Alternatives to eDeviation

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.

ValueStreamer is your digital shopfloor management tool. All your KPIs can be pinned to team-specific boards. You can manage deviations directly on the KPI, and also solve binding tasks (PDCA, PDCA, A3Report). All KPIs will automatically be accumulated across all hierarchies. Connect your existing IT infrastructure (e.g. The standadized REST API allows you to connect your existing IT infrastructure (e.g. ERP, MES, EDGE ) with ease. You can go beyond common BI solutions to create true collaboration within your company, and save tons of time and sweat. - Target/actual key figures included Automatic aggregation KPI values - Linking top issues, feedback, actions - Deviation management incl. Prioritization in the Pareto Chart T-Cards are required for process confirmation - Connectivity via REST API, e.g. MES and ERP systems - Mapping typical company processes in medium-sized companies such as AAP and product development process, CIP and Kanban

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

Ethical eAdjudication represents a cutting-edge software solution for endpoint adjudication and e-clinical needs. This cloud-based service is crafted specifically for study leaders, quality assurance personnel, and committee members, providing an exceptionally user-friendly experience. It simplifies the management of event databases, facilitates committee evaluations, and organizes meetings focused on resolving disagreements and achieving consensus within a GxP compliant framework. By utilizing Ethical eAdjudication, users can perform independent reviews and adjudication processes effectively, ensuring timely results while maintaining rigorous quality control standards. This innovative platform not only streamlines operations but also enhances collaborative decision-making among stakeholders.

Through the use of the eAdjudication® software managed service, trial leaders can effectively oversee timelines, adapt to fluctuating circumstances and results, and track trends in provider performance and adherence to protocols throughout the extended duration of trials. This innovative, comprehensive managed software service helps prevent unforeseen expenses and timeline violations in Endpoint Adjudication Studies. The eAdjudication® Managed Software Service stands out as the most effective solution for managing Endpoint Adjudication (CEC). By collaborating with the eAdjudication® platform and Ethical's staff, study teams, committee members, and clinical organizations can engage seamlessly in real-time within a user-friendly and GxP-compliant framework, eliminating the inefficiencies, costs, and errors associated with manual processes. Furthermore, the all-inclusive nature of eAdjudication® services facilitates the smooth integration and adoption of EA software across eClinical organizations, enhancing overall operational efficiency. In doing so, it empowers research teams to focus on delivering quality results without being hindered by logistical challenges.

Effectively monitor clinical trials from start to finish with Ennov’s comprehensive Clinical Trial Management software. Each year, clinical trial sponsors search for new ways to improve the efficiency and reduce the costs associated with running their trials. Investigational site efficiency and productivity can be improved by centralizing information, actively monitoring progress, automating schedules, managing finances, and providing accurate reporting and metrics. With the Ennov CTMS, trial sponsors and CROs are able to actively address all aspects of trial management from a single platform: investigator sites, patients, SAEs, deviations, inclusions, visit reports, phone contacts, investigational product management, trial facilities, and finances. Study managers can plan and track their trials in real time to make better decisions faster. With the Ennov CTMS dashboard functionality, study personnel get on-demand analytics to improve quality, control risk, and reduce costs.

Our leading solution for managing patient randomization and trial supplies is available in various formats, making it the most adaptable and customizable Interactive Response Technology on the market. Whether you're conducting Phase I or Phase IV trials, and regardless of whether your study design is straightforward or involves complex adaptive methodologies, IXRS®3 is equipped to handle any combination of study goals. Additionally, you will benefit from a dedicated team of biostatisticians and integration specialists who are available around the clock to provide support. The functions intended for site users streamline processes that are typically vulnerable to human mistakes, allowing them to correct data independently without needing to contact a Help Desk or worry about compliance issues. Instead of sifting through numerous pages of specifications and legal jargon, users can access clear visual tools that enhance understanding. Furthermore, you can monitor and respond to each development stage of the software build, which helps to prevent unexpected issues during delivery, ensuring a smoother trial experience. This comprehensive approach not only facilitates efficiency but also empowers users with greater control over their trial processes.

