Alternatives to eDeviation
Compare eDeviation alternatives for your business or organization using the curated list below. SourceForge ranks the best alternatives to eDeviation in 2026. Compare features, ratings, user reviews, pricing, and more from eDeviation competitors and alternatives in order to make an informed decision for your business.
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1
ValueStreamer
Staufen. ValueStreamer GmbH
Streamline your shop floor management with ValueStreamer, the all-in-one digital solution. Easily view team-specific KPI boards, handle deviation management on the spot, and solve problems with binding tasks using the PDCA and A3 problem solving methods. Automatically aggregate KPIs across all hierarchies. Effortlessly connect to your existing IT systems like MES, ERP, and EDGE through our standardized REST API. Go beyond basic BI and experience true collaboration within your company. Save time, effort, and money with ValueStreamer. Features include: - Target/actual key figures with automatic aggregation of KPI values - Linking of top issues, go & see, feedback, and actions - Deviation management with prioritization in the Pareto chart - T-Cards for process confirmation on the shopfloor - Connectivity via REST API to systems like MES and ERP - Mapping of typical company processes in medium-sized businesses such as AAP, product development process, CIP, and Kanban.Starting Price: $29.95 -
2
Medrio
Medrio
Medrio is on a mission to ease complexity in today’s hybrid, decentralized, and site-based clinical trials by delivering a flexible suite of eClinical technologies and services, including EDC, eCOA, ePRO, eConsent, Direct Data Capture, and Randomization and Trial Supply Management (RTSM). Trusted by CROs, sponsors, and sites across all therapeutic areas and trial phases from study startup and feasibility to post-market approval, we are industry-recognized for delivering eClinical software with intuitive interfaces and time-saving “drag and drop” configurations as well as high-touch customer engagement, onboarding, and support services. Medrio’s 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. -
3
eAdjudication
Ethical
Ethical eAdjudication is an innovative endpoint adjudication and e-clinical software solution. With an intuitive and user-friendly cloud service designed exclusively for study leaders, QA staff, and committee members, Ethical eAdjudication offers the simplest solution to seamlessly manage event database, committee assessment, and disagreement and consensus meetings in a GxP controlled environment. By leveraging Ethical eAdjudication, users are given the opportunity to accomplish independent review and adjudication procedures in an effective, timely, and quality controlled manner. -
4
ArcheMedX Ready
ArcheMedX
Pharma and biotech trust Ready by ArcheMedX to better equip their trial teams, improve decision making, and reduce study delays. Prevent the most common sources of study delays, by better understanding which sites and teams are most prepared to start and effectively conduct the study. Reduce time and costs spent resolving issues, especially early in the trial. Confidently know which sites truly understand your patient eligibility requirements. Enjoy knowing they’ll be better equipped to enroll eligible patients sooner, hit enrollment targets, and avoid screen failures. With detail down to each individual and study objective, you can know with confidence that trial team members truly understand the specifics of the protocol. Predict where risks lie so you can prevent them, and experience fewer deviations overall. -
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Ennov CTMS
Ennov
Ennov CTMS facilitates the end-to-end management of clinical trials. The software allows sponsors to be more efficient, to make better decisions, to ensure compliance, to select investigators well, to monitor patient recruitment and to manage finances. Ennov CTMS includes comprehensive directories to manage site personnel (investigators, sub-investigators, study coordinators, pharmacists) and organizations (hospitals, competent authorities, CROs, suppliers). Ennov CTMS provides functions for tracking patients, patient visits, EDC data, activities, queries, deviations, adverse events, drug supply, monitoring visits and finances. A full complement of reports and dashboards provide total visibility into the status of each study, country, site and investigator to provide the information necessary to make the best decisions possible. - Comprehensive CTMS software - Integrated with Ennov Clinical Data Management - Clear visibility into investigational sites - Integrated workflow -
6
eReconciliation
Ethical
With eAdjudication® software managed service, trial leaders have control of timelines, the flexibility to adapt to changing conditions and outcomes, and the ability to monitor trends in provider performance and protocol conformity over the duration of long trials. Avoid hidden costs and timeline breaches in your Endpoint Adjudication Study with the innovative, all-inclusive, managed software service. The eAdjudication® Managed Software Service is the most efficient way for Endpoint Adjudication (CEC) Management. Working with the eAdjudication® platform and Ethical's Staff, study teams, committee members and clinical organizations interact effectively online in real-time in an user-friendly, and GxP-compliant environment, avoiding time-consuming, costly and error-prone manual processes. eAdjudication® all-inclusive services streamline the integration and adoption of EA software throughout eClinical organizations. -
7
Next Field
Next One Technology
