Alternatives to ShareCRF

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.

OpenClinica is a leading provider of clinical data management software solutions. OpenClinica provides powerful tools to ensure that clinical trials are compliant and efficient. OpenClinica Enterprise, OpenClinica Participate and OpenClinica Randomize are the core products.

ClinCapture's mission is to create software that saves lives. ClinCapture's technology reduces the cost of clinical trials. It streamlines data capture and protects patient privacy. Clincapture is a platform that facilitates the evaluation and development drugs, biologics and devices that have the potential to treat a wide variety of medical conditions or diseases.

Complex eClinical Solutions for EDC/ERT/eCOA significantly speeds up the start and completion of clinical trials (up to 5 days), reduces costs (up to 80% for monitoring), and increases capitalization and attractiveness (recognized by 89% customers). 96% of data science specialists say it increases the knowledge and advancements of Data Management and Data Science professionals. 94% of investigators love interfaces' usability. Strong internal competence in Data Management 365 is an important part of the Data Management 365 policy. This allows us to not only better understand the challenges faced by Data Managers and improve the MainEDC™, but also to transfer technology and best practices to our clients.

Mosio allows research teams to improve subject adhesion, communications, data collection, and communication on mobile's most popular channel, text messaging. Our software helps research teams communicate more efficiently with participants by delivering interactive elements to mobile phones and messaging automation. WHO CAN WE HELP? + Clinical Trial Sponsors (Pharma & Biotech) + Cancer Centers and Clinical Research Organizations + NIH-Funded Studies + Public Health Agencies + Clinical Trial Managers/Directors and Clinical Operations Managers/Directors. Clinical Project Managers. Principal Investigators. Clinical Research (Study). Coordinators. All research staff who regularly communicate with study participants. BENEFITS + Interactive medication reminders and medication compliance alerts + Automate data collection. + Increase engagement and adherence. + Get SMS appointment reminders to fix your no-show problem. + Increase retention with automated check ins

Data management is crucial to the success and efficiency of your clinical research. Despite being complex, Quanta View, an e-CRF, makes it possible to control the processing of your data. Quanta View includes elements such as monitoring, follow up of inclusions, and project management. The application will be there to help you in all aspects of your clinical research. It is accessible via the internet and responsive. It adapts to all media (tablet, laptop, etc.). Quanta view is designed for the pharmaceutical, medical device, and cosmetic industries.

AI-powered medical image processing meets advanced clinical data automation. UNITY, available as a web-based SaaS solution or on-premises solution, is trusted by major medical equipment manufacturers and hospitals around the world to collect complete, compliant, and consistent data. The integrated modules for PROM and eCRF streamline key data collection to enable faster, more cost-efficient trials. RAYLYTIC’s Imaging Core Lab has decades of experience in high-precision, automated evaluation of musculoskeletal device performance and morphology in spine, hip and knee.

Data Management is a service we offer. We can help you with data management, statistical analysis planning, and model development. We provide all documentation required by FDA and other regulations. Our past experience has shown that more effort in the planning phase will result in a faster, more efficient trial at the end-phase. Our databases are created by data managers who have worked with many eCRFs and know the essential parts of electronic data capture system design. This allows the eCRF build to be completed in a very short time. Validation and testing of the eCRF is a mandatory part of the design. Different personnel are involved in order to receive a 100-percent detailed eCRF.

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.

TrialKit is a cloud-based platform available via both a web and native mobile app, enabling end-to-end clinical trial management for medical device, diagnostics, digital therapeutics, and biopharma 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.

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.

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.

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.

Catchtrial is an online electronic solution that allows you to manage CRFs, images and other data with efficiency and speed. Catchtrial is simple, secure, and affordable. It has been used by both large and small businesses to manage international trials. Catchtrial replaces the paper-based process and allows for cost savings. To collect paper CRF, there will not be any need to visit sites. You can also upload images and capture them, so you don't need to ship CD roms. The study progress can be accessed from sponsors' offices, giving them full control. Catchtrial is unique in that it offers flexible personalizations and functionalities that make trial management easier than other eCRF options.

