Alternatives to ez-SourceDocx

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.

In a matter of hours, you can create an eCRF that is just as easy to use and as simple as a paper one. This will help you avoid the most common problems in data collection for Pre-authorisation and post-authorisation studies. When creating an eCRF, make sure you have an EDC that is flexible. This will allow you to adapt to any type of study. The EDC includes a number of monitoring and management tools that will help you save a lot of time and effort in managing and monitoring the study. You should use a valid system that gives trust to the sponsor and allows for the collection of high quality data. Do not wait until the analysis phase to find errors in the data. Otherwise, you will have to chase down investigators to correct them. Avoid making the process of creating an eCRF long and complicated.

Clinical Ink is your guide to making confident decisions and obtaining cleaner data. Clinical Ink is a pioneer in eSource. Their technology platform and delivery capabilities give you greater certainty from source through submission. Explore Lunexis™, a connected eSource Ecosystem that provides data capture solutions tailored to your protocol at the crucial moments that matter. Lunexis makes it easy to create an integrated, simple eSource solution that gives you access to your study data from anywhere, anytime. We offer more than fast, reliable data. We also provide confidence. Your sites and patients will have a smoother experience. You can also be sure that your patients will be more cooperative and engaged, and that your protocol will be executed correctly. Lunexis can help you make informed, optimal decisions when you start the most complicated studies.

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.

Inefficient document workflows can be eliminated, which can lead to a loss of time and money and a reduction in your ability to scale up and attract new research. Florence eBinders integrates your clinical trial systems, automates eRegulatory processes and tracks study progress. It also enables secure remote monitoring via the industry-standard eRegulatory and eISF platforms. Florence eBinders integrates your clinical trial systems. It automates eRegulatory processes and reduces time for contract negotiation. It also tracks study progress and allows secure remote monitoring. Our top-ranked implementation teams and support team will quickly set up your study and get all users connected. In less than four weeks, most sites are up and running. Secure access to your monitors and remote access for your team can reduce the time spent on site monitor visits.

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.

Clinpal is the first platform for clinical research that is designed to allow virtual, hybrid, and direct-to patient studies. Patients can log in from any device, at any time. The trial's entire life span is managed by study teams that use powerful data and analytics. Sites also have all the functionality they need, which reduces burden. Clinpal Build is a point-and click studio that allows CROs and other users to quickly and easily define data, forms, and workflows. Clinpal's Single Platform provides complete clinical trial support, from patient recruitment through data capture and long-term follow-up. Data is available on-demand. Clinpal's innovative technology - Clinpal can be used in multiple formats with one online configuration. Clinpal works on all devices, including mobile and app users.

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.

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

A global, infinitely scalable, AI powered, collaborative cloud platform that is globally accessible and meets the highest standards for security and compliance. A leading, easy-to-use platform for neuroscience professionals. It was designed by data scientists and neuroimaging experts to meet the unique and challenging needs of the community. Optimized for your specific needs, whether you are conducting clinical trials, designing new algorithms, or leveraging brain-related data.

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

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.

LifeSphere eTMF provides a single source of truth for your clinical trial. Discover a flexible solution that streamlines the inspection process, ensures compliance and saves time and effort for your organization. LifeSphere eTMF is the first system that supports the TMF reference models. It aligns Clinical documentation, regulations and study protocol in one solution. Create and manage your clinical trial from a single source. Live collaboration and real-time sharing of documents will ensure the quality, timeliness and completeness of your trial master files. TMF inspections can be streamlined quickly and efficiently for any audit. Maintain compliance using embedded workflows and dashboards which allow easy trial reconstruction.

Streamline regulatory operations within your organization to improve compliance. Veeva SiteVault simplifies clinical trial management by connecting all regulatory operations. This improves efficiency and compliance. A single system that integrates regulatory and source documents supports 21 CFR Part 11 compliance and HIPAA requirements. SiteVault Enterprise provides real-time visibility across trials and speeds study activation. It also enables faster and more quality trial execution. To speed up study activation and reduce manual work, you can replace manual processes with your own workflows. Monitors will have secure, direct access into your source and regulatory documents. This will eliminate the need to redact or grant EMR access. You can create your own workflows, reports and dashboards to gain greater insight into regulatory processes and start-up timelines.

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.

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.

Korio, the Randomization & Trial Supply Management platform (RTSM), is designed for speed, flexibility, and quality. Not only built to handle clinical trial challenges when they arise, but also built to prevent them from happening in the first place. Korio can handle any trial. Legacy RTSM systems were not designed to support the trend towards increasingly complex study designs. Brittle RTSM systems do not allow for on-the-fly RTSM updates to match changes in clinical trials. Inspired by decades of practical experience. The result is a RTSM platform that combines flexibility with reliability and modernity with experience. Korio's intuitive interface is based on roles and can streamline your user experience. Everyone can work faster and with more confidence, from site users and supply manager to clinical operations and data management. Experience consistent management for your trial.

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.

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.

