Literature monitoring across 40,000 publications a month
Automated screening of scientific literature surfaced relevant safety and competitive signals without a larger team.
Category: Pharmaceuticals & Biotech
Agents for regulatory documentation, pharmacovigilance and trial operations.
Batch documentation and deviation reporting automated
Manufacturing batch records and deviation reports were generated from production data, shortening release timelines.
Accelerating clinical trial site communications
Site queries and protocol questions were answered instantly, reducing study coordinator burden across 40 sites.
Pharmacovigilance case processing at 3x throughput
Adverse event intake and coding were automated, letting safety teams handle rising case volumes within regulatory timelines.
Compiling regulatory submission documents in days, not months
Document assembly and consistency checking across study data accelerated regulatory filings for a biotech firm.