Alternatives to Flinn

Predict360, by 360factors, is a risk and compliance management and intelligence platform that automates workflows and enhances reporting for banks, credit unions, financial services organizations, and insurance companies. The SaaS platform integrates regulations and obligations, compliance management, risks, controls, KRIs, audits and assessments, policies and procedures, and training in a single cloud-based SaaS platform and delivers robust analytics and insights that empower customers to predict risks and streamline compliance. Happy with your current GRC but lacking a true analytics and BI tool for intuitive executive and Board reports? Ask about Lumify360 from 360factors - a predictive analytics platform that can work alongside any GRC. Keep your process management workflows intact while providing stakeholders with the timely reports and dashboards they need.

ViSU™ is an innovative cloud-based platform for End-to-End Regulatory Information Management (RIM) tailored for the medical device sector, allowing users worldwide to efficiently access and oversee essential Regulatory Data, including Product Master details, Registrations, and Tracking. This comprehensive tool also facilitates the management of Dossiers and Technical Files through submission planning, development, and lifecycle management, while streamlining communication with Health Authorities and Notified Bodies, tracking obligations, managing Unique Device Identification (UDI), electronic Instructions for Use (eIFU), maintaining a Regulatory Requirements Database, and controlling changes. By adopting ViSU, organizations can fully harness the power of digital transformation in regulatory processes, achieving improved connectivity, enhanced traceability, and significant automation. Ultimately, ViSU contributes to heightened regulatory management efficiency, reduced compliance risks, and lowered operational costs, making it an indispensable asset for the industry. Moreover, its user-friendly interface ensures that teams can navigate the complexities of regulatory requirements with ease.

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.

We assist clients in confidently navigating compliance choices through our innovative, patented platform. Adept effectively integrates laws, regulations, and policies to enhance compliance efforts within current systems. Additionally, Droit keeps a close watch on changes in regulations and policies, ensuring that its platform is promptly updated with every new regulatory shift or interpretation. The Adept platform offers clients a unified perspective on the application of rules and regulations. To confirm decisions, Adept produces a logic model featuring traceable paths that link back to the original source text. This level of transparency not only fosters greater understanding but also boosts operational efficiency and establishes a repeatable, defendable methodology. With the help of Adept's patented technology, clients are empowered to make well-informed decisions that lead to appropriate actions. Rapid decision-making can be executed effortlessly within your work environment by relying on digitized rules and regulations. Additionally, users can observe decision-making steps organized in clear, intuitive logic diagrams that facilitate comprehension and application. This user-friendly approach enhances the overall experience and effectiveness of compliance management.

Product Comply provides extensive 360-degree oversight of changing regulations and standards that affect your products, whether they belong to the categories of medical devices, electronics, furniture, cosmetics, or others. Our software is tailored to meet the specific compliance requirements of any regulatory environment. It adeptly manages all worldwide regulations pertaining to crucial areas like health, safety, and environmental concerns. Each regulation is systematically aligned with your product portfolio, considering components, materials, and chemicals, ensuring you remain proactive regarding any shifts in the regulatory landscape that could influence your operations. As global EHS (Environment, Health & Safety) regulations and compliance frameworks continually evolve, leveraging sophisticated software that tracks these changes is essential for minimizing monitoring workloads, thus allowing your team to concentrate on strategic initiatives that safeguard your business. This not only enhances compliance but also fosters innovation and growth by freeing up resources for more critical business strategies.

CoVigilAI is a cutting-edge solution for monitoring medical literature that leverages artificial intelligence and sophisticated data analysis to identify and manage adverse drug reactions proactively, thereby safeguarding patient well-being and adhering to regulatory standards in real time. This platform simplifies the tracking of scientific and medical literature by sourcing information from major global databases like PubMed and Embase, offering customizable search parameters that enhance the pharmacovigilance literature review process. Additionally, it systematically reviews scientific articles and publications from various local journals, ensuring comprehensive global and localized literature oversight. Utilizing advanced algorithms, the system classifies Individual Case Safety Reports (ICSRs) into three categories: valid, potential, and invalid cases, while its automated key entity recognition capability adeptly identifies essential elements such as patients, medications, adverse reactions, and relevant medical events. This holistic approach not only streamlines the monitoring process but also significantly enhances the accuracy and efficiency of drug safety assessments.

