Gain visibility into all aspects of your research operations with a comprehensive, proven, and standardized clinical trial management system built through collaboration with leading academic medical centers and cancer centers.
Clinical Conductor is a comprehensive Clinical Trial Management System (CTMS), scalable to optimize finances, regulatory compliance, and overall clinical research operations for all types of research sites, site networks, hospitals, and health systems.
Think beyond the binder. Save money, improve efficiency, and enhance regulatory compliance across your organization with a 21 CFR Part 11-compliant system designed to adapt to regulatory workflows for any size research site.
Centralize research operations within Longboat globally for all sites, sponsors, and contract research organizations (CROs) to accelerate study startup, guide efficient and compliant study conduct, enhance patient outcomes, and streamline critical coordination.
Clinical research involving human participants typically involves some type of risk. Incorporating the appropriate ethics reviews and safety oversight helps ensure stakeholder safety, data integrity, and regulatory compliance. Includes IRB, IBC, DMC, and EAC.
Our team of Advarra Consulting experts prioritizes your unique goals, challenges, and timelines. We work collaboratively with your research and development team to accelerate product development and performance, making clinical research safer, smarter, and faster.
Senior Manager, Marketing Events
Advarra
United States
