Every product Core Distro distributes meets the highest regulatory standards. We maintain rigorous oversight of our entire supply chain so your pharmacy can focus on patient care.
Core Distro is an agent of the registered FDA Importer of Record, ensuring all imported pharmaceutical products meet U.S. regulatory requirements.
All packaging components meet United States Pharmacopeia standards for identity, strength, quality, and purity.
Our manufacturing partners operate under current Good Manufacturing Practice regulations for pharmaceutical products.
Quality management systems for medical devices and pharmaceutical packaging components aligned with ISO 13485 standards.
Core Distro provides a complete documentation package with every order. No chasing down paperwork — everything you need for your quality management system is included automatically.

All packaging and equipment suppliers comply with FDA's current Good Manufacturing Practice regulations.
Our packaging components meet USP <797> requirements for sterile compounding environments.
Compliance support for pharmacies handling hazardous drug compounds.
All glass vials meet ISO 8362-1 standards for injectable pharmaceutical containers.
All suppliers undergo rigorous on-site GMP audits before any product enters our supply chain. We verify manufacturing practices, quality systems, and regulatory compliance.
Pharmaceutical-specialized temperature-controlled logistics for all temperature-sensitive products. Every shipment is monitored end-to-end with full chain of custody documentation.
Complete lot traceability from manufacturer to your pharmacy. Every product can be traced back to its origin, manufacturing date, and quality release records.