilities in security, and managing updates to legacy devices, the 3rd Medical Device Software Development Summit Europe is uniting medical device giants and innovative start-ups to share case studies and best practices in advancing and maintaining compliance of innovative software.

We will be shining the spotlight on:

Working strategies shown through examples of documentation for AI enabled medical device software
Implementing automation tools to establish feedback loops throughout the software development process
Implementing rigorous data validation and cleansing processes to ensure reliability of training datasets for AI models
Creating synergy between business and engineering through a unified data strategy
Uniquely positioned to share strategic guidance in optimising efficiency in regulatory submissions, streamlining development processes, and embedding compliant AI and ML in medical devices, join 70+ CTOs, Heads of Software, Product, RA, and QA to harmonise cross-functional objectives, accelerate time to market, and optimise updates to legacy devices.

URL:
Brochure: https://go.evvnt.com/2648359-3?pid=1356

Prices:
Conference Only - Device Developer - On the Door Price: EUR 2799.00,
Conference + Workshop Day - Device Developer - On the Door Price: EUR 3797.00,
Conference Only - Service Provider  - On the Door Price: EUR 3399.00,
Conference + Workshop Day - Service Provider - On the Door Price: EUR 4597.00

Speakers: Antoine Miguet Principal Software Engineer Medtronic, Baris Tanyeri Senior Software Engineer Philips, Christian Jensen Product Reviewer TUV SUD Danmark, David Bergstrom Director and Principal Engineer, Infusion Systems, Research and Development BD Technologies, Dominik Kowalski Senior Project Manager, Regulatory Compliance Passioned on AI Brainlab, Hariharasudan Kalidasan Head of Quality Regulatory Lightcast Discovery, Harsh Jain Senior Manager, Quality Engineering  Align Technology, Ikenna Okaro Systems Data Engineer Philips, Ilkka Korhonen Chief Technology Officer CardioSignal by Precordior, Jan Tully Senior Software Engineering Manager Medtronic, Lukas Futera Principal Platform Security Architect Roche, Mark Phillip Loria Lead Solution Architect Ypsomed AG, Mette Luxhøj Director and Head of Regulatory Affairs, Digital Health and Advocacy 3Shape A/S, Morten Andersen Safety Risk Manager Novo Nordisk, Olivier Staquet Chief Technology Officer Gabi SmartCare, Rajasekar Solai Senior Engineer, Quality Design Assurance BD Technologies, Ramin Moshavegh Head of SaMD Development Novo Nordisk, Romain Bornet Director, Firmware Engineering  ONWARD Medical, Saurabh Bhavsar Senior Leader, Digital Health Project, and Program Management Ypsomed AG, Tauseef Mehrali Vice President, Medical Safety and Regulatory Affairs Ada Health

Category: Conferences | Engineering and Technology

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Event organiser

Hanson Wade

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EUR 2799.00 - EUR 4597.00

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Location:

Holiday Inn Munich - City Centre, an IHG Hotel, Hochstraße 3, München, DE

Event links