Teckro Alternatives

OpenClinica is a premier provider of clinical data management software solutions. Offering powerful tools for efficient, compliant clinical trials, OpenClinica helps maximize the security, reliability, and compliance of every clinical research. Core products include OpenClinica Enterprise, OpenClinica Participate (helps capture data directly from study participants), and OpenClinica Randomize.

Longboat is a cloud-based clinical trial support solution provides users with an integrated Guided Compliance toolset to guide them at all times. Longboat provides the clinical trial site staff with the right resources to let them focus on patients. Longboat allows patients to view essential study information and check visit reminders. Longboat allows users to seamlessly manage the controlled rollout of the amended clinical trial protocol. Centralize the secure exchange of regulated documents between sponsors, CROs, and sites, significantly streamlining study startup and eliminating historically cumbersome processes across research stakeholders. All key stakeholders—clinical operations, monitors, site staff, and participants—access one integrated support platform with content tailored to meet their specific needs. Provide your site staff the tools and resources they need to stay engaged and compliant while focusing on the participant.

Ripple is a web-based software solution and active registry that facilitates the recruitment and management of research participants for clinical, translational and social science studies. Built from the ground up by researchers for researchers to truly transform participant workflow, Ripple is an end-to-end research participant management software that accelerates the entire research life cycle. Applying technology to solve patient recruitment and retention challenges, the #1 reason cited when clinical trials fail. The success of clinical trials and translational studies greatly depends on the ability of research teams to meet enrollment targets on time and on budget. Ripple Recruit empowers research teams with the automation tools and analytics necessary to accelerate the recruitment processes and maximize the likelihood of study success. Ripple Recruit provides critical insights into your recruitment campaign and workflows, including what sources are most effective.

Until now, the options available for managing clinical trials at an investigator site were either keeping multiple shared spreadsheets or buying expensive software unsuited to Australian conditions. MAISi is the game-changer. Beginning as a repository for clinical trials data at a major hospital in 2001, MAISi has evolved into a sophisticated workflow application to assist in most aspects of a research unit’s operations. MAISi acts as a central repository of data to store information about studies and the business units that run them. The datasets are arranged to support management decision-making. Staff in each business unit have access to the data (Studies, Patients, Investigators, Study Team Members) associated with their own business unit, whereas staff granted global access (normally Financial Officers and System Administrators) have access to all data.

Compared to other EDC solutions on the market from MediData, DataTrack, Omnicomm and others, TrialStat is the most all-encompassing suite of study management tools that can be seamlessly connected to external data sources such as EMR, wearables, and other clinical and non-clinical data and information sources. TrialStat offers a fully unified platform suitable for all phases and types of trials. Our single-sign-on, multi-tenant EDC suite includes modules for Randomization, Adjudication, Coding, Safety, Patient Diaries/ePRO, Vendor Neutral Imaging Archive, a robust Reporting and Analytics Portal and custom Machine Learning programs. With a focus on data analytics, TrialStat offers real-time reporting, data extracts on demand, and analytics across a single study, a program, or your entire research portfolio – providing all stakeholders relevant, customized, timely insight into all aspects of study data and highlighting areas of risk or potential delays.

In no other country in Europe is more research done than in Germany. Over 600 clinical and non-clinical studies are conducted annually. As is true of any study, it is becoming increasingly complex to conduct and manage. You know that: Appointments and employees have to be coordinated, study data have to be brought up to date and documents always have to be at hand for queries. Declare war on the paper economy and exchange heavy files for a handy tablet, find information in seconds with just one click and use your valuable time for what really counts: your research. The digital study management from studioMED+ will help you with this. No matter when, no matter where: With studioMED+ you get a flexible tool that adapts optimally to your requirements.