Handovers, safety rounds, condition assessments, HSEQ, QA and JSA. Whatever you do, CHECKD will make it easier for you. Log deviations and pins, delegate, follow up and extract reports. Get a complete overview of the basic drawings for the project using our WEB and field application. Workers in the field can feel secure knowing that all drawings are easily accessible in their pockets. All types of projects: construction, assignments, operations, etc. Upload your drawing files, and plot points directly on the drawings. Log deviations, tasks, observations. Extract digital reports, or export them as a PDF. Fill in our standardized checklists, such as RUH, deviations, change notifications, takeovers, etc. You can also order your own checklists. Super-simple, visual field tool for people in the BAE industry. Get all inspections, handovers, and checklists right in your pocket. Plot points directly on the drawing, and delegate to the person in charge.Starting Price: $12.00/month/user -
8
IXRS®3
Almac Clinical Technologies
Available in multiple modalities, our market-leading solution for patient randomization and trial supply management is the most configurable and customizable Interactive Response Technology available. From Phase I through to IV, simple designs to complex adaptive trials, IXRS®3 will easily accommodate any permutation of study objectives, and with it comes a team of professional biostatisticians, language and integration experts who are at the ready 24/7. The site-facing functions are designed to automate steps that are prone to human error. Site users have the freedom to make data corrections without the need to call a Help Desk for support or fear of deviating from trial compliance. Easy-to-read visual tools instead of hundreds of pages of specifications and legalese. View and react to each stage of the software build along the way, eliminating delivery surprises. -
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ClearEdge3D Verity
ClearEdge3D
Verity empowers AEC teams to generate accurate quality assessments at scale. Automatically identify deviations between your Autodesk Navisworks or Revit model and as-built point cloud data to verify the placement of installed work or validate the quality of your models. Streamline QA/QC processes, enhance your clash detection workflows, and ensure final construction matches the intended design so that you can reduce rework, schedule overruns, and overall project risk. Easily compare as-built point cloud data with your design & coordination models to identify installation or modeling errors on anything from individual elements to entire scopes of work quickly and accurately. Gain a more detailed and actionable analysis in a fraction of the time compared to traditional methods. Customizable heat maps and color-coded reports intuitively display deviation, bending, and deflection. Precise measuring tools provide you with quantitative data on how installed elements deviate from your model. -
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Clinion CTMS
Clinion
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. Our Clinical Trial Management System allows CROs and Sponsors to monitor the trial progress actively with its advanced dashboard and alert notification system. So you’ll never miss a deadline again! What can you expect? Comprehensive CTMS Software Single Source for your entire trial data On-demand Analytics for Risk-Based Management of Clinical Trials Fully Integrated with Clinion EDC and Clinion RTSM 100% web-based and hosted securely on the cloud 21 CFR Part 11 & GD -
11
delta
TIMining
Delta automatically calculates mine plan spatial compliance using actual topographical surveys and planned mining surfaces. Timely information and agility are the key in addressing spatial deviations from the mining plan. TIMining Delta aims to reduce deviations from the mining plan sequence based on actual surveys and planned surfaces or 3D plan solids. TIMining Delta automatically carries out spatial compliance calculations and outputs compliance solids to import in all major mine planning software. Spatial deviations are reduced with TIMining Delta thanks to the systematic monitoring of actual versus planned progress, in a matter of seconds. TIMining automatically calculates the spatial differences between the initial and final mine surveys and the mine plan for a given period, categorizing volumes and tonnages. It then generates exportable outputs for each of the plan compliance solids, supported by all commonly used mine planning software. -
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LANA Process Mining
LANA
Discover the possibilities of the best Process Mining tool for your processes. LANA maps processes as they actually occur. And as you have never seen them before. The target/actual comparison automatically shows critical deviations in the process flow. Thanks to Machine Learning, LANA not only finds deviations, but also their causes. All relevant data at a glance, flexible dashboards allow precise control of processes. LANA Process Mining builds a complete process model from your process data in a matter of seconds. Here you can see not only how and in how many variants your processes are actually executed in daily business. The intuitive visualization also draws your attention directly to critical values: bottlenecks, high processing times and long idle times. Whether you upload your own target model of your process or have LANA simply create a new one, the tool automatically detects all discernible process deviations by comparing the target and actual states. -
13
Ketryx
Ketryx
Ketryx enables life sciences teams to use their preferred DevTools and automation to generate evidence, real-time traceability, and prevent process deviation. Automated documentation provides teams significantly more time to focus on big risks. Ketryx embeds QMS procedures into Jira and other development tools making process deviation impossible. Release safer software faster using automation to generate documentation, traceability, and streamline processes. Ketryx can be integrated with CI/CD pipelines so that teams can guarantee their releases are fully compliant before going live. Save significant time every release cycle by automatically generating required documentation and traceability for each release. Search and use filters across the lifecycle to quickly track changes between versions, find gaps and focus efforts. -
