Intelligent Trial Management
A user-centric design that streamlines treatment allocation, subject randomization, and supply chain integration across global sites.
Trusted by leading global biopharmaceutical companies
Designed for flexibility across therapeutic areas
Fully validated and compliant with international regulatory standards
Proven in accelerating study start-up and execution timelines
A user-centric design that streamlines treatment allocation, subject randomization, and supply chain integration across global sites.
Role-based access ensures confidentiality in blinded and unblinded trials, maintaining data security and regulatory compliance.
Supports flexible randomization methods — including stratified, dynamic, and algorithm-based — aligned with your study protocol.
Automated allocation by treatment arm, dose, or investigational product, with full audit trails and compliance tracking.
Real-time tracking with pre-defined thresholds ensures investigational products are available when and where they are needed, preventing delays and protocol deviations.
A dynamic reporting engine with smart notifications, enabling study teams to respond proactively to site-level requirements.
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how we can support your next study.