Transforming the landscape of global financial regulatory rules through advanced technology aims to simplify the processes of identification and understanding, making financial regulation more accessible. With an emphasis on AI-driven compliance and effective change management, Finreg-E is at the forefront of this evolution. The platform utilizes machine learning and artificial intelligence to automatically identify crucial actions required by regulatory rules, establishing connections to internal controls while offering user-friendly workflows that address compliance gaps. Finreg-E stands out with its innovative application designed for regulatory compliance and change management, employing cutting-edge technology to enhance efficiency in the identification, analysis, and adherence to global financial regulations. By leveraging state-of-the-art tools such as natural language processing, topic modeling, and deep learning, Finreg-E seamlessly aligns regulatory mandates with internal policies and practices. This comprehensive approach not only streamlines compliance efforts but also ensures organizations remain agile in a constantly changing regulatory environment.

At ArborMetrix, our aim is to enhance healthcare through data science, while our enthusiasm lies in providing impactful, user-friendly technology and analytics. Our advanced healthcare analytics solutions are designed to yield precise, clinically-rich insights that enhance clinical outcomes, boost financial effectiveness, add value for stakeholders, and evaluate the real-world success of treatments, procedures, medical devices, and pharmaceuticals. One of the significant benefits of patient registries is their application across various medical fields, with post-market surveillance standing out as a particularly important function. To assist you in establishing a reliable data resource, we follow a systematic approach. First, it’s essential to have an effective and secure method for gathering substantial amounts of real-world data, which is crucial for thorough analysis. By utilizing the appropriate technology, you can aggregate data from diverse sources such as medical records, regulatory bodies, and patient-reported outcomes to support post-market surveillance initiatives. This comprehensive approach not only streamlines the data collection process but also enhances the overall quality of insights derived from the analysis.

Streamline tedious and repetitive tasks so you can concentrate on delivering products that are both safer and more effective, and do so at a quicker pace. IQVIA’s SmartSolve Postmarket Surveillance offers a comprehensive SaaS solution for postmarket surveillance (PMS), equipping you with best practices for the centralized management of all PMS activities. The Fusion event, tailored for SmartSolve and RIM Smart users, provides extensive education on pertinent quality and regulatory subjects, offering actionable insights and practical tools applicable across any Life Sciences organization. Initially launched as a live conference for SmartSolve users, Fusion has transformed over recent years to encompass both virtual and in-person events for the broader SmartSolve and RIM Smart communities. Enhance your compliance response times, accuracy, predictive planning, and overall efficiency through the IQVIA SmartSolve™ Regulatory Connector. This Connected Intelligence framework represents our forward-thinking, integrated strategy aimed at fostering significant operational efficiencies across the board, ultimately benefiting your organization in numerous ways. Embrace these advancements to ensure your organization remains competitive in a rapidly evolving landscape.

With our cutting-edge, adaptable application and committed support team, we stand as the leading solution for meeting operational and compliance needs. Global RADAR excels in client onboarding, customer due diligence, and transaction monitoring. We simplify the process of account openings in a secure digital space, all while adhering to international regulatory standards and utilizing advanced analytics to validate client profiles effectively. The foundation of Global RADAR rests on four robust pillars: compliance, customer due diligence, document management, and watch list screening, along with transaction surveillance. Our approach not only enhances security but also fosters trust and efficiency in financial transactions.

Infobelt assists businesses in navigating the intricate and ever-evolving regulatory environment efficiently. By implementing advanced systems and policies, Infobelt significantly mitigates the chances of non-compliance while enhancing the management and governance of regulated records. Moreover, it lowers data management expenses by optimizing processes and adopting cutting-edge technologies. The solutions provided by Infobelt empower decision-makers with essential tools and insights, ultimately boosting organizational performance and enhancing competitiveness in the market. Their products seamlessly integrate with existing platforms, ensuring straightforward maintenance without any unforeseen upgrade expenses. Furthermore, Infobelt’s platform encourages proactive engagement among teams through organized task workflows and user attestations. Users can also benefit from an extensive compliance library that consolidates in-depth regulations from various regulatory bodies, making it easier to stay informed and compliant. This comprehensive approach not only simplifies compliance management but also fosters a culture of continuous improvement within organizations.

Vixio is a comprehensive platform designed for regulatory intelligence that empowers compliance and legal teams with real-time oversight and management of evolving rules across over 200 jurisdictions and 1,400 regulatory bodies. By integrating expert human insight with AI-enhanced features, the platform offers tools such as horizon scanning, a regulatory library, a global data hub, market evaluations, and a customizable report generator to effectively track legislative and regulatory changes, assess regional requirements, and identify governance risks. In 2025, Vixio introduced Vixio Workspace, an innovative workflow and compliance-management tool that connects regulatory change insights to actionable tasks; this enables compliance teams to develop checklists, delegate responsibilities, collaborate seamlessly, monitor progress through dashboards, manage attestation records, upload supporting documentation, and maintain a comprehensive audit trail, thereby eliminating the need for disorganized spreadsheets and emails. This enhancement further streamlines compliance processes, allowing teams to work more efficiently and with greater accuracy in managing their regulatory obligations.

