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Software for MedTech - IEC 62304 Deep Dive
Wed, 15 July
|By webinar. Register for details
We explain the manufacturing process including PCB and final product assembly, with tips on how to optimise your design for manufacture.
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Time & Location
15 July 2020, 12:00 pm – 1:00 pm AEST
By webinar. Register for details
About the event
In this presentation, Geoff Sizer explains the critical role of software development for Active Medical Devices. In particular we take a close look at the pivotal standard IEC 62304. This standard specifies the requirements for firmware and software in medical devices at every stage of the product's life cycle.
Topics to be discussed:
- Software development planning
- Requirements Analysis
- Architectural Design
- Detailed Design
- Software unit implementation and verification
- Integration and integration testing
- System testing
- Software risk management
- Software release
- Software maintenance
- Software validation
Geoff Sizer is the CEO of Genesys Electronics Design and ISO 13485 certified contract designer of medical devices.
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