Compliance & Quality

COMPLIANCE ISN'T
A FEATURE.
IT'S THE FOUNDATION.

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.

Certifications

OUR QUALITY CREDENTIALS.

FDA-Registered Importer

Core Distro is an agent of the registered FDA Importer of Record, ensuring all imported pharmaceutical products meet U.S. regulatory requirements.

USP-Grade Components

All packaging components meet United States Pharmacopeia standards for identity, strength, quality, and purity.

GMP Compliance

Our manufacturing partners operate under current Good Manufacturing Practice regulations for pharmaceutical products.

ISO 13485

Quality management systems for medical devices and pharmaceutical packaging components aligned with ISO 13485 standards.

Documentation

EVERY BATCH.
FULL DOCUMENTATION.

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.

Certificate of Analysis (COA)
Batch-specific analytical results confirming product meets all specifications
Included
Material Safety Data Sheet (MSDS)
Complete safety information for handling, storage, and emergency procedures
Included
TSE/BSE Statement
Transmissible Spongiform Encephalopathy / Bovine Spongiform Encephalopathy risk assessment
Included
Sterility Certificate
Confirmation of sterility testing results for RTU/RTS packaging components
Included
Import Documentation
Complete customs and FDA import records for all imported products
Included
Vendor Qualification Records
On-site GMP audit reports and supplier qualification documentation
Included
Quality compliance documentation
Regulatory Standards

THE STANDARDS WE UPHOLD.

21 CFR Part 211

Current GMP for Finished Pharmaceuticals

All packaging and equipment suppliers comply with FDA's current Good Manufacturing Practice regulations.

USP <797>

Pharmaceutical Compounding — Sterile Preparations

Our packaging components meet USP <797> requirements for sterile compounding environments.

USP <800>

Hazardous Drugs — Handling in Healthcare Settings

Compliance support for pharmacies handling hazardous drug compounds.

ISO 8362-1

Injection Containers for Injectables

All glass vials meet ISO 8362-1 standards for injectable pharmaceutical containers.

Supply Chain

SUPPLY CHAIN INTEGRITY.

Vendor Qualification

All suppliers undergo rigorous on-site GMP audits before any product enters our supply chain. We verify manufacturing practices, quality systems, and regulatory compliance.

Cold-Chain Logistics

Pharmaceutical-specialized temperature-controlled logistics for all temperature-sensitive products. Every shipment is monitored end-to-end with full chain of custody documentation.

Batch Traceability

Complete lot traceability from manufacturer to your pharmacy. Every product can be traced back to its origin, manufacturing date, and quality release records.

QUESTIONS ABOUT OUR
COMPLIANCE PROGRAM?

Our compliance team is ready to answer any questions about our quality systems, documentation, or regulatory requirements.