Managing late-phase clinical trials can be challenging, with multiple platforms, applications, and data streams requiring constant oversight. What if all these essential tasks could be streamlined into a single, integrated platform? Lambda’s Integrated Clinical Trial Suite does just that. It’s a comprehensive solution designed to simplify trial management, offering a single-sign-on platform that integrates Electronic Data Capture (EDC), Imaging, Randomization, IP Supply Management and Trial Master Files into one cohesive system. This suite not only streamlines your operations but also serves as a single source of truth for patient data, ensuring consistency, accuracy, and compliance across all your trials.

One-Click Dashboard to Access All Applications

The Integrated Clinical Trial Suite streamlines every aspect of late-phase clinical trials, from user management to regulatory compliance, delivering significant advantages for both Lambda and our clients. By centralizing processes, it enhances the quality and accuracy of data management, reduces dependency on technical teams, and accelerates decision-making. Whether it’s improving operational efficiency, strengthening your quality management system, or facilitating seamless application integration, the Integrated Clinical Trial Suite offers a comprehensive solution that elevates clinical trial management to new heights.

Key Features:

• Cloud-Based Application: Accessible from anywhere, it ensures that your data and operations are always secured and within reach.
• Designed for Late-Phase Operations: Tailored specifically for the unique needs of late-phase clinical trials.
• Centralized User Management: Manage user access and roles across multiple applications from a single platform, minimizing the risk of data breaches.
• Dynamic Dashboard: The dashboard is a dynamic, interactive interface that allows you to jump directly into the applications and data you need.
• Project/Site-Based Access Allocation: Protect your data with project and site-specific access controls, ensuring that only authorized personnel can access sensitive information.

Overcoming Operational Challenges

Managing late-phase clinical trials often involves handling numerous applications and user permissions, which can be overwhelming. The Integrated Clinical Trial Suite simplifies this by acting as a unified platform for all your trial operations, from user activation to access deactivation, ensuring that you have complete control and visibility.

How the Integrated Clinical Trial Suite Addresses Key Challenges:

• Consolidated Operations: Instead of navigating multiple platforms, the suite allows you to manage everything in one place, from activating users to changing permissions and deactivating accounts.
• On-Demand Reporting: Need a report on user activity or access logs? The suite provides on-demand reports that give you real-time insights into your operations.
• Master Data Synchronization: Create master data in within the suite, and watch as it is seamlessly replicated across all your integrated systems, ensuring consistency and accuracy.
• Single URL for Multiple Applications: Forget about keeping track of multiple URLs and login credentials. With the Integrated Clinical Trial Suite, a single URL and a unified login give you access to all your applications.
• Unified User Credentials: No more password fatigue— with a single sign-on, simplifying access and improving security.

Benefits

This suite isn’t just about making life easier—it’s about enhancing the overall quality and efficiency of clinical trials. By centralizing and streamlining operations, the suite delivers significant benefits that impact both the quality and effiency of trials.

Quality Benefits:

• Enhanced Quality Management: By centralizing data and operations, the suite strengthens your quality management system, making it easier to maintain high standards across all your trials.
• Accurate Access Tracking: Keep precise records of who has access to what, ensuring that data is always secure and compliant with regulatory requirements.
• Timely Data Availability: Critical data is always at your fingertips, enabling faster decision-making and more efficient trial management.

Operational Benefits:

• Streamlined Processes: It simplifies the approval process, allowing direct interaction between requestors and approvers, reducing the need for technical support.
• Reduced Technical Dependency: Thanks to its user-friendly interface, It minimizes your dependency on technical teams, freeing them up to focus on more complex tasks.
• Real-Time Operational Efficiency: The real-time data access ensures that your operational activities are always up to date, reducing delays and improving efficiency.

Activities Managed:

The Integrated Clinical Trial Suite covers a wide range of activities essential for the successful management of late-phase clinical trials.

• Project Management: Oversee all aspects of your trial projects from a single interface.
• Investigator Database Management: Keep track of all your investigators and their credentials in one place.
• Site Management: Manage all your trial sites, ensuring that each one is operating smoothly and efficiently.
• Application Management: Integrate and manage multiple applications seamlessly, ensuring that all systems are working together harmoniously.
• User Management: From activation to deactivation, manage user access with ease, ensuring that only authorized personnel have access to sensitive data.
• Global Role Management: Assign and manage user roles across your entire organization, ensuring that everyone has the access they need, and nothing more.

Simplified Application Management

• Simple Configuration: Integrating new applications into your workflow is straightforward with its intuitive configuration process.
• Effortless Access Requests: Users can request access to applications with minimal information, simplifying the approval process and reducing administrative overhead.
• Real-Time Data Access: Monitor who has access to what in real-time, giving you complete visibility over your operations.
• Personalized Dashboard: The dashboard isn’t just functional—it’s personalized, allowing you to monitor pending activities and prioritize tasks based on your specific needs.
• Customizable Reports: Generate detailed reports on user access and activity with just a few clicks. The reporting tools allow you to filter and customize data without needing developer assistance.

Ensuring Regulatory Compliance

In the highly regulated world of clinical trials, compliance is not optional—it’s essential. The Integrated Clinical Trial Suite is designed to meet the highest regulatory standards, ensuring that trials are always in line with global guidelines.

• Real-Time Access Data: It provides real-time data on user access, helping you maintain compliance with regulatory requirements.
• Enhanced Quality Management: By centralizing operations, It supports a robust quality management system, making it easier to meet regulatory standards.
• Facilitates Global Audits: With this Integrated Clinical Trial Suite, you can easily facilitate global remote audits, providing read-only access to auditors, ensuring transparency and compliance without compromising security.

In the demanding environment of late-phase clinical trials, having a reliable, efficient, and compliant platform is crucial. Lambda’s Integrated Clinical Trial Suite offers a comprehensive, cloud-based solution that not only simplifies trial management but also enhances the quality and efficiency of operations. By centralizing user access, streamlining processes, and ensuring regulatory compliance, the suite is the integrated solution your trials need to succeed. Whether managing a single site or multiple projects, the Integrated Clinical Trial Suite has the tools and features to make late-phase clinical trials smoother, faster, and more efficient.

With the Integrated Clinical Trial Suite, you’re not just managing trials—you’re elevating them.