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
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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™.live 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.

  • 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/eIC, ePRO/eDiary, and remote trial workflows, supported by multilingual capabilities.
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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.

  • 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.
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Compliance and Security

GoResearch™.live is engineered with a deep commitment to protecting patient data and ensuring full regulatory compliance 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 processes, certified IT infrastructure, and built-in safeguards, GoResearch™.live delivers the trust and transparency your studies demand—without compromise.

  • 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.
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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 (RWD). 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)
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Latest Articles

ISO/IEC 27001:2022 in Clinical Trials: Turning Data Security into a Quality Standard

ISO/IEC 27001:2022 in Clinical Trials: Turning Data Security into a Quality Standard

  • Edyta Jach
  • January 26, 2026

Data security in clinical trials underpins patient protection, data integrity, and regulatory compliance. ISO/IEC 27001:2022 provides a structured, auditable framework that supports these requirements.

Read More
ALCOA++ in Practice - A New Dimension of Data Quality

ALCOA++ in Practice - A New Dimension of Data Quality

  • Edyta Jach
  • November 7, 2025

ALCOA++ principles are no longer just a good practice — they are a regulatory expectation. Learn how to translate them into system and process requirements for data collection and management in clinical trials.

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Trustworthy technologies - how to ensure the credibility of clinical trials in the digital era?

Trustworthy technologies - how to ensure the credibility of clinical trials in the digital era?

  • Edyta Jach
  • October 27, 2025

Digitalization of clinical trials offers enormous opportunities, but also demands a new approach to quality and data management.

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Welcome to GoResearch™.live!

Welcome to GoResearch™.live!

  • 2KMM
  • May 27, 2025

We’re launching GoResearch™.live, our next-generation eCRF platform — designed to meet the needs of modern clinical trials!.

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About Us

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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.

Get to Know Us

Contact or Demo Request

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2KMM Sp. z o.o.
ul. Strzelców Bytomskich 3
40-310 Katowice
P O L A N D
NIP:
634-250-79-46
REGON:
278139461
KRS:
0000180575

tel:
+48 32 479 99 90
fax:
+48 32 479 99 91