Alternatives to Infosys Regulated Document Management

RunMyJobs by Redwood is the most awarded SAP-certified SaaS workload automation platform allowing enterprises to achieve end-to-end IT process automation and unify complex across any application, system or environment without limits and with high availability as you scale. We're the #1 job scheduling choice for SAP customers with seamless integration to S/4HANA, BTP, RISE, ECC and more while maintaining a clean core. Empower teams with seamless integration with any present and future tech stack, a low-code editor and a rich library of templates. Monitor processes in real-time with predictive SLA management and get proactive notifications via email or SMS on performance issues or delays in all your processes. Redwood team provides 24/7/365 day global support with the industry’s strongest SLAs and 15-minute response times and a proven approach to migration that secures continuous operations, including team training, on-demand learning and more.

RegDesk is the most comprehensive AI-enabled RIMS platform for Medical Devices, Pharmaceuticals, and IVD companies. • Our proprietary Regulatory Intelligence for over 120+ countries is translated and accessible in a standard format. In addition, it provides alerts on evolving regulatory changes • Our AI-powered Application Builder allows RA teams to prepare and publish global applications in 1/10th of the time • Our Change Assessment capability helps RA teams understand the impact of the change(s) on an existing product(s) and the action required • Our Distributor Collaboration provides seamless workflow solutions to interact, communicate, and share documents with external business partners • Our Standards Management makes it easy for RA teams to search and manage not only international but also country-specific standards • Our Tracking & Reporting functionality allows teams to track regulatory projects across the globe, receive renewal notifications, and generate reports on KPIs within seconds For more information, visit our website.

Adaptive Compliance Engine® (ACE®) is a highly configurable, workflow based eQMS/eDMS and more that can adapt to any business process, allowing for real-time tracking, management, and reporting of all compliance, quality, and operational activities. With ACE®, you will minimize the administrative hassles and maximize ROI with productivity gains from day one – all while 21 CFR Part 11 compliant. Our one-stop software includes: -Office 365 Integration -Inspection Management -Document Management -Risk Management -Product Lifecycle Management -Learning Management -Audit Management -Quality Events -Paperless Validation -Electronic Signatures (21 CFR Part 11 Compliant) -Endless Workflow Configurations -And so much more! Empower all levels of your organization with intuitive user interfaces, easily search for all your documents and records, and transform your data into actionable intelligence with advanced analytics all on a single platform. ACE comes with everything you need, all included at one price. Every application is included, no more a la carte pricing. No more nickel and diming. One software, endless solutions.

Kalypso offers life sciences companies a cost-effective accelerator to implement a RIM system - Accel for RIM. The integrated platform allows for efficient product distribution and management, as well as a global platform to track and manage product registrations. It consolidates compliance data and quality data from different enterprise solutions into one global source of truth to facilitate product registrations and tracking in order to speed up regulatory submissions. Modern APIs are used to combine product data, regulatory documentation, and submission packages. Pre-configured for quick implementation with a valid software system. Based on industry-leading RIM practices.

It can seem like a never-ending series of tradeoffs to bring breakthrough products to market within highly regulated industries. MasterControl's GxP software simplifies workflows, so you don't have to compromise quality for cost or innovation with regulation. Complete and connected meets flexible and fast. MasterControl Quality Excellence transforms quality data and processes to a competitive edge. Modern software is the first step in modernizing your manufacturing operations. MasterControl Manufacturing Excellence, from work orders to production records (EBR/eDHR), to logbooks and work instructions, is the easiest way to digitalize manufacturing.

The regulatory affairs departments in the healthcare and life science industry are driven to improve efficiency and create intelligent systems that optimize costs, maximize accuracy, and reduce submission times. RIMTrack, a cloud-ready, artificial intelligence (AI)-based, new age regulatory information management system, addresses this concern. It was created from scratch to assist organizations in preparing submissions accurately and efficiently. It streamlines regulatory processes related to licensing, approvals, regulatory, competitive intelligence, clinical trials and reporting across global stakeholders. Integrate with existing RIM systems to achieve complete management of the regulatory lifecycle process.