CSAM Studies (previously MedSciNet Studies) is a secure, highly customizable online environment with a 20-year track record of successfully hosting clinical studies and trials of all scopes and sizes. A web-based platform for medical research, Studies offers a sophisticated online application package for hosting, maintaining, and monitoring projects of every size and complexity. CSAM MedSciNet’s standard Studies solution features the complete set of components required for setting up a fully functional study or clinical trial. The benchmark solution provides support for rich and interactive data entry forms and flexible workflow structures, as well as advanced data validation, analysis, and exporting capabilities.

Mosio enables research teams to improve subject adherence, communications, and data collection on mobile’s most popular channel: text messaging. Our software makes research teams more efficient in how they communicate with study participants through messaging automation and interactive elements delivered to participant mobile phones. WHO WE HELP: + Clinical Trial Sponsors (Pharma and Biotech) + Cancer Centers and Clinical Research Organizations + NIH-Funded Studies + Public Health Agencies + Clinical Trial Managers, Clinical Operations Managers/Directors, Clinical Project Managers, Principal Investigators, Clinical Research (Study) Coordinators, and any research staff who communicate regularly with study participants. BENEFITS: + Interactive dosing reminders and medication adherence alerts. + Automate data collection. + Increase engagement and adherence. + Fix your no-show problem with SMS appointment reminders. + Improve retention with automated check-ins.

Founded in 2010, Crucial Data Solutions (CDS) provides the most innovative low-code/no-code data and clinical trial management technology on the market today. TrialKit, our cloud-based platform available via both a web and native mobile app, enables end-to-end clinical trial management for medical device, diagnostics, digital therapeutics, and biopharm companies of all sizes. Design and deploy validated studies in days not weeks using our intuitive study builder that requires no programming. Thousands of global users have leveraged the flexibility of TrialKit to deploy over 8,000 studies across all phases of development, including Verily (a subsidiary of Alphabet), ICON, Catalyst Clinical Research, SISCAPA Assay Technologies, CDx Diagnostics, and Optinose, and many more.

Clinical Conductor CTMS is a cutting-edge clinical trial management system (CTMS) designed for hospitals, research sites, asset management companies, site networks, health systems, and contract research organizations (CROs). This cloud-based solution helps make the clinical trial process more efficient, thereby helping research organizations make better business decisions and meet every challenge. Key features include electronic data capture, study planning, enrollment management, document management, recruiting management, and more.

The Medidata Clinical Cloud is our cutting-edge platform that transforms the clinical trial experience for patients, sponsors, CROs, and research sites. As the only unified technology platform dedicated to clinical research, the Medidata clinical cloud addresses the holistic research process from start to finish. Our platform helps life science and medical device organizations cut development costs, mitigate risks, and deliver treatments and devices to market faster. No matter which products you choose for your clinical trial program, you will have access to the power of the Medidata Clinical Cloud. At Medidata, we’re leading the digital transformation of clinical research. Powered by artificial intelligence, machine learning and advanced analytics, our platform brings researchers, study managers, investigators, and patients together to accelerate research. Obtain regulatory-compliant, patient-friendly electronic informed consent for clinical trials.

Novatek’s Clinical Assay Management software is a unique information management application that provides a consistent approach to the collection, management and integrity of clinical research study data. Novatek’s Clinical Assay Management software tracks and manages all sample data throughout its whole analytical process and ensures a single verifiable version for all clinical and analytical data sets. Novatek’s Clinical Assay Management software `helps organizations manage their studies based on a particular product that is being developed. In addition, this application will give clinical studies the structure that is required to ensure all related steps are executed in a timely manner.

Flexible eCRF platform for non-commercial clinical trials, configurable to any clinical trial study protocol. Our eCRF solution was created on the basis of many years of experience of researchers and medical teams with whom we carried out research projects. The system is, above all, easy to use, user-friendly and extremely flexible. The prepared solution meets all the required quality standards, and thanks to the full control over the code, we can further develop and adapt it to the changing requirements of regulators and the clinical trials market.

