Zero-Defect Quality Assurance Architecture

Regulatory Compliance & GxP Integrity.

VeritasRx operates under an unyielding quality culture. Our standard operating procedures (SOPs) are engineered from day one to withstand rigorous third-party pharmaceutical sponsor and regulatory agency audits.

FDA 21 CFR

FDA Registered Finished Product 3PL

Rigorous Standard Operating Procedures (SOPs) governing sanitation, environmental controls, equipment calibration, personnel training, and batch quarantine controls for finished pharmaceuticals.

GxP / GDP

Good Distribution Practice (GDP)

End-to-end quality assurance ensuring product safety, temperature security, and packaging integrity throughout warehousing and flagship carrier transit.

DSCSA

Drug Supply Chain Security Act Ready

Full unit-level 2D barcode serialization scanning, transactional 3Ts data retention (TI, TH, TS), and instant quarantine protocols for suspect or illegitimate products.

DEA III-V

DEA Schedule III–V Secure Cage

Heavy-gauge locked physical wire-mesh cage with key-strike security, multi-tier access control, and 4K camera monitoring for Schedules III, IV, and V controlled pharmaceuticals.

FDA 21 CFR cGMP Compliance

100% Prepared for FDA Sponsor Audits

Current Good Manufacturing Practice in Manufacturing, Processing, Packing, or Holding of Drugs

Environmental Monitoring: continuous calibrated temperature and humidity sensor mapping across all pallet levels.
Lot Segregation & Quarantine: physical and electronic quarantine logic preventing unreleased lot allocation.
Sanitation & Pest Control: medical-grade sanitation cycles with non-toxic pest monitoring matrix.
Personnel Training: documented GxP training records on file for all warehouse technicians.
Audit Package Request

Qualified life sciences QA directors may request our complete Quality Manual, Master Facility Validation Plan, and Temperature Mapping Qualification Package.