Alternatives to Clario eCOA

TrialPoint™, electronic data capture (EDC), is simple to set up and use. Coordinators love it. Our data managers are skilled in converting clinical protocols to geek-speak (metadata dictionary for those in the know). They will set TrialPoint™, so it works for you, and not against you. The system can accept any randomization string or media upload. It can blind users to treatment assignments. To promote time-sensitive data collection. The system will calculate visit windows and send reminders to keep the team on track. Many protocols are now being implemented in trial designs that include patient-reported outcomes on health and quality of life questionnaires. TrialPoint's electronic patient outcomes (ePRO), which can be configured to suit any quality of life questionnaire, patient diary, or other criteria, is worth a look.

Medrio's Electronic Data Capture (EDC) platform and complimenting eClinical solutions such as ePRO, RTSM, eConsent, and Direct Data Capture (DDC) have been trusted by major pharmaceutical, biotech, CRO, animal health, medical device, and diagnostic companies since 2005. We are known for our easy-to-use solutions, delivering speed and simplicity to clinical trials of all phases, sizes, and complexities. Medrio users can build their databases in an average of 2.8 weeks with no programming required, make mid-study changes with just a few clicks of a mouse, and much more. From bolt-on capabilities to full-service offerings, Medrio offers flexible, modular solutions that give our customers exactly what they need – and none of what they don’t. Our innovative software, as well as the robust and flexible training and support resources we provide our customers, have earned us a 98% customer satisfaction rating.

Clin'form is a flexible and robust electronic Clinical Outcome Assessment platform (eCOA). It was designed to streamline clinical trials, improve data quality and speed up processes for research teams. It is adaptable to any protocol and population, and works with any type of questionnaire. The platform can manage studies with populations ranging from a few to over 10,000 patients in all geographical regions. Clin'form integrates seamlessly with other clinical systems to ensure a smooth workflow. It also supports flexible data collection methods, including provisioned tablet or smartphone, the patient's smartphone, web access via any browser, and interview. The embedded tele-visit function allows for planning the unexpected, and patient engagement modules ensure high compliance.

Signant Health, a global evidence generation company, helps modernize clinical trial by meeting patients where the are and reimagining how to prove. They offer a comprehensive range of clinical technology solutions including electronic Clinical Outcome Assessments, Electronic Data Capture, electronic clinician ratings and a unified eClinical Platform. Their patient engagement tools include a patient app, eConsent and telemedicine capabilities. Signant Health offers clinical data and analytics, including COA data analytics, data aggregation, and intelligence. They have over 30 years' experience and have supported thousands trials and contributed hundreds of drug approvals. This makes them a trusted partner to sponsors and CROs who are looking to deliver high-quality information for trial decisions and regulatory filings.

AssisTek, a leader in innovative technology solutions for clinical trials, offers custom clinical software to streamline and enhance data collection. Over the past 25 years, they have supported over 800 clinical research studies in 46 therapeutic areas. This includes over 500 multinational Phase I to IV clinical trials. Their eCOA solution is highly scalable, customized, and efficient. It is powered by a proven cloud-based technology platform. AssisTek offers a range of products, including TEK eCOA tablet, which supports any clinical trial questionnaire, TEK eDiary, for capturing patient reported outcomes at home, TEK Configurator, for building clinical trials from the ground up, and TEK Study Portal, for eClinical tracker, training and reports all in one place. Their systems and services make them the number one choice for collection and analysis among patients and clinicians.

Clinion eCOA allows you to conduct decentralised clinical trials, with patients participating remotely. Clinion eCOA allows study participant to report their health from their home using their smartphone. This allows clinicians to monitor patients in real time. Clinion eCOA integrates seamlessly with Clinion EDC. Trial participants can input daily outcomes directly. This eliminates data duplication and transcription errors, and provides clinicians with a real time view of patient progress. Multilingual forms are supported by the eCOA app, which makes it easier for patients to engage and provides cleaner data. The eCOA app's decentralised nature allows for faster and wider patient recruitment.

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.

