Scenario-based text systems
Clinical assistants, RAG workflows, documentation models, and coding/CDI models can be assessed when responses can be imported from approved files or collected through an approved OpenAI-compatible chat endpoint.
Synset combines versioned model access, controlled synthetic clinical scenarios, artifact checks, a scoped intervention, and held-out evaluation. Support depends on the model, access path, task, and available evidence.
A model can sometimes be assessed through its outputs even when Synset cannot change it. A hardening pilot requires a reproducible training or adaptation path, a defined output contract, and held-out real evaluation data.
Clinical assistants, RAG workflows, documentation models, and coding/CDI models can be assessed when responses can be imported from approved files or collected through an approved OpenAI-compatible chat endpoint.
Risk models are scoped case by case and require reproducible inference, a defined target, and suitable evaluation data. Longitudinal or survival models require separate review of target, horizon, censoring, and validation design.
A system may be assessed when responses can be captured through an approved path. Hardening is not available without a reproducible customer-approved training or adaptation route.
Imaging, waveform, voice, and other unsupported modalities are not current general-support claims. They require a separate partner scope and evidence plan.
Record the model task, declared use, model-facing inputs, expected output, model and data versions, and the evaluation boundary.
Create controlled synthetic records, timelines, notes, dialogue, or task-specific prompts around a measured weakness. Not every engagement uses every artifact type.
Apply configured clinical, temporal, support, metadata, and text-grounding checks. Reject failed candidates and version the retained cohort, prompt export, and manifest.
The customer may train or adapt the model. Synset may support a scoped workflow where agreed. Calibration, thresholding, abstention, workflow change, or no intervention may be the correct result.
Compare frozen original and candidate versions on customer-controlled held-out real data, then preserve observed failures as fixed regression cases.
The current controlled probe pilot uses deterministic scenario families when a compatible world-conditioned targeting path is unavailable. Universal autonomous retraining is not a current capability.
Held-out real data is a customer-controlled evaluation set not used to choose, tune, or select the intervention. Original and candidate model versions are frozen before final evaluation against prespecified success and no-regression criteria.
Subgroup and calibration checks are included where the task and data support them. A non-improving result can lead to more real evidence, a different model, a narrower intended use, or a stop decision.
Closed-loop customer-model hardening has not yet been published as a held-out public proof. Current hardening work is a selected design-partner pilot, not a universal product claim.
Institution-local evaluation is an enterprise design-partner path, not a generally available deployment. Synset does not determine clinical deployment or regulatory authorization.
Do not send PHI, patient files, model credentials, private checkpoints, or held-out evaluation rows through public email.
Start with readiness