Jeeva's patent-pending modular solution is designed from the ground up on the most powerful cloud platform with one login from any browser-enabled mobile device for remote patient screening, education, enrollment, electronic informed consent, bi-directional communications via video calling, telemedicine, SMS, email, and evidence generation including electronic patient-reported outcomes and clinical outcomes assessments, with a modern user experience. Delays in patient recruitment & retention are keeping them up at night. Generating enough evidence of safety and efficacy of investigational new medicines is critical to get timely approval from regulatory agencies. Whether you are a patient group setting up a registry or natural history study, or a biopharma sponsor of a clinical trial, or a long-term follow-up study for gene therapy, Jeeva can save you time, and money while improving user experience for study team and trial participants.

One Platform to Research, Document, and Collate your Clinical Data. Simplify your research data with the Nucleus platform. A single platform to store your study documentation, clinical datasets, submission data and compliant media. Nucleus Documents enables document management and version control for your quality documentation and media. Control, manage, and share company content with ease. Collate and control your electronic trial master file documents with ease using our centralized regulatory document management solution. Nucleus Coding enables dictionary term coding against both MedDRA and WHODrug dictionaries, either in our standalone application, or integrated into your data capture system.

OpenText™ Information Management solutions help life sciences organizations leverage insights from data and content to improve decision-making processes and accelerate product development. Integrate, manage, and securely exchange data across people, systems and things. Leverage information assets from R&D to commercialization. Freedom of choice with cloud-native software that can run anywhere. OpenText for life sciences accelerates the discovery process by extracting actionable insights that drive pipeline innovation. Capture and manage research papers into electronic lab notebooks with intelligent capture. Find insights with text mining. Extract knowledge trapped in the unstructured text contained in clinical trial reports, study protocols, clinical safety and efficiency findings. Find out how to intelligently analyze, classify and extract clinical trial documents to reduce the risk of costly stops and starts.

A simple and powerful CTMS for hospitals, site management organizations and small CROs with focus on budgeting, finance tracking and reporting. Clinicubes CTMS offers various types of useful special features that help companies successfully manage and conduct every aspect of the clinical trial. The centralized management of trial database provides the most actual information and allows better productivity. Aggregate, systematize and reorganize physicians and healthcare service institutions database. Collect, evaluate and analyze data from multiple studies and different locations on a single report. Provide with reporting options of how the trial is being carried out against pre-set criteria and targets. Communicate study performance data and other operational reports, through interactive dashboards.

Complion’s platform is the accepted standard built specifically for clinical researchers. Our solution ensures the highest level of compliance with the greatest efficiency and the least amount of work. Allowing you to focus on what really matters — advancing and improving patient outcomes. Whether you are a Research Site, Sponsor or CRO, our eReg solution can help you address any type of clinical trial challenge, now and in the future. Reduce costs, avoid redundancy, and increase staff productivity. Easily archive, get signatures and view files from anywhere or from any device. A built-in audit trail ensures accuracy and eliminates study conduct and patient safety risks. Our clients include leading cancer centers, medical centers, hospitals, and health systems, as well as multi-specialty practices and dedicated research sites.

Phoenix CTMS is a modern web application combining the capabilities of database software used in clinical research in one modular system. After years of collaborative development with trial sites at the Medical University of Graz, the Phoenix CTMS now becomes publicly available (LGPL 2.1). 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. want a CDMS that gives you unlimited Javascript form scripting support (server- and browserside). You need to deal with large eCRFs (electronic case report forms) want to try a serious open source alternative for eCRFs. Need to formulate complex ad-hoc database queries to list matching subject candidates using set operations. Conduct several trials in parallel and need to organize site staff and resources. Need a software to implement various processes for ICH GCP.

Clario CTMS is an intuitive end-to-end clinical trials management solution that brings control, efficiency for both data flow and workflow, and quality data to every study, yielding cost savings in time, labor and operational expenses. This web-based CTMS works on the go, letting you view and manage real-time operational performance — wherever and whenever. With the Microsoft Office-based work environment, Clario CTMS transforms a disjointed clinical trial into an efficient and cohesive work environment using the most widely used office productivity tools in the world. Bi-directional information exchange from Clario CTMS to SharePoint and other Microsoft products is seamless, making for a powerful, high-performance solution. Moreover, integrating Office processes with clinical operations can reduce back-office paperwork, significantly lower administrative overhead and result in low total cost of ownership.