ClinChoice manages global regulatory data with technology expertise, a deep understanding and best data management practices. ClinChoice uses its expertise in technology and regulatory affairs to help organizations manage their regulatory information. Our consultants offer general data maintenance support in regulatory Information Management System (RIMS) software. This will help ensure that applications are submitted, approved, renewed, and tracked on time. We offer the necessary support in managing and controlling the drug registration process. This allows drug and medical device manufacturers to track all regulatory information and has the ability to see it. Organizations can develop short-term and long-term strategies that meet submission deadlines with minimal impact on their day-to-day operations.

End-to-end regulatory information management from a single platform. The Vault RIM Suite streamlines global regulatory process on a single cloud-based platform. This allows life sciences companies to increase visibility, data quality, agility, and efficiency. You can respond faster to changes in regulations and improve process efficiency, from submission planning to publication. Coordinate regulatory efforts across HQ and affiliates within a single RIM platform. Assure that teams are creating reliable regulatory content with high data integrity. Veeva Vault Registrations manages product data worldwide, including variations, registration status, and interactions with health authorities. Veeva's flexible data structure supports IDMP data points, and will continue to support changing regulatory data standards. Veeva Vault Submissions automates regulatory process steps and streamlines submission planning.

RegDocs Connect provides the tools for your regulatory and operational teams to create compliant, submission-ready documents and records. This solution is built with the end user in view. It focuses on collaboration, automation, and quality. Automated workflows allow you to manage your records from draft to final. This allows your team to have complete control over your regulatory documents at any time. The mapping of document types to the EDM Reference Model and eCTD allows for organization and retrieval of documents that can be used in regulatory submissions. The powerful tools of PDF/A Publishing, document classification, unique document identifiers, and EDM reference model facilitate regulatory document management. This solution pulls together information from all levels of your organization into one easy-to-use solution. The ability to produce submission-ready and quality content has become more difficult due to electronic submissions to regulatory authorities and the complexity of drug development.

DXC RIM platform manages regulatory content, data and workflows in one central place. This helps teams accelerate innovation and reduces time to market. A unified platform is required to manage regulatory data and workflows due to the sensitive nature of regulatory affairs content (RA). All relevant data must be easily accessible to all teams. They also need an intuitive, customizable user interface that is simple to use. While configurable reporting and collaborative tools are essential for success, legacy technology can frustrate teams or slow down processes. Compliance is difficult. It is difficult to collect data and document processes. Life sciences organizations that use disparate technologies and have fragmented legacy systems can create problems. They may need to resort to spreadsheets in some cases to manage key operational processes. A centralized enterprise-grade solution is required to bring products to market and manage RA.

IQVIA Smart, our new end-to-end regulatory information management software, streamlines regulatory processes. Your team can focus on delivering high-quality products to the market instead of labor-intensive maintenance. RIM Smart, the modern regulatory information management system, is designed to improve speed, collaboration, efficiency, visibility, and performance across your entire global portfolio. It also reduces costs. IQVIA RIM Smart is a secure cloud-based solution that allows for interconnected, comprehensive, and intelligent management of all regulatory processes. IQVIA safety platform integration will increase performance and improve flexibility. Automate manual processes and increase connectivity to improve efficiency, cost savings and coordination as well as cross-enterprise visibility and visibility.

Dow Jones Risk & Compliance, a global provider, provides best-in class risk data, web based software applications, and scalable due-diligence services to help organizations manage risks and meet regulatory requirements in relation to financial crime, third party risk management, international trade, and sanctions. Dow Jones Risk & Compliance is built on the legacy of the world's trusted newsroom. It combines the expertise and knowledge of a multilingual team of researchers with the industry-leading data scientists, technologists and analysts to provide actionable compliance content. Our solutions were created in partnership with leading legal and political advisors, including former regulators, to help our clients maintain consistency among global business units and teams.

Samarind RMS is a smarter way for you to manage your medical product information. Samarind RMS allows you to only enter data once, and you can reuse it as often as necessary. An example of this is the 'INN' which can be used once and reused for all IMA submissions, renewals and variations. This concept is applicable to all key data within the system. It has been proven to improve data quality and streamline workflows. Our pragmatic approach to systems design and implementation means that our customers can manage their licenses smoothly and efficiently, safe in the knowledge that our single-place-of-truth™ approach for regulatory affairs professionals delivers a complete end-to-end system. An electronic document management system (EDMS), which includes version control, template creation, and the ability to link with external document management systems like Documentum™, SharePoint™.

