Flex Databases platform
Who Is the Company Behind Flex Databases platform?
- Seller: Flex Databases
- Year Founded: 2011
- HQ Location: Prague, CZ
-
LinkedIn® Page: www.linkedin.com
71 employees on LinkedIn®
Total Products under this Category: 220
Last updated: November 01, 2026
Why You Can Trust G2's Software Rankings:
G2's software rankings are built on verified user reviews, rigorous moderation, and a consistent research methodology maintained by a team of analysts and data experts. Each product is measured using the same transparent criteria, with no paid placement or vendor influence. While reviews reflect real user experiences, which can be subjective, they offer valuable insight into how software performs in the hands of professionals. Together, these inputs power the G2 Score, a standardized way to compare tools within every category.

Highlighted products: OnCore CTMS, Viedoc, Clinical Research Suite, Florence eBinders, Rave CTMS, Clario CTMS, Vial EDC + eSource, and TrialKit.
Underlying data: [Grid® JSON](https://www.g2.com/categories/clinical-trial-management-systems/grids.json?focus%5B%5D=oncore-ctms&focus%5B%5D=viedoc&focus%5B%5D=clinical-research-suite&focus%5B%5D=florence-healthcare-florence-ebinders&focus%5B%5D=rave-ctms&focus%5B%5D=clario-ctms&focus%5B%5D=vial-edc-esource&focus%5B%5D=trialkit)
Flow Trials is an innovative platform designed to streamline the process of connecting patients with clinical trials. By leveraging advanced AI-powered natural language search capabilities, it enables users to effortlessly find and participate in relevant medical research studies. With a database encompassing over 20,000 clinical trials, Flow Trials simplifies the search and enrollment process, making cutting-edge medical research more accessible to a broader audience. Key Features and Functionality: - AI-Powered Search: Users can describe their medical conditions or interests in plain English, and the platform's AI will identify suitable clinical trials. - Comprehensive Database: Access to a vast collection of clinical trials, sortable by condition and location, ensuring users find studies that match their needs. - User-Friendly Participation: Detailed study information is provided, and users can easily express interest by clicking 'Participate Today' to connect with researchers. - Participant Dashboard: A personalized profile allows users to view study timelines and monitor their progress throughout the trial. - Patient-First Approach: Emphasis on trial safety, trust, and efficient processes, ensuring participants' wellbeing and convenience are prioritized. Primary Value and User Solutions: Flow Trials addresses the complexities and barriers often associated with clinical trial participation. By providing a seamless, user-centric platform, it empowers patients to engage in medical research that aligns with their health conditions and preferences. The platform's commitment to patient safety, accessibility, and ethical standards ensures that participants are well-informed and supported throughout their research journey. Ultimately, Flow Trials enhances the efficiency of clinical trial recruitment, contributing to the advancement of medical research and the development of new treatments.
Gethealthkey is a comprehensive health management platform designed to empower individuals in taking control of their well-being. By integrating various health data sources, it provides users with a holistic view of their health metrics, enabling informed decisions and proactive health management. Key Features and Functionality: - Personalized Health Dashboard: Offers a centralized interface displaying real-time health data, including vital signs, activity levels, and nutritional information. - Data Integration: Seamlessly connects with wearable devices, medical records, and other health apps to aggregate and analyze health information. - Health Insights and Recommendations: Utilizes advanced analytics to provide actionable insights and personalized recommendations for improving health outcomes. - Goal Setting and Tracking: Allows users to set health goals and monitor progress over time, fostering motivation and accountability. - Secure Data Management: Ensures user data privacy and security through robust encryption and compliance with health data regulations. Primary Value and User Solutions: Gethealthkey addresses the challenge of fragmented health information by consolidating diverse data sources into a unified platform. This integration empowers users to gain a comprehensive understanding of their health, identify potential issues early, and make informed lifestyle choices. By providing personalized insights and facilitating proactive health management, Gethealthkey enhances overall well-being and supports users in achieving their health objectives.
