Alternatives to Orthogonal

Compare Orthogonal alternatives for your business or organization using the curated list below. SourceForge ranks the best alternatives to Orthogonal in 2026. Compare features, ratings, user reviews, pricing, and more from Orthogonal competitors and alternatives in order to make an informed decision for your business.

  • 1
    Matrix Requirements

    Matrix Requirements

    Matrix Requirements

    For companies looking to accelerate development of their innovative medical device technologies, our Application Lifecycle Management and Quality Management Systems (eQMS) are easy-to-use, flexible, all-in-one software solutions designed to facilitate collaboration of employees on design control, and quality management to streamline medical device design. Innovate faster with a flexible item-based approach to documentation designed to control even the most complex SxMD (Software as/in a Medical Device) product design. Enhance quality management and ensure compliance with full traceability from design input to output with a purpose-built software platform that enables a collaborative quality culture across all teams. Ensure frictionless alignment between platforms with native integrations for Jira, GitLab, GitHub, Azure DevOps and more.
    Starting Price: $500 per month
  • 2
    Claude

    Claude

    Anthropic

    Claude is a next-generation AI assistant developed by Anthropic to help individuals and teams solve complex problems with safety, accuracy, and reliability at its core. It is designed to support a wide range of tasks, including writing, editing, coding, data analysis, and research. Claude allows users to create and iterate on documents, websites, graphics, and code directly within chat using collaborative tools like Artifacts. The platform supports file uploads, image analysis, and data visualization to enhance productivity and understanding. Claude is available across web, iOS, and Android, making it accessible wherever work happens. With built-in web search and extended reasoning capabilities, Claude helps users find information and think through challenging problems more effectively. Anthropic emphasizes security, privacy, and responsible AI development to ensure Claude can be trusted in professional and personal workflows.
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    EagleView

    EagleView

    EagleView Technologies

    Property insights for smarter planning, building, and efficiency. Get reports in PDF, XML, JSON and DXF formats at any time. Import directly into third party integrations and industry workflows. Oblique to orthogonal. Mosaics to patented high-res. We have the imagery to meet your needs in an ever changing world. Reduce costs, minimize labor safety risks, and increase profitability. Get ultra-detailed contextual roof information. Virtual inspections with autonomous drones and damage detection software. Resolving claims with greater efficiency and accuracy.
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    SigmaXL

    SigmaXL

    SigmaXL

    SigmaXL was designed from the ground up to be a cost-effective, powerful, but easy to use tool that enables users to measure, analyze, improve and control their service, transactional, and manufacturing processes. As an add-in to the already familiar Microsoft Excel, SigmaXL is ideal for Lean Six Sigma training or use in a college statistics course. Version 9 adds Time Series Forecasting and advanced control charts. Click here to view the features available in SigmaXL! Automatic removal of extreme VIF or collinear terms (with alias and removal report) Specify interactions, quadratic and higher orders (all interactions or up to 3-Way). ANOVA Type I and/or Type III Sum-of-Squares with Pareto of Percent Contribution and Standardized Effects. Lenth Pseudo Standard Error for Saturated Models (Orthogonal or Non-Orthogonal) with Monte Carlo or Student T P-Values. White robust standard errors for non-constant variance (Heteroskedasticity-Consistent).
    Starting Price: $249.00/one-time/user
  • 5
    ZipQuality

    ZipQuality

    Consensia

    ZipQuality is a software-enabled service that assists medical device companies in bringing new products to market. Our collaboration platform manages rapid design changes for agile teams while ensuring regulatory compliance. Pre-configured system(processes and tools); no need to alter your quality system. The integrated system easily handles rapid design iterations for product documentation. Experienced consultants guide your team at every step. Fully-featured, scalable software tools built on the proven, powerful ENOVIA platform. Our integrated system enables rapid design changes while keeping product documentation and data in sync and maintaining all the records in an audit-ready state. Product requirements, hardware requirements, software requirements. We understand complex, software-intensive medical devices. The ZipQuality system is based on a structured documentation framework that supports good systems engineering, efficient risk management, and clear traceability.
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    ComplianceWire
    ComplianceWire is a powerful, Part 11 compliant, and fully integrated cloud-based learning management system (LMS) developed by UL Compliance to Performance. Designed as a workforce training solution for pharmaceutical, biologics, and medical device companies, ComplianceWire facilitates the management of training activities, learner proficiency, and compliance status. With its unique, role-based approach to compliance, qualification, and performance management, ComplianceWire helps users meet strict regulatory requirements as well as seamlessly manage the most complex training assignments.
    Starting Price: $15.00/year/user
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    STL Simple Viewer