Handovers, safety inspections, condition evaluations, HSEQ, QA, and JSA are all streamlined with CHECKD, which simplifies your workflow. You can easily log deviations and tasks, delegate responsibilities, follow up on progress, and generate comprehensive reports. Our web and mobile application provides you with a full overview of the essential project drawings, ensuring that field workers have immediate access to vital information right at their fingertips. This functionality extends across various types of projects, including construction, operations, and assignments. Simply upload your drawing files and mark key points directly on them, while also documenting deviations, tasks, and observations. You can extract digital reports or convert them to PDF format with ease. Additionally, you have the option to utilize our standardized checklists for multiple purposes, such as RUH, change notifications, and takeovers, or even create custom checklists tailored to your needs. This intuitive and visually engaging tool is designed specifically for professionals in the BAE industry, ensuring that all inspections, handovers, and checklists are readily available on mobile devices. With CHECKD, you can plot points on the drawings and delegate tasks efficiently to ensure smooth project execution.

Verity enables Architecture, Engineering, and Construction (AEC) teams to produce precise quality evaluations on a large scale. It facilitates the automatic detection of discrepancies between your Autodesk Navisworks or Revit models and the as-built point cloud data, allowing for effective verification of the installation positioning or validation of model quality. By optimizing QA/QC processes, improving clash detection methodologies, and ensuring that the completed construction aligns with the planned design, you can minimize rework, avoid schedule delays, and mitigate overall project risks. The platform allows for straightforward comparisons between as-built point cloud data and your design or coordination models, enabling quick and accurate identification of errors in installation or modeling, whether at the level of individual components or larger scopes of work. This results in a more comprehensive and actionable analysis that is achieved significantly faster than traditional approaches. The system features customizable heat maps and color-coded reports that clearly illustrate deviations, bending, and deflection. Additionally, accurate measuring tools furnish quantitative data regarding how installed elements differ from your original models, providing deeper insights into project integrity. Ultimately, Verity not only enhances efficiency but also fosters confidence in the quality of the construction outcomes.

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

Explore the potential of the leading Process Mining tool tailored for your workflows. LANA visualizes processes in their genuine form, providing insights you may not have encountered before. The automatic comparison between target and actual states effectively highlights significant discrepancies in the process execution. Leveraging Machine Learning, LANA identifies not only the deviations but also the underlying reasons for them. With all pertinent data displayed clearly and customizable dashboards, you can maintain precise oversight of your processes. In mere seconds, LANA Process Mining constructs a comprehensive process model from your existing data, illustrating how various process variants are performed in everyday operations. The user-friendly design also emphasizes critical metrics, such as bottlenecks, excessive processing durations, and prolonged idle times. Whether you choose to upload your own target model or let LANA generate a fresh one, the tool adeptly uncovers all detectable process discrepancies. By understanding these insights, organizations can refine their operations and enhance overall efficiency.

Delta efficiently assesses compliance with mining plans by utilizing real topographical surveys in conjunction with the intended mining surfaces. The essential elements for effectively managing deviations from the mining plan are timely data and flexibility. TIMining Delta is designed to minimize discrepancies in the mining sequence by referencing actual surveys alongside the planned surfaces or 3D model solids. This system automates the computation of spatial compliance and produces compliance solids that can be seamlessly integrated into all leading mine planning software. By continuously tracking the actual progress against the planned benchmarks, TIMining Delta significantly mitigates spatial deviations in mere seconds. Furthermore, it automatically computes the differences between initial and final mine surveys relative to the mining plan over specified periods, categorizing the resulting volumes and tonnages. In addition, it provides easily exportable outputs for each compliance solid, ensuring compatibility with all widely-used mine planning tools. This comprehensive approach enhances operational efficiency and accuracy in mine planning.

Boost revenue, volume, and profitability through comprehensive trade management processes. Empower sales leaders in consumer products to manage trade promotion planning and execution, utilize sophisticated trade management analytics, and engage in thorough customer business planning using SAP Trade Management. Leverage our unified tool for customer business planning to enhance accuracy in planning, swiftly identify deviations from the plan, and respond to those discrepancies with greater efficiency. Merge insights from both manufacturers and retailers to communicate and negotiate effectively with customers in their preferred terminology. Seamlessly integrate volume, margin, assortment, promotion, and financial planning while aligning deductions with promotional invoices to expedite the clearing process. Keep a close watch on promotional specifics and accruals, provide a centralized repository for claims reconciliation, and ensure real-time visibility into payments and funding obligations, ultimately fostering a more streamlined trade management experience. Additionally, this holistic approach not only simplifies operations but also enhances collaboration across all stakeholders involved in the trade management process.

