Clinical trial tool that enables leveraging of family health history through risk assessment and diagnosis.

Electronic data capture platform that provides the recording of patient-reported outcome data through a centralized database.

IQVIA (NYSE:IQV) is a leading global provider of information, innovative technology solutions and contract research services dedicated to using analytics and science to help healthcare stakeholders find better solutions for their patients. Formed through the merger of IMS Health and Quintiles, IQVIA has approximately 58,000 employees worldwide employees worldwide.

IBM Clinical Development from Watson Health is a global SaaS solution that can help the life-sciences transform clinical research and may accelerate the delivery of needed therapies to patients. With a powerful electronic data capture (EDC) system at its core, IBM Clinical Development affords clinical researchers access to hidden insights and visibility into their trial data. Scalable in both feature and function, we offer a robust suite capabilities that can be tailored to all clinical trials.

Clinical Ink, a global clinical technology company, offers data certainty from source to submission. Our Lunexis eSource clinical technology and configurable direct data capture, eCOA, ePRO, and eConsent modules a suite of solutions for capturing and integrating electronic data from sites, clinicians, and patients at its source naturally enhance your clinical trial workflow by reducing manual labor, providing anytime, anywhere data access, and saving resources as your trials progress.

UNITY is a web-based platform that integrates the collection of clinical data, of patient-reported outcome measures and the AI-supported extraction of radiographic data into the clinical routine. With UNITY, the planning, monitoring and analysis of clinical trials or post-market monitoring studies can be performed in a cost-effective, transparent and efficient manner while involving all stakeholders via the same platform.

Clinical trial management software that allows businesses to reduce clinical trial time, improve accuracy, drive down costs, and more.

A comprehensive clinical research management system, OnCore® Enterprise Research supports centralized operations at academic medical centers, cancer centers, and health care systems. The OnCore system includes clinical research management, billing compliance, electronic data capture, biospecimen management, patient registries, and integrations for the research enterprise.

Easy to custom and to use, fully integrated with IVRS and DSM.

SimpleTrials is a Clinical Trial Management System for Sponsors, CROs and Sites. Plans start at $124/month with no long term commitment! SimpleTrials is a validated CTMS and eTMF, including features to support site and contact management, study startup, study planning, contracts and payments, subjects, monitoring and electronic visit reports. SimpleTrials is brought to you by Trial By Fire Solutions, the clinical software provider who has been focused on CTMS and eTMF since 2008.

For organizations engaged in conducting clinical trials, BioClinica CTMS clinical trial management software create a natural next step to bring Office tools, business process workflow, and documents into the regulated world.

User-friendly software designed for recording and analysing animal tracking within an IR actimeter.

Catchtrial is a simple, cloud-based platform for capturing clinical trial data and images. Accessible anytime, anywhere, Catchtrial puts key information at your fingertips, resulting in shorter response times, improved compliance, and reduced costs.

Clinical data management system with streamlined study creation approach and detailed reporting.

Agile Health Computing's application, MAISi, is a user-friendly and sophisticated Clinical Trial Management System designed to answer the management needs of clinical research sites. By collecting and monitoring research sites clinical trial business metrics, MAISi facilitates better protocol implementation and better time and financial management which is essential in this competitive international market.

MedSciNet is a Stockholm based company specialising in design and development of web applications and on-line database systems for clinical trials and studies, quality registries, medical bio-banks, and other solutions within the medical field. MedSciNet has offices in London (UK), Vilnius (Lithuania), Stockholm (Sweden) and Cork (Ireland).

Data MATRIX is a company providing full-service data management services based on the in-house developed EDC/IWRS software. Our EDC/IWRS has been used in more than 150 international trials and data were successfully submitted to EMA and FDA. Our user-friendly software are fully validated and meet all the industry standards (CDISC, 21 CFR Part 11).

secuTrial is a powerful, web-based software solution for clinical trials. Full GCP and FDA 21 CFR Part 11 compliance all is ensured while guaranteeing the highest quality standards. secuTrial offers a high degree of conceptual freedom with regard to study design, flexibility and user friendliness. It can therefore be used in a variety of ways for all clinical trial phases, such as clinical trials for licensing approval or phase IV studies.

myClin provides you with the best documented, data-driven clinical trial oversight. It lets your clinical study team collaborate and communicate accessing training, distributing essential documents and tracking study milestones in a central, secure, and private environment.

Designed and developed with the latest technologies Clinicubes CTMS is a robust cloud-based Software as a Service (SaaS) platform for managing clinical trials. Its unique architecture based on a modular system makes it 100% customizable. This ensures you can select the modules you need and remove the ones you do not in order to optimize your workflows, speed up procedures and space unnecessary expenses.

Phoenix CTMS is a modern web application combining capabilities of database software used in clinical research in one modular system: PRS (Patient Recruitment System), CTMS (Clinical Trial Management System), CDMS (Clinical Data Management System). This unmatched feature set is geared to support all operational and regulatory requirements of the clinical front end in academic research, at CROs (Contract Research Organisations) and hospitals conducting clinical studies of any phase.

