Alternatives to GlobalSubmit

BeeCTD offers a comprehensive eCTD management system tailored for pharmaceutical companies and regulatory bodies. With its modular design and clear licensing approach, users can select the specific modules they wish to utilize, such as Reader, Compiler, and Validator. The advanced Reader provides insights into the complete lifecycle of the dossier, accommodating both eCTD and NeeS sequences, and facilitates the transition between the two formats, including baseline submissions. Additionally, the real-time sequence validator ensures compliance with the eCTD/NeeS technical specifications, incorporating best practices, while always reflecting the latest validation criteria, with older versions accessible for reference. Users can seamlessly compile their documents into an eCTD-compliant format, leveraging our eCTD compiler tool, which they can use independently or as an on-demand service where we handle the compilation for them. Moreover, the flexibility and scalability of BeeCTD make it an ideal choice for organizations seeking to enhance their regulatory submission processes.

If you're looking for the best contest software with a free trial, look no further! With its automated submission handling, streamlined organisation and robust security, our contest management platform provides the perfect solution for busy administrators, judges and candidates. Automate your projects with one platform, to make, take and judge submissions. Built-in features allow candidates to upload images, text, videos, documents, 3D models and more. Automated emails are sent to candidates and judges at every step of the process so that everyone knows exactly what they need to do next. With our submission tracking software, you can see how many of your submissions have been accepted or rejected in real time. Zealous is accessible from all devices, anywhere in the world. Users can try a free trial to gather their first submissions for free! Features: Contest Management | Submission Tracking | Bulk Processing | Blind Judging | Customisable Forms | Accept Payments | Automated Emails | Schedules & Multiple Round Publishing | Secure Data | Downloadable PDFs | Judging Management | Advanced Custom Category Scoring | Entry Collection | Anonymous Judging

RegDocs Connect equips both operational and regulatory teams with essential tools for creating thorough and compliant documents and records that are ready for submission. Designed with the end user's experience in mind, this solution prioritizes collaboration, automation, and quality as its core principles. Automated workflows streamline the management of the records lifecycle from the initial draft to the final version, allowing your team to maintain full oversight of regulatory documents at all times. By aligning document types with the EDM reference model and eCTD, this system enhances the organization and retrieval of documents necessary for regulatory submissions. Additionally, proprietary features such as PDF/A Publishing, document classification, and distinctive document identifiers create a robust regulatory document management framework that consolidates information from various parts of your organization into a single, navigable solution. As electronic submissions to regulatory bodies become more prevalent and the intricacies of drug development increase, the capacity to generate high-quality, submission-ready content is more critical than ever, ensuring compliance and efficiency in the regulatory process. Moreover, this comprehensive approach not only simplifies the documentation process but also fosters greater collaboration among teams, ultimately leading to improved outcomes in regulatory affairs.

Enhance the speed at which products reach the market by organizing, implementing, and monitoring all regulatory processes within a cohesive RIM application that offers easy access to regulatory documentation and comprehensive support for major eCTD submission standards. The integrated automation simplifies workflows, minimizing administrative tasks and increasing trust in the quality of product registration data. By utilizing this unified approach, organizations can ensure a more efficient regulatory process while maintaining high standards of compliance and accuracy.

A scalable, real-time, collaborative, out-of-the box solution for CROs, Life Science Consultants and Industry Stakeholders. Built in an Audit Ready Compliant Cloud environment (ARCC). All 21 CFR Part 11 requirements are met. GxP audit ready. Pre-configured Departmental. Communications with internal and external stakeholder. Secure data integration between remote teams. Collaboration in review and approval. Turn access on/off according to need (EX: auditors), reducing audit prep time from days to hours. Preconfigured to eTMF Reference models & EDM. Intelligent content management tools can improve workflows. Improve document management with real-time collaboration, automatic indexing and co-authoring. Pre-configured, validated system that manages documents and data electronically in accordance with eCTD mandates.

