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.
Reduce delays in study start-up and execution through process automation and real-time tracking.
Ensure data integrity, centralized access, and traceability across all trial-related documents and systems.
Maintain full GxP compliance with audit trails, version control, and structured document workflows.
Enable seamless communication between sponsors, CROs, and sites through integrated platforms.
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
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.
Pre-implementation analysis and consulting to align the system with your business goals;
Full implementation and configuration tailored to your processes and compliance needs;
Secure and accurate data migration with minimal disruption;
Customized user training to ensure smooth adoption and confident daily use;
Ongoing technical support to keep your system running smoothly;
Comprehensive system validation in line with industry regulations and best practices;
Development of dedicated solutions designed around your specific requirements.
eLife Sciences is a team of experts with unique experience in compliance, validation and quality assurance (QA). We provide services to companies in regulated industries with a special focus on life science.
