Alternatives to Condor Software

Qualio is a purpose-built quality and compliance platform for life sciences companies operating in complex, high-stakes regulatory environments. Medical device, SaMD, biotech, and pharma teams use Qualio to replace fragmented eQMS tools, spreadsheets, and consultant-driven audits with a single, validated system that delivers continuous audit and inspection readiness. Qualio combines a modern eQMS with Compliance Intelligence—an AI-driven layer that continuously evaluates how well real operating data aligns with regulatory requirements. Instead of treating audits as one-off events, teams gain always-on visibility into compliance coverage, risk exposure, and readiness across FDA, ISO, EU MDR, GxP, and software-intensive standards. Core quality workflows—document control, training, CAPA, change management, supplier quality, and design controls—are directly connected to regulatory obligations and objective evidence. Deep integrations with Jira, Azure DevOps, GitHub, TestRail, and Salesforce automatically capture proof from development and operational systems, eliminating manual evidence gathering and reducing compliance drag on engineering teams. Compliance Intelligence runs multi-standard gap analysis in under an hour, flags emerging risks before they become findings or 483s, and maps reusable evidence across frameworks to accelerate submissions and market expansion. All insights are explainable and traceable back to specific clauses and internal policies, supporting validation and audit expectations. The result: audit readiness in weeks instead of months, fewer fire drills, faster launches, and lower long-term compliance cost. Qualio turns compliance from a reactive burden into a predictable, scalable system.

To shape the future effectively, one must take proactive steps in creating it. Exigyn offers immediate access to a financial analyst right at your fingertips. You can easily design clinical trial scenarios, evaluate cash flow sustainability, and still enjoy your evening meal. By utilizing essential KPIs such as patient enrollment, site efficiency, and cost per patient, you can enhance trial expenditures. Implement our comprehensive multidimensional database for accurate and thorough tracking, down to the level of individual vendor names. With just a single click, you can swiftly adjust financial predictions, budgets, departmental structures, project listings, charts of accounts, and expenditures. Simplify personnel planning by aligning staff numbers with clinical objectives and optimizing your organizational layout. Equipped with user-friendly tools for monitoring roles, salary ranges, and anticipated hires, you can confidently prepare for what lies ahead. Moreover, our solution incorporates real-time data, automating clinical accrual processes, which allows you to conserve valuable time and resources while focusing on what matters most. Embrace the future of financial management and make informed decisions today.

At Komodo Health, we integrate an extensive understanding of patient interactions with cutting-edge algorithms and years of clinical knowledge to create our Healthcare Map, which offers the most accurate representation of the U.S. healthcare landscape. This Healthcare Map serves as the backbone for our comprehensive suite of software solutions, designed to help you provide exceptional value to your customers, colleagues, and patients alike. Relying solely on traditional scholarly data for strategic planning is now outdated. Our Aperture platform has been meticulously crafted to deliver unparalleled insights into clinical leadership and influence, enabling improvements in care standards where they are needed most—whether that involves the most referenced author, a prominent social media influencer, or the physician with the highest patient volume. Moreover, conventional open/sampled prescription and patient-level data often overlook critical patterns that are essential for accurately identifying individuals with complex care needs or uncommon medical conditions. By addressing these gaps, we aim to enhance patient outcomes and streamline healthcare delivery.

Cloud-first ERP solutions are specifically designed to meet the needs of life science companies. Merit for Life Science is a cloud-first ERP system that has been expertly crafted for manufacturers in the biotech, pharmaceutical, and medical device sectors. It enhances Dynamics 365 finance and operations, providing a seamless connection across your entire organization. This system effectively aligns resource qualifications with production needs, while also overseeing vendor relationships in procurement to ensure compliance with quality standards during manufacturing. By offering your life science organization enhanced visibility and transparency, it supports the delivery of safe and innovative products, among other benefits. Recognizing that each organization has its own distinct requirements, we are committed to understanding those needs. Explore the comprehensive solutions we provide, which are tailored to satisfy the stringent demands of the pharma, biotech, and medical device industries. Additionally, our system aids in refining your decision-making processes through dependable and auditable accounting practices, while also establishing robust financial reporting standards for acquired entities or preparing your organization for acquisition, ensuring you are always ready for the next step in your growth journey.

At Genospace, we recognize that the evolution of precision medicine is being propelled by advancements in genomics, yet the challenge of effectively scaling its implementation remains unresolved. Our mission is to bridge this gap. Our innovative platform aims to transform biomedical data into valuable insights that are easily accessible for all, particularly for those actively involved in delivering care. Equip your clinicians and researchers with essential information that empowers them to make well-informed choices while participating in our goal of utilizing intricate molecular data to enhance patient outcomes and speed up the processes of drug development and research. In this context, the significance of large-scale population data for drug discovery and research cannot be overstated. Utilize cohort-driven analyses through the Genospace platform to support your research initiatives. We have a strong focus on clinical trial research, enabling the Genospace platform to seamlessly align fragmented patient information with intricate trial requirements, thus facilitating quicker patient recruitment. Furthermore, our platform is designed to integrate genomic medicine into standard clinical care practices, making it easier than ever to harness the power of genomics in everyday healthcare. Together, we can push the boundaries of what’s possible in patient care and research.