    STL Simple Viewer

    Victor Bovio

    STL Simple Viewer is a great app to quickly view 3D STL files. Supports both ASCII and Binary STL files. Load an STL from a ZIP file. Graphic operations for rotating, panning and zooming. View your model in orthogonal or perspective mode. Obtain info on the model: triangle count, bounding box, area, and volume. Set up rendering options, faces, edges, points, and transparency. Render using a clipping plane (useful for viewing interiors). App now remembers each file graphic setting. Added buttons for graphic operations.
  • 8
    Dragonfly 3D World
    Dragonfly 3D World by Object Research Systems (ORS) is a comprehensive software platform for multidimensional image visualization, analysis, and collaboration in scientific and industrial fields. It provides powerful tools to visualize, process, and interpret 2D, 3D, and 4D imaging data acquired through modalities such as CT, MRI, electron microscopy, and more. Dragonfly supports real-time volume rendering, surface rendering, and orthogonal slicing, allowing users to explore complex structures interactively. With its AI integration, users can apply deep learning for image segmentation, classification, and object detection. It offers advanced quantitative analysis tools, including region-of-interest analysis, measurements, and statistical evaluations. Its intuitive graphical user interface enables researchers to build reproducible workflows and perform batch processing.
  • 9
    Odin

    Odin

    Odin Language

    Odin is a general-purpose programming language with distinct typing built for high performance, modern systems and data-oriented programming. Odin is the C alternative for the Joy of Programming. Odin has been designed for readability, scalability, and orthogonality of concepts. Simplicity is complicated to get right, clear is better than clever. Odin allows for the highest performance through low-level control over the memory layout, memory management and custom allocators and so much more. Odin is designed from the bottom up for the modern computer, with built-in support for SOA data types, array programming, and other features. We go into programming because we love to solve problems. Why shouldn't our tools bring us joy whilst doing it? Enjoy programming again, with Odin!
  • 10
    Requirements Portal
    Requirements Portal by Altium is a requirements management and verification tool integrated directly into Altium’s solutions, including Altium Develop, Altium Agile Teams and Altium Agile Enterprise. It enables engineering teams developing hardware products and embedded systems to create, store, and manage formalized requirements and link them to designs and verification data. Each requirement is traceable and connected to upstream system definitions and downstream design and verification artifacts, such as schematics, PCB layouts, BOMs, and test cases, providing visibility from system design through implementation, verification, handoff, and certification. This helps teams reduce rework, avoid misalignment across disciplines, and simplify compliance activities.
  • 11
    Flinn

    Flinn

    Flinn

    Flinn is an AI-driven platform built to automate and streamline regulatory and quality-management processes within the medical-device (MedTech) industry. It enables manufacturers to integrate AI into repetitive and complex workflows such as post-market surveillance, literature evaluation, complaint-handling, and safety-database monitoring, reducing manual effort and ensuring compliance with standards like the EU Medical Device Regulation (MDR). It aggregates data across sources, applies machine-learning algorithms to detect patterns and risks, generates regulatory-compliant reports automatically, and supports rapid launch and operation of high-quality products at scale. As a result, organizations can achieve up to a tenfold acceleration in process efficiency while maintaining auditability, transparency, and traceability of their compliance workflows.
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    Purple Fabric

    Purple Fabric

    Purple Fabric

    Purple Fabric is an advanced enterprise AI platform developed by IntellectAI, designed to enable financial institutions to swiftly create, deploy, and manage AI-driven solutions through a low-code, self-service approach. Leveraging the eMACH.ai framework, Purple Fabric integrates structured and unstructured data, regulatory information, market insights, and tacit knowledge into a unified system, facilitating the development of AI agents that enhance decision-making and operational efficiency. It emphasizes ethical AI by providing comprehensive governance, audit trails, and data lineage, ensuring transparency and compliance. Its modular architecture includes components like PF Imagine for AI solution design, PF Govern for governance and compliance, PF DIMS for document intelligence, PF Expert Agent for autonomous decision-making, and PF Triad for unbiased decision support. Purple Fabric's capabilities have been successfully applied in various financial services scenarios.
  • 13
    Arena QMS

    Arena QMS

    Arena, a PTC Business

    Arena’s product-centric quality management system (QMS) software enables medical device manufacturers to deliver safe and compliant products to market fast. Arena QMS streamlines new product development and introduction (NPDI) by connecting quality and product processes. Arena QMS ensures regulatory compliance to various quality standards and regulations, including FDA 21 CFR Part 820, Part 11 and ISO 13485. Arena QMS enhances visibility and traceability by controlling quality processes in context with bills of materials (BOMs), SOPs, DMRs, DHFs, specifications, drawings, and training plans.
  • 14
    AgentFlow