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Biorce Aika
Biorce
Biorce’s Aika is an AI-native clinical intelligence platform that accelerates every stage of the clinical trial lifecycle by replacing slow, manual protocol development and feasibility assessment with explainable, evidence-based automation. Built on insights from around one million real global trials, it generates first-draft study protocols, complete regulatory documentation, site feasibility assessments, risk and data management plans, and other essential trial artifacts in a fraction of the time traditional methods require, helping reduce delays and costly amendments. Aika provides full transparency into how it reaches recommendations so teams can confidently present choices to regulators and maintain expert control, blending AI speed with clinical expertise. It minimizes trial preparation timelines from weeks to days, cuts the number of amendments, and lowers overall risk while integrating seamlessly into existing workflows without heavy retraining. -
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Increase revenue, volume, and profitability with end-to-end processes for trade management. Enable consumer products sales leaders to oversee trade promotion planning and management, advanced trade management analytics, and customer business planning with SAP Trade Management. Use our integrated tool for customer business planning to plan more accurately, identify plan deviations faster, and react to deviations more effectively. Combine manufacturer and retailer perspectives and communicate and negotiate with your customers in their language. Integrate volume, margin, assortment, promotion, and financial planning and match deductions to promotion invoices to speed the clearing process. Monitor promotional details and accruals, deliver a central claims repository for reconciliation and grant real-time visibility into payments and fund liabilities.
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WizRule
WizSoft
WizRule, data auditing, automatically reveals patterns in the data under analysis and points at cases deviating from these patterns as suspected errors or frauds. A suspected fraud or error is defined as a case that deviates from valid patterns. WizRule is used by auditors, fraud examiners, forensic investigators, data-quality managers. One of their main tasks is revealing fraudulent cases and errors in data. WizRule can help in carrying out this task. WizRule is a data-auditing tool based on data mining technology. It performs an analysis of the data revealing inconsistencies and "strange" cases to be investigated. WizRule works automatically – the user just selects the data and WizRule does the analysis. WizRule checks all the relationships among the values within the various fields and reports unexpected and unlikely cases. WizRule reveals fraudulent cases missed by the standard auditing tools.Starting Price: one time licensing fee -
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QbCheck
Qbtech
QbCheck is a clinically validated, web-based ADHD assessment and monitoring tool that provides clear, quantifiable measures of the core symptom domains of attention, impulsivity, and activity by combining a structured computer task with real-time activity tracking using facial mapping and motion analysis; it generates objective data and reports that clinicians can use alongside interviews and rating scales to support diagnostic clarity and treatment decisions. Designed for flexible use, QbCheck can be administered securely in-clinic or remotely in suitable settings and integrates with clinician workflows via a portal that manages patient profiles, test progress, and results access. The test typically lasts about 15–20 minutes and benchmarks individual performance against large normative datasets matched by age and sex to highlight deviations related to ADHD traits, with instant result availability upon completion. -
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Situm
Situm
Turn indoor positioning in your best tool. The indoor navigation solution to integrate easily in your app. Make sure that your visitors find the shortest route to their destination. Improve user’s experience in your building by eliminating frustration and waste of time. Interact with clients to increase commercial profitability. Help your visitor to find their destination in Real-Time and without deviations. Make the location of their vehicle in your parking easier. Guarantee a step-by-step navigation with recalculation for deviations. Define special routes for People with Reduced Mobility (PRM). Make the location of Points of Interest like elevators or customer support points easier through maps. Reduce signage costs by implementing a more flexible solution. Increase your profitability by activating geolocated notifications and promos. Plan your spaces and services through geoanalytics on visitor habits. -
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METS
SPD Enterprises
METS is the Best Application for Project Estimation and Material Tracking. A true web-based application built and optimized for MEP contractors by people who know the business. From collaboration to accountability, METS is the most comprehensive material management solution for MEP Projects. METS's integral systems for extended validations and approval of various business processes augments the capability to "Delegate with Authorization" yet retain control and monitoring of the projects. METS's tools to perform on-demand analysis and its efficiency to get project status and deviations reports etc., all assists the team in taking prompt, reliable and accurate decisions. Prominent Challenges for HVAC projects are controlling the Scope of Work, minimizing deviations/variance, and delegating of authority. METS is the best way to accurately estimate, has robust change control management, delegates authority with limitations, and best tool for continuous monitor tracking. -
