OverviewNew case study in DeviceMed: ADMEDES digitizes production with top MES
The newly published technical paper in DeviceMed shows how ADMEDES is successfully driving forward the digitalization of its production while also reliably meeting the high regulatory requirements of the medical technology industry.
As a leading contract manufacturer of high-precision Nitinol components, ADMEDES operates in an environment characterized by strict regulations, the highest quality standards and complete traceability. This is precisely where our Manufacturing Execution Solution top MES and creates the necessary transparency and process reliability.
Digitization under the highest demands
With top MES, production processes are digitally mapped end-to-end and fully documented. This not only enables efficient production control, but also supports compliance with regulatory requirements, from MDR-compliant traceability to FDA-compliant documentation – a decisive factor in medical technology.
Transparency and efficiency in interaction
The availability of real-time data ensures clear processes and well-founded decisions on the store floor. At the same time, manual effort is reduced and processes are sustainably optimized.
The result: efficient, future-proof production that meets the increasing demands of the industry.
Practical example with a signal effect
Following the successful introduction of top MES at the headquarters in Pforzheim and at the US site in California, the solution will soon also be implemented at the plant in Costa Rica. This is an impressive demonstration of how digitalization and regulation can be successfully combined – and how companies in the medical technology sector can further develop their production in a targeted manner.
Read the full case study in DeviceMed now and find out how you too can make the switch to efficient and digital production with SAP.
