Thursday 24 Feb 2022
4:00 PM (CET) / 10:00 AM (EST) / 7:00 AM (PST)
approx. 75 min
Dr. Andreas Birk
Founder and Principal Consultant of Software. Process. Management
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Medical device development with its regulatory requirements is often viewed unsuited for Agile methods. There does seem to be a natural tension between commonplace Agile practices and regulatory compliance requirements in MedTech. However, these challenges can be overcome, unlocking Agile’s potential to bring important benefits to the development of medical devices.
This webinar highlights key characteristics of medical device development that must be considered to guide the successful implementation of Agile. During this session, we’ll present important strategies that support MedTech organizations on their journeys to Agile, helping them make the most of Agile’s enormous potential!
The webinar’s agenda:
- Does Agile contradict regulated product development?
- Advantages of Agile for medical device development
- Challenges of Agile adoption in MedTech environments
- Agile success strategies for medical device development
Our webinar is intended for:
Project Managers and Team Leaders, Product Quality and Test Engineers, Heads of Testing & QA teams, Embedded Software Developers, Business Analysts, Regulatory Compliance Analysts
Dr. Andreas Birk is the founder and principal consultant of Software.Process.Management. He helps organizations optimally design and improve their software development processes. His focus areas are software product management, Agile development, and tool-based requirements management.