Alternatives to PRA Prism

Why is HORIZON ranked among the top 10 LIMS softwares? HORIZON was designed by lab managers and is an affordable LIMS platform that can be configured and integrated with any type of lab. It is not enough to consider a laboratory information management system an afterthought. It is too important to be forgotten. There is a better option. HORIZON LIMS was designed by and for its users. HORIZON is easily integrated and can be configured to adapt to any lab's existing systems. HORIZON was designed to seamlessly integrate with existing workflows, so there is minimal disruption and fast implementation. HORIZON gives you results that you can see right away. A team of problem solvers supports our intuitive interface. HORIZON was developed by lab professionals. We understand what you need in order to deliver results. HORIZON has expert support and implementation teams that will ensure your system runs smoothly into the future.

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.

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.

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.

DFnet, a healthcare technology company, provides eClinical services, including electronic data capture, eSource and data management services. Our services offer greater flexibility, better data quality, as well as greater efficiency for clinical trials around the world. Collect data from any source, including paper crfs, EDC, other electronic sources, online/offline tablet, and ePRO entries. Install in your secure premises or let us host it in our secure cloud environment. Advanced optical recognition reduces the time required to perform SDV and RBM processes. For multi-center studies with maximum flexibility. Web-based data collection from any source is instantaneously available in a central real-time platform.

The 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.

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.

Our software provides a complete end-to-end tracking solution that can be used in clinical trials. Simply download the software to your trial managers' mobile devices, and let TruLab's blockchain technology do the rest. To spot potential problems, don't wait for samples to reach a central laboratory. Observe data anomalies as the samples progress through the clinical trial. TruLab allows remote access to samples. 20% of samples are lost in late-stage trials or deemed unusable. This is not acceptable from a logistical, ethical, and financial standpoint. Samples are not collected only at clinical sites anymore. The new world of sample collection at residences presents new challenges in sample tracking. TruLab tracks samples anywhere in the world, from home to repository.

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

A simple and powerful CTMS that can be used by hospitals, site management organisations, and small CROs. It focuses on budgeting, financial tracking, and reporting. Clinicubes CTMS has many useful features that allow companies to manage and conduct clinical trials efficiently. The central management of the trial database allows for better productivity and provides more accurate information. Systematize, organize and reorganize the database of physicians and healthcare service providers. A single report will combine data from multiple studies and locations. Reporting options are available to show how the trial is performing against pre-set criteria. Interactive dashboards allow you to communicate study performance data as well as other operational reports.

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.

FreeLIMS allows laboratories to replace paper notebooks and spreadsheets with a cloud-based Laboratory Information Management System. This allows laboratories to eliminate manual errors, improve data quality, speed up laboratory operations, and reduce turnaround times. Laboratory work has changed from being a small project involving only a few researchers to large-scale projects that involve multiple laboratories across the globe and often hundreds or even thousands of samples. FreeLIMS, a web-based SaaS LIMS system, is a one-stop shop for managing your samples through the entire life cycle. All industries, including biobanks and clinical research, testing, food, and drink, can seamlessly manage their samples, along with full genealogy and chain of custody.

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

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.

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.

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

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.

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.

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.

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.

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.

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.

The industry's best AI-powered clinical analytics platform provides actionable insights that enable your teams to manage risk, improve performance across sites, studies, and vendors. Saama's state-of-the art clintech is designed to streamline workflows, automate tedious processes, and improve collaboration across clinical operations. Saama is trusted by sponsors and CROs for data aggregation, artificial intelligence solutions, and improved decision-making. This can help to reduce drug development costs and timeframes, as well as eliminate delays. Saama can help you get on the fast track for clinical trial process innovation. Your ClinOps and medical review team will find it much easier to access all of your clinical data in one place. Data managers are often undervalued. They can now focus on the data points that are important by eliminating manual work.

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.

Lifepoint Informatics is a trusted leader in healthcare IT. We promote value-based healthcare by providing uncomplicated clinical integration, data exchange and data interoperability solutions to hospitals, clinics, diagnostic imaging, insurance companies, accountable care organizations, and health systems. Our solutions are built on a unified workflow platform and can seamlessly interoperate across multiple modalities, applications layers, and end users devices. Lifepoint customers love our simple, user-friendly data integration solutions that facilitate health info exchange, enable successful outreach connectivity and EMR integration, EHR interface, physician portal, population management, quality reporting among disparate clinic systems.

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.

HCLAB is a flexible, comprehensive and practical laboratory information system (LIS). It can be easily customized to meet the specific needs of your laboratory. HCLAB is a medical and diagnostic laboratory information system (LIS) that can be used to automate routine tasks. It is suitable for hematology and coagulation, as well as urinalysis and microbiology, as well molecular and anatomical pathology. HCLAB can be scaled to any size laboratory, whether it is a small project site or a large multi-site healthcare organization or university hospital. HCLAB provides end-to-end information management from initial test requests to results reporting and delivery. Smart client workstations from HCL allow clinical staff to access the web and request orders. Tracks and manages samples sent to outside laboratories for testing that isn't done in-house.