Rimsys provides a single, cloud platform for end-to-end regulatory process digitization and automation. Designed by and for regulatory affairs professionals, Rimsys helps medtech companies reduce repetitive administrative work, speed time to market, respond faster to changing regulations, and drive alignment across internal teams, affiliates, and partners. Only Rimsys provides a holistic platform that supports a full range of regulatory activities. Use regulatory intelligence and digital templates to guide regulatory strategy and streamline submissions. Create compliant, submission-ready content, and consolide PDF packages for electronic and print submissions. Digitally collect and maintain evidence of compliance. Link to relevant standards and get notified of changes. Get notified of changing standards, laws, regulations, and guidance documents that impact your products. Create self-service application, product, and country reports to see exactly where your products can be sold and their current registration status.

OpenText™, a leading provider of information management solutions for life sciences organizations, helps them to harness insights from data and content to improve their decision-making and accelerate product development. Integrate, manage and securely exchange data between people, systems, and things. Use information assets to drive innovation and commercialization. Cloud-native software can run anywhere, giving you freedom of choice. OpenText for life sciences accelerates discovery by delivering actionable insights that can be used to drive innovation in pipelines. Intelligent capture allows you to capture and manage research papers in electronic lab notebooks. Text mining can help you gain insights. Unstructured text in clinical trial reports, study protocol, clinical safety and efficiency findings, can be used to extract knowledge. Learn how to intelligently analyze and classify clinical trial documents and extract them to reduce the risk for costly stops and starts.

You can speed up the time to market by organizing, executing and tracking all regulatory activities within a single RIM application. This allows you seamless access to all regulatory documents and full support for all eCTD submission requirements. Automation is integrated to streamline workflows and increase confidence in product registration data quality. You can speed up the time to market by organizing, executing, tracking, and planning all regulatory activities in a single RIM application. This allows you seamless access to all regulatory documents and full support for all eCTD submission requirements. Automation is integrated to streamline workflows and increase confidence in product registration data quality.

Essenvia delivers business value to all departments and teams, and increases efficiency across the board. Centralized repository of all regulatory information allowing collaborative authoring, reporting, and eliminating technical holds, RTAs and RFIs. The regulatory affairs department is empowered to accelerate product launches, and eliminate revenue losses due to delays in submissions and missed renewals. Helicopter view over the entire regulatory lifecycle. Executive dashboards, metrics and proactive alerts are available for global registrations and submissions. Essenvia, a RIM Platform, allows you to manage regulatory workflows throughout the entire product lifecycle. It also accelerates global market access and generates exponential business value. Consolidate all regulatory activities onto one platform to bring your devices faster to market. All registration documents linked to product master information are stored in a central repository. Manage the product registration lifecycle per country.

Global regulatory affairs system that includes registration management software and support from regulatory experts around the world. This registration system is required to renew, amend, transfer, or modify your IVD market access approval or medical device. The intuitive user interface of LICENSALE®, which includes real-time data and infographic analytics, allows for project management, collaboration, future market access planning, advanced reporting, and effective project management. It allows you to take control of your global medical technology registration activities. Arazy Group's "in-country regulatory experts" review your compliance documents and assist in the preparation of your applications. They will work with authorities until you receive your desired marketing approvals. LICENSALE®, which includes compliance and submission requirements for your product in over 140 countries, as well as regulatory experts to help you with each market.

ViSU™, a cloud-based End-to End Regulatory Information Management platform (RIM), is specifically designed for the medical device industry. It allows global users to access and manage regulatory data (Product Master and Registrations, Tracking), Dossiers/Tech files (Submission planning and building & lifecycle), HA/NB correspondence and Obligations tracking. ViSU helps you embrace digitalization in regulatory. It provides connectivity, traceability, and automation which leads to regulatory management efficiency, lower compliance risks, and cost reduction.

Our enterprise document management software is the best in its class. Meridian offers a single source for truth and configurable workflows that streamline collaboration with all departments. It also ensures that every document change is versioned, audited, and reported to the regulatory authorities. Engineering document management refers to the process of finding, finding, and managing complex engineering documents, including CAD files, drawings, technical documents, and communication documents, in AEC organizations (Architecture, Engineering & Construction). Businesses in these industries can find it difficult to manage their engineering documents effectively. Meridian's document management software for engineering projects can address these concerns. Meridian can centralize documents and drawings within an organization while automating key processes.

