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M14 - Software Regulatory & Quality - CE Marking for Medical Devices Software Regulatory Requirements - Step by Step

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Part of Medical Devices Training Module 14

Dates: Monday 13 July 2025
Venue:
AMP Technology Centre, Sheffield
Cost:

£735.00 excl VAT

Type: Medical Devices
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About this course

One day course for people who need to understand the regulatory requirements for software as a medical device. This course will help you to determine how to effectively understand whether software is subjected to CE marking requirements. This is a practical case study driven training course which leaves you with no doubt as to how to approach explaining the commercialization risks associated with your software. Moreover, the day consists of project planning sessions necessary to determine the pathway to conformity with CE requirements.

Who Should Attend

This course is delivered in-house and recommended for:

  • Medical Device Product Managers
  • Medical Device Product Designers
  • Medical Device Product Testers
  • Medical Device Software Product Developers
  • Medical Device Quality Managers
  • Medical Device Quality Engineers
  • Medical Device Regulatory Personnel

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Bev Willett, Course Administrator, NSF Heath Sciences

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