Alternatives to Clinevo CTMS

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.

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

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.

VACAVA Healthcare Solutions reduces the complexity and costs of regulatory document management for clinical trials. Documents can be lost or delayed if they go through a manual workflow. VACAVA solutions streamline regulatory processes by storing forms, profiles, and documents in one easy-to-access online place. With electronic approvals, documents can seamlessly move through your workflow (21 CFR Part 11 compliant). Easy-to-read dashboards enable efficient management. VACAVA's Regulatory Document Management System was developed in collaboration with a major clinical research base to simplify operations, and dramatically increase efficiency. VACAVA's Regulatory Document Management System can be tailored to your specific needs. It is surprisingly affordable. VACAVA's solutions can be customized to meet your unique needs. They are flexible and scalable and delivered via cloud so that you don't have to worry about security and backups.

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

Datatrak International, Inc. is a software-as-a-service provider of enterprise cloud-based technologies for the life sciences industry. Datatrak's unified eClinical solution and related services improve efficiency and cost effectiveness for the clinical trial industry. Datatrak developed its multi-component, comprehensive solution using a single platform. This concept was expanded to include services delivery through Datatrak's Clinical and Consulting Services groups. The Company offers a complete range of software products that can be used to speed up the reporting of clinical research data to sponsors and regulators. This is faster than using loosely integrated technologies. Our goal is to empower workgroups with role-based access, version-controlled file management and calendar events, tasks, and contacts. All built within our eClinical software applications, including EDC, CTMS and reporting.

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.

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.

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.

Trialpack Designer is a powerful and easy-to-use tool that allows you to create blister packs and cards for clinical trials. It is especially useful for designing packages for complex blinded trials, such as dosage titrations and double-dummy. It contains configuration data for the Trialpack PC Controller and the Trialpack Controlled Dosing Systems. Easy and direct on-screen design of filling patterns, print images, and blister shapes. Access rights for users can be very precise. Workflow features that include electronic signatures. Audit trail that is 21 CFR Part 11 compliant. Reports with detailed packaging instructions.

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

A scalable, real-time, collaborative, out-of-the box solution for CROs, Life Science Consultants and Industry Stakeholders. Built in an Audit Ready Compliant Cloud environment (ARCC). All 21 CFR Part 11 requirements are met. GxP audit ready. Pre-configured Departmental. Communications with internal and external stakeholder. Secure data integration between remote teams. Collaboration in review and approval. Turn access on/off according to need (EX: auditors), reducing audit prep time from days to hours. Preconfigured to eTMF Reference models & EDM. Intelligent content management tools can improve workflows. Improve document management with real-time collaboration, automatic indexing and co-authoring. Pre-configured, validated system that manages documents and data electronically in accordance with eCTD mandates.

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

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.

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

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.

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.

Ofni Clinical is a clinical database management tool that creates and quickly implements secure, regulatory-compliant clinical trial databases. Ofni Clinical offers comprehensive search and report capabilities, strong data validation and edit-check options, flexible customization tools, and is easy to implement quickly and economically. The databases can be used to collect data from existing Case Report Forms as well as electronic data capture systems that are paperless. Most Ofni Clinical projects take less than a month from project initiation to validation. Contact us today to learn more about Ofni Clinical and how it can be used for clinical trials. It matches your existing Case Report Forms, reducing training and implementation expenses while adding electronic data capture & review capabilities. Features include extensive edit checks and data validation to detect and correct data entry errors and support data analysis.

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.

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.

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.

Unlimited trial duration, number and treatment of subjects, clinical sites, treatment arms, stratification variables, and more all for a single fee. Support for double-blinded trials is available, including kit management, replacement, and emergency unblinding. Randomize.net supports simple randomization algorithms, permuted block stratification, minimization, and permuted blocked strategy. You can configure randomization applications with exactly the options and features that you need. Randomize.net's Web Service API allows you to integrate randomization into any application. Full support for subject randomization is available. High-secure internet-based randomization service available for clinical trials.