Mednet is an eClinical technology company that specializes in healthcare solutions for the global life science community. Mednet's flexible, EDC-centric eClinical platform increases the efficiency of clinical research of all sizes. Mednet's comprehensive solution suite provides all the tools necessary to create and manage clinical research. It can also adapt to changing demands and requirements. Mednet has been trusted by CROs in every sector of the pharmaceutical, medical device, and biotechnology industries for almost 20 years. They provide the expertise, reliability, and innovation that they need to succeed. Mednetsolutions.com has more information.

Formerly eClinicalOS IBM Clinical Development is a unified cloud-based data management platform. It offers a smarter way of collecting and managing clinical data. IBM Clinical Development is a SaaS solution that allows users to access all study data and platform functions via an intuitive and simple web interface.

Calyx understands that data is key to the success of any clinical development program. Your electronic data collection (EDC), system is crucial to your success. Calyx EDC is used in more than 2,600 clinical trials around the world. It streamlines data collection and reporting through one platform. Don't give your sensitive data to anyone. We can help you make your program a success with Calyx. Calyx EDC allows you to plan, design, and carry out studies of any complexity. Calyx EDC helps you keep your trial on track with features that reduce costs, improve site visibility and drive efficiency.

You can jump-start your project with one of our applications. Are you unable to find the information you are looking for? Our intuitive visual designer allows you to create a new app. You can easily create your forms, build workflows, and design your app using our intuitive visual designer. No coding required! Drag-and-drop interface and intuitive visual designer allow you to create your study. The type of study you are doing and the data you want to collect will determine the structure of your database. You can then aggregate and review your data using specialized screens. You can check for discrepancies, manage incomplete forms and track follow-ups. Rediscover your database, and organize it according to the criteria that you choose. Use saved datasets to create filters in natural language for data analysis, workflow planning, patient management, and reporting.

Protocol First bridges the physical distance and breaks down silos in Clinical Research during the pandemic. Our solutions can also be used for "normal times". Technology, once a luxury, is now a necessity. We offer the tools you need to stay connected. Not only to help you continue your research but also to speed it up. Remote monitoring and auto-tagging. It can be used with any EDC. Protocol First focuses on breaking down silos between Sponsors, Sites, CROs, and functional areas. We offer comprehensive solutions for the many problems in Clinical Research. Protocol First is focused on getting your data right and to the right places. This includes AI/NLP/ML, both today and in the future. Your data must have an underlying structure. This is the most important aspect of AI. Protocol First's software suite ensures that data from patient to FDA can be used to harness the power of data science.

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.

Castor is an Electronic Data Capture System for Medical Research. Castor was designed by researchers for researchers. It is easy to use, complete and affordable and offers all the capabilities researchers would expect from an EDC. Top features include self-service eCFR creation (form construction), randomization, patient surveys, monitoring, easy import/export of data, EHR importer (HL7 FHIR-based), audit trails and user management.

A platform that integrates EDC, eConsent and ePRO for efficient clinical trials. Replior is a company that provides software for clinical trials. Trial Online is a suite of software that allows investigators, participants, and wearables to collect and manage data in an efficient and easy way. Trial Online supports decentralized clinical trial (DCT) by allowing trials to operate with remote visits, site visits, or as a hybrid. Our journey began 20 years ago when we were asked to create an online CRF service by one of the largest pharma companies in the world. Back then, we were an IT operations provider for pharma. This was the beginning of software that allows for data collection in clinical trials. Today, we offer a complete suite of data collection software services. Our IT operation is handled by our certified sister company Complior.

Data collection can be time-consuming and messy for researchers doing clinical research. This is especially true if you use paper forms. Teamscope was created to make it easy for you to collect data, secure it and analyze it instantly. We want you to be less concerned about your research data, and more free to do the things that you love. Teamscope makes it easy to switch from collecting data on paper to electronic in no time. Our online form builder allows you to customize your survey forms with 11 different fields. Skip logic allows you to hide or show fields based on the values entered. Skip logic allows you to create alternative paths and branches within surveys. Each path can be as complicated as you like. Our experts are available to help you create any form on Teamscope.