Ketryx empowers life sciences teams to leverage their chosen development tools and automation for creating evidence, ensuring real-time traceability, and mitigating process deviations. By automating documentation, teams gain valuable time to concentrate on significant risks that could impact their projects. Ketryx seamlessly integrates quality management system (QMS) procedures into platforms like Jira and other development tools, effectively eliminating the possibility of process deviations. With its automation capabilities, Ketryx facilitates the rapid release of safer software by generating necessary documentation, ensuring traceability, and optimizing workflows. Furthermore, Ketryx can be incorporated into CI/CD pipelines, allowing teams to confirm that their releases are fully compliant prior to deployment. By automating the generation of essential documentation and traceability for each release, significant time savings can be achieved during every release cycle. Additionally, users can efficiently track changes across versions and identify gaps by utilizing search functions and filters throughout the lifecycle, ultimately allowing teams to focus their efforts where they are most needed. This comprehensive approach not only enhances efficiency but also improves overall project quality.

Transform indoor positioning into your most effective tool by seamlessly integrating an indoor navigation solution within your application. Ensure your guests can easily locate the quickest path to their desired destination, thereby enhancing their experience within your facility and reducing any potential frustration or wasted time. Engage with customers to boost your business's profitability while providing real-time assistance to help them reach their destination without unnecessary detours. Simplify the process of locating their vehicles in your parking area and guarantee a reliable step-by-step navigation system that recalculates routes when deviations occur. Additionally, create designated pathways for individuals with reduced mobility (PRM), making it easier to find essential Points of Interest such as elevators or service desks through intuitive maps. By implementing this adaptable solution, you can lower signage costs while also increasing your revenue through geolocated notifications and promotions. Furthermore, leverage geoanalytics to strategize the organization of your spaces and services based on visitor patterns, ultimately enhancing the overall efficiency of your operations. This comprehensive approach not only benefits your visitors but also significantly contributes to your business's success.

WizRule, data auditor, automatically detects patterns in the data and flags cases that deviate from these patterns as possible frauds or errors. Any case that is suspected to be fraud or error is one that departs from the established patterns. WizRule can be used by auditors and fraud examiners as well as forensic investigators and data-quality managers. Their main task is to uncover fraudulent cases and data errors. WizRule is able to assist with this task. WizRule, a data-auditing software based on data mining technology, is available. It analyzes the data and identifies inconsistencies. WizRule works automatically. The user simply selects the data, and WizRule will analyze it. WizRule examines all relationships between the values in the different fields and reports on unusual and unlikely cases. WizRule identifies fraudulent cases that are not visible with standard auditing tools.

Agatha provides a comprehensive range of cloud-based solutions specifically designed for the life sciences sector, facilitating the centralized oversight of documents and processes related to clinical operations, quality assurance, regulatory compliance, and training activities. This platform caters to the workflows of biotech firms, pharmaceutical companies, medical device manufacturers, and contract research organizations by offering various modules, including eTMF (Inspection-Ready Master Trial File), Remote ISF (Investigator Site File) management, and tools for creating and approving standard operating procedures (SOPs) as well as managing quality documents related to CAPAs, deviations, and change controls. Additionally, Agatha enhances regulatory document handling, ensuring smooth document creation, review, approval, storage, and sharing within a single cohesive system. By promoting a paperless approach, it alleviates administrative burdens and bolsters data security, while being constructed on a global-compliance framework that meets critical standards such as 21 CFR Part 11, GDPR, and EU Annex 11. Ultimately, Agatha empowers life sciences organizations to optimize their operations and maintain compliance with industry regulations more efficiently.

METS stands out as the premier solution for estimating projects and tracking materials, specifically designed as a web-based application for MEP contractors by industry experts. Its features foster collaboration and ensure accountability, making it the most thorough material management system tailored to MEP projects. With built-in systems for extensive validation and approval of various business processes, METS enhances the ability to "Delegate with Authorization," while still maintaining oversight and monitoring of all project activities. The application's analytical tools enable on-demand assessments, providing timely reports on project status and deviations, which helps teams make informed and accurate decisions swiftly. HVAC projects often face significant challenges such as managing the Scope of Work, reducing deviations, and appropriately delegating authority; METS effectively addresses these issues by providing precise estimation capabilities, strong change control management, and a framework for limited delegation of authority, making it an essential tool for ongoing project tracking and oversight. In essence, METS empowers teams to navigate the complexities of project management with confidence and accuracy.

