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After delays in the U.S., federal DSCSA serialization regulations are in effect for manufacturers. EUFMD directives in Europe and other standards around the globe are advancing. The focus of Life Sciences manufacturers is shifting from serialization planning and preparation to serialization execution and management.

Serialization is now a standard part of designing, building and managing a pharmaceutical supply chain. We help clients design and setup serialization capabilities in conjunction with new product launch, as well as optimize their active programs to maintain compliance.

This info sheet details Converge’s approach to developing and implementing serialization programs for our clients.

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