Alternatives to ViSU

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.

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.

Dot Compliance offers the industry's first ready to use Quality Management Solution powered by the Salesforce.com platform. The Dot Compliance solution includes an extensive set of off-the-shelf ready eQMS and compliance pre-configured processes, enabling customers to deploy quickly and cost effectively. Dot Compliance ready to use solutions include full project validation services and product validation packages. Dot Compliance offers the industry’s most cost-effective quality and compliance management solution available, allowing users to quickly deploy flexible and scalable solutions. Automate core quality processes such as Document Management, Training Management, CAPA, Audits, Customer Complaints, Change Management, Supplier Quality, and more. Our solution is fully configurable and offers seamless integration abilities, with easy adaptation and implementation of customer’s specific requirements.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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™.

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.

Break down your contractual and regulatory obligations into discrete actions that can then be assigned and monitored via interactive dashboards. You can drill down into each business area to identify areas where you are vulnerable, then categorize potential risks and mitigate them. Manage IT system risk through user access reviews and contract renewal management. Establish your corporate structure and keep track of all correspondence with regulators, both at the corporate and legal level. All your licensing requirements and regulatory reporting can be managed from one place. Keep track of all incidents, complaints, and breaches. You can use the data to identify key business risks and help implement change management. Validate and verify that all controls in place are working according to compliance assurance checklists. Identify your obligations and the work you must do as part of your organization's compliance framework.

Regulatory Risks are amongst the Top 3 Business Risks globally as there are multiple Laws (Central, State & Municipal level) applicable to each business. Laws are frequently changing, are complex, and involves multiple stakeholders (internal/external) to manage. The Board needs to have oversight of their compliance and regulatory risks across the enterprise, which means understanding which Regulatory obligations map to which business processes, policies & controls. Offered as SaaS, GCMS helps businesses create a centralized framework to proactively monitor Regulatory Risks across an extensive range of Compliance obligations from all applicable Laws; enabling the Board to efficiently manage control across geography, functional, and industry mandates. Build on Twin Software Architecture, GCMS integrates Tech with Regulatory Intelligence & Updates for 1,000s of Laws, Regulations from 70+ Countries. GCMS simplifies understanding and adhering to all Compliance obligations. It creates common understanding across all stakeholders and makes compliance easier to know, adhere and report.

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.

SmartInsights™, Global Market Access Platform, is an online subscription service that allows you to quickly and easily find current, accurate, and complete regulatory requirements for global markets access. The interface is user-friendly and designed to help you achieve global compliance. Access to key regulatory data and information that is essential for the day-to-day management and strategic business decisions. This includes entering new markets and introducing new products. Access to the most current information about the regulatory landscape and new or updated regulations in your product category. The database is constantly updated to ensure you have the most current information. Access can be customized according to the country and product categories that you require.

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.

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.

Proind compliance controller, a web-based enterprise-wide solution, helps to better understand, manage and track compliance activities within an organization. This integrated view of both internal and statutory compliances across the enterprise reduces compliance management costs. PCC provides a single source of regulatory content with embedded control. This allows users to understand their obligations and associated risk. PCC gives management an automated, streamlined view of regulatory content across multiple jurisdictions, sectors, and regulators. It also helps verify regulatory compliance. PCC has powerful features that allow it to handle all compliances throughout the lifecycle of an enterprise. Reduce reputation risk, penalties, and fines for non-compliance.

Compliance Mantra is a platform that allows users to define compliance requirements according to their business, operations, statutory and regulatory requirements, schedule compliance submission targets, and assign job responsibility. Compliance Mantra also helps to organize the submitted documents and generate alerts for overdue compliances. Businesses face the primary challenge of adhering to deadlines for their regulatory and statutory obligations. There are too many compliance requirements for organizations with multiple companies and agencies. Monitoring and tracking compliance against target dates can be difficult. Compliance Mantra was created to solve the problem. It will allow the user to track their due dates, target date, and actual compliance date. Compliance Mantra generates reports based on various parameters and combinations.

