Software development is considerably more complex when the software is regulated as a medical device! Hear experts discuss the software development process; how to outsource software development; the use of tools and strategies to verify and validate.
Following MANY requests, we are now hosting this seminar about medical device software development. We will start the day discussing the content of the most commonly used standard for developing medical device software: IEC 62304.
This introduction will be followed by Medicom Innovation Partners and Medei who will share their thoughts and experience on:
- Tools to support the development process
- Risk management
- Verification and validation
- Outsourcing and third-party software components
Date: 21 November 2017
Time: 09:00 – 15:30
Venue: FORCE Technology, Venlighedsvej 4, 2970 Hørsholm
In the afternoon we will focus on outsourcing and third-party software components. We have invited experts from Oticon, Novo Nordisk and IBM to simplify this challenge and share their experience with software development outside the company – and what companies need to clarify with their subcontractors.
Target group
This seminar is targeted developers and project managers involved with medical device software. However, developers and project managers engaged with consumer products for the healthcare industry would most likely also benefit from this day’s topics and discussions.
* It is free to participate, but there will be a no-show fee of 500 kr. Maximum two participants per organization.