DSCSA serialization regulations in the U.S. and EUFMD directives in Europe are now being enforced for manufacturers. Other standards around the globe are also advancing. The focus of Life Sciences manufacturers is shifting from serialization planning and preparation to execution, management, and business value.
With manufacturer requirements in place, serialization is now a standard part of designing, building, and managing a pharmaceutical supply chain.
Converge Consulting helps clients design and set up serialization capabilities in conjunction with new product launch, as well as active program optimization to maintain compliance.