Trial leaders can control the timelines and adapt to changing conditions with the eAdjudication®, software managed service. They also have the ability to monitor trends in provider performance over long trials and to ensure protocol conformity. The innovative, all-inclusive managed software service will help you avoid hidden costs and time delays in your Endpoint Adjudication Study. The eAdjudication®, Managed Software Service is the best way to manage Endpoint Adjudication. The eAdjudication® platform allows staff from Ethical, study teams, committee members, and clinical organizations to interact online in real time in a user-friendly and GxP compliant environment. This avoids manual processes that can be costly, time-consuming, expensive, and error-prone. eAdjudication®, all-inclusive services, streamline integration and adoption EA software across eClinical organisations.

View your study data in real time through a dashboard that allows you to stay up-to date on milestones, progress of the study, and other KRIs. Mitigate risks in research by identifying issues and addressing them as they arise, improving trial performance dramatically. Lokavant's proprietary trial data can be used to optimize resources and reduce the burden on study teams. Trial data is ingested from the source and harmonized with Lokavant proprietary data and data from partners in real-time. Self-service, single view of real-time performance of studies with automated reporting and benchmarking. Daily re-forecasting is used to compare enrollment and site performance against historical performance. This provides actionable insights.

The premier clinical trial management system, specifically designed to overcome the technical challenges of managing clinical trials. CTMS Master makes it easier for users to communicate, reduces manual work, and eliminates redundant data and tasks. This allows for more efficient trial conduct. A Site Visit Report tool that integrates with an automated workflow eliminates duplicate data entry. It also facilitates the creation and distribution of out-of-the box Site Visit Reports (SVR). Standard templates can be used for site and project documents, budgets, events, milestones and site visit reports. CTMS Master offers more than 100 metrics/statistics to help you track clinical study sites, countries, and projects. It also includes 80+ standard reports and ad-hoc reporting capabilities. CTMS Master allows you to create site-specific budgets using a default template, track accrued and future obligations, and define automatic or manual approval for each payment type.

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.

The constructive IWRS ensures a well-organized, systematized supply of drugs between investigation sites. This reduces drug wastage and proactively handles complex randomization procedures for large multi-center studies. SyMetric Platform with Dynamic and Adaptive Randomization helps avoid imbalances between subjects. This results in balanced Treatment Assignment regardless of sample sizes. SyMetric Platform allows patients to handle their subjects. It offers Subject Screening and Enrollment as well as Visit Management, IP dispensing, receipt, Unblinding and Withdrawal tools. This makes it easy and efficient to manage them effectively. SyMetric Platform's robust IP supply management functionality allows drug supply mangers to closely control supplies sent to Sites and adjust supply strategies based on treatment arms and new ratios.

RealTime-CTMS (cloud-based clinical trial management software) is a leading, cloud-based system that can be used to increase efficiency and profitability of site networks and research sites. The solution includes fully-integrated services such as RealTime TEXT, RealTime TEXT, or RealTime eDOCS. This allows for faster and easier access to study and subject information through intuitive navigation. RealTime-CTMS also offers other options, including online document storage, appointment reminders and data collection.

Our market-leading solution for patient randomization, trial supply management, and patient randomization is available in multiple modalities. It is the most customizable and customizable Interactive Response Technology on the market. IXRS®, which is available in multiple modalities, can accommodate any combination of study objectives. It also includes a team of professionals biostatisticians, integration experts, and language experts that are available 24/7. Site-facing functions are designed for automating steps that are susceptible to human error. Site users can make data corrections themselves without having to call a Help Desk or fear of violating trial compliance. Instead of reading hundreds of pages of legalese and specifications, visual tools are easier to understand. You can view and react to every stage of the software build, eliminating surprises at delivery.

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.

High-quality ePRO/eClinRO can unlock more evidence. Electronic Clinical Outcome Assessments (eCOA) measure how patients feel and function during clinical trials. By capturing clinical data electronically, you can be confident that your patient's data is high-quality and regulatory-compliant. eCOA eliminates the time and quality issues that paper diaries can cause, such as illegible answers and transcription errors, inconsistent or conflicting data, and saves you both time and money. ePRO is also recommended by the FDA. Patients can report on their health using questionnaires or assessments. Examples include activity outcomes or quality of life. The outcomes were reported by the clinician. A clinician reports health outcomes. A physical exam such as PASI is an example. Performance outcomes are measures of the patient's performance in completing specific tasks. One example is performing a timed task.

We help PIs overcome common problems and limitations in setting up and selecting databases. QuesGen can also be hired by researchers to provide advice on data management best practices, and additional services to help them get their studies up and running faster. Expert partner for many academic institutions and researchers. Our flexible data platform allows for data curation and management of large data sets. Ability to quickly set up and scale research projects. QuesGen provides a complete data model, an assessment library, and curation expertise. QuesGen makes it easy to get up and running quickly and ensures compliant data so you can concentrate on the analysis. You can support multiple clinical research projects at your institution with HIPAA- and FDA 21 CFR Part 11 compliant solutions. These solutions can be integrated with your EMR, FITBIR (Federal Interagency TBI Repository), and other EMRs.

