A test plan that
survives contact with reality.
Standards mapping, timeline planning, sample preparation guidance, and cost estimation — so your testing programme runs to schedule and within budget.
We map your device's intended use, classification, and technical characteristics against all applicable standards — IEC 60601-1, EMC standards, particular standards, national annexes, and ancillary standards like ISO 10993 for biocompatibility — producing a definitive list of what must be tested.
A sequenced test programme that accounts for dependencies (EMC before safety, for example), sample availability, lab scheduling constraints, and the need for design iterations between testing phases. We build in buffer where history shows it's needed.
Realistic cost estimates for each test, lab fees, sample shipping, and re-testing contingency — based on current market rates and our direct experience placing test orders with labs.
We specify exactly what the lab needs — sample configuration, accessories, software version, labelling state, and any special preparation — so samples don't get rejected or retested for inadequate preparation.
Complete standards-mapped test programme with sequencing, owner, timeline, and cost for each test.
Itemised cost estimate with base case and contingency, suitable for project budget approval.
Precise sample requirements for each test, ready to share with the lab and your production team.
Ready to get started?
Tell us about your device and we'll map out the path to market.
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