Clinical Trial Management Software
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by IBM Watson Health
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. Learn more about IBM Clinical Development
A mobile-friendly, electronic data capture system for clinical trials, built by researchers, for researchers. Features include self service eCRF creation (form building), randomization, ePro (patient surveys), monitoring, easy import and export of data, EHR data importer (HL7 FHIR based), audit trails, user management, and much more. We are fully ISO 27001 certified, GCP & 21 CFR compliant and provide servers in US (HIPAA compliant), UK, NL, DE. Learn more about Castor EDC
Clinical Conductor CTMS is the clinical trial management system (CTMS) designed for research sites, hospitals, AMCs, site networks, health systems & CROs. Clinical Conductor CTMS allows organizations conducting clinical research to be more efficient and profitable. Clinical Conductor CTMS is the market-leading application, making the trial process easier and allow organizations to make better business decisions and meet every challenge. Learn more about Clinical Conductor CTMS
Protocols are complex. Getting data shouldn't be. With a collaborative, drag-and-drop study designer for you and mobile-friendly forms for your sites and subjects, OpenClinica is more than just data capture. It's a better experience. The result? Higher quality data for your study, at a low cost that makes budgeting easy, too. With every deployment: secure, high-performance cloud hosting on AWS | Documented validation | FDA, EMA, GDPR and HIPAA compliance Learn more about OpenClinica
Medrio provides efficient and easy-to-use Electronic Data Capture (EDC) solutions, including a suite of eSource-equipped products, for clinical trials. Our software is fully hosted in the cloud, requires no programming, and costs 75% less than traditional EDC solutions. Since our founding, some of the top pharmaceutical companies, medical device companies, and CROs in the industry have used our 21 CFR Part 11 compliant system to drastically reduce their study build time. Learn more about Medrio
Longboats clinical trial support platform creates an environment where protocol compliance is instinctive, teams are virtually guided at all times and all stakeholders have the knowledge and resources they need to conduct the trial. Clinical operations, monitors, site staff, and patients access the one integrated and consistent support platform. Depending on the users role in the study the interface, and support provided, adjusts to meet their specific needs. Learn more about Longboat
Ethical eAdjudication for Clinical Endpoint Adjudication is a GxP managed Software Service based on a Cloud Platform designed to support Study Leaders, Committee Members and the Q.A. Staff across the central review & adjudication of subjective endpoints. It provides the right tools/services to accomplish the Independent Review & Adjudication procedures in a timely, effective and quality controlled way. Learn more about eAdjudication
RealTime-CTMS is the leading clinical trial management system designed to increase efficiency and profitability for research sites and site networks. With fully-integrated services such as RealTime-TEXT, RealTime-PAY and the first fully-integrated eRegulatory document management system, RealTime-eDOCS, RealTime Software Solutions, LLC has the complete package of tools to help sites excel. No other CTMS can do all that RealTime does! Learn more about RealTime-CTMS
ClinPlus CTMS & eTMF is the core clinical trial data tracking of the ClinPlus suite offering EDC, IWRS in a unified platform, utilizing a single sign-in and a role-based tailored user interface for all functionality. ClinPlus CTMS provides end to end study start up to close out monitoring visit reports, easy navigation for quick, affordable seamless unification to avoid integration costs, and document management for all types of clinical trials delivered in 6 weeks via a secure, private cloud. Learn more about Clinical Trials Management
by Crucial Data Solutions
Clinical Studio is a true cloud-based SaaS (Software-as-a-Service) product comprised of purpose-built software that transforms clinical research, enabling companies to efficiently complete trials on a 21 CFR Part 11 compliant system. Clinical Studio redefines clinical research software by leveraging integrated software and native mobile apps to streamline the design, deployment, and management of clinical studies. Learn more about Clinical Studio
by Dacima Software
Flexible, user-friendly, web-based electronic data capture (EDC) and data management system for clinical trials, epidemiological research, web randomization (IWRS), patient registries, ePRO and web surveys. Our software provides the most easy to use and intuitive interface on the market with features and design options not available in other software products. Learn more about Dacima Clinical Suite
Story by PulsePoint makes content marketing more efficient, more effective and more trackable. We extend your targeted reach across premium social, native, and content discovery channels. Our platform optimizes to your KPIs to maximize engagement and deliver clear ROI. How it works: Upload your content via URL and create multiple headline/image variants for each channel seamlessly, choose your channels you want to advertise on. Story optimizes towards KPIs. Learn more about Story
Pristima is a fully integrated enterprise solution for preclinical data management that delivers complete life cycle automation and support for Pharmacology and Drug Safety Research Study Management, Vivarium Management, and Veterinary Care. From breeding and ordering through the study submission process, the Pristima Suite manages the planning and recording of data, controls authorized changes, and assembles the data for submission to regulatory agencies.
