Sovos stands as an international leader in delivering tax, compliance, and trust solutions that empower businesses to confidently navigate a complex regulatory landscape.
With over 100,000 clients spanning more than 100 countries, including a significant portion of the Fortune 500, Sovos is a trusted partner for compliance solutions. The company processes upwards of three billion transactions each year across 19,000 tax jurisdictions worldwide. Supported by an extensive partner network comprising over 400 members, Sovos offers a matchless global resource for businesses across diverse industries and regions. Established in 1979, Sovos has expanded its operations throughout the Americas and Europe, and currently operates under the ownership of Hg and TA Associates. With a commitment to innovation, Sovos continues to adapt to the evolving needs of its clients, solidifying its position as a key player in the compliance landscape.
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Okyline is an Executable Data Design (EDD) platform that transforms validation contracts into executable operational assets for enterprise data quality.
Instead of multiplying specifications, custom validators, monitoring scripts, tests, and reporting layers, Okyline relies on a single readable contract shared across validation, quality control, and operational monitoring activities.
The contract itself becomes executable and directly drives deterministic validation, advanced business invariant verification, multi-format processing, data quality gates, operational metrics, and historical quality analytics.
Okyline validates APIs, enterprise events, files, streaming payloads, LLM structured outputs, and distributed data flows while continuously producing measurable quality indicators, completeness statistics, validation traces, and error propagation insights.
Because contracts are created from annotated sample data, validation rules remain immediately understandable for developers, architects, QA teams, integration specialists, and business analysts.
The Community Edition includes the public specification, a free Java validation runtime, a Claude AI assistant for contract generation, JSON Schema transpilation support, and a free online studio for executable JSON contracts.
The Enterprise Edition extends the same contract-centric model to native validation of JSON, JSONL, XML, CSV, FIXED, and EDI flows, combined with operational quality dashboards, data quality gates, and long-term quality tracking capabilities, all without requiring databases, warehouses, or centralized infrastructure.
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Medidata
The Medidata Clinical Cloud is an advanced platform crafted to transform the clinical trial experience for patients, sponsors, CROs, and research institutions alike. As the only all-encompassing technological solution dedicated solely to clinical research, this platform covers the entire spectrum of research from its initial stages to final outcomes. It empowers organizations within the life sciences and medical device industries to cut down on development costs, effectively manage risks, and accelerate the launch of new treatments and devices into the market. Regardless of your choice for clinical trial strategies, the advantages of the Medidata Clinical Cloud will be at your disposal. Medidata stands at the leading edge of the digital transformation in clinical research. By harnessing the capabilities of artificial intelligence, machine learning, and advanced analytics, our platform facilitates connections among researchers, study coordinators, investigators, and patients, ultimately speeding up the research process. Furthermore, it features a regulatory-compliant and patient-centric electronic informed consent solution for clinical trials, which improves the experience for everyone involved. This seamless integration of cutting-edge technology not only optimizes operational efficiency but also significantly uplifts the overall quality and integrity of clinical research endeavors. Thus, adopting the Medidata Clinical Cloud means embracing a future where clinical trials are more efficient and patient-focused than ever before.
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ClinCapture
ClinCapture aims to develop software that has the potential to save lives. Their innovative technology not only lowers the expenses associated with clinical trials but also enhances the efficiency of data collection while ensuring the confidentiality of patient information. Additionally, ClinCapture serves as a comprehensive platform that supports the assessment and advancement of drugs, biologics, and medical devices, which can address a diverse range of health issues. By prioritizing both cost-effectiveness and patient privacy, ClinCapture is dedicated to improving the overall landscape of clinical research.
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