Automated reconciliation, reporting, compliance and reporting for trade transactions (export/import) and cash transactions across all platforms. The solution includes validations that ensure maximum accuracy in reporting. Web interfaces are used to manage processes that are not available in the current trade system. Elimination of bank-wide logins and manual input & extraction to regulatory portals. All past reconciliations and reports under regulatory can be tracked and accessed in one place. You can access your data instantly via the bank's intranet portal.

Simple regulatory monitoring. All regulatory content from around world is available in one place. You can search, organize, and search for it. You can monitor and prioritize regulatory changes that affect your business. You won't be surprised by any new or updated rules. You can view documents organized by industry-standard themes, such as cybersecurity and AML, or by your custom themes. You can work the way that you prefer to gain insight into emerging regulatory trends. You can mark documents and give them to your colleagues for their review. You can track work and make sure it is completed by managing your own obligations. All rule updates, guidance notes and speeches are consolidated in one location. To reflect the actual work of Compliance and Risk Officers, documents are organized according to key regulatory themes. Monitoring rule changes can save you 20+ hours. Ascent displays the information you are interested in.

A cloud-based, comprehensive compliance management solution that ensures compliance for all legal entities will help you protect your global business. ComplyGlobalTM, a cloud-based compliance platform, helps you manage and track your domestic as well as global regulatory requirements in real-time to manage compliance risk. Our algorithm automatically creates your real-time compliance library. Our algorithm automatically updates as regulations change to facilitate compliance activities for each legal entity. ComplyGlobal, a cloud-based compliance software, was developed by compliance and finance professionals. It puts you in charge of your compliance management. You can implement a comprehensive and efficient compliance management plan. Our compliance software will automatically manage your global compliances.

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.

Technology has revolutionized the process of identifying and understanding global financial regulatory rules. This technology will make Financial Regulation Easy. Financial Regulation is made easier by AI-driven regulatory compliance and change management. Finreg-E uses machine learning and artificial intelligence to automatically extract key regulatory actions, connect them with internal controls, and provide intuitive workflows to ensure compliance. Finreg-E's unique regulatory compliance and change management software uses innovative technology to automate and improve compliance with global financial regulatory rules. Finreg-E dynamically links regulatory requirements to internal policies and procedures, using technologies such as artificial intelligence and natural language processing.

ProcessGene is a leading provider of software solutions to manage Governance, Risk, Compliance (GRC). GRC software solutions can be implemented in days. This allows for visibility and central control. ProcessGene™, GRC software solutions create an automated workflow that reduces time and costs of GRC efforts. It also eliminates manual labor, maintenance of multiple Excel spreadsheets, and other manual labor. ProcessGene™, based on Multi-Org technology, has developed a GRC software solution for multi-subsidiary organisations. ProcessGene™, a global leader in Multi-Org technology, has been a pioneer. Over the past decade, we have developed a unique expertise in providing software solutions for multi-subsidiary organisations around the world. Our GRC software was specifically designed for multi-subsidiary organisations and provides the most comprehensive solution to complex, distributed risks management and regulatory compliance issues.

Global regulatory software to help you create and maintain your compliance program. The most comprehensive and current resource for privacy, security and third-party risk research to help you build and maintain your compliance program. DataGuidance, which is powered by 40 in-house legal experts and a network that includes over 800 lawyers, was designed to provide privacy teams with the research they need to track and interpret the requirements for the implementation global privacy laws. Get the latest regulatory news and updates from DataGuidance with daily alerts. Our network of in-house analysts and legal professionals will also provide industry research. DataGuidance Daily Alerts will keep you informed about the latest regulatory developments and news. In real-time, regulatory news and insights are posted as new developments occur. Infographics and Reports highlight the key takeaways from privacy laws and regulations that are frequently searched.

Financial institutions must be compliant with local regulations and business standards. Temenos offers a wide range products and services that will help you manage risk and stay compliant. Temenos draws on its extensive client base and vast experience to provide packaged solutions and toolkits to ensure our clients are compliant with evolving regulatory and business practices. The standard Temenos software integrates all of the regulatory compliance solutions, making it easy to adopt and use them. This solution allows banks to spend less time implementing regulatory changes, allowing them to concentrate on their business opportunities and not on technology issues that affect all banks in their area. Temenos' solution allows clients to identify and process personal information in compliance with data protection obligations.

