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.

Five of the most important regulatory agencies in the United States use MasterControl Quality Excellence solutions. A leading software-as-a-service (SaaS) provider, MasterControl helps companies get their life-improving products to market sooner. It does this by providing cloud-based solutions that manage an organizations documents, training and exams, corrective/preventive action, validation, and more. MasterControl offers solutions throughout the product's entire lifecycle.

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.

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.

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.

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.

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.

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™.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

ZippyDB™, you can save time and money on DevOps, patching, operational management, and debugging. Our consumption-based pricing is much lower than our competitor's fixed pricing. You can use all the Redis cache features such as data caching, queues, leaderboards and any other high-performance Redis in-memory storage use. A fully managed serverless Redis experience is available. Reduce the complexity of managing servers and replicas. Redis high availability, backed by our 100% uptime warranty. Redis infrastructure with hardened. Full encryption for PCI & HIPAA compliance. You only pay for what you use, and it is per-second.

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.

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.

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.

Infosys Nia™, an enterprise-grade AI platform, simplifies the AI adoption process for IT and Business. Infosys Nia supports the entire enterprise AI journey, from data management, digitization and image capture, model development, and operationalization. Nia's modular, scalable and advanced capabilities meet enterprise needs. Nia Data provides highly efficient tools and frameworks to support further ML experimentation using the Nia AML Workbench. The Nia DocAI platform automates all aspects of document processing, from ingestion to consumption. It uses AI capabilities like InfoExtractor and NLP, cognitive search, and computer vision.

Realize faster digital transformations with a unified platform. The integration of ransomware protection helps to make the transformation even easier. Achieve 421% ROI in 5 years and 63% more efficient storage management. Nutanix Unified Storage, a software-defined platform for data services, simplifies enterprise data management operations and offers the speed and flexibility required to build modern applications, services, and infrastructure, no matter whether they are deployed on the core, in the cloud, or at the edge. Consumption model to address exponential growth in unstructured information while meeting performance requirements. Integrated data security and analytics provides deep data insights for preventing, detecting, and recovering from ransomware or cyber-attacks. A consolidated platform for data services simplifies management, automation, availability, and more. Unified Storage platform can be extended across core, cloud, or edge while supporting multiple protocols.

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.

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.

Many customers of Amazon Web Services (AWS), require data storage and analytics solutions that are more flexible and agile than traditional data management systems. Data lakes are a popular way to store and analyze data. They allow companies to manage multiple data types, from many sources, and store these data in a central repository. AWS Cloud offers many building blocks to enable customers to create a secure, flexible, cost-effective data lake. These services include AWS managed services that allow you to ingest, store and find structured and unstructured data. AWS offers the data solution to support customers in building data lakes. This is an automated reference implementation that deploys an efficient, cost-effective, high-availability data lake architecture on AWS Cloud. It also includes a user-friendly console for searching for and requesting data.

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.

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.

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.

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.

Amazon S3 Glacier Deep Archive and S3 Glacier Deep Archive provide data archiving and backup services that are extremely secure and durable. They can withstand 99.9999999999% and offer compliance and security capabilities that can meet the most stringent regulatory requirements. The cost of storing data can be as low as $1 per terabyte per monthly, which is a significant savings over traditional on-premises solutions. Amazon S3 Glacier offers three access options to archives. These options range from a few minutes to several days to meet varying retrieval requirements. S3 Glacier Deep Archive offers two access options that range from 12 to 48 hours.

Conga Billing allows organizations to automate invoicing and billing management. You can bill for mixed business models such as subscription services, physical goods and professional services. Customers can choose the payment method they prefer. Conga Billing allows you to invoice customers in the way that suits your customers best. You can customize billing for partial orders, full orders, and split orders. Automated invoices are more accurate and efficient than manual billing. They are generated from assets ordered, contracted, or quoted. Automated invoice adjustments for customers based on upgrades and downgrades.

Our expertise and experience in cloud infrastructure, and all that it entails, will help you. We offer services at a competitive cost because we have multiple datacenters and unlimited resources. We offer solutions that can scale up and down to meet your needs. Personal attention and dedicated support that includes 99.95% uptime, 24/7 availability, firewall, and round-the clock DDoS protection. You have complete root and performance diagnostics, which allows for effortless flexibility, power, and control. Futuristic solutions using Tier-III datacenters and cloud ecosystems, backed up by dual redundancy parts, located in diverse geoographies. Once the customized name has been set up with system success, you can now access the addresses of files that are still in your OSS.

EKS is community-driven. It supports the latest Kubernetes version and native Kubernetes cluster administration. It is available as a plugin that supports Tencent Cloud products such as storage, networking, load balancers, and other services. EKS is built on Tencent Cloud’s well-developed virtualization technology. It also uses Tencent Cloud’s network architecture to provide 99.95% service availability. Tencent Cloud ensures that EKS clusters are isolated from each other via virtual and network isolation. You can set up network policies for specific products by using security groups, network ACLs, and other options. EKS's serverless framework ensures better resource utilization and lower OPS cost. EKS uses only the resources required by the current load. Flexible and efficient auto scaling makes sure that EKS is only using the resources necessary. EKS can integrate with many Tencent Cloud services such as CBS, CFS and COS, TencentDB products and VPC.