Best Clinical Trial Management Software of 2024

The Interactive Response Technology (IRT), systems of today are becoming more complex. Flexible and configurable IRT is important - IRT data can be used as the source of record to recruit, drop-out rates in clinical trials, patient visits, or any other vital data. You want a platform that is user-friendly, mobile-ready and comprehensive. It should also be embedded in quality, flexibility, and expertise. In today's risk-based eClinical environment, comfort is combined with complex therapeutic expertise. We empower clinical trials to deliver positive patient outcomes by combining the right technology, subject matter knowledge and a commitment to service. Clients have control over their Randomization and Trial Supply Management processes (RTSM) thanks to deep clinical and supply chain knowledge. Our innovative tools drive exceptional levels of quality control, site efficiency, and patient compliance. Our IRT platform is able to meet the needs for almost any study and allows fully validated deployment in as little time as 30 days.

TCS ADD platform speeds up speed-to-market for the pharmaceutical industry across all clinical R&D value chains and makes clinical trials more efficient and safer. TCS ADD facilitates digital ecosystems, simplifies data complexity, and provides patients faster access to effective drugs. The platform is powered with TCS Decision FabricTM cognitive artificial intelligence engine, smart analytics and IoT which provides superior business value for the pharmaceutical industry. The next-generation, end-to-end metadata-driven solution for managing industry and sponsor clinical standards. Data science-driven platform that uses AI & ML technologies to speed up study start-up, targeted interventions, and quicker decisions. This solution digitizes the entire clinical supply management process, while placing the patient at the center. This increases patient safety and overall efficacy.

The industry's best AI-powered clinical analytics platform provides actionable insights that enable your teams to manage risk, improve performance across sites, studies, and vendors. Saama's state-of-the art clintech is designed to streamline workflows, automate tedious processes, and improve collaboration across clinical operations. Saama is trusted by sponsors and CROs for data aggregation, artificial intelligence solutions, and improved decision-making. This can help to reduce drug development costs and timeframes, as well as eliminate delays. Saama can help you get on the fast track for clinical trial process innovation. Your ClinOps and medical review team will find it much easier to access all of your clinical data in one place. Data managers are often undervalued. They can now focus on the data points that are important by eliminating manual work.

Streamline regulatory operations within your organization to improve compliance. Veeva SiteVault simplifies clinical trial management by connecting all regulatory operations. This improves efficiency and compliance. A single system that integrates regulatory and source documents supports 21 CFR Part 11 compliance and HIPAA requirements. SiteVault Enterprise provides real-time visibility across trials and speeds study activation. It also enables faster and more quality trial execution. To speed up study activation and reduce manual work, you can replace manual processes with your own workflows. Monitors will have secure, direct access into your source and regulatory documents. This will eliminate the need to redact or grant EMR access. You can create your own workflows, reports and dashboards to gain greater insight into regulatory processes and start-up timelines.

Research and clinical trials were traditionally conducted outside of local hospitals and doctors' offices. Patients didn't know that research could improve their health or their outcome, and doctors weren't always informed. Elligo allows for a wider participation in clinical research. With access to more than 150 million patients and their data (and more than 150 million others), physicians can offer research as an option to patients who otherwise wouldn’t have access. Traditional methods of recruiting are limited by geographical limitations, such as the proximity of patients to research sites. Patients prefer to work with their trusted healthcare provider.

Our software provides a complete end-to-end tracking solution that can be used in clinical trials. Simply download the software to your trial managers' mobile devices, and let TruLab's blockchain technology do the rest. To spot potential problems, don't wait for samples to reach a central laboratory. Observe data anomalies as the samples progress through the clinical trial. TruLab allows remote access to samples. 20% of samples are lost in late-stage trials or deemed unusable. This is not acceptable from a logistical, ethical, and financial standpoint. Samples are not collected only at clinical sites anymore. The new world of sample collection at residences presents new challenges in sample tracking. TruLab tracks samples anywhere in the world, from home to repository.

PicnicHealth brings together patients and researchers to provide the most accurate, relevant real-world data. We can create the most comprehensive picture of patient health by working directly with patients, and not just one specialist or care site. With our established patient communities and quick recruitment through dozens if not hundreds of established direct-to patients channels, it is easy to build the right patient cohort. Patients can sign up in just 10 minutes and gain access to their medical records. Are you a part of ongoing trials or registries for patients? PicnicHealth will help you set them up. Our platform provides real-world data tailored to each patient. You can specify the data elements you want to extract from medical records. This includes narrative text, doctors' notes, and more. Patients can contribute more with our unique patient-centric approach to real world data.

Our cutting-edge platform, the Medidata Clinical Cloud, transforms clinical trial experiences for patients, sponsors and CROs. The Medidata Clinical Cloud is the only unified technology platform that focuses exclusively on clinical research. It addresses every step of the research process, from start to finish. Our platform helps medical device and life science organizations reduce development costs, minimize risks, and bring treatments and devices to market quicker. The Medidata Clinical Cloud will allow you to access the power of any product you choose for your clinical trials program. Medidata is leading the digital transformation in clinical research. Our platform, powered by artificial intelligence, machine-learning, advanced analytics, and advanced research, brings together researchers, study managers and investigators to accelerate research. Obtain regulatory-compliant, patient-friendly electronic informed consent for clinical trials.