Imagine all your regulatory information about products, registrations and submissions, correspondence, and commitments in one central place, accessible from anywhere. Ennov RIM allows life sciences companies to streamline their regulatory processes, improve data quality, quickly respond to business-critical questions, and effectively responds to health authority requests. Ennov RIM, a purpose-built application based on Ennov Process, allows for the tracking and management of therapeutic product details as well as registration information. Ennov RIM gives regulatory personnel the essential information and functionality they need to manage product portfolios globally, whether you're planning to launch a new product or handle variations to existing registrations.

EXTEDOpulse, a comprehensive RIM software solution, consists of five hubs that address all stages of product development. You can use the applications separately or combine them to get additional value based on your needs. The development of pharmaceutical products can be complex and require input from many people. Life science organizations face many challenges due to the complexity of operating in a highly regulated industry. We are able to provide you with great synergy and connection, as well as innovation, for compliance. EXTEDOpulse was designed with these aspects in view to help you connect the dots throughout the entire lifecycle pharmaceutical products. EXTEDO is familiar with the complexities involved in the regulatory pharmaceutical product journey.

Select the only solutions that you need right away. You can add more capabilities later on. The LORENZ Foundation manages Controlled Vocabularies and Repository Management, Interoperability Management, and User Management. This centrally streamlines system management, maintenance, and deployment. You can benefit from a network that integrates with other specialized systems. LORENZ solutions are compatible with third-party software. This gives you the freedom to choose the perfect fit for you, even if it is not in the LORENZ portfolio.

RIMExpert™, which addresses regulatory planning, tracking, and data management, manages the global rollout plans and automates the creation of regulatory activities, medicinal products, and regulatory applications. RIMExpert™, reduces data entry requirements, improves data quality, and increases global oversight and control. Standardize regulatory planning, tracking, and registration management processes. Increase collaboration between affiliates and headquarter. All registration activities can be done in one place. One point of contact for all applications, questions, correspondence, and commitments. To maximize the efficiency of enterprise regulatory resources, sync your efforts. You can monitor registration activities throughout the product's lifecycle, keeping track of deadlines, status of commitments, and agency questions. Interactive dashboards to monitor and control regulatory activities and registrations.

harmon.ie allows knowledge workers to easily capture and classify email and documents to SharePoint and Teams from Outlook, where they spend most of their work time. It is easy to find and share important content right from your email client. harmon.ie makes it easy to do the right things, increasing SharePoint adoption and workplace productivity as well as information governance compliance. Thousands of enterprise customers rely on harmon.ie's SharePoint- and Office 365-based user experiences products for email, records management, collaboration, knowledge preservation, and SharePoint adoption. harmon.ie is a Microsoft Partner since 2003 and has won many Microsoft Best App Awards. Our flagship solution eliminates data silos in Office 365 apps by grouping information with Descriptive Labels. harmon.ie SmartAssistant allows organizations to bring together all their information so that employees can concentrate on work.

AmpleLogic Regulatory Tracker is built using the LOW CODE AND NEUTRAL CODE (LCNC PLATFORM) and consists of two modules: ANDA Tracker and DMF Tracker. This Pharmaceutical RIMS Software will help you improve data quality, increase operational efficiency, reduce mistakes, and streamline communications across departments.

PhlexRIM dramatically improves compliance by providing you with real-time, efficient and effective access to your global registration information. PhlexRIM 2.0 includes a library of pre-configured automation "bots" and built-in regulatory use case examples based on industry best practice. The intuitive drag-and drop design tool allows regulatory teams to automate their business processes without the need for programming knowledge or IT support. Manage the entire lifecycle of pharmaceutical product registration activities. Access detailed status information and make use of the alert management feature that is part of all workflows. You can either use standard reports to illustrate your reports or create your own reports. You can create and assign regulatory tasks to your organization for management, headquarters, and affiliates.

All the information you need to register your IVD product or medical device in any market worldwide and manage your market access licence throughout the product's life cycle. REGISLATE®, which provides information about medical and IVD device-specific submission file requirements for each country, allows users to manage their market access licenses through the product life cycle. You can track milestones, timelines, estimated and actual completion dates, as well as estimated and actual completion dates, for initial registrations, renewals, amends, and license transfers, in real-time. For clear monitoring and management, infographic data and proprietary indicators are available. Collaboration tools are available to assist with the preparation and review submissions, compliance requirements, and documents. Receive progress reports in real time for current and future submissions, including market access readiness index. REGISLATE®, which includes GR-MAP registration tracking, for both country AND product.