RealTime-CTMS is a premier, cloud-based clinical trial management system (CTMS) purpose-built to boost efficiency and profitability for site networks and research sites. Comes with fully-integrated services that include RealTime-PAY, RealTime-TEXT, and RealTime-eDOCS (the first fully-integrated eRegulatory document management system), the solution promotes quicker and easier access to subject or study information using simple and intuitive navigation. RealTime-CTMS offers a host of other solutions that covers online document storage, appointment reminders, data collection, payment processing, among others.

Our Smart Protocol system aims to automate and add intelligence to clinical trial design with AI. Our Smart Protocol solution is revolutionizing the manual way research teams design clinical trials. In the digital age, humans cannot physically read and digest every bit of information relevant to a given decision. In addition, almost every company has valuable data that is not being used - more often than not, documents are living in repositories with no line of sight. As a result, companies life science companies are making important and costly decisions with incomplete information. We aim to take companies like yours from a document-driven environment into a data-driven one. We are reimagining how clinical trials are researched and planned by removing the barriers between data and end-users. We do this by mining massive amounts of trial-related documents from both customers and the public domain— so you don’t have to.

From sample size and power analysis to adaptive trial design, discover the nQuery difference today. The complete trial design platform to make clinical trials faster, less costly & more successful. See why nQuery is the #1 choice for researchers and Biostatisticians worldwide who need to tackle increasing trial complexity, spiraling costs and changing regulations. Calculate sample size for FDA/EMA submission. Fast spreadsheet-style interface with no coding required. Solutions for Frequentist and Fixed-term trials. Easy to use reporting for all trial stakeholders. Provide realistic estimates of expected timings and costs. Align your sample size with scientific & budgetary requirements. Fine-tune calculations with the specify multiple factors tool. 1000+ sample size and power calculation procedures. Rapidly calculate sample size for a multitude of scenarios

Data comes at you from all directions – EDC, EHR, smartphones, mobile devices, central laboratories. Prism assimilates data from these disparate sources and transmutes them into information and ultimately knowledge. Prism EDC combines ease-of-use with innovative features to provide a fresh solution for the collection and management of clinical trial data. Prism offers more that than form-based data collection, it aggregates and manages data from a myriad of data sources. Prism eSource is an innovative software solution that allows research teams to extract clinical trial information directly from a site’s electronic health record (EHR). This creates efficiencies and cost savings beyond the current paradigm where sites must enter the same data in multiple systems and accelerates the delivery of novel therapies to patients.

Healthcare solutions from VACAVA reduce the complexity and cost of clinical trial regulatory document management. Each time documents move through a manual workflow, it introduces the opportunity for delays and lost information. VACAVA solutions help you streamline regulatory processes by storing profiles, forms and documents in a single easy-to-access online location. Documents seamlessly move through your workflow with approvals captured electronically (21 CFR Part 11 compliant). Easy-to-read dashboards enable efficient management. VACAVA’s Regulatory Document Management System was built in collaboration with a major clinical trial research base to simplify operations and radically increase efficiency. VACAVA’s Regulatory Document Management System is surprisingly affordable and can be customized to meet your unique needs. VACAVA’s solutions are flexible, scalable, and delivered via the cloud so you never have to worry about managing servers, security, and backups.

Cloudbyz CTMS is a cloud-based trial management platform natively built on Salesforce Cloud. It is aimed at sponsors, clinical research organizations (CRO), and clinical sites for managing end-to-end clinical trial operations. Designed for clinical research, it expedites implementation and drives user adoption. Cloudbyz CTMS comes with an intuitive, straightforward design that allows for quick deployment. Boasting a rich set of features, Cloudbyz CTMS makes it easy for users to manage all aspects of clinical trials, including sites, enrolment, documents, events, milestones, site visit reports, finances, inventory, etc. Cloudbyz provides end-to-end management of the clinical trial lifecycle, including study setup, site management, study projections, monitoring, and financial management. With Cloudbyz, you can optimize your study planning, accelerate patient recruitment, and increase trial quality, while reducing costs and minimizing risk.

