Matrix Lab inc. formulates, tests and traces sterile and non-sterile preparations under pharmaceutical-grade controls — pairing analytical chemistry with end-to-end batch transparency.
Founded in Boston and operating from a purpose-built facility, Matrix Lab inc. serves prescribers, clinics and specialty pharmacies that cannot compromise on consistency. Every preparation we release carries a verifiable identity — from raw API to the vial in a clinician's hand.
Patient-specific and office-use formulations across sterile injectables, ophthalmics, hormone therapy and specialty dosage forms — prepared in classified cleanrooms.
In-house HPLC, endotoxin and sterility assays validate identity, potency and purity before release. No batch leaves without documented results.
A serialized, tamper-evident record follows each lot. Anyone holding our product can confirm its authenticity in seconds — no account required.
Pharmaceutical compounding is only as trustworthy as the data behind it. We engineer that trust into the workflow.
Our quality system mirrors cGMP expectations for outsourcing facilities. Nothing advances to the next stage until the prior one is documented and signed.
APIs sourced from FDA-registered suppliers with certificates of analysis verified on intake.
Prepared under classified air with master formulation records and dual-operator checks.
Potency, sterility and endotoxin assays performed in under 48 hours of compounding.
Each unit receives a unique, verifiable lot identity before cold-chain dispatch.
Enter the lot number printed on your Matrix Lab inc. label to confirm it was manufactured, tested and released by our facility.
Real-time lookup against our release register.
MX0312RB
MX0927KD
XX0000XX
Matrix Lab inc. is expanding access for clinics, prescribers and distribution partners. Request facility credentials and a capability dossier.
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