by Sarjen System
BizNET, A clinical trials management software offers an integrated suite of software products for CROs, Pharmaceutical, Biotech Industries and Medical device industries. Our solution blends various integrated modules that prominently support clinical trial activities like EDC/DDC data collection, IWRS & drug randomization management, CDISC SDTM. It is a validated software, compliant with 21 CFR part 11 and GCP guidelines which provide a transparent and smooth process to regulatory
by Cambridge Cognition
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.
by Clinical Systems
Delve is a cloud based solution providing a search engine allowing users to look at data across multiple streams identifying what they need. The most popular use cases that our clients have used Delve for are: 1. Automating Literature Review. 2. Pre-qualify Investigators and Sites based on the work they have done in regards to Clinical Trials and publications conducted. 3. Gather insights in regards to the different trials conducted, where they happened and so forth.
by Forte Research Systems
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.
Manage documents, signatures and deadlines with ease. Securely share documents anywhere, anytime. RDMS features trial and document management dashboards, electronic 21 CFR Part 11 compliant signature capture, dynamic data updates, automatic form population, deadline triggers, and change history. Flexible and scalable, VACAVA solutions are delivered via the cloud so you never have to worry about technology details.
by Abbott Informatics
STARLIMS Clinical Research solution grows as your labs needs evolve, providing unrivaled flexibility and support of user-configurable workflows for a wide range of research projects, clinical trials, and laboratory processes. Feel confident in your ability to meet changing investigator needs and increasingly stringent regulations, all while providing accurate research results.
by Agile Health Computing
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.
by DF/Net Research
Since 1992, DataFax has been in use by CROs, Pharmaceuticals/Medical Device companies, and Global Health Organizations for the past 23 years. DataFax is an EDC system with a hybrid approach that allows our user the flexibility of designing a study/trial by EDC, paper, or both. We provide a cloud/hosted solution or clients can host the database in-house. Users will have the option of selecting from a single study fee structure or a full license, which will allow 100 plus studies.
by Elashoff Consulting
Patient Profiles is software that reads clinical trial datasets and creates individual reports (PDF, Word, HTML) for each patient. It provides both easy access to the most common tasks - reading data and creating standard profiles, for example, as well as the flexibility to adapt to the specifics of each trial and set of datasets - changing data types and formats, deriving new variables, and transposing long, skinny data structures. Perfect for clinical data managers. 30-day demo available.
by Almac Clinical Technologies
iDiary is ideal for a wide range studies from low to high complexity, providing sponsors with flexibility to capture patient information from early clinical development through commercialization (phase IV and health outcomes 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.
Robust, flexible, SaaS-based Clinical Trial Management Solution (CTMS) delivered to Sponsors or CROs. Functionality includes: * Project Management * Supplies * CRF and DCF Tracking * Sponsor and Investigator Portal * Clinical Payments * Timesheet & expenses * Monitoring reports * SAE tracking * Offline Client
EasyTrial is an online Clinical Trial Management System for handling and administration of all tasks (operational and logistical) in clinical studies, so healthcare professionals can use their time efficiently. The system has been developed by Danish doctors experienced in conducting clinical trials. EasyTrial is compliant with Good Clinical Practice (GCP) and legislation applicable to database security and it provides maximum security, study overview and resource handling.
by Forte Research Systems
Allegro CTMS is a cloud-based clinical trial management system that efficiently manages the operational data of clinical trials for dedicated research sites, physician practices, and community hospitals. Its superior usability, coupled with the right amount of functionality is what makes Allegro CTMS the ideal system for sites who wish to gain better visibility and control of their studies, while pursuing clinical research operations excellence.
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).
