Publications

Securing High-Value Pharmaceutical Shipments in Parcel and Courier Networks

October 13, 2026

Protect Patients Beyond the Manufacturing Floor As specialty medicines, biologics, cell and gene therapies, and other high-value products increasingly move through parcel and courier networks, pharmaceutical supply chains face new security, quality, and logistics challenges. […]

Publications

Data Integrity Guide: Spreadsheet Validation

September 28, 2026

Strengthen Spreadsheet Controls. Reduce Compliance Risk. Spreadsheets remain one of the most widely used tools across pharmaceutical operations, supporting everything from laboratory calculations and stability programs to equipment maintenance, quality systems, and product release decisions. […]

Patient Safety Blog

The Next Episode | What 13 Years of DSCSA Teach Us About NDC-12 and Pharmaceutical Interoperability

September 14, 2026

The Transactions Haven’t Changed. The Network Has. Flying home from the HDA Traceability Seminar last week, I saw some news from Philadelphia that put much of what we had spent the previous few days discussing […]

Publications

When Distribution Models ​Change Faster Than Controls:​ GLP-1, DTC, and the New Pharmaceutical Risk Landscape​

July 2, 2026

Within this slide deck, you can explore how GLP-1 demand, telehealth, digital pharmacies, and direct-to-consumer distribution are reshaping the pharmaceutical supply chain and creating new patient safety and security challenges. Rx-360’s Ryan Kelly, Interim CEO […]

Publications

Supplier Assessment Questionnaire (SAQ) Guide

May 20, 2026

TURN INSIGHT INTO ACTION WITH THE RX‑360 SAQ GUIDE The Rx‑360 Supplier Assessment Questionnaire (SAQ) Guide provides a practical walkthrough of how to effectively use the SAQ within your supplier qualification program. Designed as a […]

Patient Safety Blog

What the 2026 EU GMP Annex 1 Update Means for Veterinary Product Supplier Qualification

February 10, 2026

he 2026 EU GMP Annex 1 Update Means for Veterinary Product Supplier Qualification The 2026 EU GMP Annex 1 changes mark a major regulatory shift, introducing a full separation between human and veterinary manufacturing requirements. […]

Interactive Resources

Supplier Corrective Action Report Web Form

January 12, 2026

Optimize Supplier Corrective Actions with Rx‑360’s SCAR Template The Supplier Quality Working Group at Rx‑360 has developed a standardized Supplier Corrective Action Report (SCAR) template designed to strengthen pharmaceutical supply chain integrity and improve quality […]

Publications

Rx-360 Reaffirms Compliance with NMPA Requirements | Download the Position Letter

December 30, 2025

Rx-360 is committed to supporting the global pharmaceutical industry in meeting regulatory standards worldwide. In response to the National Medical Products Administration (NMPA) release of Appendices One and Two of Article 310 of the Good […]

Patient Safety Blog

The BIOSECURE Act and the Quiet Work Ahead for Pharmaceutical Supply Chains

December 22, 2025

The BIOSECURE Act did not arrive with ceremony. It arrived embedded in the National Defense Authorization Act, debated largely in abstractions, and passed with little public attention. But for pharmaceutical and biotechnology companies operating global […]