Protocol Manager helps clinical operations manage global trials of drugs, devices, biologics, and vaccines in all phases of development. When the appropriate Standard Operating Procedures (SOPs) are implemented in your company, Protocol Manager can help you be compliant with the FDA’s 21 CFR part 11 regulations. Protocol Manager supports Web Services technology to provide seamless, automatic integration with many popular EDC and IVRS products. For systems not supporting Web Services, integration is supported via an export/import mechanism. A robust tracking tool and database designed to manage myriad trial information and metrics.

People must be at the center of research to drive health breakthroughs faster. That’s why we’ve built a platform that brings together individuals, communities, and researchers through trust, transparency, and shared value. Each of us has unique details that hold clues to the next medical breakthrough, sharing your health data helps uncover new insights. Communities bring people together to help find answers fast. Collect health experiences and data directly from participants over the course of your studies, we manage it so you can get started right away. We unite individuals and communities, putting their health data to work to answer life’s most pressing questions. When people come together with a collective vision of responsibility and fairness, it creates a force so powerful that it can alter the face of longstanding systems and institutions. Created by a team of passionate genomics and technology leaders.

With over 20 years of experience in both software edition and clinical research sectors, Arone provides clinical research organizations with a complete suite of tools for patient data entry and management. Our solutions are turnkey and our team provides you with personalized support for the proper conduct of your projects and studies. Collect and manage patient data in a single tool. Arone manages the randomization of patients by randomly assigning study participants a type of treatment in order to remove bias in the study. Empower participants of clinical trials for their daily data entry. Benefit from a customized support for your projects.

Manage your clinical trial in one platform. Zapclinica is an eClinical suite designed to manage and conduct every aspect of your decentralized clinical trial - hybrid or virtual. Automate complex processes, identify outliers, optimize resources, improve decision making and collaboration between sponsors, CROs, and sites. Zapclinica reduces the time and costs to run a successful clinical trial. Manage your clinical trial in one platform. Zapclinica is an eClinical suite designed to manage and conduct every aspect of your decentralized clinical trial - hybrid or virtual. Automate complex processes, identify outliers, optimize resources, improve decision making and collaboration between sponsors, CROs, and sites. Zapclinica reduces the time and costs to run a successful clinical trial. Cover all aspects of your study with one platform. No extra vendors, no extra third-party, choose the app you need in a single environment, including EDC, ETMF, Payments, Logistics, and many more.

LifeSphere eTMF is your clinical trial’s single source of truth. Discover a versatile solution that streamlines inspections, ensures compliance, and saves your organization time and effort. Built as the first system to support the TMF reference model, LifeSphere eTMF aligns Clinical documentation with regulations and study protocols in one solution. Create and manage a single source of truth for your clinical trial. Ensure trial master file quality, timeliness, and completeness with live collaboration and real-time document sharing. Streamline TMF inspections quickly and efficiently to handle any audit. Maintain compliance with embedded workflows and dashboards that allow easy trial reconstruction.

IBM® Clinical Development provides pharmaceutical, contract research organizations and medical device companies unified technology from start up to submission to support clinical trials. With our clinical data management system, users can organize and analyze report data from anywhere in the world. Enabling pharmaceutical organizations to deliver therapies faster to their patients. Design and launch studies without database migration. Deliver quick and easy remote consent with minimal integration.