Break down your regulatory and contractual responsibilities into specific tasks that can be assigned and effectively monitored using interactive dashboards. Explore each business sector to pinpoint areas of vulnerability, then categorize potential risks and develop strategies to mitigate them. Oversee IT system risks by conducting user access reviews and managing contract renewals diligently. Establish your corporate framework and maintain comprehensive records of all legal and corporate communications with regulatory bodies. Monitor your licensing obligations along with statutory and regulatory reporting using a unified system. Keep meticulous records of any incidents, complaints, and breaches that may arise. Utilize this data to identify significant business risks and implement necessary changes. Ensure all existing controls operate effectively by employing compliance assurance checklists for validation. Gain a deeper understanding of your obligations and delineate the scope of work necessary for your organization's compliance framework. By taking these proactive steps, you can foster a culture of accountability and transparency throughout the organization.

Capnovum’s cognitive compliance management system offers a contemporary repository for regulations, obligations, and regulatory updates, enabling regulated entities to efficiently handle compliance and resource allocation across different jurisdictions. Utilizing artificial intelligence (AI), it discerns and aligns synergies among regulations, evaluates the impact of business models, and analyzes the effects of regulatory changes. By removing the need for manual processes and the associated costs of generating and distributing static reports, Capnovum significantly reduces expenses while enhancing the quality and timeliness of information. This innovative approach, which combines automation with AI, ensures that essential insights and data are readily accessible to all critical stakeholders in your organization. In today's fast-paced environment, where distractions and time constraints are prevalent, we prioritize delivering the information you require quickly and clearly, allowing you to focus on what truly matters. With our platform, you can confidently navigate the complexities of compliance and stay ahead of regulatory challenges.

Corlytics stands out as a premier provider of regulatory risk intelligence on a global scale, assisting financial institutions, regulatory bodies, and advisors in their compliance efforts through insightful data analysis. Based in Dublin, Ireland, with additional offices in major cities like London, New York City, Boston, and Sydney, the firm specializes in regulatory monitoring, taxonomy mapping, and consultancy services designed to optimize compliance workflows. By fusing legal knowledge with sophisticated data analytics, Corlytics offers practical intelligence that empowers organizations to adeptly navigate intricate regulatory environments. Their commitment to innovation drives the continuous development of advanced solutions that aid financial entities in risk mitigation and maintaining compliance with regulatory standards. Furthermore, Corlytics’ proactive approach ensures that clients are not just compliant but are also ahead in understanding future regulatory changes.

Enhance quality and ensure GxP compliance through Vault QMS, which integrates established best practices and automated workflows to connect all stakeholders, including pharmaceutical and biotech firms, contract manufacturers, and suppliers, into cohesive quality processes for improved oversight and control. This system facilitates seamless collaboration among various departments, sites, contract manufacturers, suppliers, and testing labs, promoting a culture of continuous quality enhancement. By leveraging automated workflows, organizations can achieve greater operational efficiency while simultaneously improving risk visibility throughout products and processes via a consolidated risk management strategy. The unified suite of quality applications accelerates speed, boosts efficiency, and strengthens GxP compliance across all activities. Additionally, Vault QMS allows for the smooth implementation of essential quality management processes, incorporating built-in best practices for handling deviations, conducting internal and external audits, managing complaints, executing lab investigations, overseeing change control, addressing CAPA, and facilitating quality risk management, ultimately fostering a robust quality culture across the organization. By doing so, businesses can not only meet compliance requirements but also enhance their overall productivity and reputation in the industry.

RegPass™ serves as a compliance co-pilot designed to amplify your team's effectiveness tenfold. It seamlessly integrates every phase of the regulatory change lifecycle, from horizon scanning to assurance: Horizon Scanning → Rules Inventory → Policies & Controls → Regulatory Policy Advisor. With extensive global coverage and smart Business Profiles that tailor alerts to what matters most, you can remain proactive. Our enhanced Rules Inventory streamlines overlapping obligations into clear, canonical forms for better traceability and understanding. At the core of RegPass is AI, which extracts, ranks, and aligns obligations to your existing policies and controls, providing thorough justification for each recommendation. Every recommendation is well-documented, auditable, and primed for your approval. Developed by the specialists at Braithwate, RegPass encapsulates years of regulatory change knowledge into a dynamic knowledge graph. With its open, extensible, and inherently transparent design, RegPass ensures complete traceability, enabling teams to operate more efficiently, minimize risk, and bolster compliance. By leveraging such a powerful tool, organizations can navigate the complexities of regulatory landscapes with confidence and clarity.