Our platform provides the comprehensive support your clinical trial requires using cutting-edge cloud-hosted technology. Clinibase will make your organization more efficient and productive. Clinibase is not a plug-and play system. Why? Because every organization is unique and has its own systems and processes. Clinibase can be customized to meet your specific clinical trial requirements. We use surveys to identify areas for improvement and troubleshoot all aspects of your clinical trial processes. Our social integration tools make it easy to quickly locate and recruit eligible participants. Keep your participants engaged by providing smooth communication channels that facilitate high retention and positive participant experiences. Ensure that your trials are valid and safe by storing accurate data.

OpenText™, a leading provider of information management solutions for life sciences organizations, helps them to harness insights from data and content to improve their decision-making and accelerate product development. Integrate, manage and securely exchange data between people, systems, and things. Use information assets to drive innovation and commercialization. Cloud-native software can run anywhere, giving you freedom of choice. OpenText for life sciences accelerates discovery by delivering actionable insights that can be used to drive innovation in pipelines. Intelligent capture allows you to capture and manage research papers in electronic lab notebooks. Text mining can help you gain insights. Unstructured text in clinical trial reports, study protocol, clinical safety and efficiency findings, can be used to extract knowledge. Learn how to intelligently analyze and classify clinical trial documents and extract them to reduce the risk for costly stops and starts.

Cortellis™, a suite of life science intelligence software solutions, reveals hidden insights in data. This allows you to make better informed decisions throughout the R&D process. We have taken out the tedious work of finding, integrating and analysing data so that you can concentrate on the crucial decisions required to bring your products to market quicker. Cortellis provides unique data analysis that is rich in domain knowledge, industry insight, and therapeutic expertise. This allows you to unlock hidden insights that will allow you to make data-driven decisions that drive innovation. With the most comprehensive and deepest intelligence, you can get precise and actionable answers to specific questions throughout the R&D process. Cortellis is an indispensable part your daily work flow.

VIPER automates screening from remote patient identification (at point of diagnosis) through to qualified enrollment. VIPER uses artificial intelligence to match patients to precision trials within a narrow window of opportunity. This is done through the ingestion of lab-agnostic genomic and pathology data. It is tailored to the patient and the researcher. VIPER searches the personalized matching engine to locate the best clinical trials available for a patient's specific diagnosis--at that time. VIPER integrates workflow to send real-time notifications to the entire care team about a patient's eligibility in available clinical trials. This is done within a very limited enrollment window. VIPER provides interactive dashboards that allow you to access real-time data mining capabilities to aggregate patient data from both study and site levels to help you reach your study KPIs.

To make health breakthroughs more rapid, people must be involved in research. We have created a platform that connects individuals, communities, researchers, and others through trust, transparency, shared value, and shared benefit. Every person has unique information that could lead to the next medical breakthrough. Sharing your health data can help uncover new insights. Communities bring people together to quickly find answers. We manage your data and health experiences so you can start right away. We bring together individuals and communities to share their health data in order to answer the most pressing questions of life. People can unite with a common vision of fairness and responsibility, and it can change the face of established systems and institutions. A team of passionate technology and genomics leaders created it.

Choose Curebase to conduct your next study. You will experience more diversity, better enrollment, and better retention. Our innovative approach allows patients to participate at their own homes and with community doctors, resulting in faster, more cost-effective, and more diverse studies. Curebase offers a unique combination: Curebase has in-house virtual CRCs, paired with a global network virtual PIs working with community doctors to bring studies anywhere. Patients don't usually live near traditional research sites. Our trials bring the research into patients' homes, as well as real-world medical settings such community doctors' offices. Patients enrolled in Curebase infectious diseases trials were successful thanks to a new model that meets patients at their location through virtual and community healthcare.

DFnet, a healthcare technology company, provides eClinical services, including electronic data capture, eSource and data management services. Our services offer greater flexibility, better data quality, as well as greater efficiency for clinical trials around the world. Collect data from any source, including paper crfs, EDC, other electronic sources, online/offline tablet, and ePRO entries. Install in your secure premises or let us host it in our secure cloud environment. Advanced optical recognition reduces the time required to perform SDV and RBM processes. For multi-center studies with maximum flexibility. Web-based data collection from any source is instantaneously available in a central real-time platform.

