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    • Market Access
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      • And more…
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      • Quality management system as a service
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      • Performance evaluation of IVDs
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      • Human Factors / Usability (IEC 62366 and FDA)
      • FDA relevant documents
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May 17, 2023


Development plan versus development process

By Claudia SchmittMay 17, 2023Leave a comment

Medical device manufacturers are obliged to both describe the development process and create a development plan. Because both documents specify how medical devices will be developed, there is uncertainty as to which information belongs in which document. This article resolves this and also examines the software. It looks at the software development plan and the…

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