EvidentIQ's eCOA optimizes real-time, direct from-patient data collection. It offers a simple interface that provides advanced patient assessments to improve the patient experience and data quality. Customers can either benefit from an entire eCOA package, or choose the elements that meet their specific needs to create value. Get a demo from our experts to see how we can help you improve your study ROI. EvidentIQ's eCOA brings together data science and technology. Customers can either benefit from an entire eCOA package that covers all aspects of the process or add value by choosing elements that meet specific requirements. The solution can be used independently of any specific eClinical technologies, such as EDC systems. However, it can be integrated into any existing eClinical software. It has been created to collect any patient/clinician/observer reported outcome data in a streamlined, compliant and efficient way.

Jeeva's patent-pending modular system is built on the most powerful cloud platform. One login from any browser-enabled device can be used to remotely screen patients, educate, enroll, send SMS, email and generate evidence including electronic patient-reported outcomes. They are tired of waiting for patient recruitment and retention to happen. It is crucial to provide sufficient evidence of safety and efficacy for investigational new medicines in order to receive regulatory agency approval. Jeeva is a great tool for saving time and money for patients, biopharma sponsors, and long-term follow up studies for gene therapy.

IVR Clinical Concepts is a company that specializes in virtual clinical trial technology. They also offer patient engagement solutions. They offer electronic patient-reported outcome and patient diaries that aim to deliver better results with fewer mistakes, resulting in shorter deadlines and lower cost. They also offer outreach and recruitment services, with a focus on outreach, prescreening, real-time data collection, and data collection in real-time. The screening, registration and randomization solutions they offer are described as being modular, flexible and configurable. IVRCC also offers clinical trial management solutions that reduce workload and provide more control. They also offer eClinical Integration Services to seamlessly connect data. Their chart review services offer real-world data as well as clinical insights. IVRCC focuses on custom, modular and configurable solutions that improve the patient experience while optimizing clinical trial success.

Suvoda is a leading clinical trial technology provider specializing in managing complex trials, particularly in areas like oncology, rare diseases, and central nervous system disorders. Established in 2013, the company delivers an integrated platform featuring solutions like Interactive Response Technology (IRT), electronic Consent (eConsent), electronic Clinical Outcome Assessments (eCOA), and ePatient tools. Suvoda’s innovative software ensures streamlined processes for randomization, drug supply management, and real-time patient data collection. Focused on improving patient engagement and simplifying site operations, their solutions are designed to address the increasing challenges of modern clinical trials. With headquarters near Philadelphia and a global presence spanning Europe and Asia, Suvoda has successfully supported over 1,500 trials in more than 85 countries.

Secure and user friendly cloud-based EDC platform for managing clinical trials and studies of all sizes and complexities: ePRO, eConsent, eCOA, eSource, PROMs, PREMs, functional health assessments and participant education/engagement.

ClinAccess™, 5.1 is the next generation in our industry-leading Clinical Data Management System, based entirely upon SAS®. It simplifies clinical data management, clinical trial analysis, and electronic submissions. Your staff will be more productive if your data is directly linked into SAS®. This eliminates the need to transfer data from Oracle/SQL into SAS. ClinAccess™, which is specifically designed for ease-of use, data entry, and management, includes features to monitor and track the quality and progress of ongoing clinical trials. Your data is always available in SAS®, ready for analysis, review, and submission to FDA. The database structure was designed to facilitate and accelerate statistical analysis. This results in less time and effort to analyze data and a shorter time to market. ClinAccess™ is the best solution for security, auditing, and reliability.

Zelta is a cloud-powered platform for unified clinical data management and acquisition, designed to streamline and enhance clinical trial processes. Its modular architecture adapts to the unique demands of each study, enabling faster and more efficient outcomes. With capabilities such as electronic data capture, clinical operations management—including randomization and trial supply tracking—clinical trial management, and electronic trial master file functionality, Zelta supports comprehensive study oversight. It also enhances patient and provider engagement with electronic clinical outcome assessments and e-consent solutions. Built for studies across all phases, therapeutic areas, and global regions, Zelta offers an intuitive user experience with secure single sign-on access from anywhere. Its flexible and scalable design allows for seamless customization and integration with both native and third-party technologies, ensuring adaptability to diverse research needs.

