Clinical Trial Management System
Clinical trials are complex. Using a software system helps you manage them in clinical research.
Clinical Trial Management System (CTMS)
Clinical trials are complex. Biotech, pharmaceuticals, and other research-focused life sciences organizations run highly complicated clinical trials in the search for new medicines, devices, and the ultimate cure for many of the world’s diseases. Using a software system helps you manage clinical trials in clinical research.
In recent years, clinical trials have become even more intricate as R&D costs have increased to an average of $1.4 billion USD per clinical trial. Research sites are now spread across 200% more countries than before. Data endpoints have grown by 86% thanks in part to new technologies, and human resource turnover has averaged 55% per trial due to increased competition between sponsors.
How are organizations able to efficiently manage all of the intricate working parts of clinical trials? Enter clinical trial management systems (CTMS).
Navigate complexity with a simple, yet powerful trial management application that provides full oversight of trial activities to keep study teams aligned and on time.
Reduce study timelines with a modern, easy-to-use cloud application that streamlines study management and automates key activities across the trial lifecycle.
Streamline your clinical environment with a turn-key platform for operations that includes payments and monitoring and delivers a seamless connection with LifeSphere eTMF.
What is a Clinical Trial Management System (CTMS)?
A CTMS is a software system used by companies of all sizes for their clinical trials to help manage them and make the processes more accessible and more transparent. It serves as a single, centralized resource to support clinical research studies, enabling life sciences organizations to plan, track, and control all activities related to the set-up, conduct, and closeout of clinical trials.
Most clinical trials start small and grow as the trials advance. During these early stages, it’s not uncommon for the company who is managing the trial to use simple tools including spreadsheets and email to track and maintain the information gathered in their clinical trial. As these trials become more extensive, these bare-bones solutions become unable to manage the increasingly complex data efficiently. They require more thorough and complete systems that can not only manage compliance, regulations, patients, and project timelines, but can also control the budgeting and financials and can integrate with third-party systems that the company may already have in place.
With great advancements in mobile technology and cloud infrastructure, many clinical trial management systems are now web-based, allowing multiple sites and users to input and manage information from almost any location while processing large amounts of data.
Features and Benefits of a CTMS
Today most clinical trial management systems offer similar features to comply with and meet industry standards. There are only a few that truly stand out with their innovative approaches to the current and future complexities of the clinical trial process.
By looking at the clinical domain as a whole, ArisGlobal has developed LifeSphere Clinical as a unified end-to-end platform that delivers unparalleled efficiency gains to life sciences organizations. A core offering in the LifeSphere Clinical platform, LifeSphere CTMS is a cloud application that makes the entire clinical trial management process more accessible and more transparent for companies of all sizes:
- Enables simple, end-to-end clinical trial management in a single application, reducing complexity to empower organizations of all sizes
- Automates key clinical trial activities to enhance productivity and deliver faster trials
- Unifies clinical operations and data management in a single cloud platform
- Streamlines trial management through an intuitive interface designed for all skill and responsibility levels
- Makes site payments and monitoring fast and easy by including them out-of-the-box
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Features of a CTMS
Streamline Study Startup
Automate key study prep activities such as budget planning, site assessments, document distribution, enrollment, and site visit planning. Track submission milestones and document packages to speed up the study startup.
Simplified Trip Reporting
Supports report app authoring, review, and approval for large field teams.
Integrated Document Tracking
Fully integrated document tracking provides real-time inspection readiness.
Site Monitoring Planning
Enables monitors to efficiently conduct and document monitoring visits with an automated review and approval process governed by user-defined workflows and event-based planning.
Efficient Study Closeout
Assists independent audits and study closeout processes with versatile export capabilities and out-of-the-box unification with LifeSphere EDC. Easily provides oversight compliance to regulatory authorities without requiring them to log into the system.
Flexible Payment Modules
Included payment module allows for hassle-free configuration of payment terms so teams can easily pay as contracted.
ArisGlobal Introduces LifeSphere CTMS10, Bringing Modern Simplicity and Efficiency to Clinical Trial Management
An Easy and Intuitive CTMS for Organizations of All Sizes
LifeSphere CTMS10 is a core offering in LifeSphere Clinical’s unified cloud platform.
LifeSphere CTMS10 is an end-to-end solution that makes the entire clinical trial management process easier and more transparent for companies of all sizes.
The Evolving Role of CTMS in Risk Management
Clinical trials are a necessary and critical activity in releasing new, and often-times lifesaving, drugs and medical devices to the market. To achieve success, however, in the face of rising development costs and fewer approvals, life sciences organizations are under severe pressure to manage these trials in a way that is risk-averse and cost-effective.
The Beneﬁts of a Unified Clinical Platform
For nearly 20 years the issue of disconnected, poorly integrated systems and processes has hampered clinical R&D. The problem and its challenges have been discussed, dissected, and top of mind of most clinical operations leaders. The constant and critical push to accelerate a product’s time to market continues to push clinical teams to seek solutions that deliver greater efficiencies. After 20 years of point-to-point integrations, the time has come for a different, advanced, and unified approach.
The Clinical Domain is Evolving. Make Sure your CTMS is Evolving with It
The Evolving Role of CTMS in Risk Management takes a broad look at the challenges facing clinical trial management, how the clinical domain is changing, and how the industry can better respond.