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

Efficient submission management is essential, and Reviewr offers a cloud-based platform that simplifies the collection, oversight, and evaluation of online submissions. By utilizing Reviewr's submission management software, you can minimize the time spent on administration and maximize your impact in other areas. This all-in-one tool is designed for specific tasks, ensuring that you have the right resources for every job. Reviewr goes beyond typical submission software by providing a comprehensive digital experience that is backed by tried-and-true methodologies. Not only does it save time for administrators, but it also encourages an atmosphere conducive to growth, constructive feedback, and community engagement. Welcome to the innovative Reviewr experience, a contemporary answer to the complexities of submission management and review processes. From inception to completion, Reviewr offers a well-established submission management framework, ensuring you have everything you need. With insights gleaned from years of expertise and feedback from a multitude of clients, Reviewr's dedicated approaches effectively elevate awards, grants, scholarships, and more through specialized tools that are perfectly tailored to each task. In a world where efficiency is key, Reviewr empowers organizations to achieve more with less effort.

ConfSubmitHub simplifies the complex process of academic conference planning with a powerful, integrated platform. Organizers can manage abstract and full paper submissions, reviewer assignments, paper themes, and program agendas from one intuitive dashboard. Beyond research content, the platform handles delegate registrations, exhibition management, sponsorship tracking, and travel logistics. Its built-in communication tools make it easy to issue calls for submissions, send updates, and keep participants informed throughout the event lifecycle. With 20+ years of expertise, ConfSubmitHub is optimized to maximize efficiency and ensure smooth collaboration among committees, reviewers, and attendees. Organizers benefit from higher engagement, streamlined workflows, and measurable ROI improvements. Testimonials from institutions such as IIT Bombay highlight its flexibility, ease of use, and responsive support. For academic societies and universities, ConfSubmitHub delivers a reliable, professional-grade solution that reduces stress and improves outcomes for every event.

Sarjen's global dossier publishing software serves as a platform aimed at streamlining and automating the oversight and submission of regulatory dossiers. By enhancing the regulatory submission process through the automation of workflows tailored to specific regions and products, it significantly boosts consistency, efficiency, and precision. This automation not only expedites the creation, validation, and submission of dossiers but also minimizes the likelihood of manual errors and compliance-related issues. Designed to enhance operational efficiency, the solution ensures data consistency and that documentation remains ready for audits. Consequently, it saves valuable time while enabling quicker regulatory approvals, ultimately assisting in meeting diverse global compliance standards. Additionally, the platform's user-friendly interface empowers teams to manage submissions more effectively, leading to improved collaboration and faster turnaround times.

Dapple stands out as a contemporary submission management solution tailored for teams and organizations seeking a versatile and cooperative approach to gathering, evaluating, and overseeing submissions. Ideal for various purposes such as open calls, grant applications, contests, pitches, or program admissions, Dapple simplifies the creation of customized forms, the management of workflows, and team collaboration throughout different phases of the process. Users of Dapple can develop entirely personalized submission types or projects, determine who has access and can provide reviews, and guide submissions through a well-structured system featuring configurable stages and statuses. The platform accommodates setups involving multiple teams and organizations, offering detailed permission controls and facilitating cross-functional teamwork. What truly differentiates Dapple is its contemporary and intuitive design, enhanced by AI-driven features that optimize tasks such as submission reviews and feedback writing, ultimately making the entire process more efficient and user-friendly. This unique combination of functionality and design ensures that teams can work seamlessly together, regardless of their size or structure, to achieve their submission management goals.