Check out our quick screening tools to help you identify high-risk patients with colorectal, breast and other cancers. Progeny Clinical makes it easy to manage family history, assess risk, and determine treatment options for your patients. You can access family history data online from your patients and create pedigrees automatically before you visit the clinic. You can edit or create new pedigrees at any time. You can instantly run validated hereditary risk assessment models for cancer at the touch of one button. Ambry Genetics offers genetic testing at a fraction of the cost. You can track and view lab results without leaving the software. Save time by creating letters, notes, reports, letters, and other documents using custom templates that include patient data fields. Quickly generate custom queries or spreadsheet reports using pre-configured data entry screens. To display the most recent pedigree, add a hyperlink to your electronic medical record.

Dacima Clinical Suite, the most advanced web-based solution, combines electronic data capture (EDC), medical data management software (CDMS) and clinical trial management software into one platform. Dacima Clinical Suite is designed for clinical trials, epidemiological studies, web randomization, ePRO, surveys, and patient registers. Dacima Clinical Suite comprises three core modules: the Manager (Administrator), Designer Module, and the Data Entry Module.

IQVIA is trusted by thousands of organizations worldwide to accelerate drug development, improve product quality and safety and commercial effectiveness, get the right treatments for patients, improve healthcare delivery and access, and ultimately drive better outcomes. Connect data, technology and analytics to optimize clinical development. The result? The result? Faster decision making and lower risk, so you can deliver life-changing treatments faster. IQVIA offers specialized capabilities to customers in the healthcare industry, thanks to its foundation in data, advanced analytics and expert insights. Watch the latest from IQVIA data scientists and doctors, as well as other subject matter experts, on the topics that are important to you. You can find everything you need, from industry trends to how our capabilities are being applied to help, here.

eCOA, digital technologies, and other digital technologies, are the future of clinical and research. They bridge the gap between traditional and forward-looking, patient focused development. YPrime's eCOA services are not only high-quality patient data but also provide a better user experience across investigator sites, patients, and sponsors. YPrime uses an agile software development approach to quickly configure and customize functions to meet the needs of each study. This takes between 8-12 weeks. Clients have the opportunity to view the system at various stages of design and development before it goes live. Our pre-validated and configurable authoring environment makes it easy to set up start-up times and make post-production changes such as protocol amendments.

Clinevo electronic trial master file (eTMF), is an electronic Trial Master File in electronic format (digital content). It can be used to organize and store documents, images and other digital content for clinical trials. Clinevo electronic Trial Master File eTMF has an inbuilt DIA reference model that meets regulatory guidelines.

Maximize data quality. Capture eSource data during patient visits to ensure data quality. High-quality data can be electronically captured with built-in validation and edit checks. This reduces errors and queries and allows for remote monitoring. Study time, cost, and risk can be reduced. FDA approved eSource to streamline clinical trials. It eliminates slow, inefficient, and error-prone SDV and transcribing into EDC systems. Streamline study and site efficiency. ez-SourceDocx was designed with site users in view. It streamlines workflows, reduces workload, and ensures protocol execution. It guides sites through properly sequenced visits that guarantee all end points data and prompt quality investigator evaluation.

Carevive is an EHR-integrated platform for cancer care management that is designed to improve patient outcomes during the cancer journey. The platform optimizes decision-making by eliciting preferences, assessing interest in clinical trials, and addressing psychosocial and physical issues. Carevive allows remote symptom monitoring via electronic patient-reported outcome (ePROs), enabling symptom self management plans and guideline driven pathways to improve the quality of life and decrease hospital visits. The platform also supports the continuous monitoring of late effects reported by patients and coordinates care, including diagnostic tests to detect new or recurrent tumors. Carevive’s applied analytics also provide access to aggregated data on patient experience for continuous quality improvements and support in pragmatic research in oncology.