Organizations in the life sciences sector, regardless of their size or complexity, depend on the ICyte platform to enhance pharmaceutical market entry and therapy commercialization processes. The ICyte platform equips biotech and pharmaceutical manufacturers with exceptional services that include the aggregation of channel and patient data, management of contracts and pricing, gross-to-net forecasting, and accrual systems, as well as expert solutions for launch and pricing transparency. By utilizing ICyte, both pharmaceutical and biotech firms can significantly enhance their market access capabilities by swiftly converting patient, payer, complex transaction, and channel data into practical insights. Additionally, ICyte offers analytics-as-a-service, facilitating the deployment of standardized models and metrics as a unified service across various applications, data streams, and analytical uses. The platform integrates key performance indicators (KPIs) tailored specifically for life sciences organizations. Furthermore, it features advanced analytics tools, including forecasting, scenario modeling, and a recommendation engine powered by machine learning, which aid companies in making data-driven decisions. Ultimately, ICyte is positioned as a comprehensive solution that not only simplifies processes but also empowers organizations to navigate the complexities of the pharmaceutical landscape effectively.

FinQuery (formerly LeaseQuery) simplifies complex accounting operations by automating the flow of financial data from source documents to subledger. The platform unifies lease accounting, contract management, and prepaid and accrual accounting within a single, audit-ready system—cutting manual work by up to 80%. Designed to ensure compliance with FRS 102, ASC 842, IFRS 16, and related standards, FinQuery enables users to generate amortization schedules, journal entries, and disclosure reports in minutes. Its centralized document repository and automated abstraction tools eliminate errors while giving teams full visibility across leases, contracts, and prepaid expenses. With deep ERP integrations, real-time data validation, and AI-powered automation, FinQuery helps finance leaders accelerate close cycles and improve reporting accuracy. The platform’s managed services also allow organizations to outsource data entry, validation, and maintenance for additional flexibility. Backed by industry-leading support and a 99% customer satisfaction rate, FinQuery combines reliability, scalability, and ease of use. It’s the modern foundation for accountants seeking clarity, compliance, and control across all financial operations.

Salesforce Agentforce Life Sciences is a comprehensive CRM platform designed to support the entire life sciences value chain. It connects clinical development, medical affairs, commercial operations, and patient services within a unified and compliant ecosystem. Built on Salesforce’s deeply integrated platform, it ensures regulatory requirements are embedded into workflows. AI-driven agents assist with clinical trial recruitment, participant management, and predictive enrollment analytics. Medical affairs teams can automate inquiry responses and manage scientific knowledge exchange more efficiently. Commercial teams gain a unified view of healthcare professionals to deliver personalized, omnichannel engagement. The platform enhances patient services with automated insurance verification and proactive support programs. Real-time dashboards provide actionable insights across stakeholders and operations. Integration with Data 360, MuleSoft, Tableau, Slack, and Health Cloud expands collaboration and analytics capabilities. Agentforce Life Sciences empowers organizations to accelerate innovation, improve compliance, and drive better health outcomes.

Auditive serves as an innovative Third-Party Risk Management (TPRM) platform that facilitates ongoing monitoring, allowing both buyers and sellers to interact more confidently than ever before. By employing a distinctive network method, Auditive significantly reduces the risk review workload for companies and their vendors by up to 80%. This efficiency enables buyers to conduct third-party risk evaluations four times quicker, maintain ongoing oversight of risks throughout their vendor network, and achieve near-instantaneous insights into third-party risks, leading to a remarkable 35% improvement in vendor response rates. Meanwhile, sellers benefit from bypassing tedious questionnaires, allowing them to concentrate on higher-value projects, promote their security practices within the Auditive network, and foster trust with their clients. Additionally, the platform is designed to assess risks against industry-specific frameworks to ensure precise evaluations. Auditive's seamless integration with procurement and productivity workflows facilitates quick onboarding and constant monitoring of all vendors from a centralized location, enhancing overall operational efficiency. This comprehensive approach positions Auditive as a vital tool for organizations seeking to manage third-party risks effectively.

Streamline your company’s purchase order, vendor management, onboarding, accrual, invoicing, and payment processes to save both time and money through automation. The Accrualify platform allows you to issue and manage both plastic and virtual cards, making it easier to oversee employee expenses. By providing virtual cards for purchases typically made with personal cards, you enhance control, reduce the risk of fraud, and gain clearer visibility into company spending. You can dictate when and where employees can make purchases, while monitoring transactions in real-time for added oversight. The most appealing aspect? This module is offered at no cost*. Accrualify empowers finance teams with solutions that deliver comprehensive control and visibility over their procure-to-pay processes at month-end and quarter-end. Our tools facilitate the automation of everyday accounts payable functions, including the creation and approval of purchase orders, handling accrual requests, managing invoice collections and approvals, and processing electronic payments. Moreover, Accrualify provides enhanced vendor management capabilities, ensuring greater transparency and accountability throughout your financial operations. In this way, your organization can optimize its financial workflows and achieve better outcomes.

