Key Features of WiseCLIN
Our comprehensive platform streamlines clinical trials with intelligent risk management tools
Dynamic Risk Management
Real-time risk detection with AI-powered analytics that adapt to your specific study complexities.
Centralized Oversight
Comprehensive dashboards with real-time data visualization for immediate risk identification.
Compliance Workflows
Automated global regulatory processes for seamless compliance with ICH E6(R3), FDA, and EMA standards.
Seamless Integration
Connects with your existing systems including EDC, CTMS, eTMF, and other clinical platforms.
Why Choose WiseCLIN?
Our Risk-Based Quality Management (RBQM) system delivers measurable improvements in trial efficiency, data quality, and regulatory compliance.
Proactive Risk Management
Identify, assess, and control risks before they become costly issues with real-time risk alerts for data-driven decision-making.
Enhanced Oversight
Centralized quality tracking with dashboards to monitor vendors, track trial progress, and generate audit-ready reports effortlessly.
Regulatory Compliance
Fully aligned with ICH E8 (R1) and ICH E6 (R3) for regulatory compliance.
Cost & Time Savings
Minimize deviations and inefficiencies with smart risk prioritization, focusing resources on what matters most while cutting operational costs.
Designed For
Our platform is specially tailored to meet the unique needs of various clinical research stakeholders
Biopharmaceuticals
Qlarix’s cutting-edge WiseCLIN platform supports your entire portfolio of clinical trials, regardless of phase, therapeutic area, or study design. We offer tailored training to ensure your teams can fully leverage WiseCLIN capabilities, driving efficiency and compliance across your operations.
Portfolio-wide support
Tailored team training
Expert RBQM consulting
Efficiency and compliance
Clinical Research Organizations (CROs)
Partnering with CROs worldwide, WiseCLIN delivers innovative RBQM and oversight functionalities that align seamlessly with Sponsor expectations and regulatory requirements. Our intuitive tools and comprehensive training programs empower CRO teams to streamline trial management and enhance operational performance.
Global CRO partnerships
Innovative RBQM tools
Comprehensive CRO training
Customized trial oversight
Research Entities
Recognizing the specialized needs of academic and independent research institutions, WiseCLIN offers customizable solutions that adapt to each project’s goals and complexity. Our platform supports data integrity and risk management, ensuring the credibility and reliability of your findings.
Custom research solutions
Data and risk support
Dedicated project management
Long-term scientific impact
Medical Device Companies
Designed with the challenges of medical device development in mind, WiseCLIN accelerates your path from concept to market. Our platform provides robust support for generating reliable clinical evidence, meeting stringent regulatory requirements, and adapting to the evolving medical device landscape.
Accelerated device development
Reliable evidence generation
Regulatory-ready solutions
Confident, compliant launches