MonQual QMS is equipped with pre-configured Document Management System (DMS) and Learning Management System (LMS) functionalities. Additionally, it provides the capability to integrate seamlessly with a variety of standalone systems. This includes the integration of Laboratory Information Management Systems (LIMS), Manufacturing Execution Systems (MES), SAP solutions, Warehouse Management Systems (WMS), and more, catering to both traditional and contemporary applications. MonQual is essentially the ideal solution for quality teams, as it merges quality assurance with compliance management, advanced business intelligence tools, and enhanced productivity. The inclusion of built-in DMS and LMS services, along with automated workflows, ensures that your documentation and adherence to regulatory standards are expertly managed. While quality deviations may occur during processes, MonQual equips you with the means to prevent them in the future. It offers a systematic approach for early detection of deviations, tracking their progress, conducting root cause analyses, and meticulously documenting findings to mitigate the chances of recurrence. Ultimately, MonQual not only enhances operational efficiency but also fosters a culture of continuous improvement within your organization.

Control Tower delivers an end-to-end control tower solution that connects GPS, TMS, and ERP systems to guarantee real-time traceability and oversight of transport operations. The platform centralizes information from both owned and subcontracted fleets, enabling continuous monitoring of routes and proactive management of risks and incidents. With configurable smart alerts, automatic notifications, and unlimited reporting, businesses gain total transparency across their logistics operations. Its dedicated driver app improves communication by providing instant, direct updates from the road. Additional modules such as BI-Analytics, MAS (Service Assignment), and YMS (Yard Management System) help optimize decision-making and operational efficiency. Success stories across Latin America highlight reduced headcount costs, lower monitoring staff turnover, and increased competitiveness. By integrating GPS with business systems, ControlT eliminates silos and streamlines workflows. The result is a scalable platform that strengthens operational control and enhances customer service.

Empower sales leaders in the consumer products sector to take full ownership of profit and loss (P&L) responsibilities that enhance revenue, volume, and overall profitability. By implementing comprehensive end-to-end processes for trade management, organizations can significantly boost revenue, volume, and profitability. Equip these sales leaders with the tools needed to effectively manage trade promotion planning, advanced analytics for trade management, and customer business planning through SAP Trade Management. Leverage our integrated customer business planning tool to improve planning accuracy, swiftly detect deviations from the plan, and respond to those deviations with greater efficiency. Actively drive price, volume, and margins in alignment with corporate targets in real-time. Merge the perspectives of both manufacturers and retailers, allowing for effective communication and negotiation with customers in a way that resonates with them. Streamline the integration of volume, margin, assortment, promotion, and financial planning while matching deductions to promotion invoices to accelerate the clearance process. Furthermore, empower users to execute a seamless closed-loop process, managing everything from budget planning to execution and final settlement efficiently. This holistic approach not only supports strategic goals but also fosters a proactive environment for continuous improvement in sales performance.

Imerso stands out as the leading platform for construction monitoring, enabling the creation of highly accurate Digital Twins. By utilizing this innovative technology, users can reduce expenses, expedite project timelines, minimize travel, and enhance facility management through unmatched insights and reliable as-built data. The platform sends alerts for any deviations in fieldwork and allows users to append notes and comments directly to physical objects. Measurements are taken with millimeter-level precision, and online collaboration is facilitated seamlessly. Users can access a 3D Digital Model of the structure that reflects its current condition with pinpoint accuracy. This technology captures every phase of construction from initiation to completion. Remote teams can explore the virtual job site together from any web browser, simulating an on-site experience while taking measurements or generating status reports. Issues arising from deviations in plans can be identified within minutes, eliminating unexpected costs, delays, and conflicts with partners. With an overview of the progress and performance of all trades at a glance, stakeholders gain unparalleled insights into their teams, projects, and effective practices, ensuring continuous improvement and efficiency throughout the construction process.