ClinSoft™, was developed in-house by Innovate Research. There were no third-party acquisitions and integrations. The system is compliant to FDA regulations (21 CFR Part 11, as well as GCP and HIPAA. The system is fully auditable and validated. ClinSoft™, which is easy to use, ensures quick start-ups and close-outs. This saves you precious time and allows you to be certain that any mid-study amendments or updates to protocols will be made promptly. Innovate Research, an Indian contract research company, provides services in clinical research and regulatory affairs. US FDA 21 CFR Part 11 compliant. Electronic Signatures & Records Secure, Role-Based Access. Audit Trail. Easy to use interface for Edit Checks and CRF Set-up. Frameworks that can be reused for item, panel, visit, and page.

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.

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.

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.

uMotif, a modern eCOA/ePRO/eConsent platform, is designed to support clinical and real-world studies. The platform was developed in collaboration with patients and delivers unprecedented engagement, transforming data quality, speed, and accuracy. Combining uMotif’s eCOA/ePRO and continuous glucose monitoring data collection, the platform achieved unprecedented data compliance rates in a pan-European study on diabetes. In an immunology trial, the patient-centered eCOA/ePRO helped the sponsor meet data capture requirements six month earlier. In an FDA-required CNS trial, participants were asked to capture submission-ready data using their own devices. uMotif always puts patients first. They focus on the patient journey, and what drives their behavior. This deep understanding allows for the design of software which best meets the needs and expectations of patients, while also delivering exceptionally high levels engagement to study sponsors.

LexisNexis Health Equity and Inclusion Insights provides comprehensive and actionable data at the individual level on social drivers of healthcare (SDoH). The insights allow healthcare organizations to advance initiatives in population health, health equity, and clinical research. The solution helps identify barriers in care, improve the delivery of care, and create more diverse clinical research and healthcare options. It provides deidentified datasets which can be combined with another deidentified dataset using LexisNexis Gravitas. This tokenization solution leverages a referential layer to match deidentified records with unprecedented precision. To achieve these goals and improve health equity, it is important to identify barriers to health and predictors for poor health outcomes. This will allow targeted action that can make a difference to each patient.

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.

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.

WCG ClinSphere offers a new approach to running clinical trials from beginning to end. The platform, which uses artificial intelligence to connect sites, sponsors and CROs with participants, is a unified cloud platform. From start to finish, manage your trial from one place. The WCG ClinSphere architecture is based on four principles of efficiency. Our unsurpassed clinical data feeds into a federated AI-learning model, enabling intelligent automation across the lifecycle of clinical trials. Stay informed and make timely decision with access to the latest reports and insights. Workflows that are easy to understand will simplify tasks and improve accuracy. Streamlined operations, logistics, and processes through the entire clinical research journey. The power of massive data stores and deep analysis to make the connections needed for faster clinical research.

Medable is a software platform that allows you to conduct clinical research and studies. The software actively involves patients, who can be contacted remotely, in order to obtain the best results. Remote consent can be given by patients for digital examinations. The application also adapts to local regulations and languages. Our flexible, modular digital platform and DCT platform allows you to right-size how your protocol will be decentralized. Remote screening at scale worldwide Meet your studies enrollment targets faster. Any screening assessment can be developed. Responsive layouts on mobile and web can improve consent readability. Remote consent can be delivered to patients in a manner similar to consumer digital experiences. Global flexibility and local regulations can be accommodated. Engage patients and reduce the travel and time required for an on-site visit. Increase patient engagement and access.

Complion's platform was designed for clinical researchers. Our solution ensures compliance at the highest level with the lowest effort and the most efficiency. This allows you to concentrate on what really matters: improving and advancing patient outcomes. Our eReg solution is available to all clinical trial stakeholders, whether you are a Sponsor, Research Site or CRO. Reduce costs, avoid redundancy and increase staff productivity. You can easily archive, view and get signatures from any device. An audit trail is built into the system to ensure accuracy and eliminate patient safety risks and study conduct. Our clients include hospitals, cancer centers, and medical centers as well as multi-specialty clinics and dedicated research sites.