The RecordPoint Data Trust platform helps highly regulated organizations manage data throughout its lifecycle, regardless of system. We work with organizations in highly regulated industries to ensure their data is right where it should be - safeguarded for privacy, security, and governance.

Secure Multi-Data Archiving with a Single Interface OneVault archives email and all new data types that your organization uses today. Email, Instant Messaging and Teams, Zoom, Webex, and many other data types. OneVault gives you a single interface to archive from multiple systems. It is easy to organize consistent policies and support business continuity plans by centralizing important data in a secure cloud platform. e-Discovery is a single platform for managing and working with records. It is secure, transparent, and easy to use. OneVault combines the powerful features of our stand alone archiving solutions under one pane of glass. It is intuitive, secure, and scalable. Start with email and expand as new systems become available.

Calyx understands that data is key to the success of any clinical development program. Your electronic data collection (EDC), system is crucial to your success. Calyx EDC is used in more than 2,600 clinical trials around the world. It streamlines data collection and reporting through one platform. Don't give your sensitive data to anyone. We can help you make your program a success with Calyx. Calyx EDC allows you to plan, design, and carry out studies of any complexity. Calyx EDC helps you keep your trial on track with features that reduce costs, improve site visibility and drive efficiency.

Companies are looking for ways of increasing revenue, reducing costs, and moving quickly. Flexible pricing, managing recurring revenues and enterprise contracts the best way possible, and changing business models without restrictions, all serve as competitive advantages. However, not all enterprise billing solutions support market-paced changes. We do. The Kansys Edge provides a complete solution to charge, price, bill, settle and provide customer care. The Kansys Edge gives businesses the freedom to run their business how they want. Our flexible billing solution is tailored to your industry and business model. Subscription-based and usage-based pricing supported by a rating and pricing engine of enterprise-grade. Subscriptions generate predictable revenue, and consumption-based pricing models provide revenue that is consistent and ongoing.

The new standard for Enterprise shipping. Our high-performance shipping API provides a variety endpoints that will allow you to create the best delivery experience for customers. Our innovative technology allows you to scale faster and more efficiently and will never slow down legacy shipping software. Our reliable software is able to run at peak performance with an uptime of 99.95% You will always know the true cost of your labelling solution with our transparent pricing. Simply change carrier codes in your API requests to quickly and efficiently add new carriers. Add complex rate structures and manage worldwide shipping costs. Our label engine creates carrier-approved shipping labels in ZPL or PDF with the fastest speeds on the market. You only need one API to create the perfect delivery experience.

Data protection is becoming a top board issue and a potential source of upper hand. It is not just a compliance requirement, but a board-level concern as data volume and value grow exponentially. Data protection is a constant challenge and potential reputation bomb without a well-designed and executed data administration program. Regulators and the commercial centre are putting increasing pressure on organizations to improve how they collect, use, store, and erase individual data (PI). Its importance will only grow as technology such as the Internet of Things and Big Data creates more data and insights. Infosys Enterprise Privacy Suite (iEDPS), addresses enterprise challenges by helping companies to protect their private data while adhering to global regulatory standards like HIPAA, PIDA, GLBA and ITAR.

The HPE Consumption Analytics Portal, which is the metering and analysis component of HPE GreenLake's consumption-based IT offering by HPE Pointnext Services, is now available. It gives you the flexibility and economics of the private cloud in your own datacenter. Interactive dashboards and drag-and-drop reports give you granular insight into your usage and costs. Flexible budgets and a rules-based recommendation engine to consume-based services will help you stay on top of IT spending. Forecast demand to avoid a shortage becoming an outage. With decision-making power, you can plan your capacity. The HPE Consumption Analytics Portal, part of HPE GreenLake provides even more transparency into your usage and commitments that determine your monthly cost. You will have more power to make informed decisions and plan your workload for maximum performance.

In today's digital age, robust identity validation is essential for businesses of all types. Accurate identification is key to fraud prevention, regulatory compliance and seamless customer onboarding. ID Analyzer is a leading API for identity verification that simplifies and improves ID authentication. ID Analyzer, a cutting edge API solution, allows businesses to quickly extract, analyze and verify data from a variety of identity documents.

