01 // the challenge

Clinical AI claims face adversarial review. From regulators.

FDA expects clinical validation

SaMD submissions require evidence that goes beyond accuracy metrics. Clinical utility claims need verified support.

Benchmark gaming is everywhere

Models that perform well on standard datasets may fail in deployment. Adversarial review catches overfitting before reviewers do.

Bias claims require proof

Fairness assertions need cross-validated evidence. 'We tested on diverse populations' isn't enough for regulatory scrutiny.

02 // the axion approach

Adversarial review before regulatory submission.

656 papers indexed

656-paper clinical AI corpus

Diagnostic AI, clinical decision support, SaMD validation studies. Indexed by modality and regulatory pathway.

57% rejection rate

57% rejection rate

Claims that survive multi-model adversarial attack are stronger submissions. Claims that don't survive save you a rejection cycle.

53% fabrications caught

Citation verification

Every DOI checked against live databases. 53% of AI-generated citations contain errors.

03 // results

What the pipeline produces.

656 papers analyzed
57% hypothesis rejection
53% citation errors caught
24-48h review turnaround
the value

Pre-submission adversarial review: FDA reviewers apply adversarial pressure to your clinical validation claims. The question is whether you see the weaknesses first. Claims that survive multi-model attack are stronger submissions.

04 // start

Research audit for clinical AI work.

Send one validation claim, clinical utility assertion, or bias analysis. We run it through cross-architecture adversarial review.

One claim or validation question. We confirm review scope before work starts.

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