View your study’s data in real-time through a consolidated dashboard that enables you to be up-to-date on milestones, study progress, and other KRI’s. Mitigate research risks by identifying and addressing issues as they occur, radically improving trial performance. Benchmark trial performance against Lokavant’s proprietary data to optimize your resources and reduce study team burden. Trial data from source is ingested and harmonized in real time with Lokavant’s proprietary and partner data. A single, self-service view of real-time study performance with automated reporting and benchmarking. Daily re-forecasting of enrollment and site performance is compared against historical performance to provide actionable insights.

Study teams are increasingly being challenged to do more with fewer resources. Delays caused by disconnected systems, manual data re-entry, redundant workflows, and information silos can seriously affect a trial’s progress. You need a clinical trial management system that unifies and streamlines workflows while still maintaining full visibility, and Medidata has the solution. Rave CTMS is the only data-driven solution for faster, smarter, end-to-end trial management. As an integral part of the Medidata Rave Clinical CloudTM, Medidata provides all of the elements you expect from an industry-leading CTMS and more. Rave CTMS provides your study teams with the ability to plan and manage all of your clinical trials in a consistent and harmonized manner that standardizes activity planning and management at the study, country, and site level. Activities include study/site team creation and activation, patient enrollment and milestone tracking, site monitoring, and issue management.

Everything we do for your team starts with our blended, multi-modal platform. Comprehensive and fully configurable, Clinical StudyPal is a patient-centric technology designed to make your research faster, easier and more cost effective. As an app, it builds collaboration and engagement among sites and patients. As a web interface, it effectively manages your studies through powerful analytics. And as a notification solution, it keeps your patients and study team always in the know. What can Clinical StudyPal do for you? The real question is, what can’t it do? From our proprietary technology to our patient-centric offerings, our team is dedicated to providing yours with whatever it takes to achieve a smooth, successful trial experience.

ClinEdge is transforming the clinical trial industry by providing a comprehensive suite of services tailored for Sponsors, CROs and Sites. We creatively and collaboratively solve problems for our clients because we understand the challenges and barriers they face. ClinEdge is dedicated to improving overall trial success through every stage of every study by providing Site and Patient Access to Sponsors/CROs and enhanced Trial Solutions to Site partners. With over a decade of expertise and a deep understanding of our clients and the challenges they face, ClinEdge is focused on transforming and revolutionizing study conduct.

A Clinical Data Management System (CDMS), Clinical Trial Management System (CTMS) and Electronic Data Capture System (EDC) all in one powerful, integrated solution. All your study information can be at your fingertips with our innovative, flexible and compliant Clinical Trial Software System. Our servers or yours. Clindex® can be installed on your servers or it is available on the Fortress Medical Cloud (SaaS – Software as a Service). Cloud access is available world-wide and your data is securely stored at a SOC 3 certified data center. You can build, we can build. Clindex® provides all the tools you need to develop your own study database. Our quick start manuals and help documentation walk you through the process, step by step. Or our Clindex services team can develop a study for you.

VIPER automates the screening process from remote patient identification (at the point of diagnosis) to qualified enrollment. Utilizing artificial intelligence, VIPER identifies and matches patients to precision trials in the narrow window of opportunity through lab-agnostic genomic data ingestion, EMR and pathology data in a way that is customized to both the patient and to the research. VIPER searches the customized matching engine to find the best available clinical trials for a patients’ specific diagnosis—at the time of diagnosis. Through workflow integration, VIPER sends real-time notifications of a patient's eligibility for available clinical trials to the entire care team in the narrow enrollment window. VIPER also provides real-time interactive dashboards with rich data mining capabilities to aggregate site and study level patient data to hit your study KPIs.

eDeviation supports all the operations for Protocol Deviation assessment and management. From software design and validation to collecting supporting documents and exporting data for the TMF, eDeviation® relieves your clinical team from the risks associated with missing or wrongly assessing one-time or recurring protocol deviations. eDeviation® is part of Ethical’s eClinical Software Platforms Solutions supporting faster and more accurate clinical trials management. Whether your protocol deviation assessments are performed by an independent expert committee or by your study team, our eDeviation® software is configured to exactly match your needs. Forms, workflows and exports altogether contribute to a GxP quality and effectively managed study. Study teams, Investigators’ Sites and Committee Members, when applicable, work seamlessly online in real-time to expedite judgments, consensus and timely completion of the protocol deviation assessments and management.

