Not a sales rep. Every demo and pilot discussion is led by someone who understands PK modeling and oncology trial workflows.
Yes. Enterprise customers can import NONMEM .lst output or Phoenix WinNonlin project files. The importer reads the THETA, OMEGA, and SIGMA estimates and populates the DoseMind model parameter configuration automatically. A clinical pharmacologist reviews the import before it is activated for patient use.
The current platform requires internet connectivity for the Bayesian calculation and audit trail functions. We are developing an offline-capable mode for sites with restricted connectivity, expected in Q3 2025. Contact us to discuss your specific requirements.
A 30-day pilot includes protocol configuration, a retrospective simulation on your historical patient data (minimum 5 patients required), IQ/OQ documentation, two training sessions for CRC staff, and a readout meeting with your clinical pharmacologist and ours. The pilot is provided at no charge.
Most sites are processing real patient data within two weeks of contract execution. Start with the validation pilot.
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