Manish Garg is a Global Serialization Regulatory Compliance and Track & Trace expert and he has expertise in the enterprise architecture connecting clinical and commercial supply chain systems with large and complex global manufacturing and supply chain environment. With over 20 years of experience spanning enterprise technology and life sciences operations, Manish specializes in product identity architecture, regulatory traceability, and the systems implications of large-scale identifier transitions. He actively leads the national NDC-12 Cross-Industry Pilot Program discussions and contributes to the cross-industry and integrations working groups involving FDA, GS1, and GS1, shaping the industry’s strategy, planning, and technical response to the 6-4-2 transition. Manish serves on the Editorial Advisory Boards of Pharmaceutical Technology and Pharma Focus America and is a Senior Member of IEEE.
