Veeva Summit Europe: AI and Automation in Drug Development

Veeva Summit Europe: AI and Automation in Drug Development

Elena Rodriguez
2 min read

Veeva R&D Summit Europe Showcases AI and Automation Advancements in Drug Development

The recent 10th Veeva R&D Summit Europe held in Madrid brought attention to the pivotal roles played by AI, automation, and collaborative efforts in accelerating the process of drug development. Esteemed industry professionals, comprising sponsors, CROs, and patient advocates, deliberated on the imperative utilization of AI and automation without augmenting the existing workload. Notably, Veeva Systems is actively working on developing an application programming interface (API) to seamlessly integrate with prevalent AI technologies, with the aim of optimizing data management and regulatory interactions. Additionally, Novo Nordisk shared their ambitious vision of reducing the timeframe for trial setup to merely a day by the year 2026, leveraging AI and fostering robust partnerships with CROs. Furthermore, the summit underscored the significance of AI in exploring supplementary indications for drug candidates while ensuring adherence to regulatory standards.

Key Takeaways

  • Discussion of AI and automation at Veeva R&D Summit Europe focusing on expediting drug development.
  • Veeva's endeavor to integrate AI with customers' existing technologies via API for streamlined data management.
  • Novo Nordisk's targeted reduction of trial setup time to one day using AI by 2026.
  • AI's potential in identifying regulatory queries in trial submissions, thereby amplifying collaboration.
  • Ongoing deliberation on AI's involvement in the transfer of data from Electronic Health Records (EHRs) to Electronic Data Capture (EDC) systems due to potential site burden.


The thematic emphasis on AI and automation within the Veeva R&D Summit Europe underscores a shift towards efficiency and collaboration within the domain of drug development. Veeva's API integration strategy poses as a potential game-changer in enhancing data management for pharmaceutical companies and regulatory entities, subsequently fortifying compliance measures and alleviating workloads. Novo Nordisk's ambitious mission to significantly truncate trial setup duration has the potential to catalyze industry-wide transformation by setting new benchmarks for speed and efficiency. However, the industry's reliance on AI for data transfer from Electronic Health Records (EHRs) to Electronic Data Capture (EDC) systems raises concerns regarding potential burdens on clinical sites. While these technological advancements may expedite drug approvals, a meticulous approach is vital to prevent overwhelming healthcare providers.

Did You Know?

  • Veeva R&D Summit Europe: An annual gathering centered on research and development within the pharmaceutical and life sciences sectors, featuring discussions on technological advancements and industry trends.
  • CROs (Contract Research Organizations): Entities offering support to pharmaceutical, biotechnology, and medical device industries through outsourced research services, including the management of clinical trials and regulatory processes.
  • EHRs (Electronic Health Records) and EDC (Electronic Data Capture): EHRs serve as digital repositories of patients' medical histories, encompassing sensitive health information, while EDC systems are designed for electronic collection of clinical data primarily in human clinical trials. The ongoing debate on AI's role in data transfer from EHRs to EDC centers around the balance between efficiency and potential burden on clinical sites.

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