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.

RegulatoryOne transforms custom, labor-intensive systems into a comprehensive, singular regulatory management software solution that caters to all your compliance and regulatory requirements, enabling you to swiftly adapt to evolving regulations. The enhancements in efficiency not only accelerate your time to market but also ensure transparency throughout your organization at every product release stage as it progresses to market readiness. As a fully cloud-based regulatory management software, RegulatoryOne integrates and streamlines every element of the regulatory process, granting you clear insights into your products, their sales timelines, and their distribution locations – all accessible from a single platform. This unified approach not only simplifies compliance but also empowers your team to make informed decisions swiftly and effectively.

Technology powered by artificial intelligence allows financial organizations to completely automate their risk and compliance functions. Continuity provides a RegTech solution that streamlines risk, compliance, vendor, and performance management specifically for the financial services sector. By integrating essential risk and compliance processes, it enhances overall performance. Merging regulatory know-how with cloud technology, Continuity alleviates your regulatory challenges and reduces risk at a much lower cost. Numerous financial institutions across the U.S. reap the benefits of our innovative solution. Continuity’s enterprise risk management (ERM) technology, along with its compliance, vendor, and performance management systems, is customized to cater to the unique requirements of banks, credit unions, mortgage providers, and fintech companies, regardless of their size. This comprehensive platform is designed not only for flexibility but also for optimal efficiency in operations. As the financial landscape evolves, Continuity remains committed to providing cutting-edge solutions that support risk management and compliance needs effectively.

The Vault RIM Suite offers a comprehensive platform for managing regulatory information from end to end. By centralizing global regulatory workflows on a cloud-based system, it enhances visibility, data quality, and responsiveness for life sciences organizations. This allows companies to adapt swiftly to shifting regulations while improving efficiency throughout the submission process, from planning to final publication. The platform facilitates collaboration among headquarters, affiliates, and partners, all within a unified RIM system. Furthermore, it guarantees that teams produce regulatory content that is both reliable and maintains high data integrity. Veeva Vault Registrations oversees product registration details on a global scale, covering registration status, variations, and interactions with health authorities. Its adaptable data model is designed to incorporate IDMP data points and will keep pace with changing regulatory data standards. Additionally, Veeva Vault Submissions optimizes the submission planning process by automating various steps in the regulatory workflow, leading to significant time savings and improved outcomes. This unified approach ultimately empowers companies to navigate the complexities of regulatory compliance with greater ease and precision.

Clinevo's electronic Trial Master File (eTMF) is a user-friendly digital solution for the organization and storage of documents, images, and various digital assets related to clinical trials. This eTMF incorporates an integrated DIA reference model and complies with regulatory standards. Additionally, Clinevo offers the MICC Intake, a web-based platform designed for Medical Information Call Centers (MICC) and Pharmacovigilance (PV) professionals to efficiently log, track, and monitor Product Quality Complaints (PQCs), Medical Inquiries (MIs), and Adverse Events (AEs). Furthermore, Clinevo Safety serves as a comprehensive cloud-based system that ensures ease of use and regulatory compliance throughout the entire Pharmacovigilance process, encompassing PV Intake, Case Processing, Regulatory Submissions/AS2 Gateway, Analytics, and Safety Signals, all within a single platform. Lastly, the Clinevo Website Intake tool can seamlessly integrate with Sponsor or CRO websites, offering consumers and reporters an intuitive web interface for easy access and reporting. This innovative suite of tools enhances the efficiency and effectiveness of clinical trial management and safety reporting.

Sorcero is an innovative platform powered by artificial intelligence that aims to convert intricate medical data into practical insights for the life sciences sector. It offers a range of products such as Medical Insights Management, Intelligent Publication Monitoring, Plain Language Summaries, and Intelligent Systematic Literature Review, all of which work together to unify and interpret both structured and unstructured data from diverse sources. By leveraging AI to dissect medical themes, notes, and research findings, Sorcero provides clear and high-quality responses to challenging medical inquiries, thereby assisting teams in Medical Affairs, Pharmacovigilance, and Regulatory Affairs in making better-informed choices. The platform enhances rapid literature monitoring, facilitates content creation, and supports evidence-based decision-making, significantly improving patient outcomes while also streamlining operational processes. Additionally, Sorcero's capabilities can lead to a more effective collaboration among various stakeholders within the healthcare ecosystem.