Our submission plans are designed to grow seamlessly with your event, accommodating everything from a few entries to thousands without incurring additional fees. You can easily create and publish various forms for submissions, reviews, and decisions using an extensive selection of templates. Throughout the event, standard and customized reports can be generated to track progress and outcomes effectively. There are versatile options available for organizing abstracts, making it suitable for panels, workshops, and roundtable discussions. Maintain oversight of complex processes through intuitive workflow tools and interfaces that are easy to navigate. We offer a straightforward and accessible method for collecting and managing both abstract and paper submissions. Select from a diverse assortment of fully-editable templates for key questions to ensure you gather the precise data required. With just one click, you can publish your information and share it across your website, emails, and social media via embeddable links. You have the capability to view, delete, withdraw, edit, and download submissions and associated data, all facilitated by a multi-view table equipped with a variety of user-friendly tools. This comprehensive approach makes managing your event submissions both efficient and effective.

Renowned for its user-friendly design, sleek interface, and exceptional customer support, OpenConf has facilitated countless events and journals across more than 100 countries. The OpenConf Professional Edition stands out as a sophisticated platform that offers more than a dozen modules for enhanced peer review and event management capabilities. Beyond the features available in the Plus Edition, the Professional Edition provides priority technical assistance and allows users to customize submission forms, process payments for submissions, automatically assign reviews upon submission, submit review credits to ORCiD, perform plagiarism checks*, accept multiple file uploads per submission, and develop a program that can be published online for both web and mobile platforms. Furthermore, it includes additional functionalities that simplify copyright collection for events hosted by ACM and IEEE, ensuring a comprehensive solution for event organizers.

Discover groundbreaking startups for investment and collaboration opportunities while overseeing the complete lifecycle of your startup initiative seamlessly from one platform. Launch startup competitions to inspire and support visionary entrepreneurs tackling some of society's most pressing issues. Stay ahead of the curve by identifying emerging trends and innovations, and significantly enhance your innovation strategies through strategic partnerships with startups. Facilitate competitions for students and alumni to engage them in entrepreneurial activities. Draw in skilled entrepreneurs to your university by leveraging startup initiatives. Optimize your time by minimizing the effort spent on reviewing attachments and forms, allowing you to focus more on creating exceptional opportunities for startups. Streamline the submission process to gather entries effortlessly and establish clear evaluation workflows. Choose the most deserving winners for your scholarships based on informed assessments. Make well-informed choices regarding submissions by selecting the most capable participants and gaining comprehensive insights into all aspects of submissions at each phase. By understanding the data and demographics of your participants, you can tailor your approach to maximize engagement and support. Ultimately, fostering an environment that nurtures innovation and collaboration will lead to significant advancements in your community.

MyPoolitzer is a web-based application that allows literary agents and publishers to manage literary submissions. The platform provides services such as AI detection, advanced filtering and secure data storage. Packages range from monthly subscriptions for professionals to one-time contest management fees. Features include instant web linking, team messaging, and customizable branding. The platform ensures that all manuscript submissions are handled efficiently and securely.

ClinChoice excels in overseeing international regulatory information by leveraging advanced technology, a comprehensive grasp of both global and local regulations, and exceptional data management techniques. By harnessing its regulatory affairs and technological expertise, ClinChoice aids organizations in effectively handling their regulatory data. Our team of consultants offers essential data maintenance assistance within regulatory information management system (RIMS) software, facilitating timely application submissions, approvals, and renewals while enhancing operational efficiency and monitoring. We support the management and oversight of the drug registration process, enabling pharmaceutical and medical device manufacturers to maintain visibility and track all regulatory details. With our guidance, organizations can formulate both immediate and long-term strategies that ensure compliance with submission deadlines, all while minimizing disruption to their everyday operations, ultimately contributing to a smoother regulatory journey. This strategic partnership empowers companies to navigate the complexities of compliance with greater confidence and agility.

