The Identification of Medicinal Products (IDMP) is a set of standards created by the International Organization for Standardization (ISO) that mandates a unified data structure and vocabulary for medicinal product data submissions. IDMP standards affect various pharmaceutical functions, including regulatory, clinical, manufacturing, and supply chain. This drives the need for robust enterprise product data management solutions to ensure compliance, efficiency, and patient safety.

Building a robust product data management capability via ZS IDMP-based assets can help overcome data challenges and process inefficiencies. ZS's assets are ready-to-use and easily configurable within the client’s data management ecosystem, effectively optimizing the enterprise MDM setup journey.

Join ZS’s Master Data Management Center of Excellence to discuss how product data management can ensure compliance, efficiency and patient safety in the life sciences industry, and learn about ZS's purpose built solutions to solve your product data challenges.