QMENTA Reader handles and streamlines the medical imaging workflow in clinical trials, ensuring quality and success all over the trial: - Create your personalized imaging workflow with our experts - Upload, anonymize and classify large amounts of data from multiple sites within seconds - Use AI & data to accurately select patients based on imaging endpoints - Create collaboration teams located in multiple spaces - Ensure quality of data and analysis anytime in the workflow with automated QC

eTMF Connect helps life sciences companies better manage their clinical trial documentation. Designed using the TMF Reference Model, eTMF Connect centralizes and standardizes your essential documents, enabling sponsors and CROs to contribute and access important clinical records and information in real-time. The solution's clinical eTMF functionality, advanced collaboration features including inspector view, and scalability, create a dynamic, intuitive, and powerful experience for users.

Data management software for clinical trials that is based on GCP and regulatory compliance, user friendliness, and affordability.

Cloud-based platform that enables clinical research professionals to manage study data, prepare reports and design workflows.

Study management for post-approval research and registries conducted by bio pharmaceutical companies, and research organizations.

Cloud-based solution that allows life science companies to manage clinical trial process providing clinical trial activities planning, tracking and control.

Comprehensive SAS based clinical data management, EDC, and clinical trials reporting system

Entrypoint is a complete web-based system for creating, deploying, and administering custom data entry applications, providing data entry access anywhere you are. Entrypoint architecture relies on a modular plug-in framework for maximum flexibility. The product consists of a web application for data entry and administration and three Desktop applications: Application Studio, Desktop Workstation and Desktop System Manager. All desktop applications communicate with the server.

A web-based data management solution that can be used for recruiting patients and managing all aspects of data associated with clinical research.

A comprehensive clinical research management information system.

Electronic pen and paper technology for clinical research / CRO.

Bring order to the complex world of human studies. Phase out disjointed legacy applications and paper-based processes and replace them with a single, browser-based application that facilitates collaboration between the research personnel that support the various aspects of a trial. Features include online trial design tool, eCRF builder, participant management, robust trial financials, automated event based billing, and a single point of reference for industry and investigator-initiated trials.

Dedicated to provide leading edge solutions and equipment purpose designed for clinical trial materials packaging.

TrialPoint modules are intuitive, flexible and powerful tools to manage all aspects of clinical trial lifecycle

Clindex is a state of the art product that offers integrated clinical data management, trial management and EDC functions in a single easy to use package. Offered both as web hosted or self-hosted Clindex is one of the most flexible and complete clinical solutions on the market!

Multi-channel acquisition software with programmable experiment control and automation with lock-In amplifier and photometry extension.

Clinical Research Organization with extensive experience in conducting Clinical Trials.

Cognitive assessment and neurotechnology products accelerating clinical development from proof of concept to post-marketing. We are the leading providers of validated touchscreen cognitive tests for clinical trials developing medicines that are safe and effective in the human brain.

Octalsoft Clinical Trails Management System provides a single, centralized system to manage sponsor and CRO study management activities.

Comprehensive and secure randomization software for clinical trials run entirely on the Internet. Features include accrual reports, verification of entry criteria, multiple treatment arms, stratification. random block sizes. email confirmations, optional collection subject data

Regulatory Management System that manages and monitors the regulatory side of a clinical trial.

Clinical data management solution with data queries generation, audit trails, electronic signatures, and data reconciliation tools.

SyMetric C6 - IWRS is unique in addressing the most diverse and demanding customer scenarios and web experiences, regardless of complexity, scale and duration of a study. With SyMetric C6 - IWRS you no longer have to worry about paying for expensive infrastructure. All our products and services are hosted on our virtual servers and are made available 24x7. Fully validated, 21 CFR Part 11 compliant System that allows you to automate many aspects of the trials with added flexibility.

Set of modules that help all stakeholders effectively manage all areas of clinical and research management.

i-CDMS is an innovative cloud based system offering a complete set of features for streamlining trial monitoring and data entry with e-CRF, automated edit checks and queries resolution, patient and site reporting, real time notifications and reminders and others that are accessible from all trial participants according to their roles. i-CDMS has been built with the latest technology tools and state of art user interface consisting a fully qualified EDC for supporting clinical trials

Cronos provides end-to-end e-clinical solutions, for clinical trials, BA-BE studies, Screening and volunteer management. It has complete solution starting from subject registration till report compilation. Cronos is fully compliant to the guidelines of 21 CFR part 11 and other regulatory authorities. Customization is possible in the system as per the organization's requirements. All the modules of the system can run as a standalone and can also run on a integrated platform.

MasterControl Inc. produces software solutions that enable regulated companies to get their products to market faster, while reducing overall costs and increasing internal efficiency. MasterControl securely manages a company's critical information throughout the entire product lifecycle. Learn why over 1000 companies have chosen MasterControl to automate their CAPA, document control, change control, training, audit management, and other quality management and regulatory processes.

Cloud based solution for clinical trial leaders. Features include digital enrollment, engagement of participants, and reporting.

Electronic Data Capture (EDC) solution streamlines the initiation and management of clinical trials.