UK-based Multinational Pharma Company

June 12th, 2024 WRITTEN BY Fresh Gravity Tags: ,

Fresh Gravity worked with a multinational pharmaceutical and biotechnology company to implement an R&D Product Master solution that adheres to IDMP compliance standards and establishes a foundation for data interoperability within the enterprise data ecosystem.

Problem

The client was looking to create a combination model comprising of multiple systems and business units (vaccine and pharma) to capture and manage Product Master data, provide a platform for implementing Data Governance processes, and create the foundation for a modern cloud-based technology platform following IDMP standards within the enterprise landscape.

Solution

Fresh Gravity implemented a Product Master solution that adheres to IDMP (Identification of Medicinal Products) compliance standards. The technology of choice was cloud-based Reltio MDM system. The implementation has helped the business in streamlining the process of managing product data across the R&D business, namely, Pharmaceutical Product, Medicinal Product, Manufactured Item, Formulation along with Substance and Product Family.

This solution ensured that high-quality data was created, updated, and maintained in the Reltio system. The workflows were implemented to manage complex business requirements that ensured review and approval of data through a series of predetermined steps. The entire implementation followed strict GxP processes and procedures.

Impact

As a result of this implementation, a solid foundation providing a 360-degree view of Product Master Data (from Substance to Manufactured Item) and robust data governance to maintain the integrity of data within client’s system was established. This foundation also allowed the business to create a long-term roadmap to incorporate more elements of the drug development value chain within the MDM system.

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