In light of the constantly evolving national regulations and the intricate nature of preparing for regulatory submissions, organizations within the healthcare and life sciences sectors are increasingly focused on adopting smarter methodologies and intelligent systems to enhance efficiency, reduce costs, and shorten submission timelines. To tackle these challenges, RIMTrack emerges as a cutting-edge regulatory information management system that leverages cloud-ready artificial intelligence. Built from the ground up, its primary goal is to assist organizations in achieving precise and effective submission preparations while streamlining the various regulatory processes involved in tracking, licensing, approvals, regulatory and competitive intelligence, clinical trials, and comprehensive reporting across international stakeholders. By integrating seamlessly with existing Regulatory Information Management systems, RIMTrack facilitates a thorough end-to-end management of the entire regulatory lifecycle, ultimately empowering organizations to navigate the complexities of compliance with greater ease and accuracy. Such advancements not only improve operational efficiency but also position organizations to adapt more readily to future regulatory changes.

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.

ProposalSpace makes it easy to manage your abstract submissions and review process. ProposalSpace makes abstract management easy, regardless of whether you are a call organizer, author or reviewer. Are you responsible for organizing a conference call for abstracts, call to papers, call to speakers, or other type of "call for"? ProposalSpace is an online abstract management platform that allows anyone to create a call without any obligation. It's easy to create a call: click the "Start A New Call" button, enter a title, and you're done. There is no need to wait for a technician or "consult" with an accountant to set up things. You can customize your call to meet all your needs. You can build your submission form, set deadlines and limit your options. It's easy to create a copy of an existing phone call. Data is not included and you can control which settings are included. Copy what you want and forget the rest.

Ex Ordo is used by conference organizers to provide great experiences for their technical, scientific and professional communities. Send your call to papers and then begin collecting abstracts, papers, or speaker proposals via a custom submissions form. Track their progress and match submissions with the best reviewers. Once you are ready, notify presenters from your dashboard. You can delight attendees with an event space that includes unlimited live sessions, on demand videos, and downloadable media such as PDFs and spreadsheets. Your online conference platform will keep every piece of content for 60 days after the event ends. You can collect secure card payments, or allow attendees to pay by bank transfer. You can message reviewers, authors, and delegates and send reminders to those who need them. Your dashboard will give you a complete overview of the conference.

Kalypso offers a budget-friendly solution for life sciences organizations looking to implement a Regulatory Information Management (RIM) system, known as Accel for RIM. This platform facilitates an integrated approach to effectively oversee and monitor product registrations while enhancing the accuracy of submissions and managing global Unique Device Identification (UDI) information, thereby streamlining product distribution. It also merges compliance and quality data from multiple enterprise systems into a comprehensive source of truth for product registrations and tracking, which expedites regulatory submissions. Utilizing modern APIs, it aggregates product data along with necessary regulatory documentation and submission packages. The system is pre-configured for swift deployment and is built on a validated software framework, grounded in the best practices and successful implementations within the industry. By adopting this solution, companies can expect not only efficiency but also a significant reduction in time spent on regulatory tasks.

Software for submission management that simplifies application management, data analysis, and compliance. You can quickly create complex forms and get the media and data you need in the format that you prefer. Our expert support team can help you create complex or simple workflows. You can evaluate effectively using features like auto-tag and auto-score, self-reject, user score. Use the in-app mail to communicate directly with candidates. Use powerful analytics tools to create meaningful reports that you can control.

InfoReady is the global leader in software that manages research competitions and collaborative decisions regarding R&D. Our software solicits research proposals, then routes them to be reviewed and approved. We have over 150 research institutions and organizations around the world. We not only create software, but also forge partnerships with our clients through our exceptional client retention, unmatched customer support, and strong product referrals. We offer robust, configurable workflow automation that allows for the routing, approval, review, and review of applications, forms, and documents. We offer solutions that help our partners increase awareness and exposure of their outstanding programs, events, resources, as well as other opportunities on their campuses. Our solutions help partners break down barriers between promotion and effective process management.

