Next-Generation eCRF for Every Study Design
Design. Deliver. Discover.
Design studies your way
Audit-ready data you trust
Smarter insights, sharper outcomes
Streamline your clinical data collection process with our powerful eCRF SaaS (Software as a Service) platform. From customized study design to delivering compliant, audit-ready data, and uncovering actionable insights, we help you move faster and smarter.
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Proven. Trusted. Ready.
Recognized and trusted by sponsors and investigators, our platform has been proven across dozens of studies and countries. Built with precision, designed for confidence, and refined through real-world success, it empowers organizations to streamline research, ensure compliance, and unlock insights that drive meaningful impact— all at a truly global scale.
3,500+
investigators
50,000+
patients
14
countries
50+
studies
Role-Based Efficiency & Study Design
GoResearch™.live empowers clinical research teams with a flexible, intuitive electronic data capture (EDC) platform designed to streamline operations across every role. Whether you’re an investigator inputting data, a CRA monitoring remotely, or a project manager overseeing global studies, GoResearch™ implementation ensures seamless collaboration, greater accuracy, and accelerated study execution. From no-code form design to decentralized trial support, GoResearch™.live simplifies complexity at every step of your clinical trial journey.
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User-Centric Design
Tailored interfaces for investigators, monitors, data managers, and project teams for intuitive workflows. -
Study Design & Management
No-code eCRF designer for visit schedules and forms, plus integrated automated randomization and stratification module. -
Accessibility & Decentralized Trials
Mobile-enabled for eConsent, ePRO, and remote trial workflows, supported by multilingual capabilities.
Data Integrity & Interoperability
GoResearch™.live ensures your clinical data remains accurate, compliant, and actionable from capture to submission. With real-time validation, seamless integration, and intelligent reporting, GoResearch™ implementation enables research teams to maintain data integrity, enhance oversight, and meet evolving regulatory demands. Whether managing internal workflows or syncing with external platforms, GoResearch™.live keeps your data flowing securely and effortlessly—so you can focus on outcomes, not obstacles.
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Data Validation & Monitoring
Real-time Source Data Verification (SDV) for Risk-Based Monitoring (RBM), paired with advanced edit checks and queries modules. -
Advanced Analytics & Reporting
Customized or standard reports module to track trial progress at any level in real time. -
Integration Ready
API interoperability with ePRO/eCOA/eIC and external data sources (eSource), with CDISC data standards support for regulatory compliance.
Compliance and Security
GoResearch™.live is engineered with a deep commitment to protecting patient data and ensuring full regulatory adherence at every stage of your clinical trial. From global data privacy laws to rigorous GxP requirements, GoResearch™ implementation gives sponsors and sites the confidence to operate securely and compliantly. With validated development practices, certified infrastructure, and built-in safeguards, GoResearch™.live delivers the trust and transparency your studies demand—without compromise.
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Regulatory Compliance
Adheres to CFR 21 Part 11, GDPR, and Annex 11 guidelines. -
Validated Software
Developed under ISO 9001-certified quality processes and rigid Standard Operating Procedures (SOPs), ensuring reliability and consistency. -
Data Security
Hosted in ISO 27001-certified environments on a High Availability (HA) server cluster, with regular backups, encryption, and multi-factor authentication.
End-to-End Clinical Research Solutions
GoResearch™.live adapts to the full spectrum of clinical research—whether you’re running a tightly controlled Phase I trial or collecting post-market real-world data. With built-in flexibility and scalability, GoResearch™ implementation supports your study design of choice, from traditional site-based protocols to decentralized and hybrid models. By seamlessly managing diverse trial types within a single platform, GoResearch™.live empowers your teams to execute faster, more efficiently, and with greater confidence in every environment.
- Traditional Clinical Trials (Phase I-IV)
- Decentralized & Hybrid Trials
- Real-World Data (RWD) & Real-World Evidence (RWE)
About Us
At 2KMM, we drive innovation in the life sciences sector. GoResearch™.live is our answer to the industry’s demand for fast, precise, and reliable clinical research solutions. Built with deep sector expertise, our platform empowers organizations in healthcare, biotech, pharmaceuticals and medical devices to make smarter decisions, faster. We combine cutting-edge technology with a real understanding of market needs — helping you accelerate breakthroughs and shape the future of science.
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