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Agatha
Agatha
Agatha offers a suite of cloud-based applications tailored to the life sciences industry, enabling centralized management of documents and processes across clinical operations, quality, regulatory, and training functions. It supports biotech, pharmaceutical, medical-device, and contract-research-organization workflows by offering modules such as eTMF (Inspection-Ready Master Trial File), Remote ISF (Investigator Site File) management, SOP creation and approval, Quality document management for CAPAs, deviations, and change controls, and regulatory document management. Agatha enables streamlined document creation, review, approval, storage, and sharing in one unified system, supports paperless transformation to reduce administrative burden and strengthen data security, and is built on a global-compliance architecture addressing standards like 21 CFR Part 11, GDPR, and EU Annex 11. -
21
Control Tower
ControlT
Control Tower is a web-based platform designed to manage and monitor logistics operations in real time. It integrates data from multiple sources such as GPS, ERP, sensors, and external systems, allowing users to visualize each shipment’s status, detect deviations, and automate tracking through configurable alerts. Through a unified interface, logistics and monitoring teams can anticipate risks, respond to incidents, and improve transportation traceability—without relying on manual processes. Key Features: Integration with GPS and external systems Real-time visualization of each trip’s status Configurable alerts for: Route deviations Unauthorized stops Delays against itinerary Proximity to destination Delivery confirmation Chronological event and condition logs Operational dashboards and reporting tools Key Benefits: Complete visibility over logistics operations Automated tracking and alert handling Full traceability of cargo movement Real-time notifications -
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MonQual
MonQual
MonQual QMS comes with pre-built, DMS and LMS systems. But do you know it offers integration with various stand-alone systems too? You can integrate your LIMS (Laboratory Information Management System), MES (Manufacturing Execution System), SAP, WMS (Warehouse Management System), etc. This applies for both legacy and modern applications. MonQual is everything your quality team dreams of. It combines quality with compliance management, business intelligent tools, and business productivity. A built-in DMS and LMS services along with automated workflows takes care of your documents and regulatory standards. Quality deviations are a part of process; however, we can stop avoid them in the future. MonQual offers processes that can identify deviations at an early stage, tracks them and runs a root cause analysis and finally, records and documents them to avoid future recurrence. -
23
Imerso
Imerso
Imerso is the smartest construction monitoring platform in the industry to create true-to-life Digital Twins. Save costs, accelerate deliveries, cut travels, and improve facility management with unprecedented insight and indisputable as-built data. Alerts of field work deviations. Notes and comments appended to real objects. Measurements with millimetre accuracy. Online remote collaboration. A 3D Digital Copy of the building, representing the current status with millimeter precision. Capture all the different building stages - from start to finish. Remote teams can navigate the virtual job site collaboratively from their browser, just like being there, taking measurements or creating status reports. Problematic deviations from the plans are highlighted in minutes. No more costly surprises, delays, or partner disputes. Progress and performance of all trades at a single glance, with unprecedented insights into your teams, projects, and best practices. -
24
3D Inspection Systems
3D Inspection Systems
3DInspection is a cloud-enabled quality inspection and reporting platform that helps manufacturers, fabricators, contractors, and quality teams capture, analyze, document, and share inspection data with precision and speed using handheld 3D scanning devices, drones, or coordinate measuring machines. It centralizes inspection workflows, standards, and results in a single system so users can perform guided inspections with step-by-step checklists, collect rich measurement and alignment data, and generate professional 3D-augmented inspection reports complete with visuals, annotations, deviations, and acceptance criteria that accelerate decision-making and reduce rework. It integrates with modern digital tools and scanners so teams can import point clouds, meshes, and CAD references, compare actual parts to design tolerances automatically, and visualize deviations in real time on interactive 3D viewers accessible via browser or tablet.Starting Price: $1,199 one-time payment -
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Empower consumer products sales leaders to step up as profit and loss (P&L) owners who drive revenue, volume, and profitability. Increase revenue, volume, and profitability with end-to-end processes for trade management. Enable consumer products sales leaders to oversee trade promotion planning and management, advanced trade management analytics, and customer business planning with SAP Trade Management. Use our integrated tool for customer business planning to plan more accurately, identify plan deviations faster, and react to deviations more effectively. Drive price, volume, and margin toward company targets in real-time. Combine manufacturer and retailer perspectives and communicate and negotiate with your customers in their language. Integrate volume, margin, assortment, promotion, and financial planning and match deductions to promotion invoices to speed the clearing process. Enable users to run a closed-loop process, from budget planning to execution and settlement.