Science 37 is a company that specializes in clinical research. Its Metasite model eliminates the physical distance as a barrier to participation, allowing patients to participate anywhere. This approach allows access to more than 90% of patients that are not able to participate in site-based research. It offers the recruiting power of twenty sites in one, and provides the flexibility needed by patients to participate from anywhere. The Metasite is powered a proprietary platform which drives uniform study orchestration. It guides the workflow of study staff and patients, and captures study data without requiring manual reentry. This centralization of platforms, people, and processes ensures protocol compliance. It also ensures high-quality data. Science 37's medical teams, telemedicine researchers, and mobile nurses are experienced in conducting remote trials in various therapeutic areas.

5thPort is an eConsent, patient engagement and digital education platform. It can be used in individual practices, hospitals, healthcare systems, and clinical research. The platform uses high-quality, prescriptive media and teach-back in order to educate patients and caregivers about their diagnosis, their care plans, the risks and benefits of recommended treatments, and more. Our digital eConsent helps facilitate a meaningful discussion with your healthcare provider once the patient has been informed. 5thPort can help you achieve the following: 1. Save 15 to 20 Minutes per consultation (without any additional effort) 2. Enhance the patient experience 3. Reduce patient anxiety on the day of their appointments 4. Encourage patients to actively engage in healthcare conversations with their providers 5. Reduce nurse burnout

Koneksa, a leading digital marker company, is a leader in the pharmaceutical and biotechnology industry. They specialize in developing, testing and validating digital markers to help clients understand how their treatments affect patients. Koneksa was founded in 2013 and provides end-toend remote clinical trial assistance, leveraging digital technology, therapeutic expertise, rapid patient-friendly data collection, and remote data collection. This allows for better insights into the health of patients. Their validated, innovative data algorithms are ready for deployment in treatment development programs. This allows the identification of signals sooner and faster than traditional measurements. Koneksa’s cloud-based SaaS Platform allows multiple endpoints be fed in real time, giving immediate data access and empowering confident decisions early in the trial. The platform's ability collect remote data in high volume and with increased frequency allows for ecologically valid measures as well as opportunities to reduce sample sizes.

Deep 6 AI disrupts clinical trial enrollment by changing the way researchers identify eligible patient. DEEP 6 AI uses artificial intelligence and natural-language processing to mine structured and unstructed patient data. This allows DEEP 6 AI to find more patients that are better-matched for trials in a matter of minutes, rather than months. Deep 6 AI is used by some of the most prestigious health systems, pharmaceutical companies, and CROs around the globe. This makes the DEEP 6 platform an essential step in their clinical research workflow, greatly speeding up patients' access to clinical trial. Deep 6 AI locates more patients for clinical trials than it takes months. This allows people to receive life-saving treatments much faster. Deep 6 AI analyzes both structured data such as ICD-10 codes and unstructured clinical information, including doctor's notes and pathology reports. It also provides free-text access to important medical data that cannot be searched easily.

Lindus Health revolutionizes clinical trials by offering a single solution that delivers faster and more reliable results. Our comprehensive approach integrates CRO capabilities, site operation, and advanced technologies, streamlining all aspects of your study, from design to data collection. We use our in-house technology to expedite the setup of sites and patient recruitment. We also have access to over 30,000,000 electronic health records, which helps us accelerate enrollment. Our pay-on-results model, which is based on a fixed milestone, ensures that incentives are aligned, eliminating delays and unexpected costs. Our clinical operations team, which is responsive and experienced, has an average satisfaction rate of 9.7/10. They are committed to delivering excellence. Lindus Health has expanded rapidly its global presence by conducting over 91 clinical trials in various therapeutic areas including metabolic health and women's health. Diagnostics and medical devices are also included.