    AgentFlow

    Multimodal

    AgentFlow is an agentic AI platform that automates workflows for finance and insurance companies. The platform includes modular AI agents, such as Document AI, Decision AI, and Report AI, each specializing in different stages of regulated workflows: triage, diligence, decisioning, and reporting. AgentFlow orchestrates multiple AI agents with human supervisors and third-party systems, enabling deep transformation of how work gets done. The platform features self-learning capabilities that allow AI agents to improve over time based on subject matter experts' feedback and provides transparency through explainability features that help users understand the reasoning behind AI-driven decisions. Every action and output is fully auditable, ensuring compliance with the strict standards of regulated industries. Its main mission is to codify tacit internal knowledge in order to reliably augment high-leverage workflows and preserve the know-how across generations of talent.
  • 15
    RAMS

    RAMS

    Emergo by UL

    Emergo by UL's Regulatory Affairs Management Suite (RAMS) is a comprehensive software-as-a-service platform designed to streamline regulatory and quality management for medical device and in vitro diagnostic companies. Leveraging decades of regulatory compliance expertise, RAMS offers a suite of tools to navigate the complex and evolving landscape of global medical device regulations. Key features include product classification, which guides users through a series of questions to determine or verify device classification, and Smart Builder, a tool that provides step-by-step guidance and templated text to create accurate regulatory documentation, facilitating smoother device registration and faster market access. The Registration Tracker automates the tracking of global registrations and certifications, helping organizations avoid missed renewals and maintain compliance.
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    eTraceLine

    eTraceLine

    MAK-SYSTEM

    Integrated solution for hospital transfusion management, laboratory services, and reference labs. Robust tracking and utilization of blood components from donation to transfusion. From patient records management to ordering blood and lab requests, testing, product transformation, inventory, shipping, hemovigilance, RFID storage, and full traceability. Flexible and scalable to meet the needs of small and large centers. End-to-end automation of blood supply chain management. Interfaces with hospital information systems, lab devices, and other third-party software. Discover how MAK-SYSTEM's cutting-edge software solutions can revolutionize your healthcare management. Let's explore the future of medical technology together. eTraceLine meets the provisions of the European Medical Device Regulation (EU)2017/746. PHS is marketed under the 510(k) regulatory pathway.
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    Cognition Cockpit
    Cockpit Enterprise is our software application for medium to large medical device product development teams that integrates requirements management, test management, risk management data, and more, in a unified environment. Cockpit Enterprise is highly configurable and can be personalized to meet a company’s needs. It has a rich development framework that allows organizations to implement their Standard Operating Procedures (SOPs) and Work Instructions (WIs) in a controlled and auditable environment. Ultimately, Cockpit Enterprise helps medical device manufacturers of Class II and Class III devices author, review, and approve the documents required for regulatory submissions and audits. Cockpit Enterprise is best suited for mature organizations that have established standard operating procedures and can dedicate the necessary resources to configuring and deploying the system.
  • 18
    AuroraPrime