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Attain
RPMGlobal
Attain is the industry’s only optimization tool for open pit and underground mines that maximize alignment of the short-term plan with the long-term plan, allowing mine operators to attain the full economic value of their operations. Attain is a flexible mine schedule optimization tool enabling users to generate optimized short-term schedules that maximize alignment with the long-term mine schedule. Optimization capabilities ensure deviation from the long-term plan is minimized. Decision support with rapid rescheduling options in response to unplanned events. Avoids unforeseen loss of value caused by necessary re-planning. Identify the most frequent sources of deviation from your plan. Integrated mine planning that maximizes planning compliance. With Attain, users have a software solution that ensures operational mine planning is systematically aligned with the long-term plan. This approach ensures the operation has optimized short-term plans that are feasible. -
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PostureZone
BodyZone
Reveal imbalances and asymmetries that can lead to back pain, stress, poor health, poor performance and even make you look older before your time. PostureZone is a tool to check posture and set a benchmark for improvement. A posture picture is worth a thousand words, and provides compelling visual evidence of improvement (or decline), as well as providing important data for tracking postural changes and choosing appropriate posture exercise rehab protocols. Quickly observe deviations of misalignment between the head, torso, and pelvis over the center of the feet. PostureZone screenings measure distortions in degrees to clearly identify symmetry, balance, improvements or changes. -
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inoPLAN
inoDIGIT
The ability to react quickly to deviations from the schedule is even more important than the definition of the initial plan. The inoPLAN APS (Advanced Planning and Scheduling) system uses advanced algorithms to automatically set an optimized production plan. Unlike MRP and MRP II systems, the inoPLAN offer finite scheduling resource capacity. The plan is always up to date, because it is recalculated and optimized every time any changes occurs. Scheduling is done automatically based on your available resources. You don't have to worry about allocating resources to tasks. SaaS delivers quick and long-term ROI. Select or define the plan for your new project with a fast and easy to use tool. You can immediately check out various scenarios and the impact on other scheduled and ongoing projects. The project and all tasks are automatically scheduled. As soon as there is a deviation in any task that causes some delay in the deadline of any project, you will be alerted. -
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Amazon Inspector
Amazon
Amazon Inspector is an automated security assessment service that helps improve the security and compliance of applications deployed on AWS. Amazon Inspector automatically assesses applications for exposure, vulnerabilities, and deviations from best practices. After performing an assessment, Amazon Inspector produces a detailed list of security findings prioritized by level of severity. These findings can be reviewed directly or as part of detailed assessment reports which are available via the Amazon Inspector console or API. Amazon Inspector security assessments help you check for unintended network accessibility of your Amazon EC2 instances and for vulnerabilities on those EC2 instances. Amazon Inspector assessments are offered to you as pre-defined rules packages mapped to common security best practices and vulnerability definitions. Accelerate MTTR by using over 50 sources for vulnerability intelligence to help identify zero-day vulnerabilities quickly. -
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BREEZE CTMS
BREEZE CTMS
Electronic source documents – eSource – eliminates paper, standardizes and simplies workflow, and reduces errors and omissions. BREEZE eSource goes way beyond visit templates and scheduling. By synchronizing clinical contexts, regulatory and protocol requirements, with study procedures, BREEZE eSource ensures that users not only capture all protocol required data. BREEZE business rules make certain that the data collected are correct, complete, accurate, and compliant. Our dedicated team of clinical trial experts delivers custom, study-specific eSource documents for review and approval before study start-up and supports you throughout the trial and modifies them as needed. Modules seamlessly integrate and work together. Cross-Module Action Multiplier goes a step further by anticipating and completing automatically the additional tasks required by entries you make. For example, completing visits or procedures automatically posts to invoicing, recalculates scheduling, and more. -
31
Relecura
Relecura
Streamline your innovation ecosystem through the assimilation of the latest AI capabilities for a competitive edge. Relecura’s forte is its flexibility and adaptability to address specific problems and close-fitting solutions. The basic problem is that innovators are often not able to identify the industrial and commercial significance of their innovation as due diligence takes long days of analysis, necessitating a deviation from their regular and familiar activities. And it is a tedious iteration process. The latest custom AI capabilities help you assess the commercial value of innovation and technical due diligence can be automated to yield meaningful and immediate results. The repetitive tasks could be automated, and your time and energy could be devoted to strategic missions. -
