Serialization

White Paper: Guide to Pharmaceutical Serialization 2017

What You Need to Know When Partnering with Your CDMO

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As required by the Drug Quality and Security Act (DQSA) signed into law by President Obama on November 27, 2013, serialization for pharmaceutical manufacturers must be in place by November 27, 2018.

This guide is designed to serve as a reference for the core information, issues, and questions pharmaceutical companies must address as they work with their CDMO and other members of their supply chain.

The paper includes:

  • Serialization Basics
  • Beyond the Label
  • High Volume and Complex Data Exchange Calls for Standardization
  • Agility to Accommodate Regulatory Changes
  • Data Security
  • Serialization Collaboration with CDMO Partners
  • Network Consolidation Considerations
  • Leveraging CDMO Assistance and Expertise

Download Serialization White Paper