Alternatives to Regislate

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.

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.

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

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

High-cost contributors are essential for regulatory functions. They can be found in a wide range of regulatory content. This problem can be solved by a cloud-based solution like Infosys' regulated document management platform. Externalization, collaborative authoring, and editing. Simplify governance and processes; implement a consumption-based model. Support audit trails. Implement a proven solution that guarantees 99.95% uptime in production. Our solution allowed business users to search documents in a vast repository in just 3/4 seconds. Users also had unlimited storage on-demand. To reduce operational and maintenance costs, the DMS uses Google's application programming interfaces (APIs). The company's overheads are restricted to API usage and storage space.

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.

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.

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.

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.

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.

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.

RQM+, a global service provider for medical technology, is focused on accelerating market success and compliance. We deliver specialized solutions to medical technology companies and accelerate the journey along the entire product lifecycle, from concept through commercialization and post-market. Our portfolio of services allows us to deliver end-to-end products and solutions throughout the entire medical device lifecycle. RQM+ quality assurance engineers review materials lists, establish suppliers, and support design change processes. RQM+’s design quality engineers support any packaging, sterility or biocompatibility testing that may be required. RQM+ regulatory affairs consultants offer guidance and assistance with submissions to FDA, notified authorities, or other government agencies. Our extensive experience with the most recent reimbursement requirements and value based compensation models is what we use.

Marcaria is the global leader in domain registration and trademark registration, with operations in more than 180 countries and territories. As an ICANN accredited domain registrar they offer registration for more than 1,200 extensions including country-specific domains and generic top-level (gTLD) domains. They offer domain registration, management and hosting services, as well as free email accounts, email forwarding and URL forwarding. Marcaria offers comprehensive trademark registration and protection, guiding clients through the whole process, from feasibility analyses and application submissions, to obtaining registration certifications. Marcaria also offers trademark monitoring services to detect potential infringements. Clients can manage their domain portfolios with ease and monitor trademark statuses using an intuitive online interface.

Protect your business, meet country-specific requirements regarding drug serialization and other rapidly-changing regulations, while processing large volumes of data with intelligence. The SAP Advanced Track and Trace application for Pharmaceuticals allows you to comply with international and regional legislation. It provides a corporate serialization repository, serial numbers management, and reporting capabilities. Reduce compliance costs for current and future serialization requirements, including country-specific reporting. Increase efficiency in your supply chain by gaining greater visibility into material movements down to the sales-unit item level. Manage large quantities of serialization data and adapt to changes in legislation. Track and trace serial numbers of retail products in a corporate repository. Report serial numbers in accordance with country-specific regulations.

SmartURL is designed to simplify online marketing. Our goal is to make URLs shorter, but also to create a platform that allows for smarter marketing. smartURL redirects users to specific destinations depending on their country or device. After entering a default URL, users can choose to redirect their traffic to specific URLs for their country or device. SmartURL is the most common type and we recommend it for most campaigns. Flex smartURLs can also be configured with country-specific redirects to give users more control. Flex smartURL can be configured to handle different circumstances, such as sending Android traffic to Amazon US and Google Play Canada. Pivot smartURL creates landing pages that allow users to choose their preferred retailer. This landing page can be customized by adding links to any streaming or retail provider.

SohamLife is a web-based application that supports the entire life cycle of insurance operations. It allows you to register proposals and then settle claims by maturity or death claim. It is easy to use and provides Insurers with the flexibility and scalability they need, while also allowing for quick implementation and deployment. The solution provides an easy mechanism to view the status of the Proposal/Policy/Claim details either by an Agent or by the Life Assured himself. The solution allows seamless integration between Accounting, Claims, Reinsurance, Underwriting and Accounting departments, thereby avoiding data redundancy. The solution meets both country-specific reporting and operational processing requirements. SohamLife is multi-currency and multilingual. It is a fully integrated, component-based solution that supports core business processes and data entry into one component.

alloFactor provides a single solution that offers a variety of administrative products and services for small and medium-sized clinics. We are focused on creating value for client practices by reducing costs, and promoting productivity. To provide a unique solution for the healthcare market, we combine a world-class technology platform with a highly skilled workforce. AlloFactor is a fully integrated practice management software that covers all administrative functions, including scheduling, billing, medical records, reporting, and registration. Electronic claim submission speeds up payment and electronic remittance advice saves time. Automated eligibility verification reduces billing errors, and minimizes patient receivables. Our service division is a logical extension of your practice, taking on specific responsibilities and still allowing for flexibility. Our medical billing team works seamlessly alongside your frontdesk to maximize your revenue.

