Past event: Software Design for Medical Devices Europe 2014 Conference

The only truly international forum dedicated to medical device software standards, regulatory compliance and development

Standards, regulations and software development best practices in medical device software are constantly evolving, with more aspects to consider than ever before and teams becoming progressively more agile.
Being truly agile in such a regulated environment is a challenge, and manufacturers constantly seek to improve the quality, usability and software lifecycle of their device development.

SDMD is the only truly international forum dedicated to medical device software development & compliance, and as of 2013 is now a complete one-stop-shop for all RA/QA and Software Engineers involved in medical device development.

With a new, in-depth look into compliance and quality issues, as well as the usual popular topics of agile programming methods, new testing/V&V techniques and product usability, international medical device company QA-RA and software professionals have a real must-attend date in the calendar - the only truly international and English-language software development and compliance forum dedicated to medical devices.


So What's So Great About SDMD Europe 2014?

  • Discuss the proposed overhaul of the European medical device regulatory system
  • Get the latest updates and stay compliant with ISO/IEC standards 60601 3rd revision, 62304 software, 62366 usability and 14971 risk management; interactive Q&A and discussions led by group conveners and regulators
  • Become more agile and discover how to move away from hybrid models in safety-critical applications
  • Improve the usability and quality of your product
  • Increase the efficiency of the product software lifecycle with the latest safety testing techniques, version tracking and effective documentation
  • Network and benchmark with both QA/RA and software/R&D professionals - perfectly aligned with today's embedded industry!

See you in Munich!

 

"I look forward to attending Software Design for Medical Devices not only because I will hear about current developments and trends, but will have the chance to exchange ideas and information with colleagues who are facing the same challenges as I am, every day."
ShoeBar Associates

"Valuable for getting a view on the problems from different angles, and for making contacts with experts in this area"
Institute for Testing and Certification

"Highly valuable"
Renishaw

Register at ASDEvents and receive 15% discount.

Speakers Include:

  • Chuck Sidebottom, Director, Corporate Standards, Medtronic
  • Gerd Neumann, Standardization Expert, Siemens AG
  • Keith Reid, RA/QA Engineer, Renishaw plc
  • Conrad Dirckx, Senior Manager Software Engineering, Siemens Molecular Imaging
  • Andy Vaughan, Standards Policy, ABHI
  • Hagai Livni, Head of Software Validation, Given Imaging
  • Marco Rigamonti, Director, Design and Engineering, Flextronics
  • Marta Walker, Design Quality Manager, Roche Diagnostics
  • Brian Shoemaker, Principal Consultant, ShoeBar Associates
  • Nancy Van Schooenderwoert, Principal Consultant, Lean Agile Partners
  • Martin Schulze, R&D Project Manager, TRUMPF Medizin Systeme GmbH & Co. KG
  • Ed Israelski, Director of Human Factors, Abbott Labs
  • Celestina Bianco, QA & Regulatory Affairs Director, Systelab Technologies, S.A.
  • Edmundo Harbin, Head of Quality Assurance and Localization, ProSiebenSat.1 Media AG
  • Jan van Moll, Senior Manager Quality Management, Philips Medical Systems Nederland BV
  • Albert Farre, Project Manager, SW Development, Systelab Technologies S.A.
  • Greg Dameron, Director, Software Engineering, Medtronic
  • Lee Turl, Technical Lead, Renishaw plc
  • Arnab Ray, Senior Research Scientist, Franuhofer Center
  • Chris Ampenberger, Director of Engineering, PHT Corp
  • Klaus Ostermayer, Auditor / Technical Expert Medical Devices, BSi
  • Tony Hewer, Senior Director, Medidata Solutions Worldwide
  • Frederik Toune, R&D Manager Software, Barco NV

Register at ASDEvents and receive 15% discount.

Please fill in your name and email to receive the conference agenda of this event.

The agenda is available as PDF under downloads at the right side of the page.

Register at ASDEvents and receive 15% discount.

Venue

The venue is not yet available for this event.
Follow this event to be informed when the venue is available and stay informed on other changes.

Who Should Attend?

The following roles working in software development for medical devices, clinical data management, biobanking and any other regulated healthcare sectors:

  • Software Development Managers
  • Project Managers
  • QA/RA (Quality Assurance & Regulatory Affairs)
  • Software Engineers
  • Software Architects
  • Heads of Software Development
  • Usability Engineers
  • CTOs
  • CIOs


Venue & Accommodation

Venue to be confirmed
Munich, Germany 

Accommodation
More information to follow...

Register at ASDEvents and receive 15% discount.

Event details
Organizer : IQEU
Event type : Conference
Reference : ASDE-2940

Other interesting Medical Devices events

Virtual Seminar on Medical Device Single Audit Program (MDSAP) Implementation & Participating Country Regulatory Processes: U.S., Canada, Brazil, Australia and Japan - eLearning
Virtual Seminar on The New EU Medical Device Regulation - eLearning