Read the executive summary and first section of SCW’s NDC12 white paper on cross-functional planning, governance, data readiness, system remediation, partner coordination, and execution.
AI for Serialization and DSCSA Exception Handling | White Paper
Explore a controlled, human-in-the-loop operating model for AI-assisted DSCSA exception handling, EPCIS data quality, deterministic automation, and scalable pharma traceability operations.
White Paper: The Magic Combo: RPA and AI Agents in Pharma Supply Chains
Explore why pharma supply chains should build RPA foundations before scaling AI agents, with a practical maturity model for automation before autonomy.
Whitepaper: NDC12 – Revising the National Drug Code Format and Drug Label Barcode Requirements for the U.S. Market
This white paper blends the original high-level summary with a more detailed narrative, offering both clear structure and practical depth. It explains the new NDC format, explores stakeholder impacts, describes the implications for GTIN, and outlines concrete next steps and emerging solution options.
Whitepaper: A Comprehensive Guide to EU Medical Device Tracking Requirements
This whitepaper provides an in-depth look at the European Union Medical Device Regulation (EU MDR) and the European Database on Medical Devices (EUDAMED).
