RESOURCE LIBRARY

Battling Counterfeit Medicine Through Packaging Serialization >> Download Here

By Mario Scigliano, Global Serialization Manager, CordenPharma Latina & Christian Ahlmark, Associate Director, Sales & Key Account Management, CordenPharma International

Get informed about packaging serialization regulatory requirements & deadlines for global markets in this CordenPharma white paper discussing keys to combating the worldwide drug counterfeiting problem. Topics include serialization techniques in the supply chain such as Microscopic RFID Tags, Security Labels, Invisible Inks, and Track-and-Trace Technologies. Learn the importance and benefits of choosing the right CDMO to ensure the utmost level of support in keeping patients safe.

Minimizing Risk In API & Drug Product Development & Manufacturing: A Fully Integrated Supply Chain >> Download Here

C&EN White Paper brought to you by CordenPharma

The pharmaceutical and biopharma industry continues to experience solid growth in an expanding global market. This market growth has been accompanied by an ever-changing industry landscape, with consolidation among long-time “big pharma” leaders, ongoing mergers and acquisitions, and the emergence of start-ups and technology-based offshoots from academic laboratories. As the industry continuously adapts to evolving market pressures, the trend toward outsourcing of APIs & Drug Products to CDMOs with specialized capabilities, expertise and infrastructure remains a strong one.