Alternatives to Rave EDC

UnForm is a powerful enterprise document management and process automation solution that seamlessly integrates with any application. Our platform-independent, fully browser-based solutions provide the ability to create, deliver, capture, index, route, and store documents from start to finish so that a transaction’s entire life cycle can be accessed with one easy search. Our data extraction and workflow capabilities enable the automation of data entry-intensive processes. UnForm.Cloud, a hosting service for UnForm Document Management, is a perfect fit for those who are running cloud-based ERP systems or looking for a solution with no hardware to purchase, manage, or maintain. Implementing UnForm has never been easier. Backed by a proven hosting vendor, Oracle, you have the peace of mind knowing your data is safe and secure with well-managed data centers and cross-region backups, ensuring reliable and continues access to your data when you need it.

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.

TrialMaster, the most intuitive Electronic Data Capture (EDC), Suite on the Market, offers superior usability and flexibility. It is your EDC solution for Phase I to IV clinical trials. TrialMaster increases efficiencies and reduces workflow impact, while improving data quality, which results in faster study submissions. TrialMaster's built-in ePro enables site researchers, patients to self-report their outcomes, and sponsor staff access the platform from any device (desktop or tablet, smart phone, tablet, or laptop). All system screens adjust in real-time to the device's size. Single sign-on (SSO), which allows sponsors to use their own IdP to authenticate, reduces the need for multiple passwords and user names.

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.

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.

Study teams are being challenged to do more with less resources. Disconnected systems, manual data entry, redundant workflows and information silos can all lead to delays in a trial's progress. Medidata offers a clinical trial management solution that unites and streamlines workflows, while still maintaining full visibility. Rave CTMS is the only data-driven solution that enables faster, smarter, and more efficient end-to-end trial management. Medidata is an integral part the Medidata Rave Medical CloudTM. It provides all the elements you would expect from an industry-leading CTMS, and more. Rave CTMS gives your study teams the ability to plan and manage clinical trials in a consistent, harmonized way that standardizes activity management and planning at the country, site, and study levels. These activities include the creation and activation of study/site teams, patient enrollment and milestone tracking as well as site monitoring and issue management.

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.

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.

AI-enabled and Integrated Electronic Data Capture Software Clinion EDC is the most Integrated Electronic Data Capture System in the Industry making your clinical trials faster and better. Our Electronic Data Capture Software accelerates the speed of your clinical trial by reducing deployment time, capturing data faster, timely study close-out, and early data lock – all in a cost-effective manner providing the highest data quality, integrity, and security. Clinion EDC Software integrates all the functionalities you need into one platform, from study setup to data management and reporting.

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.

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☁️ .

Cloudbyz EDC, a cloud-native application with an intuitive user interface, is designed to store and effectively manage clinical data throughout the life cycle of a clinical trial. Our innovative solution allows clinical research teams the ability to collect, analyze and manage clinical data that is of varying complexity and size. Create your study without coding, using an interface that allows users to create forms and navigate easily to the appropriate screens for data analysis and collection.

Prelude EDC is a web-based EDC (electronic data capture) solution that helps researchers and clinicians with clinical trial management. Key features include electronic data capture, data management, project management, custom fields, and compliance management. Prelude EDC comes with a drag-and-drop functionality, which helps administrators create electronic case report forms that are configured based on parameters such as entry fields, edit checks, calculations, and more. It allows users to streamline processes for searching, report generation, statistical reporting, and data querying, in order to optimize the preparation of datasets. Plus, the system comes with an in-built library of case report forms for producing reports on metrics such as patient demographics, deviations, adverse events, and study completion rates. Prelude EDC includes an XML export capability, allowing managers to import files into statistical analysis software. Its mobile application enables researchers to collect data and schedule daily, weekly, and monthly surveys.

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.

The real open-source electronic data capture (EDC), for clinical studies. The project began with volunteers from various backgrounds, including academia, clinical research services, IT industry, and is now used by academic institutes, companies and startups.

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.

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.

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.

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.