Ripple makes it easy for you to connect with your employees. Learn what your employees love to read and how you can best promote your campaigns. SharePoint integrates intuitive tools that allow you to create beautiful, brand-branded content to connect with and engage. Visual workflow tools that are intuitive and adapt to your work style, as well as a drag-and drop calendar that allows you to create a precise comms plan. Ripple, the only internal communications tool, gives you detailed insights directly from your internal hub. You can learn from the reactions of others and refine your communications using a wide range of metrics. You can easily integrate SharePoint and M365 tools in your campaigns. You can streamline your workflow and give your audience rich, relevant content with every campaign. You can create eye-catching posts with built-in branding tools that will ensure your message is heard every time. These can be grouped into campaign themes, and rich content from all over M365 can be easily integrated.

eClinical Solutions assists life sciences organizations around world in their clinical development initiatives by providing expert data services and the elluminate®, Clinical Data Cloud -- the foundation for digital trials. elluminate, which is used by more than 100 biopharmaceutical companies worldwide, is a clinical data platform that was purpose-built to accelerate digitization efforts to manage the exponential increase in clinical data volume, variety and velocity. Gartner's 2022 Hype cycle for Life Science Clinical Development shows that life science companies are continuing to scale digital capabilities. The adoption of advanced analytics, hyperautomation, AI, and hyperautomation is becoming more mainstream. With elluminate's automated pipeline and scalable infrastructure, organizations can keep up with modern clinical trials and deliver business value across all clinical development functions.

LifeSphere eTMF provides a single source of truth for your clinical trial. Discover a flexible solution that streamlines the inspection process, ensures compliance and saves time and effort for your organization. LifeSphere eTMF is the first system that supports the TMF reference models. It aligns Clinical documentation, regulations and study protocol in one solution. Create and manage your clinical trial from a single source. Live collaboration and real-time sharing of documents will ensure the quality, timeliness and completeness of your trial master files. TMF inspections can be streamlined quickly and efficiently for any audit. Maintain compliance using embedded workflows and dashboards which allow easy trial reconstruction.

View your study data in real time through a dashboard that allows you to stay up-to date on milestones, progress of the study, and other KRIs. Mitigate risks in research by identifying issues and addressing them as they arise, improving trial performance dramatically. Lokavant's proprietary trial data can be used to optimize resources and reduce the burden on study teams. Trial data is ingested from the source and harmonized with Lokavant proprietary data and data from partners in real-time. Self-service, single view of real-time performance of studies with automated reporting and benchmarking. Daily re-forecasting is used to compare enrollment and site performance against historical performance. This provides actionable insights.

Discover the most innovative approach in the industry to clinical outcomes and data from patient-reported outcome measures. Our robust solution, for example, goes beyond simple data entry and allows a truly patient-centric research study. Our eCOA is based on behavioral science but it was also designed by clinicians in order to meet the needs of sites and sponsors. Personal identity, motivational intervals and meaningful goals. Datacubed's app is easy to use, unlike other eCOA systems. Participants can get straight to the essentials. Our intuitive, flexible and interactive app makes it easier than ever to collect data. We offer data collection in person, remotely or in combination for traditional, hybrid and virtual trials.

AI advances will eliminate the need for trial and error in medical practice. Our digital twins allow for confident and rapid clinical trials. We work in neurology, immunology and metabolic disease. TwinRCTs achieve full enrollment faster because they need fewer patients in order to achieve the same power of traditional trial designs. Enrollment time in late-stage trials can be shortened. TwinRCTs increase the power of early-stage studies without adding additional patients, allowing them to observe treatment effects. Early-stage studies can be used to make confident decisions and attract participants. TwinRCTs increase the chances of participants receiving experimental treatments because they use smaller controls groups. Position clinical trials using digital twins to achieve regulatory success. Unlearn engineers the future of medicine using artificial intelligence. We create and deploy new types generative models based on patient-level data.

Accelerating the development and delivery of life-saving medicines, and enabling cancer patients to have access to the best quality of cancer research and care. Our software revolutionizes patient access to innovative drugs & clinical trials. FICS is a software that allows the collection of regulatory standards data during patient care. FICS combines traditionally separate and noncommunicating applications to create a novel end-to-end platform. This allows clinical trials to be performed faster, easier and with greater quality.

DatStat's cloud-based platform puts patients at the centre, whether it is at the center for care or at the center for the next clinical trial. Our platform is helping clinicians, researchers, and patients connect like never before. Our cloud-based platform for patient engagement, which is used by today's most innovative and leading healthcare organizations, powers DatStat's clinical trials and clinical care solutions. The DatStat team works closely with customers to understand their specific needs. We will not hard-code your solution, but we will configure it. We can launch your project much faster than custom, paper-based, or hard-coded solutions. Patients are also involved in the process. This improves communication and helps to improve the outcomes of your team.

The Life Sciences industry has been subject to nearly $15 billion in compliance-related settlements and fines over the past few years. It is therefore critical that companies adhere to best practices in pharmaceutical, biotech, and medical device manufacturing. A well-managed clinical trial can have a significant impact on the development time, budget, and scope of a drug or medical device. OpenText™, Clinical Trial Quality Management System, (ctQMS) allows companies to remain compliant, reduce the cost of records management, and establish best practices through collaboration during, and after, the clinical trial.

Catchtrial is an online electronic solution that allows you to manage CRFs, images and other data with efficiency and speed. Catchtrial is simple, secure, and affordable. It has been used by both large and small businesses to manage international trials. Catchtrial replaces the paper-based process and allows for cost savings. To collect paper CRF, there will not be any need to visit sites. You can also upload images and capture them, so you don't need to ship CD roms. The study progress can be accessed from sponsors' offices, giving them full control. Catchtrial is unique in that it offers flexible personalizations and functionalities that make trial management easier than other eCRF options.