Harnessing actionable insights from the leading AI-driven clinical analytics platform allows your teams to effectively manage risk and enhance performance throughout studies, systems, sites, and vendor relationships. The cutting-edge technology from Saama is specifically crafted to optimize workflows, automate labor-intensive tasks, and foster improved collaboration among various clinical functions such as operations, medical review, data management, biostatistics, and pharmacovigilance. Both sponsors and CROs depend on Saama's capabilities for data aggregation and AI solutions, which facilitate superior decision-making, minimize delays, and drastically reduce costs and timelines associated with drug development. By leveraging Saama's tools, you can accelerate the pace of clinical trial innovation. When your clinical data is centralized and continuously updated, it simplifies the lives of your ClinOps and medical review teams considerably. Furthermore, Data Managers, often undervalued, can shift their focus from repetitive tasks to the critical data points that truly drive project success, ensuring that their expertise is fully utilized in the process. This transformation not only enhances efficiency but also contributes to the overall quality of clinical outcomes.

With extensive experience in the industry, our platform is uniquely tailored to cater specifically to the requirements of life science companies. R&D Logic empowers your team to analyze plans and actuals from various angles, ensuring you have a clear understanding of your business’s performance at all times. Our attentive service model guarantees that we support you comprehensively, from the initial implementation phase through training, ongoing assistance, and specialized consulting. We handle the backend maintenance to secure and protect your data, allowing you to concentrate on running your business effectively. Our commitment is to grasp your distinct needs and to customize a blend of products and logic that aligns with your objectives. The R&D Logic platform is designed to adapt as you expand, providing flexibility to add, remove, or adjust features and business rules in response to your evolving requirements. We prioritize our customers in every interaction, regardless of their size or stage, whether they are small, medium, or large enterprises, and whether they operate in pharmaceutical, biotech, or medical device sectors. Furthermore, our goal is to foster a collaborative partnership that evolves alongside your company, ensuring sustained success.

Gappify Accrual Cloud is a cloud-based software that automates the the entire accruals process. Gappify automates all aspects of accruals including vendor confirmations, PO and budget owner outreach, historical calculations, and auto-posting approved JEs into the ERP. Typical ROI is 2-5 days off your month-end close, improving completeness + accuracy of AP, and elevating your team into more strategic tasks. Eliminate hundreds of hours of manual work, drive tighter compliance, and improve the accuracy of your accounting with Gappify.

It is accurate to assert that "not all DRG vendors are equal." Although their marketing strategies may be similar, these vendors generally fall into two categories: those that cater primarily to provider hospitals and those focused on detecting overpayments for health plans and payers. Much like how attorneys often concentrate on either defense or plaintiff cases, auditing vendors tend to specialize in the distinct needs, cultures, and priorities of their respective clients. Within the realm of payer-focused vendors, a diverse array of strategies for DRG auditing and overpayment detection exists. Our service offerings also include a dedicated physician review team that generates clinical validation findings, specifically addressing cases where identified issues stem from unsubstantiated clinical diagnoses made by treating physicians, which goes beyond the capabilities of coders. Our findings consistently demonstrate that our coding compliance model yields verified savings, contributing to enhanced financial efficiency for healthcare providers. Thus, selecting the right vendor can significantly impact the financial health of both hospitals and payers alike.

FinOptimal is an innovative accounting automation solution designed to enhance efficiency by removing manual tasks within QuickBooks Online, allowing for the automation of tasks such as accruals, journal entries, spreadsheet synchronization, and real-time reporting, which ultimately helps finance teams to close their books more quickly and accurately. The flagship offerings consist of Accruer, which automates prepaid expenses, deferred revenue, fixed assets, and payroll accruals simply by specifying the time frame; Booker, which enables seamless synchronization and bulk editing of transactions in Google Sheets that are directly linked to QuickBooks; and Wrangler, which provides dynamic and customizable financial reporting based on QuickBooks data. This software seamlessly integrates with existing accounting workflows without displacing them, ensuring continuous synchronization of verified data, preventing duplicate entries, and offering users access to audit-ready backups along with valuable financial insights whenever needed. By streamlining these processes, FinOptimal not only saves time but also enhances the overall accuracy of financial reporting for businesses.

ClinicalWave.ai, built on AWS' cloud platform, is an integrated AI platform designed for life sciences companies. It uses cutting-edge NLP to extract valuable insights and automates the redaction and extraction sensitive data from clinical documents. It is made up of: 1. ClinRedact AI - Our Redaction Product that automatically identifies and removes sensitive information from clinical documents. This product saves time and ensures data integrity. 2. ClinExtract AI - The AI Data Extraction Product that uses NLP and Machine Learning to extract relevant data from clinical documents. This product provides valuable insights and streamlines workflows. 3. ClinDICOM AI - Experience the power and features of our DICOM data extraction product. It offers targeted redaction, customizable redaction rules, intelligent context analysis, audit trail compliance and a user friendly interface.