Uncover the imbalances and asymmetries that can cause back pain, increase stress levels, negatively impact health, hinder performance, and even contribute to premature aging. PostureZone serves as an invaluable tool for evaluating posture and establishing a baseline for future enhancements. A single posture image can convey an abundance of information, serving as powerful visual proof of either progress or deterioration, while also supplying critical data for monitoring postural adjustments and selecting suitable rehabilitation exercises. With PostureZone, it's easy to detect misalignments among the head, torso, and pelvis relative to the feet' center. The screenings produced by PostureZone quantify distortions in degrees, allowing for a clear assessment of symmetry, balance, and any improvements or shifts over time. By utilizing this innovative tool, individuals can take proactive steps toward achieving better posture and overall well-being.

Attain stands out as the sole optimization tool designed specifically for both open pit and underground mining operations, enabling mine operators to align their short-term and long-term plans effectively to harness the maximum economic potential of their activities. This versatile tool allows users to create optimized short-term schedules that are in harmony with the overarching long-term mine schedule. Its optimization features are geared towards minimizing departures from the established long-term plan, while also offering decision support with quick rescheduling options to adapt to unexpected events. By doing so, it helps prevent the unforeseen loss of value that can arise from necessary adjustments. Attain also aids in pinpointing the most common sources of deviation from operational plans, fostering an integrated mine planning approach that enhances overall compliance. Ultimately, with Attain, users benefit from a software solution that guarantees systematic alignment of operational mine planning with long-term objectives, ensuring that the short-term plans generated are both optimized and practical. This comprehensive integration facilitates a more efficient mining operation, leading to improved resource management and strategic decision-making.

Electronic source documents, known as eSource, replace traditional paper methods, streamline workflows, and minimize the likelihood of errors and omissions. BREEZE eSource transcends basic visit templates and scheduling functionalities. By aligning clinical contexts with regulatory and protocol requirements, along with study procedures, BREEZE eSource ensures users effectively capture all necessary data mandated by the protocol. The business rules within BREEZE guarantee that data collected are not only correct but also complete, precise, and compliant with relevant standards. Our team of clinical trial specialists creates tailored eSource documents specific to each study for review and approval prior to the trial's initiation, providing ongoing support and adjustments throughout the study duration. The individual modules integrate flawlessly, working in unison to enhance efficiency. The Cross-Module Action Multiplier further elevates functionality by predicting and automatically fulfilling supplementary tasks based on user inputs, such as automatically recording completed visits or procedures, which then updates invoicing and recalibrates scheduling effortlessly. This interconnected approach not only simplifies trial management but also enhances overall data integrity and operational effectiveness.

Responding swiftly to any discrepancies in the schedule is even more crucial than the initial planning itself. The inoPLAN APS (Advanced Planning and Scheduling) system employs sophisticated algorithms to automatically generate an optimized production schedule. Unlike traditional MRP and MRP II systems, inoPLAN provides a finite scheduling resource capacity. The plan remains current, as it is recalibrated and optimized with each occurrence of change. Scheduling is conducted effortlessly based on the resources at your disposal, eliminating the need for manual resource allocation to tasks. The SaaS model offers both immediate and long-term returns on investment. You can easily select or create the plan for your new project using a user-friendly tool, allowing you to rapidly evaluate different scenarios and their effects on other scheduled or ongoing projects. The system ensures that the project and all associated tasks are scheduled automatically. If any task experiences a delay that impacts the project deadline, you will receive an alert, ensuring you remain informed. This proactive approach enhances overall project management efficiency and minimizes disruptions.

Clin'form is an adaptable and powerful electronic Clinical Outcome Assessment (eCOA) platform that aims to simplify clinical trials for both patients and research sites, improve data integrity, and speed up processes for research teams. Its versatility allows it to be used across various protocols and demographics, making it suitable for any type of questionnaire—including Patient-Reported Outcomes (PRO), Observer-Reported Outcomes (ObsRO), Clinician-Reported Outcomes (ClinRO), and diaries—while catering to individuals of all ages, from children to the elderly. The platform is designed to handle diverse population sizes, effectively managing studies that involve anywhere from a small group to over 10,000 participants spread across multiple regions worldwide. Clin'form integrates smoothly with other clinical systems to provide an efficient workflow, supporting various data collection methods such as dedicated tablets or smartphones, the patient's personal device, web access on any browser, and in-person interviews. Noteworthy features include an integrated tele-visit option to accommodate unexpected changes and patient engagement tools that promote high levels of compliance. Additionally, Clin'form's user-friendly interface ensures that both researchers and participants can easily navigate the platform, making the clinical trial experience more streamlined and effective.