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.

sLis Enterprise®, Suite for Clinical & Radiology Laboratories, is the result of systematic design, research, and development that was based on the extensive experience and knowledge of INFOMED's IT professionals in the radiology and diagnostic fields. sLis Enterprise®, a state of the art Information System, provides the flexibility and support needed to support any Laboratory Department in a user-friendly environment. It is highly customizable and adaptable to the specific requirements and complexity of each laboratory. sLis Enterprise®, which is an advanced, fast and powerful LIS, provides a unique environment for all diagnostic departments. It can be used as a single database, allowing all users to share information. It is also a tool for Quality Control Management across all sections of a laboratory.

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.

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.

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.

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.

Sunquest Laboratory™, the core engine of your laboratory operations, is equipped with comprehensive laboratory workflows and functionality to help you provide value and service to the healthcare community. The integrated laboratory information system, (LIS), can be interoperable with microbiology, anatomic pathology and physician outreach. It also includes blood bank capabilities. You can leverage end-to-end integrated processes such as specimen labels at collection, PPID, and many more. Manage multi-disciplinary, multisite, multilab environments. Collaboration and communication are key to achieving high quality results. Automate lab processes from order to reporting. Single sign-on is a great way to support your security processes. Connect with enterprise EHRs and physician EMRs.

ApolloLIMS is a robust lab information management system (LIMS), specifically designed for toxicology and pain management laboratories of all sizes. ApolloLIMS, the flagship product of Common Cents Systems allows users to seamlessly manage workflows from specimen accession to results reporting. The core components of ApolloLIMS include customer service, quality control, specimen processing and management reports.

FormFox provides industry-leading workplace safety and health tools and technology to all employers, collectors, TPAs, MROs, and laboratories. Our web-based, software-driven service streamlines all collection and event processes, from initial order to final decision, and reporting. FormFox reduces errors, saves time and expedites data delivery, improving quality, accuracy, speed, efficiency, and productivity for our clients and the people they serve.

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.

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.

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.

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.

Agri-Labs Information Systems, (ALIS), manages all types and forms of raw laboratory data that flows out of the sample lifecycle from beginning to end. Our informatics product was designed to run on Microsoft's 32 bit operating systems. It is not just another collection Excel spreadsheets that are used as front-ends for Access databases. Our ALIS LIMS is not written in a dying language. ALIS is a inter-relational database that consists of six modules (Soil, Water and Plant Tissue), and is based on matrices of Earth's hydrologic cycle. It can be used in agricultural and natural resources laboratories and other areas. ALIS LIMS can accommodate increased sample volumes. ALIS has been kept affordable.

Omda MedSciNet improves the quality, utility and management of medical information from collection to analysis. This secure, standardized software allows clinical researchers and other professionals from medicine and academia to easily gather and analyze well managed medical data. The Omda team is specialized in designing and building clinical studies and custom database applications for medical research. The Omda MedSciNet platform is a highly customizable, feature-rich and reliable online environment that hosts and manages sophisticated study and trial systems. Omda MedSciNet is a proven platform that has hosted studies and clinical trial systems of all sizes and scopes for over 20 years. The standard implementation includes all the components needed to establish fully functional clinical trials or studies.

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.

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.

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.

Our Smart Protocol system is designed to automate and add intelligence to clinical trials design with AI. Smart Protocol is revolutionizing how research teams design clinical trials. Humans can no longer physically digest all the information necessary to make a decision in today's digital age. A majority of companies have valuable data that isn't being used. Documents are stored in repositories without any line-of-sight. Companies in life science are making costly and difficult decisions based on incomplete information. We want to transform companies like yours' from a document-driven environment to one that is data-driven. We aim to reimagine how clinical trials are planned and researched by removing barriers between data and end users. We do this by mining huge amounts of trial-related documents both from customers and the public domain.

VIPER automates screening from remote patient identification (at point of diagnosis) through to qualified enrollment. VIPER uses artificial intelligence to match patients to precision trials within a narrow window of opportunity. This is done through the ingestion of lab-agnostic genomic and pathology data. It is tailored to the patient and the researcher. VIPER searches the personalized matching engine to locate the best clinical trials available for a patient's specific diagnosis--at that time. VIPER integrates workflow to send real-time notifications to the entire care team about a patient's eligibility in available clinical trials. This is done within a very limited enrollment window. VIPER provides interactive dashboards that allow you to access real-time data mining capabilities to aggregate patient data from both study and site levels to help you reach your study KPIs.

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.

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.

limsExpress Laboratory Information Management System, (LIMS), is exactly what you are looking for. It has all the features you need, without the complexity that you hate. It is fast, simple, customizable, and most importantly, affordable. limsExpress Plus is hosted on our cloud server. All you need is a browser to log in from anywhere. We take care everything: multiple power sources and lots of bandwidth, maintaining the server and updating software, securing data, backups (we love backups), and perhaps the best feature, no upfront cost. We also offer limsExpress Client Access System (CAS) if you don't like limsExpress Plus. This program allows clients to log in to a different cloud server (we believe in security) to view their logins, retrieve reports and more. It's also included in limsExpress Plus.