Discover the future of research compliance management with mavQ's Electronic Research Administration (eRA) Suite. Specially crafted to transform your institution's handling of human, animal, bio & radiation safety protocols, and conflicts of interest. Our suite is designed to not only enhance productivity for researchers and staff, but also to expedite decision-making while ensuring rigorous regulatory compliance.
Outdated and overpriced solutions are a thing of the past. mavQ eRA Suite brings a much-needed breath of fresh air to the industry with its modern, cost-effective, secure, and user-friendly design.
Our Commitment to You:
- Experience our suite firsthand with a complimentary trial site.
- Receive a free consultation for a detailed current state analysis and a tailored implementation blueprint.
- Benefit from free active shell protocol data migration for InfoEd and IRBNet customers ready to upgrade their operations.
Key Benefits for Decision Makers:
- Streamlined Efficiency: Reduce errors and enhance automation with smart forms and advanced review features. This leads to faster decisions and a noticeable improvement in ROI.
- Affordability and Ease-of-Use: Choose between an on-premises or secure cloud-hosted solution. Our suite is budget-friendly, swift, and intuitive, reducing IT strain.
- Simplified Implementation: Rapidly deploy a fully-designed baseline system with optional universal upgrades, minimizing IT involvement. Need customization? We've got you covered.
- In-Depth Reporting: Harness comprehensive data analysis with our advanced reporting module.
- Seamless System Integration: Enjoy a unified experience with flawless HR system and CITI integration.
Advantages for Investigators and Research Teams:
- Accelerated Submissions: With dynamic, logic-driven and guided smart forms, pre-populated data where applicable, field level help and validations.
- Enhanced Teamwork: Improve coordination with task reassignment and visibility of changes.
- Complete Protocol Oversight: Easily access all historical and current protocol data, documents and lifecycle events.
- Efficient Amendment and Renewal Process: Streamline your workflow for amendments, renewals, and reporting.
- Prompt Feedback Loop: Benefit from clear, concise field-level comments for quicker revisions.
- Automated Alerts: Stay informed with reminders and notifications about key updates such as status changes, task assignments and deadlines.
Benefits for Staff:
- Smart Dynamic Forms: Our forms eliminate incomplete submissions with built-in validation logic.
- Customizable Workflow: Adapt processes to each study’s needs with real-time monitoring capabilities.
- Assured Regulatory Compliance: Utilize our advanced review system for thorough and efficient compliance. Formal responses for revisions allow field level commenting as well as collection of field level justifications.
- Automated Board Management: Effortlessly manage meetings, agendas, minutes, letters, and communications electronically.
- Comprehensive Protocol Access: Easily access all historical and current protocol data, documents and lifecycle events.
- Timely Notifications: Receive automated alerts for task assignments and status updates.
- Efficient Data Retrieval: Quickly search across all protocols with our advanced search function.
- Detailed Data Analysis: Leverage our advanced reporting module for in-depth insights.