ClinAccess™ 5.1 is the next generation of our industry leading Clinical Data Management System based entirely on SAS® 9. It leads the way in simplifying clinical data management, clinical trial analysis and preparation of electronic submissions. Having your data keyed directly into SAS® data sets enhances your staff’s productivity by eliminating the time spent transfering data from Oracle/SQL into SAS. ClinAccess™ is designed expressly for ease-of-use study definition, data entry and management with features to monitor the progress and quality of ongoing clinical trials. Whether for review, analysis, or FDA submission, your data is always in SAS®and ready for analysis. The database structure is designed to support and accelerate statistical analysis and reporting. The result is less time and effort for data analysis and a shorter time to market. For reliability, auditing and security, there is no better solution than ClinAccess™.

With eAdjudication® software managed service, trial leaders have control of timelines, the flexibility to adapt to changing conditions and outcomes, and the ability to monitor trends in provider performance and protocol conformity over the duration of long trials. Avoid hidden costs and timeline breaches in your Endpoint Adjudication Study with the innovative, all-inclusive, managed software service. The eAdjudication® Managed Software Service is the most efficient way for Endpoint Adjudication (CEC) Management. Working with the eAdjudication® platform and Ethical's Staff, study teams, committee members and clinical organizations interact effectively online in real-time in an user-friendly, and GxP-compliant environment, avoiding time-consuming, costly and error-prone manual processes. eAdjudication® all-inclusive services streamline the integration and adoption of EA software throughout eClinical organizations.

Clinpal is the first end-to-end clinical research platform purpose-built for virtual, hybrid and direct-to-patient studies. Patients log in from anywhere, on any device. Study teams leverage powerful data and analytics across the entire lifespan of the trial. And sites get all functionality all in one system, reducing burden. Clinpal Build provides a point-and-click studio, enabling CROs and others to define data, forms and workflow quickly, and easily. Clinpal’s Single Platform – provides end-to-end clinical trial support from patient recruitment and data capture through long-term follow up, with data available on demand. Clinpal’s Innovative Technology – we designed Clinpal to work in multiple formats, with a single online configuration. Configure one time, and Clinpal works for browser, mobile or app users.

Clinical trials and research traditionally existed outside of the care administered within local hospitals and physicians’ offices. Physicians weren’t always aware of what research was being conducted, and patients had little idea research that could potentially improve their outcome or benefit their health was occurring at all. Only Elligo enables broader participation in clinical research than ever before with access to over 150 million patients and their data, allowing physicians to provide research as a care option to patients who otherwise wouldn’t have access to clinical research. Traditional recruitment methods are constrained by limitations such as patient proximity to a specific site where research is conducted. Research has also shown that patients prefer to engage in a study with their trusted healthcare physician.

Streamline regulatory operations across your organization to improve compliance and advance research. Veeva SiteVault reduces the complexity of conducting clinical trials by connecting your regulatory operations to improve efficiency and compliance. Manage regulatory and source documents in a single system that supports 21 CFR Part 11 and HIPAA requirements. With a real-time visibility across trials, SiteVault Enterprise improves operational efficiency, speeds study activation, and enables faster, higher-quality trial execution. Replace manual processes and design your own workflows to support quality and speed study activation. Eliminate the need to grant EMR access or redact documents by providing monitors with secure, direct access to your regulatory and source documents. Create your own workflows, reports, and dashboards for greater visibility into start-up timelines and regulatory processes.