    AuroraPrime

    AlphaLife Sciences

    AuroraPrime is a generative AI-powered platform designed specifically for content authoring and documentation in the life sciences. It automates the end-to-end creation of complex documents such as Clinical Study Reports (CSRs), protocols, and safety narratives. Built on a modular AI and LLM framework, the AuroraPrime platform integrates flexibly with existing enterprise systems to streamline the product development lifecycle. Key features include AI automation that speeds up writing by generating accurate medical documents quickly with minimal manual effort, compliance assurance through automatic checks against standards to ensure accuracy and regulatory compliance, and content management that keeps all knowledge, templates, and documents organized for easy access and reuse.
  • 19
    LifeSphere Medical Affairs
    LifeSphere Medical Affairs is a cloud-based platform developed by ArisGlobal to enhance efficiency, compliance, and collaboration within medical affairs teams. It offers a unified workspace that seamlessly integrates medical information management with safety and quality systems, enabling end-to-end automation and real-time data sharing. The platform streamlines the intake and management of medical inquiries across multiple channels, automates the processing of product complaints and adverse events, and ensures consistent global compliance with evolving regulatory requirements. Its advanced analytics and reporting tools provide actionable insights, facilitating data-driven decision-making and improved patient outcomes. LifeSphere Medical Affairs is designed to be scalable and configurable, catering to the unique needs of organizations of all sizes.
  • 20
    aligned elements
    Aligned eQMS and Aligned Elements Design Control software are built specifically for medical device and IVD companies that need to meet global regulatory requirements without unnecessary complexity. The platform supports compliance with ISO 13485, FDA QSMR, EU MDR, and IVDR, and is trusted by experts that want full control over quality, design, and regulatory processes across the entire product lifecycle. Aligned products, designed for collaboration between quality, regulatory, R&D, and management teams, combines a complete electronic Quality Management System with deep Design Control functionality in one fully integrated environment. Design inputs, outputs, verification, validation, risk management, and change control are natively connected to the QMS, ensuring end to end traceability that stands up to audits and inspections.
    Starting Price: €1300 per year
  • 21
    OpenText Clinical Trial Quality Management
    Over the last several years, the Life Sciences industry has faced nearly $15 billion in fines and compliance-related settlements, making it critical for companies to adhere to pharmaceutical, medical device and biotech best practices. Efficient and effective management of clinical trials can also significantly impact the time, scope and budget for the development of a drug or medical device. With OpenText™ Clinical Trial Quality Management System (ctQMS), companies can remain compliant, reduce costs of records management and establish best practice through collaboration before, during and after the clinical trial lifecycle.
  • 22
    Product Comply

    Product Comply

    Product Comply

    Product Comply offers comprehensive 360-degree monitoring of evolving regulations and standards impacting your company’s products. Whether it’s medical device products, electronics, furniture, cosmetics or any other product – our software is customized around any compliance landscape. Our product compliance software successfully navigates all global regulations; related to any specific subject related to health, safety, and environment. Regulations are then mapped to your product portfolio according to components, materials, and chemicals to keep you ahead of any possible change in the regulatory scenario impacting your business. With consistently global evolving EHS (Environment, Health & Safety) regulations, laws, and compliance perimeters, it’s imperative to rely on advanced software that monitors regulatory changes to reduce monitoring efforts and to enable your team to focus on strategic decisions to protect your business.
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    Motagistic 4S

    Motagistic 4S

    Motagistics

    Motagistics LLC is a leader in the development and implementation of logistical management software for the legalized medical cannabis industry with the innovative Seed to Sale Software Suite (4S), an industry services tracking software product. Motagistics 4S is a turnkey e-commerce industrial software, the architecture of which tailors to regulatory compliance and operations of this still budding, quasi-regulated State medical cannabis markets. While also addressing the unrealized needs of State medical cannabis markets, Motagistics LLC brings this next generation of logistical software to this quickly evolving industry by partnering with the State regulatory agencies. This partnership enables the agency to affordably and effectively manage legislation through our turnkey Point of Sale (POS) software that offers next generation e-management, e-process, e-finance, e-advertising and e-marketing business functionality to all medical cannabis regulators and vendors.
  • 24
    Greenlight Guru

    Greenlight Guru

    Greenlight Guru

    Greenlight Guru’s Medical Device Success Platform is the only all-in-one solution that helps you get your products to market faster, with less risk, and advance your success in-market. The platform helps companies manufacture safer products and get to market faster, simplifies regulatory compliance, and provides a single source of truth by connecting the management of all product development, regulatory, and quality processes from documentation and design controls to submission and ongoing compliance. Device makers across the globe are replacing reactive quality management tools and shifting their focus and efforts to ensure successful product launches and in-market success of innovative, life-changing devices.
  • 25
    CaraSolva

    CaraSolva

    CaraSolva

    CaraSolva offers a comprehensive suite of cloud-based software solutions designed to empower caregivers and streamline operations for Home and Community-Based Services (HCBS), Intellectual and Developmental Disabilities (I/DD) providers, and long-term care facilities. The suite’s flagship product, MedSupport®, is an industry-leading Electronic Medication Administration Record (eMAR) system that reduces medication errors and ensures strict regulatory compliance. Beyond medication management, the CaraSolva ecosystem includes CareSupport® for tracking daily living activities (ADLs) and BehaviorSupport® for managing behavior intervention plans. Built by nurses for caregivers, the platform serves as a central hub for health outcomes, connecting care teams with pharmacies and management through real-time data, automated alerts, and secure, HIPAA-compliant documentation.
    Starting Price: Contact Us
  • 26
    Forescout Medical Device Security
    Forescout Medical Device Security is a dedicated healthcare solution that’s part of Forescout Continuum. Formerly known as the CyberMDX Healthcare Security Suite, the solution delivers continuous, real-time discovery and visibility of every medical device connected to your clinical network. It then assesses the risk of each device, factoring in their known exposures, the attack potential and operational criticality. Continuous, real-time discovery of your connected medical devices and clinical network, including devices behind firewalls and serial gateways. Clear and concise risk assessment of each connected medical device based on known exposures, attack potential and operational criticality with AI and rule-based attack detection. Custom-built security access and enforcement policy for each connected medical device. Smart isolation restricts device access, allowing only authorized nodes.
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    Neolytica.AI

