Supporting the digital transformation of clinical trials
A modern clinical environment relies on streamlined digital platforms to manage study start-up, regulatory documentation, trial master files (TMF), monitoring, site management, and more — ensuring compliance, transparency, and data integrity across all phases of clinical research.
Clinical processes under control
By implementing an advanced clinical solution with eLife Sciences, you can:
Get to market faster
Reduce delays in study start-up and execution through process automation and real-time tracking.
Get control over your data
Ensure data integrity, centralized access, and traceability across all trial-related documents and systems.
Become inspection-ready
Maintain full GxP compliance with audit trails, version control, and structured document workflows.
Get global collaboration
Enable seamless communication between sponsors, CROs, and sites through integrated platforms.
Technology neutrality in approach to clinical solutions
At eLife Sciences, we are vendor-agnostic — which means we are not tied to any single technology provider. Instead, we tailor clinical solutions that best align with your organizational needs, budget, infrastructure, and regulatory landscape. Whether you are adopting a new platform or optimizing an existing one, we bring expertise, flexibility, and a deep understanding of clinical workflows to ensure long-term success.
We support leading and proven clinical platforms used across the life sciences industry, focusing on those that ensure compliance, scalability, and performance.
Veeva Clinical brings together study start-up, CTMS, eTMF, and payments in one unified environment. It enables faster, more connected trials by eliminating manual processes and siloed data. Built specifically for life sciences, it ensures visibility and compliance across every stage of the clinical lifecycle
What sets Veeva Clinical apart is its seamless integration across the clinical ecosystem:
Get faster study activation with connected site contracts, budgets, and essential documents
Get real-time trial oversight with dashboards tracking site performance and milestones
Get audit-ready documentation managed in a compliant, version-controlled eTMF
Get centralized payments and reconciliation to reduce delays and financial discrepancies
EXTEDO Clinical Module
Secure clinical records management
EXTEDO’s Clinical Module enables secure, compliant handling of trial-related documents in a centralized system. Designed for GxP-regulated environments, it supports the creation, review, approval, and archival of clinical content across global teams.