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.
Do you have any questions about our Manufacturing Execution Solution top MES or would you like to talk to us without obligation?
Then please contact us. We look forward to your inquiry!
top flow GmbH