Entrypoint is a complete solution for creating, deploying and managing custom data entry applications. It also provides data entry and system administration access from anywhere. Entrypoint offers a range of tools that make it easy to create, deploy, and manage custom data entry applications. It also includes editing, validation, and export options. Entrypoint comes with many built-in attributes which make it easy to add advanced features like range checks and table lookups. Double-entry is the process of collecting information on paper forms and then re-entering it into a computer system. This increases the risk of errors in transcription and takes more time. Electronic forms make it easy to enter data directly into a database without the need for paper. Organizations that are facing rising data volumes and rising costs will find it more appealing to switch to electronic data capture.

A comprehensive, proven and standardized clinical trial management system, developed in collaboration with top academic medical centers and cancer centres, will give you visibility into all aspects your research operations. To ensure consistency across different teams and systems, centralize billing designation information. You can improve your budgeting, route charges correctly, and audit/monitoring billing compliance more accurately. With a standard system developed in collaboration with top research institutions, you can gain visibility and insight into all aspects clinical research. Integrate OnCore into your existing EMR, including turnkey interfaces to Epic and Cerner, in order to improve patient safety, reduce duplicate entry, improve billing compliance, and increase operational efficiency.

All-in-one solution for clinical trials using diamond SaaS. Data MATRIX has been working with clinical data since 2009. We analyze data and create documents that can be accepted by the Russian Ministry of Health and FDA. Our products automate clinical trials and allow users to monitor and manage the progress of their projects online. To ensure that the project runs smoothly, we adjust and validate the software before it starts. Our team has completed 180 projects for pharmaceutical and biotech firms and CROs. Six of the 10 top Big Pharma companies have seen their R&D costs drop by 15% using Data MATRIX products. Our employees are proud members of professional groups that include clinical data specialists (CDISC), medical writers (EMWA and AMWA), and data managers (ACDM.SCDM).

Welcome to Dotter.science. This online platform supports clinical research. Dotter is an online platform for health research organizations and researchers. It allows you to be supported in your research and stay focused on the important things. You can easily collect and analyze clinical research data. Dotter.science makes it easy to create collection forms and optimizes the entry of clinical research databases. This will facilitate statistical analysis and publication. Dotter is a time-saving tool for professionals, students, and researchers. Dotter features. Optimized data collection. Our user-friendly interface allows you to design electronic logbooks (eCRFs) and then quickly add your patients using our real-time data consistency testing tools. Simple statistical analysis. Dotter eliminates the need for paper! Your data is protected on certified servers throughout the study and can be exported in structured formats.

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☁️ .

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.

Fusion is Axiom’s proprietary, cost-effective and easy-to-use eClinical solution. It is aimed at small to medium-sized device, pharma and biotech companies. Axiom's Fusion eClinical Suite allows you to add-on any Modules that meet your study needs. Are you running a small study? You can choose the base configuration with EDC and DM, as well as AE/SAE tracking. Are you looking for something more? To make managing your study easier, you can include powerful Modules like Inventory Tracking, RTSM, Safety Management. You can save time by electronically capturing your study data - even offline! Once you have an internet connection, your data will sync to your Fusion databases. Real-time records available for subject screening activities. Fusion Safety Database allows you to manage pharmacovigilance events.

GoResearch™ is a fully validated, innovative internet platform for electronic data capture(EDC) created by 2KMM for research projects such as clinical/observational studies andpatients registries. It supports such projects in many areas, including: configuration of the information flow, the Adverse Events management processes (including automatic e mail notifications to safety departments), random allocation to a treatment arm via the built-in randomization modules, data collection with the use individualized case report forms (eCRF), to meet the requirements for each study, and ePRO and eSource data integration through dedicated mobile and/or Web applications or flexible API (API).

The Datimbi Platform is ideal for applications that require large amounts of structured data from many collaborators. It also has built-in quality assurance controls. You can monitor and control the quality of your collection process in real time and perform reporting and analysis. You need to get things set up quickly. Our platform is optimized to handle solutions such as eCRFs in Clinical Trial Management, Social Case Management or any other workflow-driven data collection or processing. You can usually get your platform up and running in one week if your need falls within one of these categories. An easy-to-use web interface allows you to set up roles, workflow transition states, data collection forms, processing rules and lists of values, as well as custom email alerts. These tools can be managed either by your staff or via a Datimbi service.

