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In today’s competitive clinical research landscape, effective risk management and compliance with Good Clinical Practice (GCP) are critical.

Qlarix is your partner in smarter, Risk-Based Quality Management (RBQM).
Let us help you ensure the success of your clinical studies.

WiseCLIN is the ultimate Risk-Based Quality Management (RBQM) designed to empower your clinical trial teams with insightful risk management, seamless oversight, and enhanced efficiency.

Streamline Oversight. Strengthen Compliance.

Request a Free Demo Today

Discover how our WiseCLIN Risk-Based Quality Management (RBQM) can help you:

  • Reduce trial risks by 30% or more.
  • Cut trial costs by up to 20%.
  • Save hundreds of hours on manual quality oversight.
  • Achieve compliance with the latest ICH E6(R3) requirements effortlessly.

Key features of WiseCLIN Risk-Based Quality Management (RBQM)

Dynamic Risk Management Boards tailored to study complexity

Centralized Oversight with real-time data visualization

Customizable Dashboards for progress tracking and compliance

Integration-Friendly: Seamlessly connect with CTMS, eTMF, EDC, and other trial systems

Compliance-Driven: Built to meet global requirements, including ICH E6(R3), ICH E8(R1), and ICH Q9 standards

Discover our RBQM Tech

Why Choose WiseCLIN Risk-Based Quality Management (RBQM)?

Proactive Risk Management
  • Identify, assess, and control risks before they become costly issues.
  • Fully aligned with ICH E8 (R1) and ICH E6 (R3) for regulatory compliance.
  • Real-time risk alerts for data-driven decision-making.
Enhanced Oversight for Sponsors, CROs and Research Entities
  • Centralized tracking of quality metrics.
  • Monitor vendor performance and trial progress via customizable dashboards.
  • Generate audit-ready reports effortlessly.
Streamlined Collaboration
  • Minimize protocol deviations, vendors and site inefficiencies, and regulatory non-compliance through smart risk prioritization.
  • Focus resources on critical trial aspects while reducing operational costs.
Cost & Time Savings
  • Minimize protocol deviations, vendors and site inefficiencies, and regulatory non-compliance through smart risk prioritization.
  • Focus resources on critical trial aspects while reducing operational costs.
Connect with an RBQM Expert

Designed For

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. For teams requiring additional support, our consultants are ready to collaborate until your organization achieves full independence in risk-based quality management.

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. By customizing our approach, we ensure both you and your Sponsors achieve superior trial outcomes and compliance excellence.

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. With dedicated project management and long-term support, we help research entities advance research discoveries and achieve meaningful 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. We help you maintain confidence and compliance while ensuring your devices reach patients efficiently and effectively.