    Neolytica.AI

    Neolytica.AI

    Neolytica, a subsidiary of QPharma, is a healthcare analytics firm leveraging data science and artificial intelligence to enhance medical communication and commercialization activities for life sciences companies. Their flagship product, Ti Expert, offers comprehensive data on Key Opinion Leaders (KOLs) and Community Opinion Leaders (COLs), including professional spheres of influence, social relationships, and promotional activities, enabling effective engagement planning. Additionally, NotifyMe provides real-time, enterprise-scale monitoring of KOL social activities, delivering actionable alerts to keep teams informed of relevant developments. Neolytica's solutions are designed to bridge the gap between medical and commercial teams by providing a single platform with strict compliance firewalls, facilitating collaboration while maintaining regulatory standards. Their innovative approach includes sentiment analysis tools to measure the impact of medical communications.
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    CaptureITPro

    CaptureITPro

    AmbalSoft

    CaptureITPro is a comprehensive medical imaging and reporting software developed by AmbalSoft, designed to facilitate the capture, storage, and management of high-definition medical images and videos. It supports a wide range of medical devices, including endoscopes, laparoscopes, bronchoscopes, gastroscopes, colonoscopes, cystoscopes, arthroscopes, and surgical microscopes. It allows for the recording of images in various formats such as BMP, JPG, and DICOM, and videos in AVI and MPEG formats. CaptureITPro offers high-definition video capture capabilities, supporting resolutions up to 1080p at 50/60fps, utilizing H.264 compression for efficient storage. It features a Picture-in-Picture mode for displaying multiple video sources simultaneously, enhancing the visualization of procedures. It is DICOM-compliant, enabling integration with Hospital Management Systems (HMS) and Picture Archiving and Communication Systems (PACS), supporting modalities like ultrasound.
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    Medication Management Platform
    Antares Vision Group has developed a digital healthcare solution for automating drug and medical device logistics, which eliminates or reduces activities that do not generate value for the patient while introducing a new paradigm of process efficiency for healthcare providers. The Medication Management Platform eliminates non-value-added activities that can help hospital systems optimize the time of medical and nursing resources to focus on patient and patient safety. The Medication Management Platform allows the complete traceability of the flow of medicines and medical devices, combined with automation systems that can help improve efficiency and operational excellence within healthcare institutions. The combination of automation systems and traceability allows for the better management of reorders and stocks, both at the central and peripheral levels, avoiding the waste of materials due to expiration.
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    Teammately

    Teammately

    Teammately

    Teammately is an autonomous AI agent designed to revolutionize AI development by self-iterating AI products, models, and agents to meet your objectives beyond human capabilities. It employs a scientific approach, refining and selecting optimal combinations of prompts, foundation models, and knowledge chunking. To ensure reliability, Teammately synthesizes fair test datasets and constructs dynamic LLM-as-a-judge systems tailored to your project, quantifying AI capabilities and minimizing hallucinations. The platform aligns with your goals through Product Requirement Docs (PRD), enabling focused iteration towards desired outcomes. Key features include multi-step prompting, serverless vector search, and deep iteration processes that continuously refine AI until objectives are achieved. Teammately also emphasizes efficiency by identifying the smallest viable models, reducing costs, and enhancing performance.
    Starting Price: $25 per month
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    BrightInsight

    BrightInsight

    BrightInsight

    BrightInsight accelerates time to market for our customers’ digital health products, including apps, algorithms, medical devices, connected combination products, diagnostics, and Software as a Medical Device (SaMD) across therapeutic areas. BrightInsight replaces the need for lengthy and complicated ‘build from scratch’ implementations and instead offers a pre-built and proven digital health platform designed under a Quality Management System to support global security, privacy, and regulatory requirements. We helped Roche launch a Software as a Medical Device (SaMD) dosing calculator for hemophilia A in 6 months in Europe, and accelerated a Top 10 Biopharma companies remote patient platform from project kickoff to commercialization in less than a year. We are experts at building and maintaining biopharma and medtech regulated digital health products, with multiple commercial launches in the last year alone.
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    ViSU