In-app IMAP email and collaboration tools enhance your interactions with clients, vendors, and colleagues, making it easier to coordinate with all parties involved in compliance. Rumzerbot takes charge of keeping you updated on regulatory changes, allowing you to concentrate on running your business effectively. Every subscription plan provides updates regarding declarable substances and pertinent regulations. Rumzer empowers you to have better oversight of your compliance procedures and communication within your supply chain. We operate as your dedicated compliance software solution, eliminating the need for a middleman. You can conveniently manage all compliance-related emails in one centralized location. Setting up the system is as straightforward as configuring email on your mobile device—simply input your email credentials and you're ready to go. Users can be added or removed easily, and you can also integrate third-party service providers into your organization to assist with your compliance efforts. This flexibility ensures that your compliance management remains efficient and tailored to your specific needs.

DataGuidance offers a comprehensive global regulatory research platform that assists organizations in establishing and upholding their compliance frameworks. With the most current and extensive resources available for privacy, security, and third-party risk analysis, teams can effectively manage their compliance obligations. The platform is enhanced by a dedicated team of 40 legal analysts alongside a vast network of over 800 legal professionals, ensuring that privacy teams receive the critical research required to navigate and understand the complexities of global privacy legislation. Stay ahead of the curve with timely updates and daily alerts on regulatory news, all curated from our expert network. By subscribing to DataGuidance Daily Alerts, you can ensure you are continuously informed about the latest developments in regulations that affect your industry. Regulatory insights are disseminated in real-time as new information surfaces, while infographics and reports succinctly summarize key points for frequently referenced privacy laws and regulations, making compliance management more efficient and informed. Furthermore, our tools empower organizations to proactively address compliance challenges and adapt to evolving legal landscapes.

RQM+ stands as a prominent global provider of medical technology services, dedicated to accelerating compliance and ensuring market success for its clients. With a wealth of expertise and deep industry insight, we offer tailored solutions that streamline the entire product lifecycle for medical technology firms, guiding them from initial concept through to commercialization and beyond. Our comprehensive suite of services facilitates seamless end-to-end solutions that encompass every stage of the medical device development process. The quality assurance engineers at RQM+ meticulously evaluate material lists, establish supplier networks, and assist in navigating the design change process. Likewise, our design quality engineers are instrumental in overseeing crucial aspects such as packaging, sterility, biocompatibility, and required device testing. Our regulatory affairs consultants play a vital role by providing expert guidance and assistance with submissions to the FDA, notified bodies, and other regulatory agencies. Additionally, we leverage our significant experience with current reimbursement requirements and value-based compensation frameworks to enhance our clients' market positioning. Ultimately, RQM+ is committed to empowering medical technology companies to achieve their goals efficiently and effectively.

Statt is transforming the landscape for public policy and regulatory experts by delivering a groundbreaking real-time data stream, coupled with AI-enhanced automated insights and analyses. This innovative platform provides exceptional clarity regarding policy and regulatory risks and public sentiments, empowering users to efficiently search, monitor, and evaluate every significant policy issue, industry, and key influencer. With its unique software-as-a-service model, Statt’s web-based system integrates effortlessly with current infrastructures, granting users a comprehensive perspective on all pertinent case data accessible from any device. The platform's inclusive approach to financial wellness is crafted for easy adoption and tailored to meet specific business requirements, featuring user-friendly financial evaluations, straightforward implementation, and customization options that align with organizational objectives. Furthermore, Statt's enterprise solutions are shaped by a wealth of experience in engaging with communities and stakeholders, ensuring that clients receive not only data but also strategic insights to navigate the complex regulatory landscape effectively.

AccelSafety is an all-encompassing pharmacovigilance solution crafted by Techsol Life Sciences, centered around the Oracle Argus Safety application, designed to streamline the unified gathering, medical evaluation, and regulatory reporting of safety surveillance data for both clinical and post-marketing purposes. This fully managed cloud-based platform empowers emerging biopharma companies, device manufacturers, and service providers to effectively handle safety data while ensuring their business decisions align with global compliance standards. Among its primary advantages are expedited Argus Safety implementation, migration, and validation that reduce effort by 70%; secure transfer of existing safety data to the AccelSafety Cloud; and enhanced case processing efficiency through tailored configurations and built-in automation. Additionally, users benefit from extensive operational insights provided by advanced reporting tools, line listings, and analytics packages, as well as round-the-clock support from the Argus Safety Service Desk for user inquiries, incident resolutions, and change management needs. Overall, AccelSafety stands out as a pivotal tool for organizations looking to optimize their pharmacovigilance processes and uphold regulatory obligations effectively.