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.

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

EasyTrial.net can be accessed from anywhere because it is a web-based system. EasyTrial.net allows you to easily involve others as you have individual access control which allows you to share data and block access if necessary. EasyTrial.net can be used as a GDPR-compliant storage solution. You have complete control over your data. You are the investigator and EasyTrial.net is the data processor. If requested, they will enter into data handling agreements. We are a specialist in IT and cyber security and are a professional supplier of data security. EasyTrial.net has been used in thousands of clinical trials over the years. This system is approved by many hospitals, data legislation authorities, and educational institutions across many countries.

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.

EDGE, a cloud-based Clinical Trials Management System, has been successfully integrated into the UK's clinical research infrastructure and the devolved countries. Currently, EDGE is used in 80% of England's NHS regions, Scotland, and Northern Ireland. EDGE is the leading research management system in the UK. EDGE was launched in 2000 and adopted by the National Cancer Research Network. It has seen tremendous growth and has a growing number international subscribers from countries which include Canada, Belgium, New Zealand, South Africa and India.

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

Our platform provides the comprehensive support your clinical trial requires using cutting-edge cloud-hosted technology. Clinibase will make your organization more efficient and productive. Clinibase is not a plug-and play system. Why? Because every organization is unique and has its own systems and processes. Clinibase can be customized to meet your specific clinical trial requirements. We use surveys to identify areas for improvement and troubleshoot all aspects of your clinical trial processes. Our social integration tools make it easy to quickly locate and recruit eligible participants. Keep your participants engaged by providing smooth communication channels that facilitate high retention and positive participant experiences. Ensure that your trials are valid and safe by storing accurate data.

CSAM Studies (previously MedSciNet Studies), is an online environment that allows for secure and highly customizable hosting of clinical trials and studies of all sizes. It has a 20-year history of hosting successful clinical trials and research of all types. Studies is a web-based platform for medical research. It offers a sophisticated online application package that allows you to host, maintain, and monitor projects of any size or complexity. The standard Studies solution from CSAM MedSciNet includes all the components necessary to set up a clinical trial or study. The benchmark solution supports rich and interactive data entry forms, flexible workflow structures, advanced data validation, analysis and exporting capabilities.

Cloudbyz eTMF is a cloud-based solution that offers a repository of all clinical trials documents, including images, files, information, etc. Store, manage, and easily share all documents related to clinical trials in a digital format. Manage trial documents, remain inspection-ready, and provide real-time visibility to CROs and sponsors, as well as monitors and other stakeholders.

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.

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.

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.

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.

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.

Complete control. Full visibility. LifeSphere CTMS is an intuitive trial management system that allows clinical operations teams to reduce complexity, speed up timelines, and stay organized. A modern, user-friendly cloud application streamlines study management and automates key tasks throughout the trial's lifecycle. A simple yet powerful trial management app that gives full oversight of trial activities helps you navigate complexity. Streamline your clinical environment by using a turn-key platform that allows for payments and monitoring, and connects seamlessly with LifeSphere eTMF.

Teckro clinical trial software connects all stakeholders to crucial information. Every time. Everywhere. Every day, we find answers from our smartphones. The same applies to clinical trials. Research staff and CRAs always have access to the most current study information. Research staff can access the most important details via their mobile devices by simply tapping a button. Site staff and monitors can be notified in real time if any updates or amendments are required. Teckro, a cloud-based clinical trial software that runs quickly and requires no installation, is quick and easy to set up. It's easy, intuitive, and simple. Teckro is secure hosted and in compliance with major industry regulations, such as FDA 21 CFR Part 11. You don't need to worry about version management as long as you have the approved version of the study documents.

Ripple, a web-based software solution that allows for the management and recruitment of research participants in clinical, translational, and social science studies is an active registry. Ripple was developed by researchers to transform the participant workflow. It is an end-to–end research participant management system that speeds up the entire research process.

