News & Insights

Insights from Europe's leading regulatory conference. Our key takeaways on data governance, EMA PMS' progress, and our joint talk with Boehringer Ingelheim.

Empowering pharmaceutical companies with trusted, standardized product data

How a Top 10 Pharma Company Built an IDMP-Aligned Knowledge Graph in Under 100 Days with ACCURIDS

Facing a 2026 EMA deadline, one global pharma leader achieved a 200% ROI and reduced manual work by 75% in under 12 months.

Why the management of reference data management cannot be centralized, and how easy-to-use global lookup services effectively increase findability, reuse, and interoperability.

Insights from the DIA 2024 workshop on tackling "standards fatigue" with a domain-focused IDMP strategy that delivers measurable value and reduces industry burnout.

Discussions at the summit confirmed the industry's digital transformation, with Regulatory Affairs evolving into a strategic partner driven by structured data, AI, and global standards.

At the Madrid Connectathon, we collaborated with UMC and NOMA to integrate PhPIDs and GSIDs into FHIR, demonstrating improved global medicine traceability via a Knowledge Graph.

The message from LIMICS Day was clear: facing challenges like supply shortages, the time to act is now to accelerate medicine digitalization with ISO IDMP.

Highlights from the ISO TC 215 / WG6 meeting, where discussions reinforced that industry-regulator collaboration is critical to streamlining global processes and improving data interoperability.

A recap of our intensive three-day workshop at the Uppsala Monitoring Centre, focused on advancing the WHODrug Knowledge Graph through collaborative, hands-on efforts.

The conference reinforced a shared vision: Semantic standards and governance are key to unlocking automation, interoperability, and building more efficient global healthcare systems.

Highlights from the DIA RSIDM conference, where industry leaders agreed that deep collaboration and strong data governance are essential for unlocking the value of global standards.

Following the Global Pharmaceutical Regulatory Affairs Summit, here are the key takeaways on advancing IDMP with semantic standards, collaborative PoCs, and industry benchmarks.

Avoid costly implementation delays and failures. These 6 steps create a sustainable, data-centric foundation that turns regulatory pressure into a strategic advantage for your enterprise.