Greenlight Guru is the only product development and quality management platform designed specifically for medical device companies. The Medical Device Success Platform helps companies get safer products to market faster, simplifies FDA and ISO regulatory compliance, and provides a single source of truth by connecting the management of all quality processes like CAPAs, risk, audits, document control, training, design control, and more. Device makers across the globe are replacing their outdated paper-based and general-purpose legacy quality systems with Greenlight Guru to push beyond baseline compliance and achieve True Quality.

Easy Medical Billing Professional was established in 1994 as a cutting-edge software program for medical billing. Our billing software is specifically designed for Medical Billing and includes features that are specific to the needs or Surgical Assistants, Chiropractic, Physical Therapy, and Billing Services. We are proud to keep up with industry changes and offer affordable medical billing packages. We offer ICD-10 coding and have met the 5010 electronic submission requirements. Let's show you our amazing report engine. It allows you to customize search categories as well as create custom forms. We offer custom reports with exports for your Excel Templates. (charges do apply). Our mission is to offer the best medical billing software on the market, while making it easy to use and affordable.

Real-time submission, verification and authentication of claims. With effective reporting, you can see exactly where your stand regarding payments from patients and medical assistances. You won't have to waste time or resources chasing payments or doing unnecessary member administration. Our fully hosted solution is 100% internet-based and can handle all your practice management needs. You don't have to worry about Medprax updates, tariff changes or legislative requirements. We take care of it all. Access your database and other information securely and confidentially from anywhere in the world. Synchramed provides South African doctors with a variety of practice management solutions. This has been going on for over a decade. These solutions include outsourced credit control, debt collection, and medical practice management software.

Susan.one is an accounting software that simplifies complex accounting operations. It's fast and simple. You can manage employees, run country-specific payslips, create sick leave reports, and calculate overtime and salary deduction worksheets. Susan can help you increase your productivity, create sales and purchase invoices, and insert inventory and other business assets. The application can run offline and generate all mandatory tax reports automatically. There is no need to manually enter tax rates in the system. You can add as many users you want to the software license without incurring additional fees.

Our device-specific matching ensures that you get the right solution at exactly the right time. This means you don't have to waste time looking for the right driver for your devices. You can enjoy the full potential of your devices quickly. Our service is available wherever you are. You can use our service at home, at work, in your favorite coffee shop, or wherever you go on your travels. Our continuous monitoring of your device ensures that we keep our promise to protect you. You can be sure that your productivity will improve. Driver Support uses automated support to resolve the most common problems that computer users experience. Only Driver Support matches the driver based upon the make and model of the consumer's computer. All other services match drivers based on the date/version recommended by the manufacturer. For those cases when automation is not enough, we also offer human technical assistance!

GridMarkets will ensure that your project is delivered on schedule. GridMarkets' render service offers powerful CPUs and GPUs, flexible pricing plans, and scalability options to suit every budget and deadline. Envoy, Envoy's secure render manager, allows you to easily submit your 3D models from your 3D software directly to our render farm. GridMarkets provides the 3d software licenses required to run your simulation or render at scale. No local licenses required for submission. GridMarkets credit is required to pay for our rendering or simulation services. To render or simulate, you need a positive GridMarkets balance. We also offer managed services, where a GridMarkets member joins your team to help prepare and optimize your scene to submit within your budget and timeframe. GridMarkets offers a credit overdraft that kicks in when your credit balance is zero.

Cockpit Enterprise, our software application for medium-sized to large medical device product developers, integrates requirements management and test management in a single environment. Cockpit Enterprise can be customized to meet the needs of any company. It offers a rich development environment that allows organizations to implement Standard Operating Procedures (SOPs), and Work Instructions(WIs) in a controlled, auditable environment. Cockpit Enterprise is a tool that helps medical device manufacturers of Class II or III devices to author, review, and approve documents necessary for regulatory submissions. Cockpit Enterprise is best for mature companies that have established standard operating procedures, and can devote the necessary resources to configuring the system and deploying it.

