Medical Device Software Regulations and Standards Training
This course provides a foundation for understanding the regulatory landscape for medical device software development.
Comply Guru offer IEC 62304 training for those working with Software as Medical Device (SaMD) in Ireland.
IEC 62304 defines the life cycle requirements for medical device software. The set of processes, activities, and tasks described in this standard establishes a common framework for medical device software life cycle processes. This standard was last reviewed and confirmed in 2021, remaining current.
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Training Guide
This course provides a foundation for understanding the regulatory landscape for medical device software development.
This course provides an in-depth look at both the SDLC and IEC 62304 (2006).
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