StarWind VTL allows businesses to move beyond costly physical tape backups without compromising regulatory data archiving and retention requirements. StarWind VTL uses on-premises Virtual Tape Libraries that offer cloud and object storage tiering. Keep your backups "air-gapped", which is a virtual tape that stores them, to protect them from ransomware. For maximum security and cost-efficiency, you can duplicate and tier backups to any public cloud. You can also store any industry-standard object storage.

Ennov Doc is part of Ennov's ECM platform for regulated industries, especially the Life Sciences Sector. Our solution is recognized by Gartner as a relevant actor in the Life Sciences sector (mentioned in Gartner's Hype Cycle for Life Sciences Reports as a Regulated SaaS EDMS, as well as for eTMF and QMS) , and suitable for large as well as small organizations. It comprises in the same interface and completely integrated : Document management (EDMS), Business process management (BPMS), Dossier management (composite documents management), Report management, Traceability and security (21 CFR part 11 compliance). With a very intuitive 100% web interface, deployments are easy and user adoption extremely high. Another key point is that document management is "metadata oriented", meaning that documents navigation and search is completely configurable using metadata rather than folder structures. Users can very quickly find documents based on what they are rather than where they are.

StockQuery is an inventory management system hosted in the Cloud. StockQuery tracks the stock count and generates a list to be reordered. StockQuery offers customizable transaction and inventory reports that allow you to cross-check physical inventory with inventory records. All your inventory data is securely stored in the Cloud, and can be accessed from any web browser. StockQuery uses industry-standard SSL encryption to encrypt data communication between our Servers and your Web Browser. This technology is used by banks and brokerage houses for secure communication. We use strong passwords and take other security measures that are specific to each application. StockQuery is hosted on Microsoft Azure Platform, which guarantees 99.95% uptime. All data is automatically backed-up. StockQuery is available at a special price of $5 for the first 30 days (non-refundable).

Brainloop CollaborationRoom. The dataroom solution that offers unlimited security worldwide. Brainloop CollaborationRoom is the foundation for secure collaboration between staff and external partners. This means that it works in your company as well as outside. Complete encryption at the highest standards at rest and transit, on mobile devices (apps/client), and encrypted local storage ensures that sensitive data doesn't fall into the wrong hands. It integrates compliance intelligence so you can implement both internal and external regulations. The integrated audit trail keeps a record and the integrated audit log of all activities keeps a log of all activities. Each time your data are accessed. Brainloop CollaborationRoom provides secure document editing, sharing, and storage. You can rest assured that confidential data is protected and that your team's collaboration is efficient.

Features With its integrated variable-length duplication technology, Dell EMC Avamar allows for fast and efficient backup and recovery. Avamar is optimized to provide fast, daily backups of virtual and physical environments, NAS servers and enterprise applications, as well as remote offices and desktops/laptops. Avamar can be purchased as a virtual edition, or as a component in Dell EMC Data Protection Suite. This suite offers you a complete set of data protection software options.

Cloud computing is made easy by Otava Gen3 Cloud. VMware Cloud Director allows you to quickly add and configure resources within your environment. This will allow you to dream big. Consumption-based billing gives you full transparency at every level of usage and volume. This allows you to easily access the entire set of interoperable VMware Cloud Infrastructure capabilities as a service. This is just one more way Otava makes cloud computing easy. Our passion for excellence drives us to find new solutions and share them with our clients and partners. We overcome all regulatory and security challenges through innovation and collaboration and execute with fierce determination. We will do what we promise and we won't allow anything to stop us. Hybrid cloud computing that is secure and compliant for service providers, channel partners, and enterprise clients.

Spectral is a lightning fast, developer-first cybersecurity solution. It acts as a control plane over source code and other developer assets. It detects and protects against security mistakes in code, configurations, and other artifacts. Spectral is the first hybrid scanning engine. It combines AI and hundreds upon detectors. This allows developers to code with confidence and protects companies from costly mistakes. You can map and monitor hidden assets, such as codebases, logs and other intellectual property, that are not visible in public repositories. SpectralOps' advanced AI-backed technology with over 2000 detectors can be used to provide extensive coverage and detect issues, as well as keeping your organization safe.

Diligent Workflow is a leading workflow solution that streamlines secure management, approval and compliance of sensitive or regulatory documents. Diligent Workflow automates document and media creation. This improves efficiency in project management, approval and distribution, archiving, archiving, and audit trail for all your policy documents and contracts. You can see how Diligent Workflow features can automate your approval process to improve efficiency and transparency in document creation.