In today's competitive market, efficiency and ease of use are essential. Our web-enabled Rate, Quote, and Issue solutions can be adapted to meet the needs of large volume environments. Our Workflow Framework is flexible enough to meet your internal and external needs. MGAs, MGUs and Carriers can all offer their products in a controlled, secure manner. TopSail makes it easy to manage your underwriting portal. It covers everything from the basics of rate and quote to full forms management/policy issuing and endorsement processing. TopSail provides rich email messaging, alerts, automated renewal processing, as well as the ability to feed any back-end systems. After the submission and underwriting cycles are complete, you will have a rich collection of data that can be used to harvest Management Information essential for staying competitive.

InSync Healthcare Solutions EHR/PM allows healthcare professionals to provide quality healthcare that meets regulatory requirements. This ONC-ATCB and CCHIT-certified ambulatory EHR/PM product is suitable for both solo and large multi-specialty practices. InSync allows you to choose between an upfront license and a subscription that is web-based. InSync integrates both EHR and PM, resulting in a medical office system that eliminates duplicate records and allows for workflow management throughout the practice. InSync's system can be adapted to meet any practice's requirements with features such as scheduling calendars and e-prescribing. The package also includes a user interface that allows users to create custom fields and layouts.

ClearVAT allows for e-commerce that is border-free. ClearVAT allows for rapid expansion into European markets, portfolio expansion and scaling, efficiency gains, outsourced VAT risks, and the exclusion of declaration obligations. ClearVAT makes it possible to sell goods to B2C customers in all EU-27 countries plus the UK without VAT. ClearVAT allows you to display all prices in your online shop. This includes the current country-specific TVA. This means that a French retailer will pay 19% in Germany, 23% or 22% in Poland for the prices. ClearVAT calculates the final cost of the goods, even if the delivery address is changed during check-out. ClearVAT takes the purchase price from the customer. The retailer ships the products directly to its customers. ClearVAT deducts VAT from the destination countries' authorities and pays the principal amount to merchant. A transaction fee of 1.25% - 4.75% is retained.

All-in-one award management system, including grants, scholarships, grants, mentorship programs, fellowships, and scholarship applications. We assist universities, associations, and other organizations in streamlining their form submission processes. We make it simple for applicants and reviewers. We make it easy to manage your program from beginning to end. It is easy to submit required information and support documents, as well as request e-references. It is easy for committee members and reviewers to access submissions and make comments. You can effectively manage your program, run complex and simple reports, and communicate with the users. Digital marketing, which includes social media and online ads, can help you expand your program's reach and presence. You can configure the system to suit any online submission program, from simple to complex.

Brokers are seeing a huge growth in the SME market. However, your business must have the technology necessary to differentiate your products and services from the rest. Applied Policy Works allows you to generate submissions quicker by allowing you collect important risk information and then automatically send it out to as many underwriters you wish. This eliminates the need to manage individual submissions and reduces the risk of E&O. Automate your commercial lines process, from marketing to renewal, with standardized workflows. This will empower your CSRs and marketers to serve customers faster and increase your bottom line.

DELTA ID is the main solution. It focuses on the secure, efficient, and automatic registration and reading of identity documents. It is designed to simplify and optimize user registration and check-in, from any device. It does this quickly, securely, and conveniently. It can be used to identify documents and identity cards from up 200 countries. It can be integrated into your management system using our complete SDK API. Or, it can be used with our software (in the cloud or on the client's servers), which allows for automatic data dump in real-time. Integrated identity document reader that allows for fast uploading of data to your system. Easy-to-disinfect, quick-to-use readers. You can identify almost 200 types (Passport, DNI, Driver's License) and share one scanner with multiple jobs. To improve data collection, it has been integrated and approved by a large variety of PMS and HIS available on the market.

Tracking and managing submissions. Automated error and oversight detection. Dynamic target rate engine. You can conduct 1 tender to cover all volumes. You can manage your spot volume in the tool throughout the year. The tool allows you to issue amendments or general rate increases (GRI). Waterfall approach to awards. Based on carrier acceptance, dynamic allocation. Scenario optimization as part of the award process. Ability to modify the bid template (add/remove column, adjust column order and hide columns from carrier. Ability for the carrier to automate fees types and rates. Acuitive listens first and then solves second for every client. Acuitive will then create a project plan that includes key milestones and deliverables. It is a seamless process to manage your ocean, air, and drayage rates & contracts.