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.
by Phoenix Software International
Entrypoint i4 is a complete web-based system for creating, deploying, and administering custom data entry applications, providing data entry access anywhere you are. Entrypoint i4 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.
by BSI Business Systems Integration AG
Our CTMS software is easy to operate, thereby saving you time and costs. The software adapts to your requirements, and not the other way around. BSI CTMS seamlessly integrates into your system environment, interfacing all necessary peripheral systems as a cloud or on-premise solution. This makes BSI CTMS the central hub for all aspects of your clinical trials.
by Progeny Software
Progeny Clinical simplifies the process of managing pedigree and family history data, used by genetic counselors, clinicians and research institutions worldwide. Use online family history questionnaires to collect patient data before the clinic visit. Assess risk for hereditary cancers, order/track genetic testing and results, run custom reports, generate patient letters, integrate with your EMR and much more. Plans include pre-configured free version to fully customizable premium options.
by Study Manager
Since 1993, Seattle-based StudyManager has been an industry-leading provider of Clinical Trial Management Software (CTMS) solutions to organizations who conduct clinical trial research. StudyManager Reveal, our Site CTMS solution, helps Sites and Hospitals organize and centralize clinical research through groundbreaking ease-of-use, power, and flexibility.
by InfoEd International
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.
by Axiom Real-Time Metrics
Axiom Real-Time Metrics, is a leading eClinical technology and data management services provider offering cost-effective, unified EDC/DM tools focused around the unique needs and budgets of small-to-mid size device and biotech companies, CROs, Universities and Institutions. Axiom is unique to the marketplace in that we offer more functionality and tools in one easy-to-use unified platform, at a cost-competitive price, than any other EDC provider in the space.
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.
by Flex Databases
Flex Databases is a company providing e-solutions for clinical trials. We offer a unique platform which allows combining traditional features related to management of clinical trials (CTMS, EDC&IWRS) with the functionality for running internal pharma companies and CRO processes as well as a capability to manage financial data, invoicing and expenses. All modules developed by Flex Databases are validated and 21 CFR Part 11 compliant.
by MedNet Solutions
iMedNet eClinical delivers an innovative, cost-effective, and easy-to-use technology platform that allows non-technical research personnel to quickly build their own clinical studies...in just a matter of days, not months. And iMedNet's low Software-as-a-Service (SaaS) pricing makes it affordable for ALL study types. iMedNet eclininical has been built from the ground up based on MedNet Solution's proven, decade-long experience developing practical eClinical solutions for sponsors and CROs.
The premier EDC clinical trial software, eCaseLink combines novel technology and unmatched industry experience to help reduce clinical trial time, improve accuracy, drive down costs/improve ROI, prevent risk, and use clinical trial data more effectively. The most successful clinical trials begin and end with the highest quality, clean data. Data that is collected in the most streamlined and efficient way possible. An EDC system is a computerized system designed for t
by BioPharm Systems
Siebel Clinical Trial Management System accelerator designed to help life sciences organizations manage all aspects of clinical trials efficiently and effectively.
The DATATRAK ONE Unified Experience removes clinical research complexities, accelerating the ultimate outcome of every trial. The inherent strength of DATATRAK solutions is the intrinsic connection to the DATATRAK ONE platform, with all products powered by a single data source, providing unsurpassed system reliability, eliminating integration and downtime, and delivering an unsurpassed easy-to-use interface. These attributes deliver better site compliance, better data, and a safer trial.
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.
OpenText Clinicals is designed to manage the capture and review of all trial-related information throughout the setup, conduct and review of clinical trials. It is a highly scalable platform that is already being used by some of the largest pharmaceutical companies and clinical research organizations (CROs) to manage their multiple, global clinical trials, as well as by smaller biotechnology companies and academic research centers.
by Catalyst eClinical
Catalyst is a secure, cloud based Clinical Trials Management solution that enables clinical researchers to increase engagement with study participants while minimizing time spent managing bloated technology. Built with simplicity in mind, Catalyst can either be used as a standalone solution or it can easily integrate with other systems allowing researchers to continue using complimentary web based software they value.
by Blue Sky eLearn
Designed specifically for the communication needs and compliance requirements of life sciences and research facilities, Path Clinical reduces costs and maximizes efficiency by quickly connecting trial investigators in any location to improve retention and increase compliance.
