Software Design for Medical Devices 2017
Ground-breaking innovations, cutting-edge ideas and out-of-the-box development techniques are making the medical device marketplace more competitive every day. At the same time, increasingly rigorous standards and regulations are making regulatory compliance more difficult than ever before.
So how can medical device software remain efficient and compliant, and help devices get to market faster?
Are you currently:
Wondering how the new Medical Device Single Audit Program can help you get inspection while saving time and money? GE Healthcare tell you all about the program.
Striving to perform powerful Root Cause Analysis on your med-device software pre and post release? Philips are doing it, and will tell you how.
Trying to avoid software failures by embedding risk analysis into your agile development cycle? Diagnostic Grifols share their strategies.
Trying to get ahead of the competition with innovative verification and validation processes? Medtronic prove why they are a market leader.
Seeking clarification on the FDA’s new Postmarket Cyber Security Guidelines, or Usability regulations? Abbvie’s Human Factors Director explains everything.
And back in 2017 by popular demand, we bring you a FULL DAY training course on introducing agile adoption for regulated medical software - the business and regulatory impacts.
To find out about all the exclusive case studies and interactive discussions, download the agenda now.
Senior Quality Site Leader
Principal System Engineer
Manager, Software Design QA
Senior Engineer Medical Software
Project Manager (SW), Multisite Scaled Scrum
Head of Quality Management System, Audits & Compliance
Instruments R&D Director
Department Head Release Management, Digital Factory Division, Factory Autom
Former Director Human Factors
Senior Quality & Regulatory Affairs Director
Lean Agile Partners
Head of Global Software Standards
Principal Technical Consultant
Technical Project Leader Measurement Engineering
Roche Diabetes Care
R&D SW Development Manager
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