ClaimBook streamlines the insurance claims process by facilitating quicker settlements, enhancing accountability, and reducing the likelihood of rejections. It is equipped with comprehensive features that cater to all aspects of claims management and evidence submission. Furthermore, ClaimBook promotes international patient care through specialized workflows, thereby fostering medical tourism. The platform includes a built-in Rules Engine that prevents incomplete submissions and ensures that all necessary information and documents are provided. This leads to submissions that are accurate, thorough, and pre-authorized. Additionally, ClaimBook incorporates Smart Data Extraction technology, which can interpret uploaded documents to retrieve pertinent information from a connected Hospital's Information System, eliminating the need for manual data entry. Another valuable feature is Integrated Emailing, which creates a virtual inbox directly within your dashboard, allowing users to compose emails with a familiar design similar to that of Microsoft Outlook. This integration not only enhances productivity but also ensures seamless communication throughout the claims process.

ProcEdge Regulatory Information Management System (RIMS) provides companies with a powerful, centralized platform to manage complex regulatory requirements for their entire global product portfolio. Moving away from traditional Excel-based tracking, it offers a single source of truth that connects multiple departments, providing 360-degree visibility and real-time updates on product registration, license maintenance, and post-registration activities. The platform enables detailed planning and tracking of submission timelines tailored to country-specific regulations, helping users meet compliance standards and reduce costly errors. It features configurable data models, automated email notifications, and a robust workflow engine that streamlines query management and response tracking. ProcEdge RIMS complies with global standards like IDMP and regulatory frameworks including GxP, GDPR, and Part 11. By eliminating redundant systems and manual data entry, it significantly reduces operational expenses and accelerates health agency approvals. The system’s audit trails and electronic signature capabilities ensure data integrity and regulatory reliability. Overall, it empowers regulatory professionals to make faster, informed decisions and maintain product marketability efficiently.

PharmaPendium serves as a robust platform that grants users access to a wide array of FDA and EMA drug approval documents, encompassing essential aspects like pharmacokinetics, pharmacodynamics, and safety evaluations. This resource delivers in-depth insights into drug-drug interactions, side effects, and outcomes from clinical studies, thereby empowering stakeholders to make well-informed decisions during the drug development process and when making regulatory submissions. Its rich database aids researchers and healthcare practitioners in assessing both the efficacy and safety of medications, playing a pivotal role in the progression of pharmaceutical research and enhancing patient care. Users can explore historical regulatory submissions and leverage past precedents to better understand and anticipate agency requirements. The interface allows for a seamless transition from tabular data to dynamic charts, graphs, and other visual tools, making it easier to analyze and interpret findings. Additionally, users can search for information related to adverse events (MedDRA), therapeutic targets, drug indications, and endpoints utilizing standardized data. Result pages effectively connect preclinical research with clinical applications, facilitating a comprehensive understanding of the drug development landscape. Overall, this platform not only streamlines the research process but also fosters collaboration and knowledge-sharing among industry professionals.

Introducing a comprehensive global regulatory affairs platform, featuring registration management tools and expert support from regulatory professionals worldwide. This system is essential for initiating, renewing, modifying, or transferring market access approvals for your medical devices or IVDs. With LICENSALE®'s user-friendly interface and real-time data capabilities, you gain access to complete project management tools, infographic analytics, a seamless collaboration space, future market access strategies, and detailed reporting features. This empowers you to oversee your global medtech registration processes effectively. Regulatory specialists from Arazy Group meticulously examine your compliance documents, providing guidance in the preparation and submission of your applications, and they liaise with authorities until you secure the necessary marketing approvals. Furthermore, LICENSALE® encompasses specific submission and compliance requirements tailored to your product across over 140 countries, with dedicated regulatory experts available to assist in navigating each market's unique challenges. By leveraging this system, you can streamline your regulatory processes and enhance your overall market entry strategy.