Proind compliance controller offers a comprehensive web-based solution that enables organizations to effectively grasp, oversee, monitor, and govern their compliance activities on an enterprise scale. By providing an integrated perspective of both statutory and internal compliance requirements, this solution significantly lowers the costs associated with compliance management. PCC serves as a centralized resource for regulatory information, complete with built-in controls that help users recognize their obligations and the relevant risks to their organization. Additionally, it offers management a cohesive, automated overview spanning various jurisdictions, sectors, and regulatory bodies, ensuring adherence to compliance standards. The robust features of PCC are designed to manage all compliance types throughout their entire lifecycle within the organization. Implementing this system can lead to a reduction in fines, penalties, and risks to reputation stemming from non-compliance, ultimately fostering a culture of accountability and diligence within the enterprise.

Introducing the Secure Audit, Risk, Compliance & Quality Software, which provides both On-Premise and Cloud-based deployment alternatives. Auditrunner ensures the highest level of security with granular encryption and role-based access control for all audit files and documents that are stored. Your data transfers are safeguarded, enhancing overall security. We have streamlined over 3000 business processes for organizations globally, with our GRC platform modules forming just a portion of these solutions. Whether you choose Cloud-based or On-Premise, you can deploy and begin utilizing the software quickly. Our hassle-free integration process guarantees that you will experience the platform’s advantages within weeks of initiation. Built on a low-code framework, our system is entirely customizable, ensuring compliance with any relevant standard or regulation. Adapt swiftly in today’s dynamic regulatory landscape and effortlessly comply with various legislations without needing external support. The user-friendliness of our platform stands unrivaled, making it an exceptional choice for businesses of all sizes.

Mitigate losses and minimize risk occurrences through proactive risk visibility. Foster a contemporary and cohesive risk management strategy that leverages real-time, consolidated risk intelligence to assess their influence on business goals and investments. Safeguard your brand’s reputation, reduce compliance costs, and cultivate trust among regulators and board members. Keep abreast of changing regulatory demands by actively managing compliance risks, policies, case evaluations, and control assessments. Promote risk-conscious decision-making and enhance business performance by aligning audits with strategic priorities, organizational goals, and associated risks. Deliver prompt insights on potential risks while bolstering collaboration among different departments. Decrease vulnerability to third-party risks and enhance sourcing choices. Avert incidents related to third-party risks through continuous monitoring of compliance and performance. Streamline and simplify the entire lifecycle of third-party risk management while ensuring that all stakeholders are informed and engaged throughout the process.

Sentria is a cutting-edge platform that utilizes artificial intelligence to manage adverse event cases and conduct post-marketing surveillance. This software solution is user-friendly, highly customizable, and automated, ensuring it meets industry regulations to improve the efficiency, speed, and accuracy of adverse event handling. It supports pharmacovigilance compliance with international ICH guidelines while adhering to local regulatory requirements for the assessment of adverse events. By providing an easy-to-use interface enhanced with pharmacovigilance automation, Sentria minimizes reporting errors through smart alerts and simplifies report processing by employing international coding standards such as MedDRA and ATC/WHO. The platform enhances analytical capabilities through the use of semantic artificial intelligence tailored for pharmacovigilance needs. Notably, Sentria offers features like secure access controlled by user credentials, comprehensive auditable logs to ensure compliance, and a secure encrypted cloud environment for data protection. These functionalities collectively empower organizations to manage adverse events more effectively, contributing to better patient safety outcomes.

Compliance Star is an innovative compliance software solution designed for on-demand use, providing essential tools for effective risk management and monitoring. It enables efficient remote oversight of FCA Authorised Firms along with their associated Units and Agents, thanks to its real-time data gathering and reporting capabilities. This technology-driven compliance platform streamlines management, workflow, and oversight of firms regulated by the Financial Conduct Authority (FCA). A key feature of Compliance Star is its robust, calendar-based task management system, which supports both automatic and manual task assignments, sends notifications for necessary actions, integrates deadlines into a calendar, issues reminders, and tracks task completion status. By significantly alleviating the compliance workload, this platform is currently leveraged by top regulatory networks. Furthermore, it allows for comprehensive tracking of internal regulatory procedures and delivers a centralized access point for up-to-date data, along with the functionality to generate reports required by the FCA. Consequently, Compliance Star enhances operational efficiency and ensures regulatory adherence for its users.

