Clinical research organizations (CROs), big pharma, and biotech can all benefit from MainEDCTM. Its use of artificial intelligence (AI) simplifies even the most complex trials and studies. As an advanced eClinical Solution for EDC/ERT/eCOA, it drastically reduces the time it takes to launch clinical trials (by as much as 5 days), saves money (by as much as 80% for monitoring), and raises your company's market value and appeal (as indicated by 89% of clients).

The tools help boost the quality and efficacy of the research as real-time data collection from patients is possible with DatStat. As a result, tedious, error-prone manual processes are unnecessary. The DatStat cloud platform enables remote management of clinical trials and complies with 21 CFR Part 11 and HIPAA. This makes it possible for you to access your trial from any computer, anywhere in the world.

The tool helps in improving efficiency in terms of finances, regulatory applications, and overall clinical research operations in any business. It gives you the ability to go above and beyond the constraints of standard procedures for conducting clinical trials. This clinical trial software is essential to maintaining a rigorous and transparent procedure as trials become more sophisticated and increasingly worldwide.

With Encapsia, you're no longer constrained by the location of your study's participants, opening up opportunities to boost productivity. The platform lighten patients' load, and forge stronger bonds between researchers and their patients. It contributes to higher patient retention rates. When used in combination with eSource DDC, Encapsia's seamless integration with features like eConsent and IRT services, can yield significant time and money savings.

It allows research professionals quicker access to real-time data, which improves their ability to monitor patient recruitment and keep tabs on the status of their studies in real-time. EDGE's collaborative features and structure fully encourage data exchange and do away with redundant efforts. Better care and faster treatment may be provided to patients thanks to EDGE's improved efficiency, which also improves the quality of research data.

All documents pertaining to study participants and researchers can be stored in an accessible and secure location. As a result, you may tailor your processes to the specifics of your research and the requirements of your site. In addition, features like audit trails, user permissions, version control, etc., that automate compliance, are included into the programme.

They are able to cater to the needs of any client because their staff is both diverse and cohesive. Dacima Clinical Suite is cutting-edge software for managing clinical trials. It combines a CDMS with a CTMS and an EDC with a centralised database. When it comes to administering clinical trials, Dacima Clinical Suite has you covered. It also gives you the option of building your own bespoke databases to meet your specific requirements.

Ripple helps teams work together by providing a centralised location for members to discuss and share their research. Players' success is communicated to team members via email, which is updated often. Ripple is a front-end patient journey-focused programme that extends the functionality of your CTMS. Even though Ripple shares many similarities with a CTMS, the way it operates is somewhat different.

The software allows companies to fully automate the research request process and the associated portfolio management responsibilities. Financial management, electronic document and data management, and customised workflows are just some of the many benefits it offers. Compatible with Research Manager's Electronic Data Capture and Ethical Review Management System.

Its ability to track protocol deviations and alert you to those made by users or the system is priceless. As part of this process, they keep track of the actions taken to correct their path and enhance their operations. They use automated technologies to solve any problems that arise. CTMS Master's robust capabilities in the realm of financial management allow for simplification of budgeting, payment, and approval processes.

By syncing with the Electronic Trial Master File (eTMF), this CTMS software provides enterprises with a specific CTMS platform that includes all the bells and whistles necessary for more effective efficiency, accuracy, and security when combining clinical data. Experts in clinical trial management make sure that their evidence generation tools are grounded in the latest research in therapeutic areas and endpoints.

For researchers and biostatisticians faced with rising trial complexity, escalating costs, and fluid rules, it is a great tool. nQuery is web-based software for a trial design that supports Classical and Bayesian statistical approaches, adaptive trials, and trial prediction. It can be used by clinical research organisations in academia and industry. The robust features and utilities available on the platform, such as automatic sample size computation, were designed to facilitate the optimization

The tool helps to automate their central business operations and document management tasks. Managing the massive amount of data, artefacts, and documents that make up a full TMF is a challenging and error-prone task that is accomplished by MasterControl. When it comes to keeping up with the ever-changing needs of clinical trials, the MasterControl CTMS Software is an excellent resource. Researchers and patients can collaborate in a setting that encourages the free flow of information.

The company's Virtual Data Capture technology developed by the firm is used in conducting clinical trials remotely. Some examples of these components are the electronic patient record, electronic informed consent, electronic clinical outcomes assessment, and electronic source. And because it's built on a modular framework, it's easily adjusted to meet the needs of a particular study, institution, or group. ClinCapture is a complete Clinical Trial Management Software for SMEs, Enterprises.

Medrio provides electronic data capture (EDC), electronic patient-reported outcomes (ePRO), electronic consent, direct data capture (DDC), real-time safety monitoring (RTSM), and the ability to conduct decentralised clinical trials. The three main products from Medrio, an enterprise data management software vendor, are all geared toward the healthcare and medical industries. It offers a wide range of eClinical solutions, including on-premise EDC and CloudEDC, to a large customer base.

With the platform's automated recruitment options, assembling your panel is a breeze. The use of ARCS's tailored screening tools allows for the identification of the most suitable study volunteers. In addition to streamlining the scheduling process, this platform frees up staff time by allowing study participants to establish their own schedules based on their preferences and availability.

When using LifeSphere CTMS, you'll have a much easier time monitoring the current status of your study in real time. It streamlines the study-running process and gives CROs insight into how each site's paperwork is being handled. It's helpful for scheduling subsequent appointments and maintaining tabs on previous ones. LifeSphere CTMS facilitates on-site audits and enhances workflow management. If your organisation works in the life sciences, you need LifeSphere CTMS.

Electronic permission forms and participant report forms are two examples of how this software aims to streamline the research participant experience. This software solution features DCT modules that can be helpful for businesses who have not yet implemented decentralised research or are in the midst of performing hybrid clinical trials, in addition to its comprehensive Electronic Data Capture (EDC) system. Castor EDC is a protected EDC platform for managing clinical trials and studies.

VISION was created by Prelude Dynamics, as a world-renowned provider of eClinical solutions and services, and it can be utilised in clinical trials. Subject-level dispensing is interfaced with site-level inventory management and tracking. Reordering happens automatically such that IVP/CP is always on hand. As tasks are completed on sites or as monitors verify completion, the technology automatically adds costs to invoices. It keeps track of which versions of files are downloaded and how often.