Plantvision, together with Swedish MedTech, invites you to the second webinar of three focusing on medical software!
The medical device industry is innovative and fast-moving. This is especially true when we look at medical device software. Development moves at a rapid pace, which gives rise to demands for new regulations and guidelines from authorities. This in turn requires manufacturers and developers to take a new approach to the so-called state of the art.
From the contents:
- What is the current regulatory landscape for medical device software development?
- Which points are fixed and which are moving?
- How do the different regulations, guidelines and guidance documents relate to each other?
- What is the common thread?
Other
There will be time for questions. The link will open at about 08:20 and then we will check that the technology works for everyone.
Location : Via zoom to which you will receive a link well in advance of the event.
A warm welcome!
Gustav Hoppe, Senior Expert consultant Medical Device and IVD, Plantvision.
With over 20 years in the medtech industry and experience from both test houses, manufacturing companies and the consulting industry, Gustav has a solid base with expertise in topics such as Regulatory affairs, testing, AI, software, electrical device, cyber security etc.