Amazon Inspector serves as an automated service for security assessments that enhances the security and compliance posture of applications running on AWS. This service efficiently evaluates applications for potential exposure, vulnerabilities, and deviations from established best practices. Upon completing an assessment, Amazon Inspector generates a comprehensive list of security findings ranked by their severity levels. Users can access these findings either directly or through detailed assessment reports available via the Amazon Inspector console or API. The security assessments conducted by Amazon Inspector enable users to identify unwanted network accessibility of their Amazon EC2 instances, as well as any vulnerabilities present on those instances. Furthermore, assessments are structured around pre-defined rules packages that align with widely accepted security best practices and vulnerability definitions. To expedite mean time to recovery (MTTR), the service leverages over 50 sources of vulnerability intelligence, which aids in the rapid identification of zero-day vulnerabilities. This comprehensive approach ensures that organizations can maintain a robust security framework while efficiently addressing potential risks.

Longboat is a cloud-based solution designed to support clinical trials, offering an integrated Guided Compliance toolset that assists users consistently throughout the process. By supplying clinical trial site personnel with essential resources, Longboat enables them to concentrate on patient care. Additionally, it allows participants to access vital study details and receive reminders for upcoming visits. The platform facilitates the streamlined management of any amendments to the clinical trial protocol, ensuring a smooth and controlled rollout. Furthermore, it centralizes the secure sharing of regulated documents among sponsors, CROs, and sites, which significantly enhances the startup process and simplifies traditionally labor-intensive tasks for all research stakeholders. Through a unified support platform, all key participants—including clinical operations teams, monitors, site personnel, and trial participants—can access customized content that addresses their individual requirements. This comprehensive approach ensures that site staff are equipped with the necessary tools and resources to remain engaged and compliant while prioritizing the needs of participants. In doing so, Longboat not only improves operational efficiency but also elevates the overall experience for everyone involved in the clinical trial.

Enhance your innovation ecosystem by integrating cutting-edge AI technologies to gain a competitive advantage. Relecura excels in providing flexible and adaptable solutions tailored to specific challenges. A common issue faced by innovators is the difficulty in recognizing the industrial and commercial relevance of their innovations, as thorough due diligence often requires extensive analysis, diverting them from their usual tasks. This process can be painstakingly repetitive. With the newest custom AI functionalities, evaluating the commercial potential of innovations becomes more efficient, and the technical due diligence process can be automated to deliver significant and prompt insights. By automating these routine tasks, you can redirect your focus and efforts toward more strategic initiatives while fostering a culture of innovation. This shift not only enhances productivity but also allows for a more agile response to market demands.

Clinical One RTSM is capable of accommodating various randomization strategies, ranging from the most straightforward to highly intricate studies, all without requiring any programming or coding, which consequently reduces the duration of user acceptance testing. You can take charge of your study with self-service configurations, allowing you to develop a study in just a matter of days rather than weeks. Additionally, you can assess the drug inventory status and make real-time adjustments without needing to consult the vendor, thereby avoiding unnecessary costs and change requests. By implementing changes swiftly, you can eliminate expenses associated with change requests and prevent delays, enabling you to launch your studies almost instantaneously. This platform stands out as the only one that genuinely integrates individuals, processes, and data to streamline and expedite the future of clinical trials. Moreover, the inclusion of virtual components in clinical trials enhances patient engagement and significantly elevates the quality of trial data. To keep pace with the rapidly evolving landscape, it is essential to adopt transformative digital strategies that facilitate quicker study initiations, harmonize data from diverse sources, and optimize workflow efficiency. Such advancements are pivotal for the successful execution of modern clinical research initiatives.

At last, there is an easy-to-use and adaptable centralized system for managing metrics. This system allows for the creation of indicators related to strategic goals, locations, departments, functions, plant zones, roles, units, and critical assets. It emphasizes the importance of addressing notable target deviations while minimizing exceptions, eliminating the need to wait for outdated reports. Moreover, analytics are directed towards identifying substantial gaps, and the system is designed to work with various data sources, providing real-time insights, relational data, and compatible with both ERP and manual data entry. This innovative approach empowers organizations to enhance their performance tracking efficiently.