Cytobank serves as a cloud-driven platform that facilitates the analysis, storage, and sharing of flow and mass cytometry data. Being entirely web-based, users only need a web browser and an account to gain access, eliminating the need for any software or hardware installations, updates, or maintenance. This makes Cytobank especially suitable for individual researchers or small teams. For larger research groups, pharmaceutical and biotech research and development teams, as well as clinical research organizations, Cytobank offers a shared cloud option, while also providing a private cloud solution that allows for controlled access managed by a designated administrator. Furthermore, it supports enhanced computational capabilities, particularly for advanced functionalities like viSNE, making it a versatile tool for diverse research needs. Overall, Cytobank streamlines the process of data management and enhances collaboration among researchers.

Sapio Sciences delivers a cutting-edge AI-driven lab informatics platform that integrates Laboratory Information Management Systems (LIMS), Electronic Lab Notebooks (ELN), and a Scientific Data Cloud into one seamless ecosystem. It is tailored to advance scientific research, clinical diagnostics, drug discovery, and manufacturing through configurable, no-code solutions. The Sapio LIMS® automates complex workflows with full configurability, removing the need for programming. Sapio ELN® offers a flexible, adaptable electronic lab notebook that supports diverse experimental needs. The platform’s Scientific Data Cloud consolidates instrument and research data enterprise-wide, paving the way for AI-driven insights. By unifying these components, Sapio simplifies data management and boosts productivity across the lab lifecycle. The platform is accessible for a wide range of industries and research applications. It aims to reduce administrative burden and enhance collaboration within scientific teams.

In recent years, the Life Sciences sector has incurred nearly $15 billion in fines and settlements related to compliance, underscoring the importance for firms to follow best practices in pharmaceuticals, medical devices, and biotechnology. Additionally, the way clinical trials are managed can greatly influence the timeline, scope, and financial resources allocated for the development of drugs or medical devices. Utilizing OpenText™ Clinical Trial Quality Management System (ctQMS) allows organizations to maintain compliance, lower record management expenses, and foster collaboration to implement best practices throughout the entire clinical trial lifecycle. This strategic approach not only enhances operational efficiency but also contributes to the overall success of product development initiatives.

Stripe Revenue Recognition simplifies the process of accrual accounting, allowing for a swift and precise closing of your financial books. By automating and tailoring revenue reports, it aids in adhering to IFRS 15 and ASC 606 revenue recognition standards effortlessly. As your business expands, managing revenue can quickly turn into a cumbersome and error-prone task. That's why we've integrated a revenue recognition feature directly into Stripe, enabling you to automate the accounting process for your transactions and billing agreements. Our solution adeptly manages intricate situations, including upgrades, downgrades, prorations, refunds, and disputes without hassle. With reliable data at your fingertips, you can prepare financial statements that are ready for audits and attain a complete understanding of your business operations. You can easily access all your Stripe transactions and terms while also importing data from non-Stripe sources through the dashboard. Plus, you can generate accounting reports that come pre-configured, eliminating the need for dedicated engineering resources and allowing you to focus on what truly matters—growing your business. This seamless integration ensures that all aspects of your revenue accounting are handled efficiently, giving you peace of mind.

Combine and liberate your disorganized health information through an interactive AI and NLP solution that provides valuable health insights for various stakeholders. This innovative technology serves Providers by hastening the data abstraction process and ensuring the clinical information validation found within notes, thus minimizing the time and costs associated with identifying care gaps, assessing the quality of care through dashboards, and producing registry reports. For Payers, it facilitates the integration and analysis of claims alongside clinical notes, enhancing the management of high-risk and high-cost member populations. In the realm of Life Sciences, this solution enables swift patient matching to clinical trials using databases alongside clinical note data, maximizing the potential of real-world clinical evidence. Ember offers a comprehensive approach that merges NLP with predictive analytics, streamlining healthcare analytics for unstructured data to boost quality, efficiency, and outcomes in the healthcare system. As a result, stakeholders can make informed decisions that lead to improved patient care and resource allocation.

LexisNexis® MarketView™ provides medical claims-based insights tailored for healthcare payers, providers, life sciences enterprises, and health IT organizations throughout the United States. This platform offers actionable intelligence designed to enhance competitiveness, enabling businesses to uncover valuable insights and visualize transformative strategies. Regardless of whether you represent a life sciences firm, a health insurance plan, a healthcare system, or a health IT service provider, MarketView can significantly enhance critical business processes such as marketing, sales, strategic planning, physician engagement, outreach, market research, network optimization, talent acquisition, pricing strategies, contracting, and clinical management, among others. To stay ahead in the competitive landscape, your organization requires the most relevant insights available. However, determining the right areas to focus on can be challenging when the overall picture lacks clarity. MarketView addresses this issue by providing insights into various aspects such as referral trends, strategies for aligning with physicians, the performance of clinically integrated networks, and patient volume metrics, ultimately empowering organizations to make informed decisions. By leveraging these insights, businesses can drive innovation and improve their operational effectiveness.