To meet ICH M7 guidelines, predict genotoxic and carcinogenic endpoints for impurities and degradations. Impurity profiling Suite is a tool that can be used in your ICH M7 workflow to help you prepare regulatory submissions and stay compliant.

cubeSAFETY is an advanced pharmacovigilance platform designed to assist safety teams in efficiently managing adverse-event reporting, regulatory submissions, and case processing in a compliant manner. It adheres to ICH E2B and various regional reporting standards, facilitating submissions to agencies like the FDA, EMA, CDE, MFDS, and PMDA through specialized gateways, while also automatically converting and formatting data for CIOMS and XML export. The platform boasts AI-driven medical coding suggestions, duplication detection, the capability to import CIOMS PDF files, and dynamic dashboards for real-time submission tracking. Additionally, it offers complete integration with other CRScube modules, including cubeCDMS. cubeSAFETY is crafted to enhance the safety-case entry process, guarantee superior data quality through embedded validation features, and streamline workflows for compliance with global regulatory requirements, all while decreasing manual labor and financial overhead. Ultimately, this innovative platform aims to redefine pharmacovigilance efficiency and accuracy across the industry.

Compliance Mantra offers a comprehensive platform that allows users to establish compliance requirements tailored to their specific business needs, operational processes, or legal obligations; it also enables scheduling of compliance submission deadlines and designating job responsibilities. In addition, the platform organizes submitted documents and sends alerts for upcoming and overdue compliance tasks. A significant obstacle for businesses is meeting the deadlines for their legal and regulatory commitments, especially for organizations with multiple subsidiaries and diverse compliance demands, making it challenging to track and monitor compliance timelines effectively. To address these issues, Compliance Mantra empowers users to manage their due dates, target dates, and the actual dates of compliance completion. Furthermore, the platform produces detailed reports based on various criteria and combinations, enhancing visibility and control over compliance processes. This robust solution ultimately streamlines compliance management for organizations of all sizes.

Essenvia enhances business value and improves operational efficiency across various teams and departments. It serves as a centralized hub for all regulatory data, facilitating collaborative document creation and reporting while helping to prevent technical holds, RTAs, and RFIs. This platform empowers the regulatory affairs team to speed up product launches, thus avoiding revenue losses associated with submission delays and missed renewals. It provides a comprehensive overview of the entire regulatory lifecycle, complete with executive dashboards, key performance indicators, and proactive alerts for global registrations, submissions, and change assessments. Essenvia acts as a Regulatory Information Management (RIM) Platform that streamlines regulatory workflows throughout the entire product lifecycle, enabling faster global market access and delivering significant business advantages. By consolidating all regulatory activities into one unified platform, businesses can accelerate their market entry. Additionally, it includes a central repository for all registration documents, which are linked to product master data, allowing users to effectively manage the product registration lifecycle on a country-by-country basis while ensuring compliance and efficiency.

Medi-EHR is designed to accommodate medical practices of all sizes and varying scopes. This highly customizable platform empowers healthcare providers to utilize an electronic health record (EHR) system that seamlessly integrates with their specific workflows. Featuring a cutting-edge Ambulatory Surgery Center (ASC) system, Medi-EHR ensures that every aspect—from scheduling and documentation to post-operative care—is crafted for both efficiency and user-friendliness. Each component of the system can be tailored to meet the unique requirements of your facility. It serves as a comprehensive and intuitive solution for managing your organization, facilitating everything from therapy notes to tracking compliance with regulations and submitting bills with minimal human input. Additionally, Medi-EHR includes a specialized module for Residential Treatment Facilities, specifically designed for Addiction Treatment Facilities with residential patients, offering scheduling options for both in-facility and outpatient services. The billing module, developed by experienced billing professionals, provides an effective solution for billing, available as both a product and a service, thereby equipping your in-house billing team with a powerful and efficient system. This versatility makes Medi-EHR an invaluable asset for any healthcare organization looking to enhance its operational capabilities.

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.

CommunityForce is a trusted partner for organizations passionate about making a difference in their communities through grants, scholarships, and other impactful programs. With its comprehensive features, advanced technology, CommunityForce empowers organizations to create positive change.

