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Medical Device Industry
How devices reach and stay on the market: development, evidence, post-market surveillance, interoperability and the workforce behind it all.
From Prototype to Market
The work between a working model and a device that can be sold and supported responsibly.
Post-Market Surveillance Explained
How real-world use feeds back into design, labelling and safety communication.
Interoperability in Healthcare Technology
Why devices and systems must exchange information reliably, and what breaks when they cannot.
The Healthcare Technology Workforce
Why skilled device and sterile-processing staff are in short supply, and what makes people stay.
Right to Repair in Medical Device Service Contracts
Ownership often stops at the enclosure. Where service barriers sit, how manufacturers defend them, and which contract terms preserve access years later.
Single-Use Device Reprocessing: Rules, Risks and Reality
A single-use label is a validation boundary, not a cleaning verdict. How reprocessing is regulated, where risk concentrates, and what the economics leave out.