Who We Are

We are a GMP-aligned pharmaceutical quality control laboratory starting with small-molecule Chemistry and Microbiology testing, with an internal LIMS undergoing CSV. Future expansions will include biopharmaceutical quality control, small-molecule drug manufacturing, and biomanufacturing.

What We Aim to Do

Deliver audit-ready analytical data with speed, rigor, and transparency while building a scalable, compliant QC platform that bridges science and technology. We are building long-term trust and brand recognition.

Why Work with Us

We combine scientific rigor with lean execution, delivering reliable results that meet global compliance standards. Led by a multi-disciplinary founding team and chemical analysts with decades of combined experience, we are committed to operational excellence, transparency, and client success.

Operational Status

Pre-MVP. Building the LIMS MVP and CSV suite (VP, URS, FRS, SDS, IQ/OQ/PQ, RTM, etc.). We are not currently seeking investors and are not yet accepting client samples.

Future Roadmap

TruoX's long-term development is composed of multiple phases:

Phase MVP

LIMS MVP & CSV documentation

Phase I

GMP QC Laboratory

Phase II

SaaS Division: TruoX LIMS

Phase III

Small Molecule Contract Manufacturing

Phase IV

Small Molecule Generics Production

Phase V

Biomanufacturing and ML-Driven Optimizations

For a more detailed plan, please see our Future Roadmap.

Welcome to TruoX Laboratories