Raycaster/ Eval

APEX-Agents · Law

World 420_LB_02

Best published3/3Pass

APEX-Agents task World 420_LB_02 in AI Agents for FDA and Pharma Promotional Compliance. Compare dual-harness agent runs across models, scores, and public traces.

AI Agents for FDA and Pharma Promotional ComplianceLaw World 420Dual harnessGrader: rubric
task_1918e229773b46699fe5576f1b11d7a2
Law World 420
message_in_console
7 models · dual config

Task prompt

What the agent was asked to do

Identify for each item below whether it could be used by the U.S. Food and Drug Administration (FDA) as evidence that Bencontra is intended by Livyra for use in pediatric patients: 1. bencontra_provider_contact List.xlsx 2. Livyra sales representatives disseminating to doctors unaltered reprints from peer-reviewed medical journals that discuss use of Bencontra in pediatric patients 3. BENCONTRA - dosage - children.pdf, if disseminated to doctors alongside a source publication supporting the dosage recommendations For each item, be sure to specify clearly whether it “could” or “could not” be used by the FDA as evidence that Bencontra is intended by Livyra for use in pediatric patients. Alternatively, if the answer cannot be determined without more information, please say that and explain what additional information is needed. Otherwise, no explanation is needed. Provide your response in a message to the console. Please consider the following additional sources when responding: 1. 21 CFR 201.128.pdf 2. Guidance from FDA on Unapproved Uses.pdf

Published trajectories

Agent runs on this task

Curated dual-harness runs (parsed + original sandbox). Best scored run per model.

ModelHarnessScoreResultLinks
Gemini 3 Flashdual3/3Pass
GPT-5.4 minidual3/3Pass
Gemini 3.1 Produal2/3Fail
GPT-5.4dual2/3Fail
GPT-5.4 nanodual2/3Fail
GPT-5.5dual2/3Fail
fireworks models Kimi K2dual1/3Fail

Grading rubric

Rubric criteria

Runs are graded against these criteria. Open a run for model-specific verdicts.

  1. States that the U.S. Food and Drug Administration could use Livyra’s provider contact list as evidence that Bencontra is intended for use in pediatric patients

  2. States that the U.S. Food and Drug Administration could use the dissemination by Livyra sales representatives of unaltered reprints from peer-reviewed medical journals that discuss the use of Bencontra in pediatric patients as evidence that Bencontra is intended for use in pediatric patients

  3. States that the U.S. Food and Drug Administration could use the dissemination by Livyra sales representatives of the pediatric dosage sheet alongside a source publication as evidence that Bencontra is intended for use in pediatric patients