Science 37 is a pioneering clinical research organization that focuses on decentralized clinical trials through its innovative Metasite model, which eliminates the need for physical proximity, allowing patients to engage in studies from virtually anywhere. This method significantly broadens accessibility, reaching over 90% of individuals who might be excluded from conventional site-based research, and harnesses the recruiting capabilities equivalent to 20 sites in one location, thereby offering patients the flexibility they desire. The Metasite operates on a proprietary platform that not only streamlines study orchestration but also facilitates the workflow for both patients and research staff, all while efficiently capturing study data without manual reentry. By centralizing personnel, processes, and technologies, this approach guarantees built-in protocol compliance, which leads to enhanced compliance rates and the collection of high-quality data. Science 37's dedicated in-house medical teams, telemedicine investigators, and mobile nursing professionals are well-versed in the conduct of remote trials spanning various therapeutic areas, thus ensuring comprehensive outreach. This commitment to innovative trial methodologies positions Science 37 at the forefront of transforming the landscape of clinical research.

BrickControl is a cloud-based platform designed to streamline the management of your projects, making the process straightforward and efficient. It offers a variety of features such as estimates, progress reports, certifications, and cost analyses, addressing the diverse needs of professionals and organizations involved in construction. This tool significantly simplifies the workflow for construction firms of all sizes, including architects, engineers, remodelers, project managers, interior designers, financial departments, and educational institutions. With BrickControl, users can create budgets, review project documentation, oversee daily construction activities, and manage any deviations from the project plan. Additionally, the platform enhances collaboration among team members, ensuring a smoother project execution.

Oversee your clinical trial seamlessly through a single platform. Zapclinica offers an eClinical suite tailored to manage and execute every facet of your decentralized clinical trial—whether hybrid or entirely virtual. By automating intricate processes, it helps in spotting anomalies, optimizing resources, and enhancing decision-making alongside collaboration among sponsors, CROs, and study sites. This comprehensive solution significantly cuts down the time and expenses associated with running a successful clinical trial. With Zapclinica, you can handle all study components without the need for additional vendors or third-party services; instead, select the necessary applications within one unified environment, including EDC, ETMF, Payments, Logistics, and much more. Embrace the efficiency of a single platform to streamline your clinical research efforts.

Avela envisions a world in which opportunities are more efficiently and equitably distributed, starting with education. We empower families and give them the tools they need to make fair decisions. Our platform is also used by nonprofits and governments to allocate talent and resources in a fair and effective manner. Our products cover every stage of the admissions or selection process. This ensures that your selection committee makes fair and informed decisions, regardless of whether you are selecting students for your school, recipients of your scholarship, or fellows to your program. Our founding team also includes a Nobel Laureate as well as a Clark Medalist. Our methods resulted in a 90% decrease in dissatisfied families in school districts. This has real learning implications - MIT research showed that students who enrolled at their first choice school had an improvement in math achievement of 0.4 standard deviations.

Tecplot RS is a comprehensive visualization and analysis tool specifically designed for professionals in the oil and gas reservoir engineering field. It streamlines the handling and analysis of reservoir simulation data by offering detailed XY plots, 2D cross-sections, and 3D grid visualizations. By allowing users to import data from multiple simulation platforms, it helps in organizing outcomes, validating models, and sharing insights effectively among team members. The latest updates, including the 2023 R1 release, have introduced improvements that enhance the evaluation of history match quality through the ability to create selection sets based on deviation bands. Furthermore, the software has expanded its capabilities by incorporating the visualization of negative values in stamp plots, which is crucial for examining fluid behavior patterns within reservoirs. With an intuitive interface, Tecplot RS promotes a quick adaptation process for new users, alongside providing comprehensive technical support and complimentary online training resources. This approach not only fosters user confidence but also encourages collaborative efforts in analyzing complex reservoir data.