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. The solution benefits are listed below- 1. Secure, reliable & scalable 2. Faster time to value 3. Monitor study progress & risks from planning to close-out 4. Seamless collaboration among sponsors, CROs & sites 5. Improved clinical team efficiency

The industry's best eSource, CTMS and eRegulatory software. CRIO's electronic source is the best in its class and allows you to capture source data instantly and in real time. You can eliminate up to 90% of paper and improve data quality by as much as 80%. CRIO's intuitive clinical trial management system will help you take control of your operations. You can schedule patients, track financials, streamline recruitment, and much more. Electronic regulatory binders are now ready for the 21st Century. This includes the first ever electronic delegation log, all 21 CFR Part 11 compliant. Clinical trial sponsors can now remotely monitor your sites' source data, and regulatory documents via an online portal. Join our network of 500+ clinical research sites from around the world. Our mission is to help your business grow. We help you streamline your site's operations so that your studies don’t stop because you aren’t in the clinic.

Clinical One RTSM supports a randomization scheme for the simplest and most complex studies, without the need for programming. This eliminates the need to conduct lengthy user acceptance tests. Self-service configurations allow you to take control of your study and create a study within days, not weeks. Assess the status of drug inventory in real-time and make changes without having to contact the vendor or incurring costs and change requests. Eliminate the need for change requests and avoid delays with quick implementation of changes and promotion of your studies. The only platform to truly unify people, processes and data in order to simplify and accelerate clinical trials for the future. Virtual components in clinical trial allow for greater patient participation, and improve the quality of clinical trial data. To accelerate study start-up, we need to transform digital strategies to harmonize and streamline data from all sources.

Data can come at you from many directions - EDC and EHR, smartphones, mobile devices and central laboratories. Prism combines data from many sources and transforms them into information and knowledge. Prism EDC offers a new way to collect and manage clinical trial data. It combines simplicity with innovative features. Prism does more than just collect data via forms. It also aggregates and manages data coming from many sources. Prism eSource, an innovative software solution, allows researchers to extract clinical trial information directly form a site's electronic medical record (EHR). This allows for cost savings and efficiency beyond what is currently possible. It also speeds up the delivery of new therapies to patients.

This company offers a variety of clinical trials management solutions suites for various CROs, Pharmaceutical and Biotech industries. BizNET-CTM is a multi-functional platform that allows a CRO (Contract Research Organization), to plan, manage, design, execute, monitor and analyze trial-related activities and data in compliance with regulatory requirements and protocol obligations. A complete solution suite that addresses all aspects of clinical research projects, from Project Management to feasibility assessment to patient or volunteer enrollment using iris recognition technology to capture clinical trial data and multi-level review to data archiving. BizNET-CTM Suite is designed to manage all documents, tasks and processes, audits, relationships, audits, training, and other information that are required throughout the life of a clinical study.

We create solutions that connect and empower clinical trial ecosystems. The Enrollment Performance Monitoring platform that sponsors love and sites rely on. It is used by over 2,000 research sites in 26 countries, and half of the top-20 global biopharma firms. Sites are able to move patients forward by spending less time on redundant and manual tasks. Sites do less double work. Sites and sponsors will have fewer logs, phone calls, emails, and emails. With real-time access and real-time data, sponsors can optimize enrollment. It is simple and easy to use, with over 1,800 sites in 26 countries using it for patient recruitment. To run more predictable and faster clinical trials, access powerful enrollment and recruitment insights. You can stop wasting time and get back to what matters most: helping patients. You can manage recruitment across all sponsors, trials, and CROs. Once you enter information, it will go where you need.

TrialStat, in comparison to other EDC tools on the market such as MediData, DataTrack and Omnicomm, is the most comprehensive suite of study management tools. It can seamlessly connect to external data sources like EMR, wearables and other clinical and nonclinical data and information sources. TrialStat is a fully integrated platform that can be used for all types and phases of trials. Our multi-tenant, single-sign-on EDC suite includes modules to randomize, adjudicate, code, safety, patient diaries/ePRO and Vendor Neutral Imaging Archive. It also has a robust Reporting and Analytics Portal and custom Machine Learning programmes. TrialStat focuses on data analytics and provides real-time reporting, data extractions on demand and analytics across a single study or a program. This gives all stakeholders timely, relevant, customized insight into all aspects and highlights areas of risk or potential delays.