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Clin'form
Kayentis
Clin'form is a flexible, robust, and comprehensive electronic Clinical Outcome Assessment (eCOA) platform designed to streamline clinical trials for patients and sites, enhance data quality, and accelerate processes for research teams. It is adaptable to all protocols and populations, effective for any type of questionnaire (PRO, ObsRO, ClinRO, Diary), and caters to all age groups, from pediatric to older patients. The platform accommodates any population size, capable of managing studies ranging from a handful to over 10,000 patients across all geographic regions. Clin'form offers seamless integration with other clinical systems, ensuring a smooth workflow, and supports flexible data collection modes, including provisioned tablets or smartphones, the patient's own smartphone, web access from any browser, and interviews. Key features include an embedded tele-visit feature to plan for the unplanned, patient engagement modules to ensure high patient compliance. -
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Vizion OE
IT Vizion
Finally, a simple and flexible centralized metric management system. Create indicators for strategic objectives, sites, departments, functions, plant areas, roles, units, critical assets. Focus on significant target deviations and limit exceptions, no delay waiting for out-of-date reports, analytics to focus on significant gaps, data source agnostic, real-time data, relational data, ERP, and manual entry data. -
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BrickControl
BrickControl
BrickControl is a “cloud-based” application that helps you manage all of your projects in an easy, simple, and efficient way. Estimates, Project Progress Reports, Certifications, Costs Analysis and more. BrickControl covers a range of needs, making the work of professionals and companies involved in a project much easier. Small, medium, and large construction companies, architects and engineers, remodelers, construction managers, interior designers, cost controllers and financial departments, and universities. Create budgets and study your project’s documents. Manage the day-to-day activities of the construction. Manage project deviations. BrickControl is a “cloud-based” application that helps you manage all of your projects in an easy, simple, and efficient way. Estimates, Project Progress Reports, Certifications, Costs Analysis and more.Starting Price: $25 per month -
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Oracle Clinical One
Oracle
Clinical One RTSM can support a randomization strategy for the simplest to the most complex studies without the need for programming or coding, which eliminates the need for prolonged user acceptance testing. Take control of your study through self-service configurations and build a study in days instead of weeks. Assess the status of the drug inventory and make modifications in real-time without reverting to the vendor and incurring cost and change requests. Eliminate change request costs and avoid delays by quickly implementing changes and promoting your studies in seconds. The only platform that truly unifies people, processes, and data to simplify and accelerate the clinical trials of the future. Virtual components in clinical trials allow greater patient participation and significantly improve clinical trial data quality. Transformative digital strategies are needed for faster study startup to harmonize data from any source and to streamline workflow. -
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Longboat
Advarra
Longboat is a cloud-based clinical trial support solution provides users with an integrated Guided Compliance toolset to guide them at all times. Longboat provides the clinical trial site staff with the right resources to let them focus on patients. Longboat allows patients to view essential study information and check visit reminders. Longboat allows users to seamlessly manage the controlled rollout of the amended clinical trial protocol. Centralize the secure exchange of regulated documents between sponsors, CROs, and sites, significantly streamlining study startup and eliminating historically cumbersome processes across research stakeholders. All key stakeholders—clinical operations, monitors, site staff, and participants—access one integrated support platform with content tailored to meet their specific needs. Provide your site staff the tools and resources they need to stay engaged and compliant while focusing on the participant. -
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Avela
Avela
Avela envisions a world where opportunities are more equitably and efficiently allocated, starting with education. We give enrollment, admission, and award officers the tools to make equitable decisions and empower families. Governments and nonprofits also use our platform to allocate talent and resources fairly and effectively. Our suite of products covers each stage of the admission or selection journey. Whether you are choosing students for your school, recipients for your scholarship, or fellows for your program, It ensures your selection committee makes informed, equitable decisions. Our founding team includes a Nobel Laureate and a Clark Medalist. They showed that school districts see a 90% reduction in the number of dissatisfied families when using our approaches. This has real learning implications - their research at MIT showed that students who enrolled in their first choice school improved math achievement by 0.4 standard deviations. -
