Medical device software - key insights to meet regulatory requirements
Podcast #29
Medical device software - key insights to meet regulatory requirements
In today's episode, we dive into the tangled jungle of regulatory requirements for medical device software. What do you need to consider when developing your product? What common mistakes should you avoid? And how can you ensure your software meets all requirements before it reaches the market? Listen in as one of our Consulting Managers Sara Kyrkander talks to colleague and subject matter expert Gustav Hoppe who has many years of experience working with medical device software. Gustav shares his insights on development methodology, software architecture and cybersecurity, as well as practical advice on how to navigate the key regulatory requirements.