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Partners with serialization solutions provider to comply with EU FMD serialization regs
November 1, 2017
By: Tim Wright
Editor-in-Chief, Contract Pharma
Spanish-based pharmaceutical manufacturer, Normon Laboratories, has selected Tracelink for its serialization solutions to comply with the EU Falsified Medicines Directive (FMD) requirements. The first generics pharmaceutical manufacturer in Spain, Normon Laboratories has grown to be a global player, supplying products to multiple markets. With high volumes of pharmaceuticals shipped throughout Spain and exported across the rest of the world, and offering additional contract manufacturing capabilities for customers, the company needed a serialization solution that could accommodate its various roles in the pharmaceutical supply chain and ensure compliance for its customers, as well as its own product lines. Normon selected TraceLink for its ability to scale at the enterprise level and its seamless integration with multiple contract manufacturing organizations, in order to enable compliance with the EU FMD serialization regulations. “At Normon, we uphold our commitment to developing the safest and highest quality medicines at affordable prices for everyone. Our dedication to ensuring patient safety was a key factor in selecting a partner with a proven solution to comply with the EU FMD,” said Gonzalo Fernández Govantes, chief operating officer, Normon Laboratories. “We selected TraceLink for its demonstrated EU and country compliance capabilities and enterprise scalability. As Normon continues to expand its business through ongoing innovation, we are confident that TraceLink can provide the breadth of support needed in order for Normon to successfully comply with EU and global regulations.” Shabbir Dahod, president and chief executive officer, TraceLink, said, “We are pleased to be working with Normon Laboratories, a pioneer in the development of generic medications, and one of the leading pharmaceutical companies in Spain. At TraceLink, we understand and value the need to implement an EU FMD compliance strategy that can scale quickly to accommodate for rapid growth and impending deadlines for serialization and individual country compliance. Drug traceability and serialization is a global initiative and we look forward to working closely with Normon Laboratories to meet the approaching EU FMD deadline for serialization and ultimately, help secure the integrity of its products for patients across Europe.”
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