Streamline your approach to data governance, risk management, and regulatory compliance using IBM OpenPages, an advanced, scalable, and AI-enhanced GRC platform. IBM® OpenPages® provides a comprehensive governance, risk, and compliance (GRC) solution that operates seamlessly on any cloud through IBM Cloud Pak® for Data. This platform facilitates the centralization of disparate risk management processes within a unified framework, enabling organizations to efficiently identify, manage, monitor, and report on risk and compliance in today’s dynamic business environment. Equip your organization for future challenges with a customizable, integrated enterprise risk management solution that can accommodate tens of thousands of users. Additionally, foster widespread GRC adoption across all business lines with an intuitive, task-oriented user interface that streamlines task completion and enhances productivity. By leveraging these capabilities, organizations can better navigate the complexities of risk and compliance while driving organizational resilience.

We are excited to introduce Compfie, our comprehensive global e-Compliance Platform designed to help you reduce or entirely eliminate the risks associated with non-compliance while providing the flexibility to monitor all your compliance obligations and their progress from anywhere. Now you can digitize your compliance documents and meet all your regulatory requirements effortlessly, all through a single user-friendly interface that ensures you remain fully integrated in compliance matters. Leverage our cutting-edge digital technology to boost operational efficiency, adhere to regulations, and foster growth. In today's rapidly changing business landscape, maintaining robust control over your operations with a reliable system is crucial. Compfie represents a forward-thinking SaaS compliance framework that allows businesses to oversee, manage, and fulfill their regulatory responsibilities, assess performance, and streamline internal processes, thereby reducing potential future risks. With Compfie, you can gain a comprehensive overview of your organization's compliance status at any time, ensuring you are always informed and prepared. Staying compliant has never been easier or more efficient.

Simplifying regulatory monitoring is our goal. Access, search, and arrange global regulatory information seamlessly in one centralized location. Stay on top of regulatory developments that impact your business by monitoring and prioritizing relevant changes. You’ll find Rule Updates, Filings, Proposals, and Amendments included, ensuring you’re always informed about new or revised regulations. Documents are categorized by widely recognized themes, like cybersecurity or anti-money laundering, as well as your personalized themes. This flexibility allows you to work in a way that enhances your understanding of emerging regulatory patterns. You can flag documents and assign them to colleagues for further evaluation. Additionally, you can create and oversee your own obligations to keep track of tasks and ensure they are completed. Every regulatory document, including rule updates, guidance notes, and speeches, is gathered in one accessible location. The categorization of documents based on essential regulatory themes aligns with the workflow of Risk and Compliance Officers. By utilizing this tool, you can save over 20 hours per regulation while keeping up with rule changes. Ascent pulls together the information that matters most to you, streamlining your regulatory monitoring efforts. This comprehensive approach not only improves efficiency but also enhances your ability to respond proactively to regulatory changes.

RegAlytics leverages innovative technology to collect and organize regulatory data, which is then enhanced by our team of regulatory specialists. Our platform is featured in the FINRA verified compliance vendor directory, serving a diverse clientele that includes major entities such as the New York Stock Exchange/Intercontinental Exchange, as well as smaller financial consulting and FinTech companies. We have frequently observed organizations caught off guard by unexpected fines or regulatory changes, leading them to incur substantial costs in their attempts to rectify these issues, only to face new penalties due to evolving regulations that they were unaware of. This insight drove us to create RegAlytics, providing risk and compliance teams with access to the most thorough and up-to-date stream of regulatory information available. Unlike other solutions that only track about 70-100 regulators and often come with high costs and usability challenges, our platform minimizes redundancy and streamlines the search for relevant updates. As a result, organizations can stay ahead of regulatory changes and mitigate risks more effectively.

CUBE RegPlatform stands as a premier SaaS solution, delivering unparalleled and extensive regulatory intelligence tailored for large global financial institutions. This innovative platform seamlessly integrates top-tier technology with expertly validated insights to ensure a continuously updated service that effectively navigates the intricacies of compliance across multiple jurisdictions. With a collection of customizable modules, RegPlatform allows users to adapt the product to meet their specific business and compliance requirements. For expansive financial organizations aiming to enhance their regulatory compliance efforts internationally, RegPlatform emerges as an essential ally for compliance teams. Central to our approach are the Three R’s: providing real-time, pertinent regulatory insights that help reduce compliance risks. We achieve this by employing cutting-edge artificial intelligence methodologies, including both machine learning and natural language processing, to optimize the delivery of regulatory information. Consequently, RegPlatform not only simplifies compliance but also empowers organizations to stay ahead in a constantly evolving regulatory landscape.