Phoenix CTMS is a web application that combines the capabilities of database software used for clinical research in one modular system. The Phoenix CTMS is now publicly available (LGPL 2.0) after years of collaboration with trial sites at Medical University of Graz. This feature set is unrivalled and designed to meet all regulatory and operational requirements of the clinical front end of academic research at CROs (Contract Research Organisations), hospitals and clinics conducting clinical studies at any phase. A CDMS that supports unlimited Javascript form scripting (server-side and browserside) is what you need. You will need to deal with large electronic case report forms (eCRFs) Want to explore an open-source alternative to eCRFs. To create complex queries in ad-hoc databases to find matching candidates using set operations, You will need to conduct multiple trials simultaneously and organize staff and resources at each site. You will need software to implement different processes for ICH GCP.

Management of clinical data. Comprehensive solution for managing clinical trial information. Easy data entry and creation of CRFs. Support for multi-center complex studies. Data validation and processing is accelerated Multilingual capabilities. Global deployment, cloud-based and on-premise. Clinical researchers understand the importance of reducing time and costs when conducting clinical trials. This is especially true when it comes to the collection, processing, and management of study-specific data. To ensure that the necessary patient data was recorded and sent to the sponsor for analysis and processing, study coordinators used paper Case Report Forms (CRFs). The days of paper CRFs are long gone. The industry now understands that electronic data capture (EDC), systems increase efficiency and improve data quality.

You can manage your clinical trials data with ease and elegance. Clincase's eClinical Technology Solutions gives you access to a comprehensive set of features, services, and additional functionality from one login. Clincase is a seamless, flexible and robust EDC software that keeps data managers, sponsors, and monitors connected to study progress and performance. It also encourages increased investigator and site participation. Clincase is a time-saving, easy-to-use software that makes data available in real time. Clincase is a zero footprint solution that uses secure, encrypted data transfers. The secure environment where clinical trial data is stored in Germany ensures that the highest standards of physical security are maintained. Our system is redundant. Data is constantly mirrored to secondary data centers for assurance. Daily backups are also made.

Cost-effective data capture. LifeSphere EDC offers sponsors and CROs an economical way to capture, manage, and report clinical research data. It combines disparate systems into one unified database, eliminating the need to reconcile and integrate them. The site captures clinical data directly, eliminating the need to enter data and fill out paper CRFs. Study development time is reduced and changes to live studies can be easily implemented. Integrate with the LifeSphere Clinical cloud platform – including LifeSphere eTMF, LifeSphere EDC – to seamlessly connect operations and data management. Single sign-on functionality allows easy access to a variety of applications. Open architecture allows for rapid integration with third-party applications via API.

Effectively monitor clinical trials from start to finish with Ennov’s comprehensive Clinical Trial Management software. Each year, clinical trial sponsors search for new ways to improve the efficiency and reduce the costs associated with running their trials. Investigational site efficiency and productivity can be improved by centralizing information, actively monitoring progress, automating schedules, managing finances, and providing accurate reporting and metrics. With the Ennov CTMS, trial sponsors and CROs are able to actively address all aspects of trial management from a single platform: investigator sites, patients, SAEs, deviations, inclusions, visit reports, phone contacts, investigational product management, trial facilities, and finances. Study managers can plan and track their trials in real time to make better decisions faster. With the Ennov CTMS dashboard functionality, study personnel get on-demand analytics to improve quality, control risk, and reduce costs.

Your clinical trial technology partner...together we create better trials. We offer state-of-the-art software solutions, but we believe in the human touch. We will work with you to make sure your next trial is the best. It takes only days to set up your study. You can either hire us to set up your study, or build it yourself. Any device can be used for investigator or subject-led data collection. All the features you need in one intuitive and integrated application. You can achieve your business and regulatory goals. A skilled, experienced human being will answer your query and prioritize its resolution. We are currently helping medical device companies to meet their compliance and business requirements.