The Thrana Safety Database is a cloud-centric system focused on pharmacovigilance and drug safety management. Crafted to prioritize user experience, this comprehensive solution effortlessly combines essential features like PV Intake, Case Processing, Regulatory Submissions via AS2 Gateways, Regulatory Reports, and Analytics, all conveniently available from a single, unified platform. This integration enhances efficiency and streamlines workflows for users across the industry.

Advanced clinical data analytics is essential for expediting and minimizing risks associated with regulatory approvals, thanks to our innovative automated analytics and validation platform. Unlike any other clinical data analytics software, our solution enhances data integrity and reduces the risks tied to submissions. By automating manual quality processes, you can avoid the hassle of QC reruns, eliminate instances of data duplication and inconsistencies, and maintain robust data traceability, all while ensuring a transparent quality assurance process. This leads to a faster time to market, allowing businesses to generate revenue sooner and reduce validation times effectively. Moreover, this efficiency frees up valuable resources and cuts costs, thereby accelerating the journey to regulatory approval. The demand for precise clinical data validation and top-tier data output is increasingly critical in today’s fast-paced environment. Verify is dedicated to managing and analyzing clinical data to minimize risk and hasten the approval process for new drugs and vaccines, ensuring that quality, speed, and success are at the forefront of your clinical trials. Ultimately, our platform empowers organizations to respond swiftly to market needs while maintaining high standards of compliance.

Utilize the Cygnet Tax Tech compliance tracker solution to monitor global tax and compliance submissions, ensuring that no deadline is overlooked, and empower users with specific rights and roles while keeping an eye on their activities as needed. In order to enhance collaboration between internal tax departments and external consultants, the system delineates user roles and responsibilities effectively. You can create and organize tax documentation, tailored packages, client profiles, employee records, and additional resources through user-friendly web applications for improved operational efficiency. The solution offers both automated and manual oversight regarding document statuses, allowing you to view the assignments, historical tracking, and workload of team members. Effortlessly communicate with users through calls or automated emails and in-app notifications to remind them of submission and approval tasks. You can monitor all your tax submissions, prompt users for outstanding actions, and manage your documents efficiently, among other capabilities. Additionally, leverage our expertise in utilizing GST data for insightful analytics and fraud detection, ensuring a comprehensive approach to tax compliance management. By integrating these features, organizations can significantly streamline their tax processes and enhance overall productivity.

Samarind RMS offers an intelligent solution for overseeing your medical product information more effectively. With Samarind RMS, you can input data just once and utilize it repeatedly as needed. For instance, an ‘INN’ can be registered once and applied to all associated IMA submissions, renewals, variations, PSURs, and XEVMPD submissions. This principle is applicable to all essential data maintained within the system, which has demonstrated its ability to enhance workflow efficiency and boost data quality. Our practical approach to system design and implementation allows clients to handle their licenses with ease and confidence, knowing that our single-source-of-truth™ strategy for regulatory affairs experts provides a comprehensive end-to-end solution. Additionally, our platform includes an electronic document management system (EDMS) equipped with version control, the creation of templates, and the capability to connect to external document management systems such as Documentum™ or SharePoint™, ensuring a seamless integration of all your documentation needs. Ultimately, Samarind RMS empowers users not only to manage their information but also to improve collaboration across different departments.

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.

Judgify is a versatile system designed for managing abstracts and awards across various contest formats and nomination categories. This intuitive award management platform streamlines the automation of competitions, regardless of their scale or nature. Engage your audience through a personalized awards landing page, establish your own submission guidelines, and enable judging or public voting accessible from any device, while also benefiting from detailed reporting. Judgify serves as a complimentary event planning solution for contests that provide free entry. Leverage the advantages of automated event management tools to create a meaningful influence within your community. Moreover, with Judgify, you can tailor custom solutions to meet the needs of organizers, judges, participants, and marketers, ensuring that each feature aligns with the specific attributes of the event type and audience size. This makes it an ideal choice for anyone looking to enhance their award management experience.

