07/10/2026 | Press release | Archived content
Today we're announcing TriClick 3.0. Highlights across generation quality, submission documentation, reviewer transparency, and a new protocol-to-CRF capability.
Each of the three clinical generation agents was benchmarked against internal accuracy suites.
TriClick 3.0 adds support for the Analysis Data Reviewer's Guide (ADRG), Study Data Reviewer's Guide (SDRG), and Define.xml - the reviewer-facing submission artifacts that accompany datasets in an FDA filing.
Alongside the datasets and TLFs, TriClick 3.0 delivers a customer-facing Audit Package with:
Clinical teams see what was generated, what was checked, and what still needs review.
A new Lineage Graph traces how the AI moved from study inputs to final deliverables, capturing source data, specifications, CRFs, shells, intermediate decisions, generated code, checks, and final outputs.
For every supported output, TriClick 3.0 exposes the source evidence used, intermediate artifacts, assumptions, checks performed, and review status. No black-box answers.
TriClick 3.0 adds the Data Management Agent, which turns a study protocol PDF into a structured first-draft CRF. It extracts visits, assessments, SOA, eligibility, safety, dosing, and follow-up requirements.
TriClick 3.0 does not claim every generated result is 100% correct. It generates high-quality outputs while making uncertainty, evidence gaps, and review needs visible. For pharma and CRO teams: faster generation with a stronger foundation for QC, handoff, and audit prep.
Congratulations to our engineering, biostatistics, and regulatory teams who shipped this release.