Medical Device Software Development Plan
$119.00
$119.00
per item
The Medical Device Software Development Plan provides detailed instruction on the creation of a software development plan that is harmonized with the requirements of IEC 62304 and FDA guidance.
- IEC 62304:2015 Compliant
- ISO 13485:2016 Compliant
- FDA QSR Compliant
- MS Word Format
- Instructive Document
- Instant Download - Digital Content
SKU:
SD-PLAN
Medical Device Software Development PlanThe Medical Device Software Development Plan provides detailed instruction on the creation of a software development plan that is harmonized with the requirements of IEC 62304 and FDA guidance.
Medical Device Software Development Plan-OverviewThe Software Development Plan addresses content contained within IEC 62304:2015, IEC 12207 and FDA Guidance. The Medical Device Software Development Plan helps the user to organize the necessary roadmap, phases and tasks required throughout the development lifecycle, regardless of which life cycle model or approach is employed.
Medical Device Software Development Plan-ComplianceThe Medical Device Software Development Plan is IEC 62304:2015, ISO 13485:2016 and FDA QSR compliant.
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