Globally accessible, infinitely scalable, AI-powered, collaborative cloud platform meeting the highest standards of security and compliance. An industry-leading and simple-to-use software platform, purpose-built by neuroimaging and data science experts to meet the distinct and challenging needs of the neuroscience community. Optimized and tailored for your needs, whether you are conducting research, running clinical trials, at the point of care, developing novel algorithms or leveraging brain-related data. Global data aggregation, and consolidation of imaging-based studies in one cloud platform. Streamlined, end-to-end clinical, real-world data and medical imaging data management. End-to-end expert and personalized support to ensure your study success. Centralized reading and the ability to compare quantitative results to a normative database. Highest quality, shareable reporting and data exporting for submissions approval.

The industry’s leading eSource, CTMS, and eRegulatory software for clinical trial sites. Capture source data seamlessly and in real-time with CRIO’s best-in-class electronic source. You’ll eliminate up to 90% of your paper and improve data quality by 80%. Take control of your operations with CRIO’s intuitive Clinical Trial Management System. Schedule patients, track financials, streamline recruiting, and more. Introducing electronic regulatory binders fit for the 21st century, which includes the first-ever electronic delegation log — all 21 CFR Part 11 compliant. For clinical trial sponsors: conduct 100% remote monitoring of your sites’ source data and regulatory documents in a secure, online portal. Join Our Network of 500+ Clinical Research Sites From Around The World. Our mission is to help you grow your business. We do that by streamlining your site’s operations, so that your studies don’t stop just because you aren’t in clinic.

Mednet is a healthcare technology company specializing in eClinical solutions designed for the global life sciences community. Mednet’s flexible, electronic data capture (EDC)-centric eClinical platform improves the efficiency of clinical studies of all types and sizes. Beyond simply EDC, Mednet’s comprehensive solution set provides the tools required to build and manage all types of clinical research, while adapting to evolving demands and requirements. Pharmaceutical, medical device, biotechnology and Contract Research Organizations (CROs) around the world have trusted Mednet for nearly 20 years to deliver the technology innovation, experience and reliability they need for success. For more information, visit mednetsolutions.com.

Today’s Interactive Response Technology (IRT) systems are increasingly complex. Flexible and configurable IRT matters - with IRT data as the source of record for recruitment, clinical trial drop-out rates, patient visits, and other crucial data. Choose a platform that’s user-friendly, mobile-ready, and comprehensive - embedded in quality, flexibility and expertise. Choose comfort with complex therapeutic expertise in today’s risk-based eClinical environment. Combining the right technology, subject matter expertise and commitment to service we empower clinical trials to deliver patient outcomes. Deep clinical and supply chain knowledge drives innovation and provides clients with control over their Randomization and Trial Supply Management (RTSM) processes. Our innovative suite of tools drives distinctive levels of quality control, site efficiency and patient compliance. Our IRT platform can meet the needs of almost any study, enabling fully validated deployment in as little as 30 days.

Ennov CTMS facilitates the end-to-end management of clinical trials. The software allows sponsors to be more efficient, to make better decisions, to ensure compliance, to select investigators well, to monitor patient recruitment and to manage finances. Ennov CTMS includes comprehensive directories to manage site personnel (investigators, sub-investigators, study coordinators, pharmacists) and organizations (hospitals, competent authorities, CROs, suppliers). Ennov CTMS provides functions for tracking patients, patient visits, EDC data, activities, queries, deviations, adverse events, drug supply, monitoring visits and finances. A full complement of reports and dashboards provide total visibility into the status of each study, country, site and investigator to provide the information necessary to make the best decisions possible. - Comprehensive CTMS software - Integrated with Ennov Clinical Data Management - Clear visibility into investigational sites - Integrated workflow

DFnet is a healthcare technology company that provides eClinical solutions, including electronic data capture, eSource, and data management services. We bring more flexibility, better data quality, and greater efficiency to clinical trials everywhere in the world. Collect data from any source – paper crfs, EDC and other electronic sources, online/offline tablet and ePRO entries. Install within your controlled premises or allow us to host in our secure cloud environment. Accelerate SDV and RBM processes with advanced optical recognition that shaves time off manual data entry. Built for maximum flexibility of multi-center studies. Web-based data capture from any source is instantly available in a centralized real-time platform.