Despite the advancements in AI technology, it remains flawed, prompting us to utilize our automated verification tools to evaluate AI models for safety and reliability while providing a warranty to ensure their efficacy. This allows vendors to market their AI solutions with greater assurance, and gives buyers the confidence that they can recover their investment should their AI model underperform. Armilla, our dedicated AI assessment and auditing service, fosters trust based on solid evidence in your AI solutions. Additionally, we safeguard against risks posed by third-party AI through our systematic model risk evaluations and thorough vendor assessments. As pioneers in AI and machine learning model auditing, we leverage state-of-the-art technology and automated testing methods to guarantee the dependability and security of your models, which ultimately enhances the accuracy of the underwriting process for our AI warranty. Whether you are a business owner or a consumer, it is natural to have reservations about the AI solutions available to you; thus, we are committed to addressing these concerns with transparent and rigorous evaluations. By prioritizing trust and safety, we aim to reshape the landscape of AI deployment and adoption.

Mednet is an eClinical technology company that specializes in healthcare solutions for the global life science community. Mednet's flexible, EDC-centric eClinical platform increases the efficiency of clinical research of all sizes. Mednet's comprehensive solution suite provides all the tools necessary to create and manage clinical research. It can also adapt to changing demands and requirements. Mednet has been trusted by CROs in every sector of the pharmaceutical, medical device, and biotechnology industries for almost 20 years. They provide the expertise, reliability, and innovation that they need to succeed. Mednetsolutions.com has more information.

Cytel stands out as a prominent global innovator in software for clinical trial design, biometrics, and advanced analytics, focusing on maximizing the efficiency of clinical trials while aiding pharmaceutical companies in harnessing the full scope of both clinical and real-world data. Established in 1987 by renowned statisticians Cyrus Mehta and Nitin Patel, Cytel has consistently been a leader in adaptive clinical trial technology and the field of biostatistics. Its software solutions, notably the East Horizon platform, facilitate accurate trial design and simulation, employing adaptive and Bayesian methodologies to enhance protocols and expedite the drug development process. The East Horizon platform serves as a comprehensive integration of Cytel's reliable software offerings, featuring R integration that significantly improves trial design functions. Furthermore, Cytel provides the Xact software suite, which is an all-encompassing toolkit designed for statistical analysis of small datasets, including those with sparse and missing data. By continuously innovating and expanding its product offerings, Cytel remains committed to providing cutting-edge solutions that meet the evolving needs of clinical research.

The deal management component captures the terms of agreements, establishes approval workflows, manages financial transactions, accommodates contract modifications, and maintains a historical record with an audit trail. Meanwhile, the rights management aspect facilitates the searching and creation of deals, organizes IP rights hierarchies, oversees advances and guarantees, tracks payment schedules, sets royalty rates, and performs collision checks along with rights clearance and holes analysis. The royalty management section is responsible for processing sales and usage data, calculating and verifying royalties both in and out, allowing for deductions or recoupments, addressing violations, providing analytical insights, and producing royalty statements. Additionally, the finance management module encompasses revenue recognition and accruals, expense oversight, a comprehensive accounting engine, an accounting sub-ledger, and seamless bi-directional integration with financial systems through ERP. This interconnected system enhances efficiency and accuracy across all financial and contractual dealings within the organization.

Flatiron Health's Evidence Solutions provide a versatile method for generating real-world evidence, both prospective and retrospective, which aids life sciences companies in efficiently meeting their oncology research objectives. At the heart of these offerings is Flatiron Horizon, a comprehensive platform that combines a rich database of more than 5 million anonymized patient records and 1.5 billion data points, coupled with advanced curation techniques and disease-specific machine learning models. This innovative platform is designed to facilitate various phases of the biopharma lifecycle, including discovery, clinical study design, regulatory submissions, and post-marketing commitments. Furthermore, Flatiron's services deliver customized real-world data configurations that cater specifically to oncology, enabling prospective evidence generation through minimally invasive studies and optimizing protocols for better patient identification. Additionally, the platform ensures a streamlined transfer of data from electronic health records to electronic data capture systems with the functionality of Flatiron Clinical Pipe, enhancing overall research efficiency and effectiveness. Such capabilities position Flatiron Health as a leader in transforming oncology research through the power of real-world data.

Efficiently generating reports for NGS-based clinical tests necessitates a well-established and sophisticated platform that can automatically prioritize variants, interpret clinical data, and create comprehensive reports. Strand Omics serves as a rapid, HIPAA-compliant cloud platform that enhances our clinical diagnostics efforts, having been refined over four years through the analysis of more than 10,000 clinical reports and numerous peer-reviewed studies. This platform integrates advanced bioinformatics algorithms with curated databases, intuitive visualization tools, and robust reporting features. It is designed with specialized workflows tailored for both rare inherited conditions and somatic tumor profiling assays. Additionally, the system boasts a library of over 10,000 somatic variants that have been curated for their oncogenic potential, alongside 100 genes selected for their druggability across various cancer types, as well as 500 drugs that have been validated for efficacy against multiple cancers. Furthermore, its comprehensive approach ensures that healthcare professionals have access to critical data, ultimately facilitating informed decision-making in patient care.