In-system protocol and its training program. Equipted with fingerprint attendance. Cronos offers highly customizable if/workflows that can be used to conduct derma/ patch/ other early phase BA-BE/ phase studies. You can capture, cleanse, and manage your data from paper-based or EDC based trials. Data extraction in desired datasets is possible using standards such as CDISC (SDTM) EDC tool that allows for real-time activities. Its Bedside Data Collection capabilities allow for faster and paperless assessments. It also includes a sample inventory and tracking facility. Compliance-ready data repository.The facility of data e-printing from almost all BA instruments/software and online review of data in defined workflow with e-stamping and e-signature.Project-wise view, export & archival of data. High-quality statistical reports (tables and listings) can be generated in fixed/desired formats.

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.

Sofpromed offers electronic data capture (EDC), systems for pharmaceutical, medical device, and biotechnology companies that are conducting phase I-IV clinical trial. An EDC system can be described as a software tool that is used to collect, clean and export data during clinical trials. The EDC application by Sofpromed is used worldwide in clinical trials across many therapeutic areas, including oncology and hematology, cardiovascular, metabolic (CNS), dermatology as well as infectious diseases, respiratory disease, pain, and other diseases. Clear design, intuitive and easy to use Navigation and data entry are quick and easy. Data encryption and access control. No installation required. Service that seamlessly integrates data backups daily. It works on multiple devices, browsers, operating systems, and devices. Monitoring, data management, reporting tool. Conforms to HIPAA, GCP and 21 CFR. Convenient billing model Monthly flat rate

CSAM's Registries platform, previously known as MedSciNet Registries, provides a rich and flexible online environment for hosting registries. It features powerful tools that can be used for all phases of the project's development, from data collection to analysis. CSAM's Registries platform design is based on our decade-long experience in developing web-based software for medical research. It offers a sophisticated online application package that can be used to host, maintain, and monitor registry projects of any size or scope. The standard registry system implementation by CSAM includes all the components necessary to set up a functional registry. The system supports sophisticated data entry forms and flexible workflow structures. It also allows for advanced data validation, monitoring and analysis.

Flexible eCRF platform that can be used for non-commercial clinical trials. It can be configured to any clinical trial protocol. Our eCRF solution was developed from the many years of experience gained by researchers and medical teams who collaborated on research projects. The system is easy to use, user-friendly, and very flexible. The prepared solution meets all quality standards. We have full control over the code and can continue to develop it and adapt it to meet the changing needs of regulators and clinical trials market.

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.

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.

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.

Flex Databases is an innovative, unified, and compliant electronic clinical platform that provides software solutions for clinical trials: pharmaceutical companies and CROs. Our system is composed of: - Clinical Trial Management System - Electronic Trial Master File - Project Management & Budgeting solution specifically designed for the clinical trials industry - Pharmacovigilance System - Learning Management System It was possible to create a flexible platform thanks to our unique experience and a qualified team of more than 100 professionals with a deep understanding the clinical trial process.

DSG, Inc., a global leader in eClinical, offers a complete suite of innovative technology solutions as well as data management services to the global clinical research community. DSG's eClinical platform offers a competitive advantage and on-time delivery. DSG solutions have been used in thousands clinical trials across the globe using our award-winning eCaseLink™, platform and eCaseLinkDesign for enterprise licensing. The company was founded in 1992 and is proud to have been awarded the SCDM Data Driven Innovation Award.

secuTrial®, a professional, browser-based GCP compliant EDC system for collecting patient information in clinical or non-interventional research and patient registries. SecuTrial®, which has been used in over 600 international and national studies and long-term projects by universities, CROs and pharmaceutical companies, has been a strong testimony to its superior product quality and universal applications. secuTrial®, a web-based software solution for clinical trial, is powerful. It allows patient data to be collected and managed completely online for multi-center clinical trials. It ensures compliance with all data privacy and licensing regulations, while maintaining the highest quality standards.

SlimEDC, a cloud-based platform for EDC (Electronic Data Collection), is an EDC solution. The study editor makes it easy to launch retrospective and prospective studies, patient surveys (ePRO) and market research projects. SlimEDC can be purchased as software that is managed by the research sponsor, or as a service where the entire process, from the collection of data to its evaluation, is handled by a professional SlimEDC staff. SlimEDC has been adapted to the EU legislation and environment. The software generates all of the required reports for regulatory agencies. SlimEDC is ISO 9001 & 27001 compliant. Our team has received pharmacovigilance and BHBIA certifications. Independent authorities conduct strict GDPR audits on the legal and data security.