In this seminar you will learn the relevant standards, laws, regulations, guidelines and methods, for example how to implement your agile software development compliant with regulatory requirements, you will learn how to integrate third party software („SOUP`s“) into your medical device compliant with standards and how to document it.
By means of practice-relevant exercises, the handling of the standard will be deepened and the implementation with regard to process design and documentation will be practiced. The aim of the seminar is to learn the requirements for the development and approval of medical software and to be able to implement them for your own application.
This basic course is also suitable for participants with no or little previous knowledge. For newcomer and start-ups, this course offers an optimal introduction to the implementation of IEC 62304 and IEC 82304-1.
This basic course is part of our online course: Medical Software Specialist!
Content:
- Definitions of terms
- Overview of relevant regulations and standards and connection with other essential standards for medical devices
- Requirements of the software standard IEC 62304 (Software for medical devices – Software life cycle processes)
- Software Safety Classification
- Software-Development Process
- Software Maintenance Process
- Software Risk Management Process
- Software Configuration Process
- Software Problem Solving Process
- Overview IEC 82304-1 (Health software — Part 1: General requirements for product safety)
- Validation of medical device software
- Implementation of the standard in existing medical software (Legacy Software)
- Group work & exercises