A clinical trials electronic data capture application available both as a mobile app and via the internet, quickly set up for your needs. Quick to set up for your specific needs with many features. Able to store supporting documents, images, audio and video. Can upload existing CRFs or data collection templates or start from scratch. Free and non-obligation custom configuration and trial available - just contact us for details.
by Intrinsic Clinical Systems
Are you tired of using a CTMS that is overcomplicated, has a poor user interface and costs way too much money? At Intrinsic, we solved these problems by developing an easy to use practical CTMS that is cloud based. Intrinsic has 4 key clinical software productsCTMS, eTMF, study portals, and investigator portalsthat help pharma companies more easily manage their trials and CROs. Each module can be purchased separately, or users can enjoy the benefits of an integrated suite of clinical systems.
Data+ is a revolutionary data management solution for clinical research. We deliver an all-in-one solution for research organizations - connecting the organization, researchers, and patients together. Our focus is on insights - to improve care, team and time management, and patient engagement as well as compliance using informative feedback.
by Clinical Research IO
An intuitive eSource, lab routing, and CTMS solution for research sites. Using CRIO, sites can save favorite procedures; build own source templates; capture source data quickly and accurately; mark up labs; and share visits with their monitors for review. Recruiting helps manage patients and campaigns, and enables one-click calling and texting. Finances calculates receivables and invoiceables as the visits are being completed. We are a premium service at an affordable price.
by Target Health
Target Health eSource EDC is aimed at helping organizations of all sizes with all their clinical trials software needs. As "Champions of the Paperless Clinical Trial", our patented eSource EDC software suite goes beyond direct data entry and electronic data capture (EDC), to include a clinical trial management system (CTMS), eInformed Consent, ePRO (patient reported outcomes), and includes integrated RBM reports. Backed by a CRO, we are the one-stop-shop for your EDC needs.
by Clinic Software
Awarded The Most Innovative Fully Comprehensive Software Solution for Clinics, Salons and Spas! Clinic Software .com gives your entire company a 360-degree view of your customers, appointments and facilitates collaboration across your organization, helping you build strong customer relationships to run and grow your business. Grow Sales. Save Time. Get Organized. Start today! Businesses of all sizes succeed with ClinicSoftware .com Advanced Features. Everything you need, all in one place.
by Novatek International
Clinical Assay Management Software is a unique system that provides a consistent approach to the collection, management, and integrity of all clinical research study data. Along with including a full documentation management solution, the Clinical Assay Management Software tracks and manages all data generated and ensures a single verifiable version for all clinical and analytical data sets.
by Medical University of Graz
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.
by Fortress Medical Systems
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!
by Lormarc Development Group
Clinical trial management software has never been easier to use. Clinical Trial Administrator (CTA) is clinical trial management software that assists clinical research sites conducting research studies. It is also 21 CFR Part 11 compliant. If you are trying to manage a study, patients, recruitment, or finances, CTA helps you get it done. Clinical Trial Administrator assists you in making well-informed decisions. Think of it as your decision-making assistant.
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
by SyMetric Systems
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.
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
by Data MATRIX
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).
by Prelude Dynamics
Prelude Dynamics helps companies focusing in the Pharmaceutical, Biotechnology, Medical Device, and Academia focusing on Human & Animal Health industries to streamline and accelerate their clinical development pipelines with a cost-effective and flexible study EDC/CTMS solutions. [8:55] VISION simplifies, standardizes, and automates the collection and cleaning of data for clinical trials, in near real-
by Ripple Science
Ripple is a web-based recruitment-focused patient and study management tool for clinical and translational studies. Ripple provides clinical sites with a centralized software to manage all aspects of recruitment and post-enrollment tracking of patients in clinical trials. Ripple helps clinical trial sites enroll more patients, increase retention, simplify reporting, and automate tasks in order to provide an excellent, patient-centered experience to trial participants.
by INTUIT Micro Technology
Software made with an objective. Using technology we wanted to provide better care for patients and increase the revenue of the service providers. We started looking for products do just that. Since we couldn't find one, we made SimplexHIMES. SimplexHIMES is a cloud-enabled Clinic management software that is highly configurable to suit any type of customer. The regional plugin provides local requirements and regulatory needs of any region. Enterprise level product that can scale up on demand.