Extensive modules and features are available for the implementation of the Medical Device Regulation (MDR) at level 3:
modules
User and rights management
Audit Trail (in all modules)
Customer / target market management
item management
Work order management/ process order management
Serial number management (optional)
line management
interface management
label layout management
features
Create / edit / import work orders / process orders
Reporting to n markets/customers/databases
Parameterization and communication of connected line managers (level 2)
Overview of assigned work orders / process orders of a line
Communication to Level 4 and Level 5 systems