The medical technology industry faces massive challenges in 2026:
High regulatory requirements (FDA, MDR, ISO 13485), bureaucracy, pressure to innovate and rising production costs.
ADMEDES has decided to secure these requirements directly in the production system – with the Manufacturing Execution Solution top MES.
top MES supports medical technology companies in implementing strict regulatory requirements:
Electronic, FDA-compliant documentation
✔ Support for electronic records and electronic signatures
✔ Compliance with the requirements of the US health authorities in accordance with FDA 21 CFR Part 11
Standard-compliant labeling & traceability
✔ Labeling according to ISO 13485 and EU Medical Device Regulation (MDR)
✔ Specially developed labeling app with mandatory fields for complete and correct labeling
Quality assurance directly at the workplace
✔ Start of production only after completion of all mandatory preparations
✔ Automatic checking of employee qualifications by the machine
✔ Use only approved materials in accordance with the parts list (barcode scan)
You would like to know if top MES is also suitable for your production?
We offer you a proof of concept as part of a test installation:
✔ Non-binding & with little effort
✔ Test installation in your own SAP test system
✔ Test with own data and processes
✔Founded basis for decision-making – without obligation
Or register for our non-binding webinar and learn all about the functions, benefits and optimization potential of top MES for your production.
top flow GmbH
