GoResearch logo

GoResearch

by 2KMM · Since 2003
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ActiveAvailable globallyCloud
Quick facts
Vendor2KMM
Year launched2003
StatusActive
Location2KMM Sp. z o.o., ul. Strzelców Bytomskich 3, 40-310 Katowice, Poland.
Countries servedGlobal
Languages11
Integrations
Free tier
Free trial
Contact salesYES

About GoResearch

GoResearch is a project management software from 2KMM [designed for Life Sciences IT services]. It provides project planning, resource and budget management support, and profitability analysis so users can effectively manage their projects. Additionally, it supports project and task-based activity reporting and progress monitoring, along with offering a repository for document segregation and classification, versioning, and responsibility and time scope assignments. GoResearch allows teams to track project milestones and ensure alignment with budgetary constraints. Users can benefit from improved visibility into project performance and documentation management. Key capabilities: project planning resource and budget management progress monitoring document segregation profitability analysis Best for: Life Sciences organizations that need comprehensive project management solutions.

GoResearch.live is a highly-specialized, next-generation Electronic Data Capture (EDC) platform engineered to simplify and accelerate data collection for a variety of research initiatives, including clinical trials, observational studies, and patient registries. Its primary purpose is to provide a comprehensive and compliant solution that empowers research teams to execute studies faster and with greater confidence in data quality. A key strength of the software is its no-code design, which allows for the rapid creation and customization of electronic Case Report Forms (eCRFs) without requiring specialized programming knowledge. This feature significantly enhances its user-friendliness and accessibility, making it an ideal tool for professionals across various roles. The user interface is built with a user-centric approach, featuring tailored interfaces for different team members—such as investigators, monitors, and data managers—to ensure that workflows are intuitive and efficient. This design philosophy streamlines the entire data collection process, reducing potential errors and simplifying navigation for all users involved in a study. The platform's robust functionality extends beyond its user-friendly design to a comprehensive suite of features essential for modern clinical research. GoResearch.

Pros & Cons

What users like
  • +Strong regulatory compliance posture (21 CFR Part 11, GDPR, Annex 11).
  • +No-code eCRF design speeds study setup and reduces reliance on programmers.
  • +Real-time validation and RBM/SDV features improve data quality and monitoring efficiency.
  • +API/CDISC support enables interoperability with ePRO/eSource and downstream submission workflows.
  • +Hosted in ISO-certified environments with HA — good security and availability posture.
What users flag
  • Pricing details and public plans are not published on the site (requires contact).
  • No public marketplace or clear third-party app ecosystem listed.
  • Public documentation/knowledge base not visible (may require onboarding to access).
  • Specific country coverage and local regulatory/localization details beyond “14 countries” are not listed.
  • No obvious self-serve trial or public sandbox details visible on the site.

Features

Key features

Full Regulatory Compliance
Meets GCP, 21 CFR Part 11 and Annex 11, GDPR (site states adherence).
No-Code Study Build
Drag-and-drop/no-code eCRF designer for rapid form and visit schedule creation.
Real-Time Data Validation & Monitoring
Edit checks, real-time validation, SDV and RBM support for higher data quality.
Role-Based Interfaces
Tailored UX for investigators, CRAs/monitors, data managers and project teams.
API Interoperability
API-ready for integration with ePRO/eCOA/eIC, eSource and other external data sources; CDISC standards support.
Advanced Randomization & Stratification
Integrated automated randomization and stratification module.
Mobile & Decentralized Trial Support
Mobile-enabled eConsent/eIC, ePRO/eDiary and remote workflows with multilingual capabilities.
Real-Time Analytics & Reporting
Customizable/ready-to-use reports and dashboards for study progress and decisions.
High Security & HA Hosting
Hosted in ISO 27001 environments on HA clusters, encryption, backups, MFA.
Validated Software Development
Built under ISO 9001 quality processes and SOPs for validated delivery.

Additional features

User-Centric Design
role-specific UIs for investigators, monitors, data managers, PMs.
Study Design & Management
no-code eCRF designer, visit schedules, forms management.
Automated Randomization & Stratification
built-in randomization tools.
Accessibility & Decentralized Trials
mobile eConsent, ePRO/eDiary, remote workflows, multilingual support.
Data Validation & Monitoring
real-time SDV, RBM, edit checks, queries module.
Advanced Analytics & Reporting
standard and customizable reports, trial tracking.
Integration Ready
APIs for ePRO/eCOA/eIC, eSource, mHealth; CDISC compatibility.
Regulatory Compliance
CFR 21 Part 11, GDPR, Annex 11 compliance.
Validated Development & Quality
ISO 9001 processes, SOPs for software validation.
Data Security & Infrastructure
ISO 27001 hosting, HA server clusters, backups, encryption, MFA.
End-to-End Trial Support
support for Phase I–IV, decentralized & hybrid trials, RWD/RWE collection.

Pricing

Free trial
Free version
Request a quote
Promo Offer

Countries & Languages

Global
Countries served
11
Interface languages
12
Billing currencies

Interface languages

EnglishSpanishFrenchGermanItalianPortugueseDutchRussianChineseJapaneseKorean

Billing currencies

🇺🇸USD🇪🇺EUR🇬🇧GBP🇦🇺AUD🇨🇦CAD🇯🇵JPY🇨🇳CNY🇮🇳INR🇷🇺RUB🇧🇷BRL🇰🇷KRW🇲🇽MXN

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