How Salesforce Life Sciences Cloud and Cloudbyz Unified eClinical

Clinical trial operations still run on disconnected systems — separate CTMS, EDC, eTMF, and safety platforms that require manual reconciliation and create compliance gaps. The result is slower study timelines, administrative overhead, and risk that compounds across the trial lifecycle.

This white paper examines how Salesforce Life Sciences Cloud and Cloudbyz Unified eClinical — built natively on Salesforce — work together as a single, connected platform to eliminate these inefficiencies across clinical, regulatory, and safety operations.

What's inside:

• How a unified data model replaces fragmented eClinical systems across CTMS, EDC, eTMF, RTSM, and pharmacovigilance
• AI-driven automation for site activation, compliance tracking, adverse event reporting, and study monitoring
• Compliance architecture supporting 21 CFR Part 11, ICH-GCP, HIPAA, and GDPR
• Real-world case studies from a global pharma company, a biotech startup, a medical device manufacturer, and a CRO
• Future directions: Salesforce Agentforce, decentralized trials, and digital twin technology