    ViSU

    DDi

    ViSU™ is a cloud based End-to- End Regulatory Information Management (RIM) platform designed specifically for the medical device industry enabling global users to access and manage Regulatory Data (Product Master, Registrations, Tracking), Dossiers/Tech Files (Submission planning, building & life cycle), HA/NB correspondence, Obligations tracking, UDI, eIFU, Reg Requirements DB and Change Control. ViSU helps you embrace digitization in regulatory that delivers connectivity, traceability and automation leading to regulatory management efficiency, less compliance risks & cost reduction.
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    Axivion Static Code Analysis
    Axivion helps development teams deliver safer, cleaner, and more maintainable C, C++, and CUDA code by automatically detecting coding standard violations, security vulnerabilities, dead code, and code clones. It provides actionable recommendations and detailed analytics, helping teams track, resolve, and prevent defects early in the development process. Axivion also supports architecture verification, enabling teams to maintain modular and scalable codebases. Designed for safety-critical industries like automotive, aerospace, medical devices, and industrial automation, Axivion supports functional safety standards including MISRA, ISO 26262, and IEC 61508. By combining static code analysis with architecture verification, it helps teams maintain long-term code health, accelerate certification readiness, and deliver high-performance software while reducing technical debt and ensuring compliance.
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    RQM+

    RQM+

    RQM+

    RQM+ is a global medical technology service provider focused on accelerating compliance and market success. Through our unparalleled expertise and industry knowledge, we deliver specialized solutions and expedite the journey along the full product lifecycle for medical technology companies, from concept to commercialization to post-market. Our portfolio of services enables the delivery of end-to-end solutions across the complete medical device product lifecycle. RQM+’s quality assurance engineers review material lists, set up suppliers, and support the design change process. RQM+’s design quality engineers help support packaging, sterility, biocompatibility, and device testing that may be needed. RQM+’s regulatory affairs consultants provide guidance and help with submissions to the FDA, notified bodies, or other government agencies. We use our extensive experience with the latest reimbursement requirements and value-based compensation models.
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    HCL RTist

    HCL RTist

    HCL Software

    HCL RTist is a development environment for creating complex, event-driven and real-time applications. It is specifically designed to help software engineers with feature-rich tooling for design, analysis, building and deploying embedded, real-time systems and IoT applications. Helps developers design applications at higher abstraction level than code. Meet the only tool you need to develop stateful, event-driven and real-time applications. Embedded systems developers are looking for a developer tool to deliver secure, high-quality production code with quick, agile methodologies allowing them to react to new business requirements while minimizing the maintenance cost of long-lived applications running on many different device preferences of their users. Also, companies strive to implement strict, continuous delivery processes to ensure code integrity and a stable, highly available production deployment of these real-time applications.
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    Patched

    Patched

    Patched

    Patched is a managed service that leverages the open-source framework Patchwork to automate development tasks such as code reviews, bug fixing, security patching, and documentation. By utilizing large language models, Patched enables developers to build and deploy AI-assisted workflow, referred to as "patch flows", that autonomously handle post-code activities, thereby enhancing code quality and accelerating development cycles. The platform offers a user-friendly graphical interface and a visual workflow builder, allowing for the customization of patch flows without the need to manage infrastructure or LLM endpoints. For those who prefer self-hosting, Patchwork provides a self-hosted command-line interface agent that integrates seamlessly with existing development pipelines. Patched emphasizes privacy and control, enabling deployment within an organization's infrastructure using its own LLM API keys.
    Starting Price: $99 per month
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    Latta

    Latta

    Latta

    Latta AI is an innovative platform designed to streamline the software development process by automating the detection and resolution of bugs. By recording user sessions and applying AI-driven fixes, Latta AI enables developers, project managers, and testers to focus more on feature development, thereby boosting productivity and accelerating release cycles. The platform integrates seamlessly with popular version control systems like GitHub and GitLab and maintains strict security protocols to ensure code privacy and protection. Additionally, Latta AI offers a plugin for JetBrains IDEs, allowing developers to access its bug-fixing tools directly within their development environment. This integration facilitates quick identification and resolution of issues without the need to leave the IDE. Overall, Latta AI aims to reduce the time developers spend on debugging by up to 40%, enhancing efficiency and allowing teams to focus on innovation.
    Starting Price: $0.05 per fix
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    PureOHS
    Boost your operational efficiencies while staying OSHA compliant with PureOHS™. Companies and health care providers use PureOHS, UL’s Occupational Health Medical Record system, to support their occupational health initiatives in critical areas such as regulatory compliance and surveillance programs. With PureOHS you can track encounters and easily distribute information to appropriate people and programs. Track cases including diagnosis, cause of injury, appointment scheduling, treatment plans, and medical notes. Record, manage, and report incidents, near misses, or other conditions that could lead to injury or illness. Easily export required forms ready to upload to OSHA and identify key areas for safety improvement. Whether you work for a manufacturer, a healthcare facility, a municipality, or any other organization that is struggling to track your employees’ medical compliance for OSHA, the CDC, or internal regulations, PureOHS can help by streamlining medical recordkeeping.
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    Agentverse

