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For Pharma R&D

Compress discovery-to-decision loops with private medical AI.

Surface signal from millions of pages of literature, internal SOPs, and trial data — without exposing molecules or pipelines to a third-party API.

−60%

literature triage time

faster protocol drafting

100%

of data stays in your VPC

Where it hurts

Bench-to-bedside, accelerated.

Below are the friction points we hear from teams in this function — and the agents that resolve them.

  • Literature volume outpaces what humans can read.
  • Protocols drafted from scratch each cycle.
  • Sensitive IP can't leave the company perimeter.

Target rationale assistant

Synthesizes mechanistic evidence across PubMed, internal decks, and patent corpora.

Protocol drafter

Generates trial protocol skeletons grounded in your therapeutic area precedents.

Competitive intelligence agent

Daily digests of pipeline moves, ClinicalTrials.gov updates, and regulatory filings.

Why teams choose Evarx for this

  • Custom SLM fine-tuned on your therapeutic area.
  • Air-gap deployment for early-discovery teams.
  • Audit trail for every retrieved citation.