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.

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.

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☁️ .

All the power and functionality of a powerful, integrated clinical data management system (CDMS), Clinical Trial Management System(CTMS) or Electronic Data Capture System(EDC). Our innovative, flexible, and compliant Clinical Trial Software System can provide all your study information. Your servers or ours. Clindex®, which can be installed on your server or on the Fortress Medical Cloud (SaaS – Software as a Service), is available. Cloud access is available worldwide and your data is stored in a SOC 3 certified data centre. We can build what you can dream of. Clindex®, provides all the tools necessary to create your own study database. The help documentation and quick start manuals will guide you through each step. Our Clindex services team can also create a study for your company.

BSI CTMS impresses with its innovative interface and intelligent visualization of data. Our clinical trial management software is more than just an attractive interface. It includes functions that assist pharma, biotech, and diagnostics sponsors as well as CROs and academics (SMOs) in their daily lives for managing clinical trials in a targeted manner. BSI CTMS continues to be developed based on market needs and in close collaboration. BSI CTMS is unique because it offers CTMS, eTMF and Study Startup functionality in one integrated platform. Excel and other standalone solutions are overrated.

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 aspects of your clinical trial can be managed from one platform. Zapclinica, an eClinical suite, is designed to manage and execute every aspect of your hybrid or virtual decentralized clinical trial. Automate complex processes, identify outliers and optimize resources. This will improve decision making and collaboration among sponsors, CROs, sites, and other stakeholders. Zapclinica makes it easier to manage a clinical trial. All aspects of your clinical trial can be managed from one platform. Zapclinica, an eClinical suite, is designed to manage and execute every aspect of your hybrid or virtual decentralized clinical trial. Automate complex processes, identify outliers and optimize resources. This will improve decision making and collaboration among sponsors, CROs, sites, and other stakeholders. Zapclinica makes it easier to conduct a clinical trial that is successful. All aspects of your study can be covered with one platform. You can choose the app that you need in one environment, with no additional vendors or third-party.

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.

Accelerating the development and delivery of life-saving medicines, and enabling cancer patients to have access to the best quality of cancer research and care. Our software revolutionizes patient access to innovative drugs & clinical trials. FICS is a software that allows the collection of regulatory standards data during patient care. FICS combines traditionally separate and noncommunicating applications to create a novel end-to-end platform. This allows clinical trials to be performed faster, easier and with greater quality.

AcceleTrial™, takes the guesswork out identifying and activating clinical trial sites. Our Study Start-up Management System is based on objective data, not self-identification. AcceleTrial™, a global database of thousands of sites, is indexed and ranked based on: Objective Site-specific Therapeutic Expertise and Objective Site-specific Clinical Test Experience. Objectively match the right sites with objective data on expertise, patient data, and experience to your clinical trials. AcceleTrial™, an automated "push-and-pull" structure, allows you to quickly launch the right sites and begin enrolling patients. It is available in multiple languages. Collect required documents accurately using pre-filled templates. Track activities in real time. You can immediately start using the system - a cloud-based solution that requires minimal IT setup or training. Integrate AcceleTrial™, CTMS, or other clinical trial system.

TCS ADD platform speeds up speed-to-market for the pharmaceutical industry across all clinical R&D value chains and makes clinical trials more efficient and safer. TCS ADD facilitates digital ecosystems, simplifies data complexity, and provides patients faster access to effective drugs. The platform is powered with TCS Decision FabricTM cognitive artificial intelligence engine, smart analytics and IoT which provides superior business value for the pharmaceutical industry. The next-generation, end-to-end metadata-driven solution for managing industry and sponsor clinical standards. Data science-driven platform that uses AI & ML technologies to speed up study start-up, targeted interventions, and quicker decisions. This solution digitizes the entire clinical supply management process, while placing the patient at the center. This increases patient safety and overall efficacy.