Technology Foundation for Product Development

³Ô¹Ï±¬ÁÏ Development Cloud is the technology foundation for product development that brings together applications for clinical, regulatory, and safety to help organizations drive end to-end business processes. Today, product development systems are not well integrated, which creates inefficiencies and slows down critical operations. ³Ô¹Ï±¬ÁÏ is the first and only company to offer unified suites of applications that are connected on a single cloud platform. This enables organizations to centralize content and data across global departments for greater efficiency and compliance.

³Ô¹Ï±¬ÁÏ Connections

³Ô¹Ï±¬ÁÏ Connections are ³Ô¹Ï±¬ÁÏ-delivered integrations that seamlessly transfer data and documents across clinical, regulatory, and safety Vaults. Designed to streamline cross-functional business processes, the Connections break down silos and provide greater visibility, and automate manual tasks. View the ³Ô¹Ï±¬ÁÏ Connections Resource Hub for a full list of available ³Ô¹Ï±¬ÁÏ Connections.

³Ô¹Ï±¬ÁÏ Clinical Operations

Simplify and standardize clinical trial execution.

³Ô¹Ï±¬ÁÏ Clinical Operations unifies clinical systems and processes on a single cloud platform to enable end-to-end trial management.

  • ³Ô¹Ï±¬ÁÏ eTMF ¨C Enable active eTMF for real-time inspection readiness.
  • ³Ô¹Ï±¬ÁÏ CTMS ¨C Enable proactive trial management.
  • ³Ô¹Ï±¬ÁÏ Payments ¨C Pay clinical research sites faster.
  • ³Ô¹Ï±¬ÁÏ Study Startup ¨C Accelerate time to site activation.
  • ³Ô¹Ï±¬ÁÏ RTSM ¨C Randomize subjects and manage trial product supply.
  • ³Ô¹Ï±¬ÁÏ Site Connect ¨C Automate information sharing.
  • ³Ô¹Ï±¬ÁÏ Study Training ¨C Streamline and automate training.
  • ³Ô¹Ï±¬ÁÏ Disclosures ¨C Centralize clinical trial disclosures.
  • ³Ô¹Ï±¬ÁÏ OpenData Clinical ¨C Provide investigator and site data.

³Ô¹Ï±¬ÁÏ Clinical Data

Accelerate study timelines with modern, innovative applications for clinical data.

³Ô¹Ï±¬ÁÏ Clinical Data helps clinical teams collect, aggregate, clean, and manage trial data with agility and speed.

  • ³Ô¹Ï±¬ÁÏ EDC ¨C Collect, clean, and review study data.
  • ³Ô¹Ï±¬ÁÏ DQS ¨C Manage complete and concurrent study data.
  • ³Ô¹Ï±¬ÁÏ eCOA ¨C Capture responses directly from clinical trial participants.

³Ô¹Ï±¬ÁÏ RIM

Bring speed and agility to your regulatory team with unified RIM.

Unify regulatory systems and processes on a single cloud platform for end-to-end submission and registration management.

  • ³Ô¹Ï±¬ÁÏ Registrations ¨C Track global registrations.
  • ³Ô¹Ï±¬ÁÏ Submissions ¨C Plan and manage submissions.
  • ³Ô¹Ï±¬ÁÏ Submissions Publishing ¨C Publish to health authorities.
  • ³Ô¹Ï±¬ÁÏ Submissions Archive ¨C Access submissions history.

³Ô¹Ï±¬ÁÏ Safety

Safety suite of applications operate as a unified pharmacovigilance system on a single cloud platform to maximize operational efficiencies and improve patient safety.

  • ³Ô¹Ï±¬ÁÏ Safety ¨C Real-time management and oversight for adverse events.
  • ³Ô¹Ï±¬ÁÏ SafetyDocs ¨C Centrally manage pharmacovigilance content.
  • ³Ô¹Ï±¬ÁÏ Safety Workbench ¨C Run advanced reports, queries, and analytics.
  • ³Ô¹Ï±¬ÁÏ Safety Signal ¨C Reliably detect, validate, and manage potential safety signals.

To learn more, watch this 13 minute demo of the ³Ô¹Ï±¬ÁÏ Development Cloud in action.

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Copenhagen | 28-29 May, 2026

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