RegAdvisor Pro alerts you to any federal regulatory changes that may affect your institution. This streamlines compliance management. Our regulatory experts provide concise summaries and suggested implementation steps to help reduce the time required to read and review these changes. Intuitive task delegation gives you the tools to create, assign, and track implementation steps. This includes updating your policies and procedures, system upgrades and training, or creating custom tasks that are specific to your institution. Continuity makes it easy to execute your compliance strategy. RegAdvisor Pro provides you with a complete analysis and all the tools you need for implementing federal regulatory changes. Our regulatory experts analyze every federal regulatory change and inform you when it will take effect, what steps you need to take to implement it.

You can easily adapt to changing regulatory requirements, and accommodate different interpretations of Basel II and III guidelines across multiple jurisdictions. Our flexible solution allows you to easily evolve your system so that you are always up-to-date. You can quickly get up to speed with regulatory compliance by using pre-defined regulatory environments, sample reporting and a banking-specific model. The parallel processing capabilities of SAS Infrastructure for Risk Management execution platform, which are integrated within SAS Risk Stratum, result in a reduction of 50% or more in processing time compared to previous versions. SAS Solution for Regulatory Risk management leverages the foundational capabilities from SAS Risk Stratum. This allows you to use your investment in multiple uses.

Pentana Compliance (previously Redland Solutions), is the market-leading software for individual accountability. It helps financial service firms comply with regulatory requirements such SMCR, IACG, and training and competency obligations. It protects managers and organizations from the risks of non-compliance and helps raise standards and increase productivity. It will help regulators and other stakeholders to ensure that all aspects of process and people regulation are addressed. All the tools you need for effective regulatory compliance are available in one central, easily accessible, and accurate system of records. Pentana Compliance allows you to create and manage MRMs or SoRs, conduct F&P assessments, support certification processes, and provide dashboard reporting for stakeholders.

Waymark's cutting-edge technology will provide you with the regulatory insight, oversight, collaboration tools and support you need to satisfy regulators. The combination of automated workflow and improved collaboration across all lines saves time and money, allowing you to spend more time on higher-impact activities. Key developments are automatically identified and tracked down to completion. Management and directors have the evidence, insight and confidence they need to meet their obligations. Change management audit trails and reports give them that information. Waymark's AI tools automatically classify, sort, and classify an unmatched variety of sources: News, regulatory changes, legal insights, enforcement actions, and other updates.

Product Comply provides 360-degree monitoring of the evolving regulations and standards that impact your products. Our software can be customized to suit any compliance landscape, whether it's electronic products, medical devices, furniture, cosmetics, or any other product. Our product compliance software is able to navigate all global regulations related to any subject related to safety, health, and the environment. The regulations are then mapped to your product portfolio based on components, materials, or chemicals to ensure you stay ahead of any regulatory changes that could impact your business. Advanced software that monitors regulatory changes is essential to ensure your business is protected.

Capnovum's cognitive compliance platform allows regulated entities to manage compliance and resource usage across jurisdictions. Artificial intelligence (AI), which is a form of artificial intelligence, is used to identify and understand synergies among regulations, assess the footprint and impact of regulatory updates and assess the business models. Capnovum eliminates the manual work and external expenditure that are traditionally required to produce and distribute static reports. Capnovum reduces cost, improves timeliness, and increases quality. Combining automation and AI allows for critical information and insights to be instantly available and flow seamlessly between all stakeholders within your organization. We recognize that distraction and pressure on time have become the norm. It is important to cut through the noise to get the information you need quickly and concisely.

