@@ -15,3 +15,10 @@ Physicians and scientists must disclose valid information about the processes, e
## EAM.4: The quality requirements are documented and prioritised.
The software as a whole is seen as a prototype and therefore not intended for productive usage. Nevertheless, it is intended to let people test the software as soon as an appropriate development stage is reached (e.g. the software runs stable and the results of the text analysis are mostly reliable).
## EAM.5: User groups and their tasks are documented in the respective usage context.
There are mainly two user groups:
- People that are supposed to read and understand an ICF and as result make a self-determined, informed consent or refusal (e.g. patients or participants).
- People that must disclose valid information about the processes, effects, and risks associated with a particular treatment (e.g. physicians and scientists).