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Science 37
Science 37
Science 37 is a clinical research company specializing in decentralized clinical trials through its Metasite model, which eliminates physical proximity as a barrier, enabling patients to participate from anywhere. This approach expands access to over 90% of patients who are unable to participate in traditional site-based research, offering the recruiting power of 20 sites in one and providing the flexibility patients need to participate from anywhere. The Metasite is powered by a proprietary platform that drives uniform study orchestration, guiding the workflow of patients and study staff, and capturing study data without the need for manual reentry. This centralization of people, processes, and platforms delivers built-in protocol compliance, ensuring greater compliance and high-quality data. Science 37's in-house medical teams, telemedicine investigators, and mobile nurses have extensive experience in remote trial conduct across various therapeutic areas, ensuring broad reach. -
39
Validfor
Validfor
Validfor is a secure, modular digital validation platform that centralizes the entire validation lifecycle on a single, paperless system. Designed specifically for regulated industries, Validfor enables efficient validation while ensuring full compliance with GAMP 5, 21 CFR Part 11, and EU Annex 11. The platform supports electronic records and advanced electronic signatures with full audit trails, role-based workflows (Author, Reviewer, Approver), and complete CSV compliance. All documents and records are securely managed in a centralized repository, capturing every change with full traceability to protect data integrity and Quality Assurance. Validfor offers integrated modules for Change Management, Deviations, Testing, and Periodic Reviews, enabling seamless impact assessments, CAPA tracking, Computer Software Assurance (CSA), and audit-ready lifecycle management. -
40
Tecplot RS
Tecplot
Tecplot RS is an integrated visualization and analysis software tailored for oil and gas reservoir engineers. It facilitates the management and interpretation of reservoir simulation data through comprehensive XY plots, 2D cross-sections, and 3D grid visualizations. The platform supports data import from various simulation sources, enabling users to efficiently organize results, validate reservoir models, and effectively communicate findings across teams. Recent updates, such as the 2023 R1 release, have introduced features enhancing the assessment of history match quality by allowing the creation of selection sets based on deviation bands. Additionally, the software now supports the visualization of negative values in stamp plots, aiding in the analysis of fluid behavior trends within reservoirs. With a user-friendly interface, Tecplot RS ensures a short learning curve, complemented by full technical support and free online training. -
41
Effcon (Effective-Control)
Effcon
MONAROV & Co. Consulting’s Effcon system (effective – control) is a unique automated system which was developed based on over 20 years of experience in the fields of Internal Control and Fraud Prevention Engagements. The system facilitates the maintenance of an automated, continuous and independent control system for purposes of identifying control weaknesses, fraud and irregularities, reducing operational risks and assessing the effectiveness of internal control in the organization. The system constitutes a major tool in assisting organizations in achieving their business objectives. Our firm assists organizations in installing the Effcon (Effective control) system which contains defined sets of analytical rules. The set of analytical rules is defined by a team of experts with vast experience in discovering deviations in various fields, based on many years of experience in our firm, in the fields of control and risk management. -
42
Mereo
Mereo
Integrated platform for managing people and organizations . We have the right tools to align people's results with companies' results. Everything you need to achieve your results in one place . Use each of our solutions separately or in an integrated way. Fully automated system to maximize your results. More assertive decisions through effective targets and indicators to generate alignment. Assess skills and improve your team's performance. Structured and transparent processes for calculating variable remuneration. Manage training and monitor the evolution of your team. Evaluate your talents through competencies, provide feedback and carry out PDIs. Plan and track goals, analysis of deviations and action plans in an automated way. Measure your team's engagement and make data-driven decisions. Have a variable compensation plan with analytical reports and simulation of results.Starting Price: $20 per month -
43
Zapclinica
Zapclinica
Manage your clinical trial in one platform. Zapclinica is an eClinical suite designed to manage and conduct every aspect of your decentralized clinical trial - hybrid or virtual. Automate complex processes, identify outliers, optimize resources, improve decision making and collaboration between sponsors, CROs, and sites. Zapclinica reduces the time and costs to run a successful clinical trial. Manage your clinical trial in one platform. Zapclinica is an eClinical suite designed to manage and conduct every aspect of your decentralized clinical trial - hybrid or virtual. Automate complex processes, identify outliers, optimize resources, improve decision making and collaboration between sponsors, CROs, and sites. Zapclinica reduces the time and costs to run a successful clinical trial. Cover all aspects of your study with one platform. No extra vendors, no extra third-party, choose the app you need in a single environment, including EDC, ETMF, Payments, Logistics, and many more. -