Financial institutions can fully automate their compliance and risk management processes with AI-driven technology. Continuity, a RegTech solution, automates risk, compliance and vendor management for the financial service industry. It integrates the required processes of compliance and risk to improve performance. Continuity reduces regulatory burden and mitigates risks by combining cloud technology with regulatory expertise. Our solution has been adopted by hundreds of financial institutions in the United States. Continuity's enterprise-risk management (ERM), compliance, vendor, performance management, and compliance systems are designed to meet the needs of banks, credit unions and mortgage companies of all sizes. A robust platform designed for efficiency and flexibility.

Compfie, our global e-Compliance Platform, is proudly presented by Compfie. It helps you reduce or eliminate non-compliance risk and gives you the convenience to access all your compliance requirements and status wherever you are. You can now digitize all of your compliance documents and satisfy all compliance criteria in one easy-to use form. This will make it 100% compliant integrated. Our innovative digital technology will help you improve operational efficiency, regulatory compliance, growth, and profitability. It is vital to have a system in place to manage your business in this ever-changing business environment. Campfire, a futuristic SaaS-based compliance platform, allows companies to track, govern, and take care the regulatory requirements, performance evaluations, and internal operations. This helps mitigate future risks. You can view a complete overview of your company's compliance status at any time.

Compliance Star is an online compliance software that provides the right tools to manage risk and monitor performance. Compliance Star allows remote management of FCA Authorised Firms, its operating Units/Agents and their operations via real-time data collection. It also provides reporting and reporting. Compliance Star, a technology-enabled compliance platform, facilitates compliance management, workflows and monitoring of firms authorized by the Financial Conduct Authority. Compliance Star is built on a calendar-based task management system that is 'fail safe'. This system allows for manual and automatic task setting, notifies actions, populates deadlines in a calendar, issues reminders, and monitors for completion. Leading regulatory networks are currently using the platform to reduce compliance burden. It allows for complete tracking of internal regulatory processes. It allows for single-point data access and the ability to generate FCA-required reports.

We are the best solution for compliance and operational requirements because of our innovative and customizable application. Global RADAR is the market leader in client onboarding and customer due diligence. Global RADAR makes it easy to open accounts in a safe digital environment. We also ensure compliance with global regulatory requirements. We also leverage sophisticated analytics to ensure clients' suitability. Global RADAR is built upon four solid pillars: customer due diligence, compliance, document management, watchlist screening, transaction surveillance, and document management.

Complius®, the next-generation compliance management software. Complius® is a perfect combination of compliance checklists and intuitive workflows & integration with email, as well as automated reminders for compliance tasks. This platform does everything: it determines the applicable statutory compliance laws to your business, assists your compliance team automates the process, stores all proofs of compliance in one central repository, and sends regular status reports to your management. Sign up today for this cloud-based legal tech SaaS platform. Complius®, has been created to ensure that your business is compliant with all applicable laws and regulatory bodies. Complius®, integrates directly into your email inbox. All tasks are sent to your email client. You can also access them via email. Your team doesn’t need to learn new software!

Software/tool for automating regulatory and statutory compliance management in India. This software/tool can be used to monitor compliance risk across all types industries and operating units. You can easily identify and comply with applicable laws by having a central compliance repository. Continuously monitoring amendments and updating the compliance repository. Pre-determined email alerts are sent to task owners and escalated if breached of certain thresholds. The compliance management system India allows for control over the compliance process with defined workflows and flexible escalate mechanisms. This India compliance management software allows you to assess the status and potential risks of pending violations. Real-time status reporting - granular analysis according your requirements.

Complinity is a comprehensive Governance, Risk & Compliance Software that includes rich modules such as Compliance, Contracts and Registrations, Litigation Assessments, Legal Updates. Audit, Insurance, Document Management. Secretarial, Task Tracker, and many more. You can find out more at!

Tandem is an online tool that reduces regulatory compliance burdens and improves security posture. This is your all-in one information security and compliance solution. Tandem is our product because it works in partnership with you - in tandem. Tandem brings together your organization's knowledge and your needs. Tandem also offers software designed by information security professionals to help you organize, manage and monitor your information security program. Tandem will handle the new guidance, data tracking and structure, as well as report generation. You will be amazed at what you can do with the right tool for your job.