What is Advarra?

Advarra is a leader in clinical trial management, offering a unified platform designed to streamline all phases of clinical research, from planning and study startup to conduct and closeout. Leveraging advanced technology, Advarra connects stakeholders—sponsors, sites, and contract research organizations (CROs)—to promote efficient collaboration, data consolidation, and accelerated trial outcomes. Their solutions prioritize regulatory compliance, enhance patient safety, and optimize every stage of the trial lifecycle for maximum transparency and speed.

Trusted by thousands of institutions and investigators, Advarra delivers seamless document organization, integrated study reviews, and secure communication workflows. Their platform’s patient-centric approach, combined with robust data management and analytics capabilities, empowers research professionals to improve efficiency, ensure audit readiness, and deliver better trial results, making Advarra a central technology partner in the clinical research industry.

Features

Unified Platform: Manage all aspects of clinical research through a single system.
Stakeholder Collaboration: Connects sponsors, sites, and CROs efficiently.
Document and Workflow Management: Organize and track regulatory documents and trial protocols.
Regulatory Compliance Tools: Facilitate IRB, IBC, and other ethics reviews.
Data Analytics and Visualization: Enhance research insights and reporting capabilities.
Patient-Centric Tools: Prioritize participant safety and engagement throughout trials.
Customizable Workflow Automation: Expedite startup, conduct, and closeout stages.
Secure Communication: Protect sensitive clinical trial data and support collaboration.