Organiser: Taipuva
Risk management in product development is complex, because risks are related to almost everything in the technical file. This “everything” should be on the move constantly, as the MDR says that risk management is a continous process over the product lifecycle.
Join the webinar on 23 November to hear:
- What do regulations require of (medical) product risk management
- What are the typical methods and tools – and associated problems
- How is it possible to solve these problems?
- Taipuva presents an example of a holistic digital solution
- How to obtain the advantages of this?
There is a Finnish language version of this webinar organised on 8 November – read more.