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At Cloudbyz, we understand the pivotal role that clinical trials play in the Vaccines, Blood & Biologics industry. Recognizing the distinct complexities and regulatory nuances that come with these processes, our solutions are designed to simplify these tasks, enhancing efficiency and delivering accurate, actionable results.
Our unified clinical trial management system offers an integrated approach to managing intricate trials in the Healthcare Provider industry. By unifying the end-to-end clinical trials management process, our platform acts as a comprehensive hub for patient recruitment, trial operations management, budgets and financials, study start-up, data capture, safety, and reporting.
Seamless End-to-End Clinical Trial Operations
Real-time Visibility on Budgets and Payments
Improve Trial Management with Real-time Collaboration
Accelerate study build and data capture
Integrated randomization and trial supply management
Unified Safety adjudication and reporting
Our system seamlessly unifies all components of your trial, from participant recruitment, study start-up, trial operation management, financials, regulatory document management, clinical data management to safety management and reporting.
Crafted with simplicity and efficiency in mind, our platform ensures your team can effortlessly navigate its features, maximizing productivity.
Whether you're an innovative pharmaceutical startup or a well-established multinational corporation, our system adjusts to your needs, facilitating growth while maintaining superior performance.
Equipped with robust data management capabilities and stringent security standards, our solutions ensure your data is accurate, trustworthy, and safeguarded.
Centrally manage all aspects of your biological product trials, from initiation to closure, ensuring optimal resource allocation and efficient trial conduct.
Securely collect, manage, and analyze trial data with our robust data management tools, ensuring data integrity and compliance with industry and regulatory standards.
Ensure that all trial activities and data meet regulatory guidelines with our built-in compliance management features. Our solution supports compliance with FDA, EMA, PMDA and other global regulations.
Foster effective communication and teamwork among clinical teams, sponsors, and other stakeholders with Salesforce's robust collaboration tools. Real-Time Reporting and Analytics: Drive insights, improve trial design and management, and boost operational efficiency with access to real-time data and analytics.
Streamline your trial management process, reduce manual tasks, and optimize resource allocation.
Ensure adherence to regulatory standards, reduce the risk of non-compliance and enhance product safety
Safeguard sensitive trial data and patient information with our secure platform.
Enhance collaboration among your teams and with stakeholders for successful trial outcomes.
Leverage real-time data and analytics to make evidence-based decisions that can drive product innovation and market competitiveness.
With seamless EMR & EHR integration, enhance patient experience throughout the trial process.