Infosys Cobalt consists of a range of services, solutions and platforms that act as a force multiplier to enable cloud-powered enterprise transformation. InfosysCobalt assists businesses to redesign their enterprise from the core and build new cloud-first capabilities that create seamless experiences in public and private cloud across PaaS and SaaS landscapes. Infosys Cobalt's community power allows enterprises to quickly launch solutions and develop business models that meet changing market demands while adhering to the strictest industry, regional, and global regulatory and security standards. Enterprises can harness the full potential of the cloud ecosystem, Infosys Cobalt’s vibrant community of technology innovators, and drive greater business value.

Smartswim is a cloud-based swimming school application. Smartswim supports both Mac and PC and requires no additional software to install. It also has a 99.95% uptime guarantee. Smartswim's full range of features is available to you for a free 30 day trial. Trial access is free and without restrictions. All browsers can cache web pages to make it easier to access them. Browser Caching allows the browser to store a copy of pages and websites it has previously visited in its own storage container, which makes it easier to load the next time the site visits. This is a tricky process because every browser handles it differently. Smartsports Pty Ltd is happy to announce the availability of Smartswim 4. This new version will run in parallel to Smartswim 3.0 Silverlight for approximately. 60 days pending user acceptance. Both systems' data is to be considered "live" as they both point to the same database.

Acuvity provides the most comprehensive AI governance and security platform for your employees and apps. DevSecOps allows developers to focus on AI Innovation while DevSecOps implements AI Security without code changes. Pluggable AI security ensures complete coverage without outdated libraries or inadequate coverage. By utilizing GPUs only to run LLM models, you can reduce costs. Full visibility of all GenAI models and apps, plugins and services that are being used and explored by your teams. Granular observability of all GenAI interactions, with comprehensive logging. AI usage in enterprises needs a specialized framework that can address new AI risks and comply with emerging AI regulation. Employees can use AI with confidence, without exposing confidential information. Legal wants to make sure that AI-generated content is free of copyright or regulatory issues.

GAS MANager is a program that generates gas bills based upon the actual or estimated amount of gas consumed over a billing period. GAS MANager was originally designed for natural gas cooperatives, but can also be used to bill any metered consumption-based utility such as water. GAS MANager was released in 1997. Since then, the software has been enhanced to allow for the management additional information that isn't directly required in the preparation and payment of gas bills but is essential in the operation of a natural-gas co-op. Many of these enhancements were integrated into GAS MANager for the benefit all users. However, some of them have been added to the program as add-on modules. GAS MANager users can choose the features they want to use, while keeping the cost of GAS MANager low.

FileQuest®, enables Web-based data discovery to accelerate litigation, investigations, regulatory compliance, and privacy protection. FileQuest®, Digital Mountain offers Web-based solutions that allow for the acceleration and control of the entire electronic discovery process. FileQuest®, a Web-based data discovery tool that empowers law firms, corporations, and government agencies to perform data extraction, filtering and processing, review, and production of documents. FileQuest®, a robust, fully integrated platform that dramatically reduces time for data discovery, eliminates the need for any software or hardware maintenance, and makes it easy for organizations to get rid of all unnecessary software. FileQuest®, in other words, provides data discovery that is fast and easy with no upfront costs. FileQuest®, allows you to: Import data. As discovery happens, it is updated continuously. An audit trail allows you to track all electronic evidence.

BluLogix is a leading SaaS-based recurring revenue monetization platform, offering B2B enterprises a powerful platform to catalyze growth through streamlined subscription and usage billing. Designed for companies with complex billing challenges, the BluIQ platform offers flexible, scalable solutions to streamline operations and boost innovation. BluLogix provides end-to-end automation and seamless integration across the revenue process, tailored for businesses with complex billing needs. It is built to adapt rapidly to evolving business requirements, ensuring customers can capitalize on the subscription economy with efficiency, accuracy, and speed. With BluLogix, businesses can enjoy increased revenue, enhanced profitability, and higher customer satisfaction thanks to comprehensive automation and seamless system integrations. Tailored to adapt to your dynamic needs, our platform ensures you efficiently leverage the subscription economy. As a recognized leader in managing recurring revenue, BluLogix optimizes our customers’ quote-to-cash processes, fostering sustainable growth, and delivering exceptional customer experiences.