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.

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.

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.

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☁️ .

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.

Ready by ArcheMedX for Pharma and Biotech Trusts to better equip their trial team, improve decision-making, and reduce study delays By understanding which sites and teams are best equipped to conduct the study, you can avoid the most common causes of study delays. Reduce the time and cost of resolving problems, especially early in a trial. You can be confident that the sites you choose truly understand your patient eligibility requirements. You'll feel more confident that they will be better equipped to help you enroll eligible patients faster, meet enrollment targets, and avoid screen failures. You can be confident that the trial team is fully conversant with the protocol, down to the individual and study objectives. You can predict where there are risks so that you can avoid them and have fewer deviations overall.

Longboat, a cloud-based clinical support solution, provides users with an integrated Guided Compliance toolet to help them at all times. Longboat gives clinical trial staff the resources they need to focus on patients. Longboat allows patients access to essential study information and reminders for their visits. Longboat makes it easy to manage the controlled rollout and revision of the clinical trial protocol.

The options for managing clinical trials at investigator sites were limited to either using multiple spreadsheets or purchasing expensive software that was not suitable for Australian conditions. MAISi is a game-changer. MAISi began as a repository of clinical trials data at a major medical center in 2001. It has since evolved to be a sophisticated workflow application that assists in all aspects of a research unit’s operations. MAISi is a central repository for data that stores information about studies and business units that manage them. The data are organized to support management decision making. Each business unit's staff has access to the data (Studies and Patients, Investigators, Study Teams Members) that is associated with their business unit. Staff granted global access (normally Financial officers and System Administrators) have all data access.

Clindata Cloud is able to receive pre-clinical, clinical, and Risk Metric data from multiple sources/sites. It empowers clinical operations teams with submission-ready data sets and analytics, as well as risk-based monitoring alerts and risk-based monitoring alerts. Consolidate and harmonize study data from multiple sources into a comprehensive data model. Validate the data received for completeness, accuracy and consistency. To eliminate noise and create submission-ready data set in real-time, standardize data according to CDISC data standards. Based on standard data, generate submission-ready analytics in real time.

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.

Clinical Conductor CTMS (Clinical Trial Management System) is a cutting-edge system for managing clinical trials. It's suitable for hospitals, research sites and asset management companies. Site networks, health systems, contract research organizations (CROs), and other healthcare facilities. This cloud-based solution makes clinical trials more efficient and helps research organizations make better business decisions. The key features include electronic data capture and enrollment management, document management, recruitment management, and many more.

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.

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.

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.

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.

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.

One platform to research, document, and collate your clinical data. The Nucleus platform simplifies research data. One platform to store all your study documentation, clinical data, submission data, and compliant media. Nucleus Documents allows you to manage and control your media and quality documentation. You can easily manage, control, and share company content. Our centralized regulatory document management solution makes it easy to manage and collect electronic trial master files. Nucleus Coding allows you to code dictionary terms against both WHODrug and MedDRA dictionaries. It can be used in our standalone application or integrated into your data capture software.

Intrinsic's clinical trials management system (Intrinsic CTMS®,) was designed with the end user's in mind. It minimizes data entry and focuses on proactive study management. Intrinsic is cloud-based and features a simplified interface, the ability of managing studies at any level, as well as a task-based design. This new era in trial management tools has been introduced. Intrinsic®, the first global CTMS, is natively integrated with all Microsoft applications including Outlook, Excel and SharePoint. Users can import bulk data from CROs and study updates using the CRO clinical trial management system. Dynamic Worksheets allows users to quickly create 'live exports' for ad-hoc analysis or reporting. Intrinsic CTMS® also uses Power BI, a cloud-based report tool that allows users to report on data from other clinical system, such as EDC or IRT without having to build expensive data warehouses.

Clear design, intuitive, easy to use, quick data entry, navigation, access control, and SSL encryption. Fully web-based, no installation required. Built-in monitoring, data management, and reporting tools. Monthly flat rate (SaaS), adjusted for study size and duration. Quick data collection via a user-friendly interface, review of data completion status using visual indicators, edit checks and manual queries to detect discrepancies. Remote reviews with integrated buttons allow for remote reviews and tracking of changes, including author, date, hour and reason of modification. CSV) for statistical analysis.

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.

OpenText™, a leading provider of information management solutions for life sciences organizations, helps them to harness insights from data and content to improve their decision-making and accelerate product development. Integrate, manage and securely exchange data between people, systems, and things. Use information assets to drive innovation and commercialization. Cloud-native software can run anywhere, giving you freedom of choice. OpenText for life sciences accelerates discovery by delivering actionable insights that can be used to drive innovation in pipelines. Intelligent capture allows you to capture and manage research papers in electronic lab notebooks. Text mining can help you gain insights. Unstructured text in clinical trial reports, study protocol, clinical safety and efficiency findings, can be used to extract knowledge. Learn how to intelligently analyze and classify clinical trial documents and extract them to reduce the risk for costly stops and starts.