    Agentverse

    Fetch.ai

    ​Agentverse is an intuitive platform designed for creating, testing, and deploying customizable AI agents. It offers a cloud-based integrated development environment that simplifies agent development, allowing users to build, train, and integrate agents into various systems without extensive coding knowledge. It provides pre-built agent templates and use cases, enabling quick deployment and customization to serve a variety of purposes. Agents hosted in Agentverse are registered in the Almanac, facilitating discovery and interaction within the Fetch.ai network. It also supports collaborative development through its Teams feature, allowing multiple users to work together on agent projects. Security is emphasized with containerized environments ensuring data protection and compliance with industry standards. Additionally, Agentverse offers a marketplace where users can explore and connect with other registered agents.
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    Onpoint Healthcare

    Onpoint Healthcare

    Onpoint Healthcare

    OnPoint Healthcare Partners delivers an AI-powered autonomous practice management platform and suite of healthcare technology solutions that optimize clinical documentation, coding, care coordination, revenue cycle, and administrative workflows so providers and care teams can focus more on patient care. At the core of its offering is the Iris Medical Agent AI Platform, a cloud-based system that uses agentic and generative AI with clinical oversight to execute tasks across the full care continuum, including AI-enhanced charting, coding accuracy and compliance, longitudinal patient management (HCC risk adjustment, care gap closure), and real-time care coordination and referral/prior authorization support, all integrated seamlessly with existing EHR systems to minimize disruption and reduce manual work. OnPoint’s Practice Management as a Service model combines these autonomous AI workflows with operational expertise to reduce staffing burdens, lower costs, and more.
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    Verisk 3E

    Verisk 3E

    Verisk 3E

    Ensuring product safety, managing regulatory compliance and promoting responsible design, development and management of products throughout their lifecycle is a difficult job. Increasing consumer scrutiny and shrinking resources make it even harder. With Verisk 3E™ as your single trusted source for global regulatory expertise and compliance solutions you will be able to proactively anticipate and manage regulatory changes, respond quickly to changing customer requirements, avoid supply chain disruption and accelerate time to market. We deliver the most comprehensive and powerful suite of intelligent compliance solutions for product safety and stewardship. With limited resources, continually changing regulatory obligations, rapid fire customer demands, and information locked in siloed systems, R&D professionals are required to be more agile than ever before.
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    smol developer

    smol developer

    smol developer

    smol-developer is an open-source library that enables developers to integrate a powerful AI-powered "junior developer" agent into their applications. This agent uses natural language processing to generate, scaffold, and assist with the development of code. Unlike conventional approaches, smol-developer allows for a more interactive development process, where the AI agent iterates and refines the code based on feedback, making it ideal for building project-specific scaffolds and automating repetitive tasks. Developers can leverage this tool to speed up the development cycle, create customized codebases, and collaborate with AI on development tasks in real-time.
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    Arena PLM

    Arena PLM

    Arena by PTC

    Arena PLM is a cloud-native and helps high-tech, medical device, life science, and aerospace and defense companies design, produce, and deliver innovative products quickly. By unifying all product information in a single, secure source of truth, product teams can collaborate anytime, anywhere. Arena streamlines new product development (NPD) and new product introduction (NPI) processes while ensuring regulatory compliance for FDA, ISO, ITAR, EAR, and environmental compliance.
    Starting Price: contact vendor
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    OneTrust Tech Risk and Compliance
    Scale your risk and security functions so you can operate through challenges with confidence. The global threat landscape continues to evolve each day, bringing new and unexpected risks to people and organizations. The OneTrust Tech Risk and Compliance brings resiliency to your organization and supply chain in the face of continuous cyber threats, global crises, and more – so you can operate with confidence. Manage increasingly complex regulations, security frameworks, and compliance needs with a unified platform for prioritizing and managing risk. Gain regulatory intelligence and manage first- or third-party risk based on your chosen methodology. Centralize policy development with embedded business intelligence and collaboration capabilities. Automate evidence collection and manage GRC tasks across the business with ease.
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    PydanticAI

