For pharmaceutical and biotech companies
One specification, many facilities, evidence that survives audit.
You need assays run to a specification, on a schedule, across more than one site, with a record that stands up when someone asks how the result was produced.
What you get
The programme is written once, in capabilities
Work is expressed as what has to be done, not as a product from one supplier. Any qualified facility can be routed the work and quote for it, and the platform does not depend on a single vendor.
Comparisons that are not vendor theatre
Every provider record carries its equipment and the rate it publishes. Where no rate is published, the platform writes "needs a quote" and stops. No figure is estimated and presented as a price.
An audit trail per run, not per programme
Material identity, plate maps, instrument run records, QC decisions, deviations and the result hash are captured as the run happens.
What is true today
- No facility has been contacted and none has been verified. The provider registry holds named facilities, their capabilities and their published rates, and every entry stays "named, not verified" until someone calls them.
- No physical run has been performed. The execution path is built and proved with synthetic data.