Viedoc designs engaging software that modernizes clinical research so that necessary treatments can reach the people who need them faster. We believe in life and science, in people, and in our collective power to change the world and build a healthier future. That unmatched driving force is what pushes us to innovate, accelerate and improve every aspect of modern clinical studies. Since 2003, Viedoc has united scientists and clinical trial professionals in a shared mission of pushing life-changing research forward. Our solution has been used to power thousands of studies, by collecting data from over a million patients and allowing it to flow smoothly across sites and countries. We take great pride in helping bridge the gap between patient and researcher – and, in the best of cases, between research and breakthrough.

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.

Flask Data offers life science R&D teams same-day clinical data as well as patient safety solutions. Flaskdata.io's cloud API platform unifies data collection applications for patients, researchers and site coordinators. It also connects devices and drugs. Our data management and safety monitoring solutions can help you reduce the risk to clinical data, patient safety and protocol compliance. Flaskdata.io is scalable, automated, and adaptable to your clinical trial's needs. Flask Data, a technology company that specializes in clinical data monitoring and management, is Flask Data. We have the expertise to provide our customers with the best possible way to obtain high-quality clinical data while ensuring patient safety. There is no one solution that will work for every clinical trial. We take the time to get to know you and your situation. We will work with you to find the best solution for your unique situation.

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.

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.

Our application offers a web-based interface that can be used to collect data from a variety clinical situations or study types. The flexibility of the application's data capture methods for collecting patient outcomes allows data to be adapted to any specialty, patient population, research study, or other situation. Improve the quality of patient care by using population analytics and tracking patient-reported outcomes. It is compatible with both personal computers and tablets via a secure web-based interface. Researchers can generate reports in real-time. This allows them to manage the entire process of single-center and multi-center studies regardless of their geographic location. DADOS Platform offers a user interface (UI), and do-it yourself tools for researchers and clinicians to create programs and studies that bridge the gap between clinical care and research. DADOS is easy to use and accessible from anywhere.

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.

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.

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).

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.

FormsCenter by Medforce Technologies is an electronic data capture tool that allows you to connect and track your businesses. FormsCenter makes it easy for users to find the information they need and ensures that all data is correct. FormsCenter makes it possible to centrally store large amounts of data and reduce the risk that missing information is discovered. FormsCenter allows users to export data in many formats.

CORE (Clinical On Demand Research) offers a range expert services that include the design, construction and running electronic forms for clinical trials in the UK and abroad. CORE not only creates the forms you need but also provides randomization, data management, and all the necessary statistics. CORE provides vital data to researchers in both the academic and commercial worlds. CORE has forged a strong partnership with FormsVision. The Unit first engaged with FormsVision under a FP7 EU funding scheme. CORE has successfully deployed the ALEA eCRF to support trials in the UK and New Zealand. CORE offers a range services, including database build. (CRFs and randomisations, drug supply management, and ePRO (ALEA). Data hosting (ALEA hosting for data/videos/images/documents). Expert advice (including writing a protocol advice, statistics support, and funding application).

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

CloudShark delivers secure storage, organization, user and group access control, and elegant, powerful analysis tools all through a web interface that enables packet analysis from any device. An Enterprise solution, CloudShark is easily deployed on-prem or in the cloud. CloudShark combines all of the analysis capabilities of Wireshark, Zeek, Suricata IDS, and more into a single solution that enables your team to solve problems faster by eliminating duplicate work and streamlining investigations and reporting. CloudShark is brought to you by QA Cafe, a dynamic software company composed of experts in networking, consumer electronics, and security. We develop industry-leading network device test solutions and network analysis tools for business use while providing our customers with world-class support.

Don't reduce manual invoice data entry. Skip it entirely. Parashift can instantly eliminate 100% of your invoice data entry. Parashift requires no infrastructure, licensing, or complicated implementation. Variable costs are only charged for the volume of processed documents. There is no minimum consumption. Start small. You can scale up and down quickly thanks to an extremely scalable cloud infrastructure. Parashift goes beyond OCR, Data Capture and Data Capture. Parashift validates extracted data for you so you don't have. You can greatly improve your accounts payable processes. The most common purchase to payment documents are processed by us, which greatly increases the efficiency of our accounts payable department. - Offer - Place an Order - Oder confirmation Delivery statement - Pro-Forma invoice - Invoice / Receipt Credit note - Dunning (with overdue penalties) Parashift integrates with your existing Purchase to pay Software

