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BREAM/SIGNALS

INSIGHT BANK · 28 LIVING CARDS

Follow a question. See what changes.

Evidence, technologies, people and the next test—connected, but not confused.

Linked entity: ARPA-H · Clear

R&D Allocationv1 · 09.23

Who Will Build the Systems to Oversee Clinical AI? ↗

Who checks clinical AI decisions, and how is that supervision itself evaluated?

ARPA-H announced ADVOCATE development plans covering patient-facing AI, supervision, implementation and independent evaluation.

  1. Program and awardsRecorded
  2. DevelopmentUnverified
  3. Clinical evaluationUnverified
  4. AuthorizationUnverified
New question opened

Published the analysis and recorded the next checks.

NEXT CHECK

Missed errors, false alarms, appropriate clinical handoffs and evaluation in routine care.

R&D Allocationv1 · 09.29

Transporting Cell Therapies Without Refrigeration ↗

Can cells retain their function through room-temperature storage and transport?

BoSS announced three development teams and independent testing by ATCC, with up to $87 million planned over four years.

  1. Reports and agreements reviewedRecorded
  2. Further validationUnverified
  3. Adoption and benefitUnverified
New question opened

Recorded a new question and follow-up checks from the approved manuscript.

NEXT CHECK

Storage duration by cell type, recovered function and independent ATCC testing.

R&D Allocationv1 · 10.09

What does an AI business sell when it helps run a clinical trial? ↗

Who pays for the work of making AI-enabled trials viable, and what do they buy?

SURPASS calls for validation in real trials, with initial public support and a route to continuing operations. Participation does not establish an automatic allocation of drug development or commercial rights.

  1. Reports and agreements reviewedRecorded
  2. Further validationUnverified
  3. Adoption and benefitUnverified
New question opened

Examine continuing operations and payment for AI-enabled trials through the SURPASS solicitation.

NEXT CHECK

Selected teams, trial execution, payment by later sponsors and terms for model and patient-data use.

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