Data Management & Identification of Medicinal Products (IDMP) Services

Ensuring Adherence to New Standardized Data Formats

Identification of Medicinal Products (IDMP) is a series of worldwide standards requiring organizations to capture and manage significantly more regulatory data than ever before. While the result is overall improved patient safety, its implementation can be burdensome, requiring a clear strategy based on a cross-functional approach, which impacts multiple information management systems.

ProPharma Group’s global and local regulatory expertise in information technology, business, and regulatory affairs helps to ensure a painless transition to IDMP compliance.  Working closely with your quality management group, we start with a thorough analysis of the data context, subsequently advising on the best path forward, taking resources, technology, and regulatory requirements into account. Our unique and proven methodology, together with our knowledge and experience, ensure the proper acquisition, management, and transfer of data throughout the product lifecycle.  

In the EU, our IDMP services can support with the practical registration and data handling within SPOR, the structured, IDMP-compliant EU-register of product substance and company information.