"There are many regulatory compliance providers – so why Metecon?"
Simple: Because we don’t just know what needs to be done – we know how to do it. Together. Whether MDR, IVDR, EC-REP, software validation, or clinical evaluation – at Metecon, more than 60 experts from all regulatory disciplines work hand in hand: with expertise, heart, and conviction.
We don’t just advise – we act.
We don’t just support – we think ahead.
And we don’t speak in buzzwords – we speak at eye level.
What we offer:
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Regulatory Affairs – from classification to full RA strategy
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Clinical Affairs – clinical and performance evaluations that truly convince
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Quality Management – not just certified, but fully integrated
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Biological Safety – well-founded and clearly documented
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Verification & Validation – for software, processes, and even ideas
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Technical Documentation – audit-ready, traceable, and human-readable
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Digitalization & RIMS Consulting – because Excel isn't enough
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EC-REP, CH-REP & PRRC – for secure market access in the EU and Switzerland
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Post-Market Surveillance – so you know what’s really happening out there
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Academy – training that sticks and breaks down silos
Sounds like a lot? It is – but with us, it becomes manageable.
Meet us at the Swiss Medtech Expo in Lucerne – or reach out today:
👉 Book a meeting with Fabiola Hartung-Linz
💬 Send us a message
We look forward to real conversations, clear questions, and shared solutions – maybe with you?
