Advarra
VS
SimpleTrials
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.
SimpleTrials
SimpleTrials is a validated clinical trial management system (CTMS) and eTMF solution designed for sponsors, clinical research organizations (CROs), and sites. It combines robust document management, subject tracking, site visit planning, automated workflows, and integrated analytics in a secure, compliant environment. Users benefit from flexible subscription plans with no multi-year contracts and scalable options tailored to team size and study complexity.
The platform supports seamless collaboration and oversight by offering integrated tracking for studies, documents, calendars, contracts, payments, and more. Features such as automated notifications, customizable trackers, risk management, and compliance documentation empower research teams to efficiently manage specialized studies or large portfolios while maintaining regulatory requirements and data integrity.
Pricing
Advarra Pricing
Advarra offers Contact for Pricing pricing .
SimpleTrials Pricing
SimpleTrials offers Paid pricing with plans starting from $599 per month .
Features
Advarra
- 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.
SimpleTrials
- CTMS & eTMF Integration: unified management for studies, sites, and documents
- Compliance and Security: validated, 21 CFR Part 11 compliance, and dedicated compliance portal
- Custom Trackers: tailor data tracking for unique research needs
- Automated Alerts & Workflows: automated notifications via email and in-app for tasks and milestones
- Calendar & Site Visit Tracking: centralized scheduling and visit planning
- Subject and Enrollment Tracking: monitor screening, enrollment, protocol deviations and subject visits
- Contract and Payment Management: integrated solution for contracts, accrual reporting, and site/vendor payments
- Data Import & Integration: support for EDC/IRT integration and data workflow automations
- Advanced Reporting: real-time dashboards, ad-hoc report generation, analytics
- Premium Support: user manuals, videos, knowledge base, sandbox study, and help desk
Use Cases
Advarra Use Cases
- Coordinating multi-site clinical trials between sponsors, sites, and CROs
- Streamlining regulatory document submission and review processes
- Ensuring compliance with institutional and biosafety requirements
- Optimizing study startup, protocol activation, and timeline management
- Automating trial workflows for improved operational efficiency
- Enhancing data analysis and visualization for clinical research teams
- Preparing trial documentation for audits and regulatory inspections
SimpleTrials Use Cases
- Managing and tracking clinical trials for pharmaceutical or biotech sponsors
- Electronic document management and regulatory compliance for clinical research organizations
- Coordinating site operations, subject enrollment, and visit scheduling in multi-site studies
- Automating workflows and notifications for study teams to ensure milestone completion
- Integrating with EDC, IRT, and other systems for streamlined data collection and reporting
Advarra
SimpleTrials
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