The PegEx Platform, a cloud-based hazardous waste management platform, is designed for waste brokers, haulers, disposal facilities, and other users. The PegEx Platform can be used to create and print regulatory documents, eManifest submission, safety management, job tracking and operations management, customer support and sales management. The PegEx Platform can help you increase productivity, reduce risks, and maximize revenues in your waste management business. Get a free demo.

Signant Health operates as a worldwide leader in evidence generation, striving to transform the landscape of clinical trials by connecting with patients in their environments and rethinking the route to validation. Their extensive range of clinical technology solutions includes electronic Clinical Outcome Assessments (eCOA), Electronic Data Capture (EDC), electronic clinician evaluations, and a cohesive eClinical platform. Additionally, they offer patient engagement solutions featuring a user-friendly app, eConsent for informed consent processes, and telemedicine functionalities. Furthermore, Signant Health delivers clinical data and analytics services, which include COA data analysis as well as the aggregation and interpretation of data. With a rich history spanning over three decades, they have played an instrumental role in supporting numerous trials and have been pivotal in hundreds of drug approvals, establishing themselves as a reliable ally for sponsors and CROs eager to provide high-quality data for informed trial decisions and regulatory submissions. Their commitment to innovation continues to shape the future of clinical research.

SafetyEasy by EXTEDO is a robust software solution for managing pharmacovigilance and multivigilance, aimed at simplifying the handling of safety cases and vigilance information. It adheres to a wide range of drug safety regulations such as E2B(R3) and HL7 eMDR, while facilitating the necessary creation of regulatory documents including PSUR, PBRER, and DSUR. The software is equipped with features that optimize workflows through email alerts and online dashboards, allowing users to efficiently monitor project progress and adhere to submission timelines. Additionally, SafetyEasy features sophisticated tools like CasEasy AI, which leverages Natural Language Processing to streamline the automation of case creation, alongside a Business Intelligence module that offers an insightful 360° perspective on scientific data, thereby improving case evaluation and safety signal identification. This cloud-based platform is not only quick to deploy but also designed for ease of use, requiring very little training for effective operation. Furthermore, the integration of these advanced functionalities makes SafetyEasy an invaluable asset for organizations aiming to enhance their pharmacovigilance processes.

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.

A comprehensive solution for managing awards encompasses fellowships, scholarships, grants, mentorship initiatives, and any other application processes that necessitate evaluation and selection. Our platform aids associations, organizations, and universities in optimizing their form submission workflows. We ensure a seamless experience for both applicants and reviewers, making it straightforward for them to fulfill their responsibilities. Our system simplifies the overall administration of your program, facilitating the submission of essential information, supporting documents, and requests for electronic references. Reviewers and committee members find it easy to access, evaluate, and provide feedback on submissions. Effectively oversee your program while generating straightforward and intricate reports, and maintain communication with all users. Moreover, broaden the visibility of your program through digital marketing strategies, including social media engagement and online advertising. Our solution is customizable, adapted to fit the requirements of any online form submission, whether simple or complex, ensuring efficient management throughout the entire process. By leveraging advanced technology, we empower organizations to enhance their outreach and maximize the impact of their award programs.

FurtherAI is a specialized AI workspace tailored for the commercial insurance sector, streamlining repetitive functions in areas such as submission intake, underwriting audits, policy comparisons, and claims processing. The platform includes an AI Assistant capable of reading, writing, comparing, classifying, summarizing, and reasoning about various insurance documents and data, all integrated into modular workflows that reflect actual insurance procedures. It is specifically optimized for policy language, underwriting guidelines, and compliance standards while facilitating seamless connections with over 100 enterprise systems. With a modular and flexible architecture, FurtherAI can efficiently manage submissions, audits, or policy oversight, leveraging a combination of large language models to enhance task accuracy. Additionally, it incorporates a human-AI interface that promotes collaboration and oversight, thereby ensuring greater precision in handling sensitive operations. This innovative approach not only improves efficiency but also enhances the overall quality of decision-making in the insurance industry.