Most Easy-to-Use Clinical Trial Management System (CTMS) 𝐂𝐥𝐢𝐧𝐢𝐨𝐧 𝐂𝐓𝐌𝐒 integrates seamlessly with Clinion EDC and Clinion RTSM to provide detailed and faster access to the entire trial process to address all aspects of Clinical trial management from a single platform: investigator sites, patients enrollment, SAEs, deviations, inclusions, visit scheduling, IP management, milestones, finances, custom reports, and on-demand analytics enables you to improve quality, control risk, and reduce costs. Clinion CTMS is modular in design These modules are available: Admin Module Project Management Site Monitoring Activities Finance and Budget Management Safety Reporting Management of IP Inventory Document Management System Audit/Activity Log Comprehensive dashboards Comprehensive Reports

Our clinical trials management software is compatible with virtually any controlled clinical trial. The software can be configured to generate paper CRFs (Clinical Report Forms) and eCRFs (electronic CFR). Software can be configured to capture data using a variety of techniques and forms. You can also define specific rules to ensure integrity and quality control. The system can also be used to directly capture electronic data (EDC), i.e. eCRF or to print paper CRFs that could be entered into the system. You can attach audio, video, and documents, with the limitations of your storage. The system supports Double Data Entry and provides detailed exception reporting. This allows you to lock records after they have been matched to prevent any further changes.

eDeviation supports all operations related to Protocol Deviation management and assessment. From software design and validation to gathering supporting documents and exporting data to the TMF, eDeviation®, relieves your clinical staff from the risks of missing or incorrectly assessing protocol deviations.

Electronic source documents - eSource – eliminate paper, standardize and simplify workflow and reduce errors and omissions. BREEZE eSource does more than just schedule visits and create templates. BREEZE eSource synchronizes clinical contexts, regulatory requirements, and protocol requirements with study procedures. This ensures that users capture all protocol-required data. BREEZE business rules ensure that data collected is accurate, complete, accurate, and in compliance with regulations. Our dedicated team of clinical trial specialists delivers customized, study-specific eSource documents to review and approve before study start-up. They also support you throughout the trial by modifying them as necessary. Modules work seamlessly together. Cross-Module Action Multiplier takes things one step further, anticipating and completing automatically any additional tasks you enter. For example, the completion of visits or procedures automatically posts invoicing, recalculates scheduling, etc.

Streamline your clinical studies with Clinvigilant, your global cost-effective eClinical tools provider for CROs, Pharma, Biotech, Nutraceuticals and Academic organizations in clinical and post-marketing stages. Most of our clients choose and stay with us for thanks to our: ♦ Fast EDC set-up (less than 4 weeks). ♦ Cost-effectiveness. ♦ 3rd party integrations (including legacy systems). Our cloud-based suite (Microsoft Azure) is HIPAA, ICH-GCP, GDPR & 21 CFR part 11 compliant and we have been audited by the FDA, EMA and MHRA. The Clinvigilant eClinical suite includes: EDC, CTMS, eCRF, eTMF, eSource, IWRS, ePRO, eConsent and eCOA. Just pick the tools that you need and we will integrate them within your existing software ecosystem. Every interaction and data exchange creates Audit Trails, which provide compliant real-time data visibility across all relevant roles. Our products are modular, highly customizable, and available on the web, iPad, and Mobile App for both Android and iOS. We also support Patient's Own Device (BYOD) and interface with Devices and Wearables. Clinvigilant💊, your one-stop🌐solutions provider for clinical trials☁️ .

Clinion RTSM makes it easy to manage clinical trial supply and patient randomization by using Interactive Response Technologies (IWRS). The Inventory module, which integrates with the Clinion RTSM Software's Randomization module, allows you to implement simple or complex randomization strategies according to protocol specifications. Clinion has one of the best integrated EDC/RTSM platforms available in the industry. Site users can perform Randomization, drug allotment, returns, and re-allotment without having to log in to two systems or worry too much about reconciliation Our predictable and affordable pricing model allows you to lower the cost of RTSM ownership while not sacrificing quality or functionality. You can gain more by integrating EDC and RTSM modules