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Gain an understanding of the medical device software lifecycle processes, classification rules and development activities to meet regulatory requirements.
This course is designed to provide you with knowledge of how the Medical Device Regulation (MDR (EU 2017/745)), standards and guidance documents impact medical device software; software as a medical device; and medical devices with software.
It will help you to understand how EN 62304 Medical device software - software lifecycle processes can improve your medical device software development, validation and lifecycle process.
This course will help you to:
On completion of this training, you’ll be able to:
This course is intended for individuals or organizations involved in software within the medical device industry.
Pre-requisites
You should have an awareness of Medical Device Regulations and some basic knowledge of medical device software to benefit from this course.
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