Based on your existing checklists, create advanced mobile forms. To conduct inspections, you can use our mobile data collection app. Automatically generate reports Data charts provide insight. Track the status of tasks on-site. Transform paper forms and spreadsheets to powerful mobile checklists. Include logic, location & rich media. Simple to use app that allows you to access real-time data, generate reports automatically and automate workflows. Follow key metrics to make data-driven decisions. Integrate with existing systems. Record audio and video, take photos, scan QR-codes and use bluetooth to capture data at points of interest. Digital signatures are used to verify reports on-site. Poimapper Plus Product, a mobile app that displays correct site information, guidelines, and form templates to field teams is easy to use. While offline, data collection and editing are possible. Final reports are automatically generated with your branding and sent to you by email. Eliminate the need to manually prepare reports in the office.

Marvin is a software platform that provides solutions for Clinical Data Management. This includes EDC (including IWRS/Drug Management and WebPRO), reporting, and more. ), Coding and Composer (CDISC ODM based study design including SDTM map), SDTM visualization, Clinical Document Management, (eTMF), and a mobile app for direct communication between Investigators & patients. Our software and technical support help accelerate clinical trials around the world. Founded in 2002, XClinical is an international eClinical vendor. Marvin, the company's software platform, provides solutions for Clinical Data Management such as EDC (including IWRS/Drug Management and WebPRO), reporting, and more. ), Coding and Composer (CDISC ODM based study design including SDTM map), SDTM visualization, Clinical Document Management, (eTMF), and a mobile app for direct communication between Investigators & patients. Our software and technical support help accelerate clinical trials around the world.

BLU DELTA, a next generation invoice capturing app, uses real AI to capture digital receipts and automate. Easy, professional, and quick. Real AI reduces lead times. Reduced acquisition costs. No setup and no training. Increased recognition rates immediately. Cloud, on-site or API. Digitization can be more valuable with real AI than just OCR. Features: Real AI instead OCR: You can reduce the workload of your employees by automating your invoices with an exceptionally high recognition rate of up to 99 percent, even for those in unfamiliar formats. A forecast is available upon request Simple setup and a pragmatic licensing model keep costs low and ensure that your company gets a quick return on investment. Our support and optimization services are included in the price. BLU DELTA Capture Service can be used as an MS Azure cloud solution or onsite. Your company data is safe in any case!

A comprehensive suite of professional products that allows you to dynamically share preclinical study data within an enterprise and around world. It features cutting-edge functionality and industry-accepted standards. Seralogix StudyManager™, a new platform, aims to standardize and streamline preclinical studies through an elegant interface. The platform is both scalable and adaptable to large research organizations. It uses sophisticated computing power to simplify your experimental design, data collection and reporting. This suite of tools will allow you and your team confidence in the quality of your data and provide instant reporting. It can be difficult to plan your experimental design correctly. Seralogix Study Manager guides you through the process for experimental design in order to attain the statistically rigorous results that are necessary to ensure your success.

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.

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.

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.

Clinical research is a time-consuming and demanding task. This puts a lot of pressure on the project team and makes it difficult to manage everything. The solution was designed to save you time when it comes to electronic data capture in clinical trials. Our data management department provides everything you need to collect clinical data. This will allow you to spend your time on what is most important. We can implement non-usual features or unique project-specific requirements. The EDC system is also flexible in budget terms. It is well-suited for low-budget clinical research. Our team has fully configured the Electronic Data Capture tool to meet your project requirements. Don't waste your time on system validation and configuration. The EDC system source code as well as the database are stored in the European Datacenter, or in any other country you choose. Multilevel backup also ensures the safety of clinical data.

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.

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.

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.

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.

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

Encapsia continues to push the boundaries of modern concepts, and is already revitalizing clinical trials with the most flexible and efficient system. Responsive image Encapsia was built in the age of smart phones and leverages modern concepts to revitalize clinical trials. Encapsia eSource is available for direct data capture (DDC). It's the same system that provides medical coding, third-party data Loads, and industry-leading data visualisations. Encapsia is the most powerful and innovative system that allows you to collect and manage clinical trial data. Live is real. All data are available immediately after being entered. This gives you the ability to monitor trial progress and make informed management decisions.