Validfor is a robust and secure digital validation platform that consolidates the entire validation process into a single, paperless system, specifically tailored for industries that are heavily regulated. This platform not only streamlines validation tasks but also guarantees adherence to critical standards such as GAMP 5, 21 CFR Part 11, and EU Annex 11. With capabilities for handling electronic records and advanced electronic signatures, Validfor ensures complete audit trails, role-specific workflows (including Author, Reviewer, and Approver), and thorough CSV compliance. It securely organizes all documentation and records within a centralized repository, meticulously tracking every modification to maintain data integrity and uphold Quality Assurance. Additionally, Validfor provides integrated modules for Change Management, Deviations, Testing, and Periodic Reviews, thereby facilitating smooth impact assessments, tracking of CAPA, Computer Software Assurance (CSA), and management of audit-ready lifecycles. This comprehensive approach not only enhances operational efficiency but also strengthens compliance across various validation activities.

An all-in-one platform designed for the effective management of individuals and organizations enables businesses to synchronize employee performance with corporate outcomes seamlessly. With a comprehensive set of tools, everything necessary for achieving your objectives is conveniently located in a single interface. You can utilize our various solutions individually or merge them for a cohesive experience. Our fully automated system is engineered to enhance your success rates significantly. By implementing precise targets and indicators, you can make more informed decisions that foster alignment within your organization. Evaluate your team's skills to boost their performance and promote development through structured, clear processes for calculating variable compensation. Additionally, you can oversee training programs and track your team’s growth effectively. Assess talent based on competencies, provide constructive feedback, and conduct Personal Development Initiatives (PDIs). Furthermore, automate the planning and tracking of goals while analyzing deviations and strategizing action plans. Gauge your team's engagement levels and leverage data-driven insights to inform your decisions. Moreover, your variable compensation framework will be enhanced with analytical reports and simulations that predict potential outcomes. This holistic approach ensures that your organization not only meets its goals but thrives in its competitive landscape.

MONAROV & Co. Consulting has developed the Effcon system (effective – control), an innovative automated solution crafted from over two decades of expertise in Internal Control and Fraud Prevention. This system enables organizations to maintain an automated, continuous, and independent control framework designed to identify weaknesses, detect fraud and irregularities, mitigate operational risks, and evaluate the efficiency of internal controls. As a vital resource, Effcon plays a significant role in helping organizations achieve their strategic goals. Our firm supports clients in implementing the Effcon system, which features a comprehensive set of analytical rules. These rules are meticulously crafted by a team of seasoned professionals who specialize in identifying deviations across various sectors, drawing on extensive experience in control and risk management to ensure effectiveness. Consequently, the Effcon system not only aids in compliance but also enhances overall operational integrity.

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.

LifeSphere eTMF serves as the definitive source of truth for your clinical trial. Experience a flexible solution that simplifies inspections, guarantees compliance, and reduces the time and effort required by your organization. As the pioneering system designed to adhere to the TMF reference model, LifeSphere eTMF integrates clinical documentation with regulatory requirements and study protocols into a unified platform. Establish and oversee a singular source of truth for your clinical trial to enhance efficiency. With features that promote live collaboration and real-time document sharing, you can ensure the quality, timeliness, and completeness of your trial master file. Expedite TMF inspections swiftly and effectively to manage audits seamlessly. Furthermore, uphold compliance through built-in workflows and intuitive dashboards that facilitate straightforward trial reconstruction, making the process smoother for all stakeholders involved.

Quality Collaboration By Design (QCBD) offers a comprehensive quality management software solution tailored for the manufacturing sector. This cost-effective, Windows-compatible application streamlines the process of obtaining and sustaining compliance with various quality management standards, including ISO 13485, ISO 9001, TS 16949, AS9100, and SQF 2000 / ISO 22000. Developed by CAMA Software, QCBD encompasses a wide range of modules that facilitate training management, supplier oversight, process deviation tracking, document control, equipment management, and additional functionalities. With its user-friendly interface, QCBD not only enhances operational efficiency but also ensures that businesses can easily adapt to evolving quality requirements.

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.

CANEA Workflow, a case management tool, allows users to speed up, automate, and quality assure their organization's administrative processes. CANEA Workflow makes it easy to create process-driven applications without the assistance of an IT professional. CANEA Workflow's design tool makes it easy to create, deploy, and improve forms, workflows, and business logic. CANEA Workflow allows users to manage all types workflows including HR-processes and risk, audits, deviations, claims, and audits.