Reduce errors and save time. Receive real-time visibility into commission accruals, and payouts. Your rules can trigger payouts. Your data can be centralized in one source of truth. Our commission plan designer makes it easy to set up complex calculation logic. Trust is built with transparent and auditable commissions that are paid on time. Calculate commissions automatically in real time. You can save time and let your team concentrate on what is most important. Palette gives your sales team personalized performance dashboards that are updated in real time. This ensures transparency and visibility. Your commission data can be used to answer the most critical questions for your business. You can A/B test your compensation plans to see how they might impact your cash flow, and your business goals. Optimize ramp-up, set better quotas and budget commission costs, and forecast future payouts. Extract mission Critical insights

Orbiq serves as a Trust Center platform that transforms internal compliance efforts into externally verifiable evidence for buyers, auditors, and regulatory bodies. By linking their existing Information Security Management Systems (ISMS), SharePoint, Confluence, or Drive to a customized Trust Center (trust.yourcompany), companies can implement layered access controls—public, restricted, or NDA-protected—ensuring that each stakeholder has access to the appropriate level of information. Designed to meet the demands of the NIS2 and DORA regulations, Orbiq transcends traditional document sharing by offering features such as real-time vendor registers, incident reporting with detailed audit logs, AI-enhanced questionnaire answers, and ongoing monitoring, providing regulated companies with the necessary third-party visibility essential for modern procurement. Unlike other tools that primarily aim to minimize the number of questionnaires, Orbiq delivers a structured and always up-to-date proof layer that financial institutions, regulatory agencies, and corporate buyers now require and expect—stored securely in the EU, incorporating watermarking, download tracking, and comprehensive audit trails. By streamlining compliance and enhancing transparency, Orbiq empowers organizations to navigate the complexities of regulatory requirements with confidence.

Circit is a centralized platform designed for the collection of audit evidence and confirmations, aimed at enhancing the efficiency of audit and accounting firms, their clients, and evidence providers by automating and securing essential components of the auditing process. By automating the generation and handling of audit confirmation requests—including those related to banks, legal matters, and funds—directly from source systems, it significantly cuts down on time spent and manual efforts, while also boosting data accuracy and the overall quality of audits. The platform facilitates connections between auditors and various third-party providers such as banks, law firms, fund administrators, and custodians across the globe, delivering real-time access to verified transaction-level data, a comprehensive audit trail, and collaborative tools that enable teams and clients to communicate and address inquiries within the context of the audit, all without the need for email. Furthermore, Circit enhances the overall audit experience by ensuring that all stakeholders have access to pertinent information at their fingertips, thereby fostering a more transparent and efficient auditing environment.

MyAmici is a comprehensive cloud-based LabOps platform that consolidates procurement, inventory, purchasing, and supply-chain software specifically designed for biotech and life-science laboratories into a cohesive system. By linking the internal systems of a lab—such as ERP, inventory databases, supplier catalogs, and invoicing tools—with external vendors and suppliers, it facilitates real-time information exchange, allowing labs to uphold a dependable and consistent “single source of truth” regarding procurement, inventory levels, consumption patterns, invoices, and delivery updates. This seamless integration guarantees that any changes in product catalogs, order placements, deliveries, and invoicing are automatically aligned between the supplier systems and the internal lab records, thereby eliminating the need for manual data entry and significantly minimizing error risks. MyAmici adeptly manages complete lab procurement processes, encompassing requisition, purchase orders, order tracking, receipt handling, inventory management, and oversight of both assets and consumables. Furthermore, this platform enhances operational efficiency, ultimately contributing to more streamlined lab management and improved research outcomes.

Koop is an innovative platform that utilizes artificial intelligence to unify compliance, security, and insurance processes into one streamlined system tailored for tech-focused organizations. It accommodates prominent frameworks such as SOC 2, ISO 27001, HIPAA, and GDPR, providing expertly crafted policy templates, seamless integrations with over 200 different systems, and comprehensive audits conducted by vetted auditors based in the U.S. Users benefit from the ability to oversee contractual obligations, which includes extracting requirements, managing evidence, and tracking the status of counterparties. Additionally, Koop automates workflows related to third-party risks, encompassing vendor onboarding, outbound requirements, and trust monitoring, while also simplifying the management of security questionnaire responses, such as VSA, SIG, and CAIQ, through both standardized and customizable formats. On the insurance front, Koop facilitates the acquisition of essential coverage options, including general liability, cyber liability, technology errors & omissions, and management liability, ensuring that compliance efforts are integrated into the risk management framework to assist in securing advantageous insurance conditions. This comprehensive approach not only streamlines processes but also enhances the overall efficiency of tech companies navigating the complexities of compliance and risk management.

Revolutionizing medical coding and auditing through artificial intelligence, our platform enhances the efficiency of manual inpatient coding processes, elevates the quality of documentation, and empowers your team to concentrate on more valuable tasks. Leading hospitals are experiencing significant advancements thanks to Semantic Health’s innovative solutions. By leveraging bespoke clinical AI and natural language processing algorithms, developed from millions of medical records by our exceptional AI experts, we can analyze clinical and coded data with precision. This enables our coding and auditing systems to grasp intricate clinical contexts, adapt to evolving coding guidelines, and identify high-quality coding and auditing prospects, all supported by clear evidence from clinical documentation. By integrating AI into the traditionally labor-intensive processes of medical coding and auditing, you can save time and enhance your revenue cycle. Furthermore, Semantic Health provides hospitals and healthcare systems with a powerful inpatient auditing platform designed to conduct comprehensive pre-bill reviews of claims data, ensuring that every detail is meticulously checked before submission. Ultimately, this approach not only streamlines operations but also significantly reduces the risk of errors.

