Company Capabilities Quality Verify a Batch
FDA-registered  ·  503B Outsourcing Facility

Precision compounding for the next standard of patient care.

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.

99.9%
Potency accuracy
14k+
Batches traced
<48h
Release testing
21
CFR Part 11 compliant
USP <797> Sterile Compounding USP <800> Hazardous Drugs cGMP 21 CFR 210/211 ISO 14644 Cleanroom Class 7 DSCSA Track & Trace USP <71> Sterility Testing USP <797> Sterile Compounding USP <800> Hazardous Drugs cGMP 21 CFR 210/211 ISO 14644 Cleanroom Class 7 DSCSA Track & Trace USP <71> Sterility Testing
Who we are

A laboratory built around the integrity of a single batch.

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.

Compounding

Patient-specific and office-use formulations across sterile injectables, ophthalmics, hormone therapy and specialty dosage forms — prepared in classified cleanrooms.

Analytical Testing

In-house HPLC, endotoxin and sterility assays validate identity, potency and purity before release. No batch leaves without documented results.

Traceability

A serialized, tamper-evident record follows each lot. Anyone holding our product can confirm its authenticity in seconds — no account required.

Matrix Lab inc.
Capabilities

What sets the bench apart.

Pharmaceutical compounding is only as trustworthy as the data behind it. We engineer that trust into the workflow.

  • 01Closed-system formulationHazardous and sterile preparations handled in ISO Class 7 isolators with continuous environmental monitoring.
  • 02Release-by-dataQuantitative HPLC potency and USP <71> sterility results are attached to every lot record before dispatch.
  • 03Cold-chain assuranceValidated, monitored logistics from our suite to point-of-care with full temperature audit trails.
  • 04Public batch verificationIndependent authenticity lookup available to clinicians and patients — built into this site.
Quality & Compliance

Four checkpoints between formula and patient.

Our quality system mirrors cGMP expectations for outsourcing facilities. Nothing advances to the next stage until the prior one is documented and signed.

STAGE 01

Sourcing

APIs sourced from FDA-registered suppliers with certificates of analysis verified on intake.

STAGE 02

Compounding

Prepared under classified air with master formulation records and dual-operator checks.

STAGE 03

Release Testing

Potency, sterility and endotoxin assays performed in under 48 hours of compounding.

STAGE 04

Serialization

Each unit receives a unique, verifiable lot identity before cold-chain dispatch.

Authenticity

Verify a batch.

Enter the lot number printed on your Matrix Lab inc. label to confirm it was manufactured, tested and released by our facility.

Batch Authentication

Real-time lookup against our release register.

Try a sample lot: MX0312RB MX0927KD XX0000XX

Bring the standard to your patients.

Matrix Lab inc. is expanding access for clinics, prescribers and distribution partners. Request facility credentials and a capability dossier.

Request Access