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.

How will I benefit?

This course will help you to:

  • Understand the key concepts and requirements of EN 62304
  • Gain knowledge of the implementation steps of the medical device software lifecycle processes
  • Correctly classify your medical device software as per the MDR
  • Perform the necessary risk management and software lifecycle management activities 

Đào tạo trực tiếp: luôn sẵn sàng khi bạn cần

Khi bạn đã sẵn sàng cho việc đào tạo trực tiếp tại văn phòng BSI, chúng tôi sẵn sàng chào đón bạn.

Khi tất cả chúng ta điều chỉnh thói quen đi lại sau khi kiểm soát dịch, BSI luôn tăng cường các biện pháp kiểm soát nhằm đảm bảo sự chuẩn bị an toàn cho các khóa đào tạo tổ chức tại địa điểm BSI.