Clinithink stands out as a premier technology firm in the healthcare sector, focusing on artificial intelligence solutions that convert unstructured medical information into valuable insights. The company's proprietary CLiX platform leverages Clinical Natural Language Processing (CNLP) to decipher intricate clinical narratives, which empowers healthcare providers to improve both patient outcomes and operational productivity. Clinithink delivers customized solutions across various domains, including life sciences, revenue cycle management, and population health, effectively tackling issues such as identifying patient cohorts, maximizing reimbursement, and monitoring disease progression. With its cutting-edge technology, Clinithink has earned the confidence of top pharmaceutical and healthcare entities globally, establishing its leadership in the realm of healthcare AI and digital health progress. Moreover, the CLiX platform is adept at comprehending a wide array of unique and intricate clinical concepts, including but not limited to certainty, severity, laterality, and temporality, further enhancing its utility in clinical settings. As the demand for innovative healthcare solutions grows, Clinithink remains committed to advancing its technology to meet the evolving needs of the industry.

Agatha provides a comprehensive range of cloud-based solutions specifically designed for the life sciences sector, facilitating the centralized oversight of documents and processes related to clinical operations, quality assurance, regulatory compliance, and training activities. This platform caters to the workflows of biotech firms, pharmaceutical companies, medical device manufacturers, and contract research organizations by offering various modules, including eTMF (Inspection-Ready Master Trial File), Remote ISF (Investigator Site File) management, and tools for creating and approving standard operating procedures (SOPs) as well as managing quality documents related to CAPAs, deviations, and change controls. Additionally, Agatha enhances regulatory document handling, ensuring smooth document creation, review, approval, storage, and sharing within a single cohesive system. By promoting a paperless approach, it alleviates administrative burdens and bolsters data security, while being constructed on a global-compliance framework that meets critical standards such as 21 CFR Part 11, GDPR, and EU Annex 11. Ultimately, Agatha empowers life sciences organizations to optimize their operations and maintain compliance with industry regulations more efficiently.

Syntropy is a robust cloud-native platform specifically designed for healthcare and life sciences entities, facilitating the integration, harmonization, analysis, and optimization of intricate biomedical and clinical data. It provides a cohesive environment that merges internal silos with external partnerships, allowing for data orchestration accompanied by purpose-specific access control, comprehensive provenance tracking, and detailed governance. The platform supports complete workflows, starting from data intake and ingestion, progressing through semantic mapping and harmonization, and culminating in advanced analytics and workflow automation. This empowers researchers, clinicians, and partner organizations to extract valuable insights from extensive compound datasets while ensuring the integrity of the source data remains intact. Syntropy prioritizes transparency, accountability, and secure collaboration; data owners maintain control over their sharing preferences, all actions are meticulously audited and attributed, and the platform adheres to essential regulatory standards such as HIPAA, GDPR, and GxP. Ultimately, Syntropy aims to revolutionize how healthcare and life sciences organizations leverage data for improved outcomes and innovation.

Datatrak International, Inc. is a software-as-a-service provider of enterprise cloud-based technologies for the life sciences industry. Datatrak's unified eClinical solution and related services improve efficiency and cost effectiveness for the clinical trial industry. Datatrak developed its multi-component, comprehensive solution using a single platform. This concept was expanded to include services delivery through Datatrak's Clinical and Consulting Services groups. The Company offers a complete range of software products that can be used to speed up the reporting of clinical research data to sponsors and regulators. This is faster than using loosely integrated technologies. Our goal is to empower workgroups with role-based access, version-controlled file management and calendar events, tasks, and contacts. All built within our eClinical software applications, including EDC, CTMS and reporting.

The Medidata Clinical Cloud represents our innovative platform designed to revolutionize the clinical trial journey for patients, sponsors, CROs, and research institutions. As the sole comprehensive technology solution focused exclusively on clinical research, the Medidata Clinical Cloud addresses the entire research spectrum from inception to completion. Our platform enables organizations in the life sciences and medical device sectors to reduce development expenses, manage risks effectively, and expedite the introduction of treatments and devices to the marketplace. Whatever selection you make for your clinical trial initiatives, you will benefit from the capabilities of the Medidata Clinical Cloud. At Medidata, we are at the forefront of the digital evolution in clinical research. With the power of artificial intelligence, machine learning, and sophisticated analytics, our platform connects researchers, study coordinators, investigators, and patients, thereby hastening the research process. Additionally, it provides a regulatory-compliant, patient-friendly electronic informed consent solution for clinical trials, ensuring a smoother experience for all parties involved. This integration of advanced technology not only streamlines operations but also enhances the overall quality of clinical research.