    PydanticAI

    Pydantic

    PydanticAI is a Python-based agent framework designed to simplify the development of production-grade applications using generative AI. Built by the team behind Pydantic, the framework integrates seamlessly with popular AI models such as OpenAI, Anthropic, Gemini, and others. It offers type-safe design, real-time debugging, and performance monitoring through Pydantic Logfire. PydanticAI also provides structured responses by leveraging Pydantic to validate model outputs, ensuring consistency. The framework includes a dependency injection system to support iterative development and testing, as well as the ability to stream LLM outputs for rapid validation. It is ideal for AI-driven projects that require flexible and efficient agent composition using standard Python best practices. We built PydanticAI with one simple aim: to bring that FastAPI feeling to GenAI app development.
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    Ona

    Ona

    Ona

    Ona, formerly Gitpod, is a modern development platform that provides mission control for software projects and engineering agents. It allows developers to keep momentum on any device by offering sandboxed, API-first environments in the cloud or within a company’s VPC. These environments come pre-configured with tools, dependencies, and controls, ensuring a consistent and secure setup for professional software engineering. Ona Agents further enhance productivity by assisting with tasks like scoping, writing, reviewing, and documenting code across the entire development lifecycle. Enterprise-ready guardrails deliver fine-grained permissions, policies, and audit trails, giving organizations full control over compliance and security. Trusted by millions of developers and Fortune 500 companies, Ona integrates seamlessly with tools like GitHub, GitLab, AWS, Copilot, and Amazon Bedrock.
    Starting Price: $20/month
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    Sphinx

    Sphinx

    Sphinx

    Sphinx is an AI agent platform that automates KYC (Know Your Customer) and KYB (Know Your Business) compliance workflows for banks, fintechs, and other regulated financial institutions. The platform deploys intelligent AI agents that handle the manual, time-intensive work traditionally performed by compliance analysts, dramatically reducing operational costs while improving accuracy and consistency. Core Functionality: Automated Customer Onboarding & Verification, Transaction Monitoring & Alert Triage, SAR (Suspicious Activity Report) Preparation, AML (Anti-Money Laundering) Case Management, Regulatory Change Management.
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    InjureFree

    InjureFree

    Agency for Student Health Research

    Modernize your sports organization management with mobile-based incident reports sent in real time to medical staff, administrators, coaches, parents, and other authorized users - all in the connected care ecosystem. Increase both convenience and security by going paperless on an entirely digitized system. No more paper forms, stored in cardboard boxes, waivers misplaced by athletes or parents, or missing doctor’s notes. Decrease compliance concerns with incident processes that are HIPAA- and FERPA-compliant. Personal information is not stored on any local devices, and only authorized users can access the system. InjureFree is not an electronic medical record. Manage risk and easily access athlete rosters from a smartphone, tablet, and other mobile smart devices. See critical risk management and safety updates in real-time, like seeing who has been cleared by a medical professional to Return-to- Play/Learn.
    Starting Price: $2.50 per user per year
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    Quanticate

    Quanticate

    Quanticate

    Quanticate offers comprehensive pharmacovigilance services, including the provision and management of pharmacovigilance safety databases. A pharmacovigilance safety database serves as the central repository for individual case safety reports collected globally for a company's medicinal products. It is essential that these databases are up-to-date with the latest regulatory requirements and validated to meet international standards and business needs. Quanticate emphasizes the importance of selecting the right database by considering factors such as implementation and maintenance costs, hosting model availability (internal infrastructure, third-party hosting, or vendor cloud options), prior experiences, and compatibility with other systems. They caution that while many commercially available databases claim compliance with standards like ISO ICSR ICH-E2B, true compliance requires careful setup, validation, and management.
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    Flexib+

    Flexib+

    3i Infotech

    With more and more organizations adopting digital transformation and using DevOps and agile methodologies to deliver software projects, there is a demand for increasing agility, speed, and reduced costs. While DevOps has broken silos that once existed between testing, development, and operation teams, several organizations fail to address the safety and performance requirements in software development. With FlexibTM+, organizations can embrace testing in DevOps, create automated build & test pipelines, accelerate functional testing, perform application monitoring, and integrate security early in the DevOps cycle. With over two decades of experience in software testing services, we understand the pulse of the customer. We provide both independent testing services and testing for applications developed as part of application development services as an integral part of the software development life cycle.