BrightInsight significantly shortens the time it takes for clients to bring their digital health solutions to market, which encompasses apps, algorithms, medical devices, connected combination products, diagnostics, and Software as a Medical Device (SaMD) across various therapeutic domains. By utilizing a pre-built and validated digital health platform that adheres to a comprehensive Quality Management System, BrightInsight eliminates the need for time-consuming and complex custom implementations while ensuring compliance with global security, privacy, and regulatory standards. For example, we assisted Roche in launching a Software as a Medical Device (SaMD) dosing calculator for hemophilia A in just six months in Europe, and we expedited a remote patient platform for a Top 10 Biopharma company from the initial project kickoff to market readiness in under a year. Our expertise lies in the development and maintenance of regulated digital health products for both the biopharma and medtech sectors, having achieved multiple successful commercial launches within the past year alone. This proficiency enables us to respond swiftly to industry demands while maintaining the highest standards of quality and compliance.

In India, there exists automated software designed for managing regulatory and statutory compliance, serving various industries and operational units by effectively monitoring compliance risks. This system features a centralized repository that helps organizations identify and adhere to relevant laws. It continuously tracks legislative changes and ensures the compliance repository is updated promptly. Task owners receive predetermined email notifications, which are escalated if certain thresholds are breached. This compliance management tool in India streamlines the compliance process through established workflows and adaptable escalation procedures. Furthermore, it allows users to evaluate both the current compliance status and the potential risks associated with outstanding requirements. The software also provides real-time status updates, offering detailed analysis tailored to specific user needs, thereby enhancing overall compliance efficiency. Ultimately, it empowers organizations to maintain a proactive stance in managing compliance obligations.

Our SmartInsights™ Global Market Access Platform is an online subscription service designed to provide you with swift and straightforward access to the most current, accurate, and comprehensive regulatory requirements necessary for global market entry. This platform features a user-friendly interface specifically crafted to facilitate your journey towards achieving global compliance. With immediate access to essential regulatory data, you can effectively manage the complexities of multistage product development cycles and make informed strategic business decisions, such as launching into new geographic markets or introducing additional product lines. You will benefit from real-time updates on the constantly evolving regulatory environment, ensuring you have easy access to any new or revised regulations pertinent to your product category. The information within the database is continuously refreshed to guarantee that you receive timely and relevant requirements, and access can be tailored specifically to the countries and product categories you require, ensuring that your regulatory needs are met efficiently. Overall, this platform serves as a vital resource for navigating the complexities of global market access.

RegAdvisor Pro keeps your organization informed about relevant federal regulatory changes, enhancing your compliance management efforts. Our team of regulatory experts distills complex regulations into concise summaries and offers actionable implementation steps, significantly minimizing the time required to comprehend these updates. With our user-friendly task delegation features, you can easily create, assign, and monitor various implementation tasks, whether it involves updating your policies, upgrading systems, providing training, or developing custom tasks specific to your institution's needs. Trust in Continuity to confidently execute your compliance strategy, as RegAdvisor Pro equips you with comprehensive analysis and essential tools for implementing federal regulatory changes. Each time a federal regulation is modified, our experts conduct a thorough analysis to keep you informed about its effective date, necessary completion timelines, and specific steps required for compliance. This proactive approach allows your organization to remain ahead in managing regulatory demands efficiently.

A centralized platform for integrating compliance within business operations across any team, tool, or process is essential for modern enterprises. Specifically designed for financial institutions, it empowers them to develop, tailor, and oversee regulatory controls across highly distributed teams while effectively steering the organization’s risk management strategy. Users can swiftly access intricate details regarding the decision trees and intelligent policies that form the foundation of their compliance frameworks. The Apiax View module allows for interaction with and examination of verified regulatory content, whether accessed through our platform or incorporated into internal systems, ensuring seamless integration. Furthermore, organizations can adapt regulatory insights to align with their specific language, organizational structure, and risk tolerance. With our user-friendly digitalization environment, experts can transform their knowledge into digital compliance rules, making this critical information readily available to all stakeholders. Additionally, by unlocking Rule View, users gain insight into the comprehensive characteristics of the regulatory components that underpin over 6,500 rulesets, enhancing their understanding of compliance requirements. This robust capability not only streamlines compliance processes but also promotes a culture of transparency and accountability within the organization.

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VERMEG’s award-winning modular regulatory reporting platform offers agility to meet your business and technical goals, providing solutions from last-mile template-based reporting to enterprise-wide automation with risk calculations, available on-premise or as a SaaS model.