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LifeSphere eTMF
ArisGlobal
LifeSphere eTMF is your clinical trial’s single source of truth. Discover a versatile solution that streamlines inspections, ensures compliance, and saves your organization time and effort. Built as the first system to support the TMF reference model, LifeSphere eTMF aligns Clinical documentation with regulations and study protocols in one solution. Create and manage a single source of truth for your clinical trial. Ensure trial master file quality, timeliness, and completeness with live collaboration and real-time document sharing. Streamline TMF inspections quickly and efficiently to handle any audit. Maintain compliance with embedded workflows and dashboards that allow easy trial reconstruction. -
45
QCBD
CAMA Software
Quality Collaboration By Design (QCBD) is a fully integrated quality management software solution designed specifically for manufacturing businesses. This affordable, Windows-based application reduces the cost of achieving and/or maintaining compliance with quality management standards such as ISO 13485, ISO 9001, TS 16949, AS9100, and SQF 2000 / ISO 22000. QCBD by CAMA Software offers a host of modules for training management, supplier management, process deviations, document control, equipment management, and more. -
46
Jeeva eClinical Cloud
Jeeva Informatics Solutions
Jeeva's patent-pending modular solution is designed from the ground up on the most powerful cloud platform with one login from any browser-enabled mobile device for remote patient screening, education, enrollment, electronic informed consent, bi-directional communications via video calling, telemedicine, SMS, email, and evidence generation including electronic patient-reported outcomes and clinical outcomes assessments, with a modern user experience. Delays in patient recruitment & retention are keeping them up at night. Generating enough evidence of safety and efficacy of investigational new medicines is critical to get timely approval from regulatory agencies. Whether you are a patient group setting up a registry or natural history study, or a biopharma sponsor of a clinical trial, or a long-term follow-up study for gene therapy, Jeeva can save you time, and money while improving user experience for study team and trial participants.Starting Price: $100/mo/user -
47
CANEA Workflow
CANEA ONE
CANEA Workflow is a case management solution that allows users to quality assure, speed up, and automate their organization's administrative processes. With CANEA Workflow, users will not need the help of an IT expert in creating process driven applications. CANEA Workflow's design tool is easy to define, deploy, and improve on forms, workflows and business logic. CANEA Workflow also allows users to manage all types of workflows including HR-processes, risk, accidents, audits, deviations, and claims.Starting Price: $6.00/month/user -
48
Fusion eClinical Suite
Axiom Real-Time Metrics
Fusion is Axiom’s proprietary easy-to-use and cost-effective eClinical solution that is focused on small to medium sized device, pharma, and biotech companies. With Axiom’s Fusion eClinical Suite, you can add-on any Modules to meet your study requirements. Running a small study? Just choose the base configuration with EDC, DM and AE/SAE Tracking. Running something more complex? Include powerful Modules such as Inventory Tracking, RTSM, Safety Management to make the management of your study so much easier. Save time by capturing your study data electronically – even when offline! Data syncs to your Fusion databases once an internet connection is established. Access real-time records for Subject screening activities. Safety Database for the management of pharmacovigilance events directly within Fusion. -
49
Transition Technologies eCRF
Transition Technologies Science Sp. z o.o.
Flexible eCRF platform for non-commercial clinical trials, configurable to any clinical trial study protocol. Our eCRF solution was created on the basis of many years of experience of researchers and medical teams with whom we carried out research projects. The system is, above all, easy to use, user-friendly and extremely flexible. The prepared solution meets all the required quality standards, and thanks to the full control over the code, we can further develop and adapt it to the changing requirements of regulators and the clinical trials market.Starting Price: $45k licence -
50
Zelta
Merative
Zelta is a cloud-based unified clinical data management and acquisition platform with adaptable modules that can be tailored to meet the unique needs of your clinical trials program and accelerate outcomes. It offers features such as electronic data capture, clinical operations tools like randomization and trial supply management, clinical trial management system, electronic trial master file, and patient and provider engagement solutions including electronic clinical outcome assessments and electronic consent. Zelta is designed to manage clinical studies across all phases, therapeutic areas, and regions, providing a user-friendly interface and seamless access through single sign-on from anywhere in the world. The platform emphasizes flexibility and scalability, allowing for customization to align with specific study goals and the integration of solutions from both Zelta and other technology vendors.