AuditUtopia serves as a real-time Inspection Management System designed for hosting inspections and audits, gaining the trust of life science organizations across the globe. With features such as logging inspection notes, chatrooms, instant updates, and customizable request and scribe note reports, AuditUtopia simplifies the inspection process. It aims to be the cornerstone of your inspection and audit management strategy, enhancing efficiency and reducing response times for requests. As a preferred choice for many organizations, AuditUtopia® facilitates seamless collaboration within teams to improve the speed of responding to inspection inquiries. Our belief is that software should be both cost-effective and intuitive, enabling our clients to gain a competitive edge. By utilizing our system, you can effectively manage requests while ensuring that normal business operations continue uninterrupted. Whether you're conducting routine checks or comprehensive audits, AuditUtopia is your reliable partner in achieving operational excellence.

Genoox is revolutionizing the field of genomics through its dynamic and expanding community, which enables the accumulation of the most pertinent database and facilitates the delivery of actionable, real-world genomic insights that significantly affect lives, enhance clinical outcomes, and influence healthcare business practices. By harnessing community power, Genoox merges public data with community-generated information to optimize the journey from DNA sample to clinical report, thereby improving patient care through the accessibility and applicability of genomic data at critical moments. The company's innovative solutions are transforming the landscape of genomics, while also supporting research and life sciences enterprises with an insightful platform that leverages real-world data and evidence, bolstered by comprehensive genomic analytics, which assists researchers in simplifying intricate genomic information and achieving meaningful breakthroughs with cutting-edge genetic tools. Moreover, Genoox collaborates with biosystems firms like DNA sequencing companies to integrate its advanced genomic engine with specialized assays, further enhancing the capabilities of the entire genomics ecosystem. Ultimately, Genoox stands at the forefront of genomic innovation, consistently aiming to empower healthcare professionals and researchers alike.

From managing sales leads to generating invoices, overseeing customer deposits, tracking balances and receipts, and handling sales management, to all essential aspects of revenue oversight. This includes processes from purchase orders to acquisitions, advance requests to various expenses, reimbursements or settlements, as well as vendor balances and payments. The system supports dynamic management of products and variants, along with services and transactional items, project billing and reporting, and managing bills of materials to production and warehousing. It also integrates direct bank feeds and payment connections with prominent financial and payment service providers in Cambodia. Users can utilize four types of budgets to effectively track and report on budget performance. Both cash and accrual accounting methods are recorded within the same journal, providing a versatile reporting framework. Streamline your payroll operations and confidently prepare your tax and financial reports with ease. All necessary tools are at your disposal to effectively manage your business operations. Experience every feature of our online accounting platform without any obligation, as no credit card is required for a trial. Additionally, our user-friendly interface ensures that even those new to accounting can navigate the system easily.

FairPath is an innovative platform that leverages artificial intelligence for the management of remote care and compliance, aimed at empowering healthcare providers to effectively implement Remote Patient Monitoring, Remote Therapeutic Monitoring, Chronic Care Management, and Advanced Primary Care Management programs while maintaining complete control over revenue and ensuring readiness for audits. By eliminating the need for ambiguous vendor services that can siphon off profits and monopolize data, FairPath equips healthcare practices with essential tools that enable them to manage their own workflows, maintain data ownership, and ensure compliance documentation is readily available, all while automating various clinical operations and billing processes. Utilizing AI technology, the platform efficiently captures patient interactions and time spent, transcribes and summarizes outreach communications, evaluates patient eligibility, adheres to specific CMS guidelines (including minimum monitoring durations), and uncovers compliance issues prior to submitting claims, effectively minimizing the likelihood of audits and claim denials. Additionally, FairPath creates clear, verifiable claims and documentation records, complete with timestamped event logs, and seamlessly integrates with current electronic health records and operational workflows, fostering a more streamlined healthcare management experience. This comprehensive approach not only enhances operational efficiency but also contributes to improved patient care outcomes.

Oversee your clinical trial seamlessly through a single platform. Zapclinica offers an eClinical suite tailored to manage and execute every facet of your decentralized clinical trial—whether hybrid or entirely virtual. By automating intricate processes, it helps in spotting anomalies, optimizing resources, and enhancing decision-making alongside collaboration among sponsors, CROs, and study sites. This comprehensive solution significantly cuts down the time and expenses associated with running a successful clinical trial. With Zapclinica, you can handle all study components without the need for additional vendors or third-party services; instead, select the necessary applications within one unified environment, including EDC, ETMF, Payments, Logistics, and much more. Embrace the efficiency of a single platform to streamline your clinical research efforts.

Loftware Cloud Clinical Trials is a robust solution tailored to meet the stringent compliance needs of clinical trials. It enables organizations to efficiently manage the creation, approval, and distribution of clinical trial labels and booklets. With an intuitive interface, Loftware ensures adherence to regulatory standards, such as FDA and EMA, by providing templates, barcode functionality, and real-time updates. The platform's seamless integration with existing systems enhances productivity and reduces the risks associated with manual labeling processes, making it ideal for global clinical trial operations.