Connect G2 to Claude or ChatGPT for answers grounded in G2's trusted reviews, comparisons, and pricing from real user insights.
Next-generation eCRF & EDC software for faster, audit-ready clinical trials. GoResearch™.live (https://goresearch.live) is a cloud-based eCRF/EDC platform for clinical trials, observational studies, and patient registries. Supporting traditional, hybrid, and decentralized trial designs, it helps research teams move from study setup to compliant, audit-ready data faster. GoResearch™.live combines the simplicity of no-code study design with powerful clinical data management capabilities for studies of any scale. Build and personalize eCRFs in minutes. Capture high-quality data with instant edit checks, intuitive query management, configurable Source Data Verification (SDV) with Risk-Based Approach, and integrated randomization. Seamlessly connect ePRO/eCOA platforms, external data sources, and third-party systems through open APIs. Real-time dashboards, analytics, and customizable reports provide complete operational visibility, enabling faster, data-driven decisions throughout every stage of the study. Hosted on ISO 27001-certified infrastructure and developed under an ISO 9001-certified quality management system, GoResearch™.live is designed to support compliance with ICH GCP, 21 CFR Part 11, EU Annex 11, GDPR, and HIPAA requirements out of the box.
Health Studio is a clinical data platform built exclusively on Google Cloud. This low code platform allows organizations to build AI-enabled clinical solutions in a fraction of the time, unlocking all Google cloud resources and APIs with clicks not code. This allows organizations to introduce AI-enabled workflows and agent based applications with lower risk and cost and accelerate the time to realize the benefits. Further Health Studio's modular and customizable design integrates with existing technology, allowing customers to introduce this change in a pace that makes sense to their organization.
**HEKMA.ai** is an AI-powered clinical intelligence platform transforming how patients, healthcare providers, researchers, and life sciences organizations connect with clinical research. By combining intelligent patient matching, secure healthcare data integration, and advanced analytics, HEKMA.ai accelerates clinical trial recruitment, streamlines research workflows, and improves access to life-changing treatments. Committed to innovation, security, and inclusivity, HEKMA.ai is helping shape a smarter, faster, and more connected future for clinical research.
Hipp Health offers an AI-native platform that streamlines and automates behavioral health practice management operations.
Imagene AI is democratizing precision medicine with multi-modal foundation models and an end-to-end OI Suite.
ImproWise is your all-in-one, 100% web-based, secure, and HIPAA-compliant solution for Clinical Trial Management (CTMS) and Clinical Data Management (CDMS). Designed for flexibility, speed, and security, ImproWise integrates CTMS, CDMS, EDC, CTBM, CTPM, eTMF, ePRO, and RBACS functionalities, enabling rapid study setup, seamless multi-trial and multi-site management, and effortless customization. Our feature-rich and scalable platform caters to every stakeholder in clinical trials—from sponsors and investigators to data managers, site staff, and regulatory professionals—ensuring seamless collaboration, efficiency, and compliance at every stage.
Inductive EDC is a cost-effective & compliant platform to help you collect, analyse and manage clinical trials data in mammoth quantity reducing your dependency on the paper-based process. IEDC removes all the roadblocks to achieving a seamless data management environment that expedites your study, improves data quality, and complies with regulatory standards. Our EDC system allows you to configure the CRFs for any specific need including academic, biotech, and pharmaceutical study. It ensures greater data privacy and security, along with inherent compliance.
InfoEd Clinical Trials Software links trials to related protocols, grants, contracts, publications, conflict of interest information, and patents with a true clinical trial document management system. Accessible at any time, from any computer with Internet access, InfoEd’s Clinical Trials software and Clinical Trials Management System reduces administrative burdens and workloads with clinical data software by consolidating information in a single location that facilitates collaboration between all the research personnel supporting your trial.
Insight68 is a cloud-based platform for cell and gene therapy manufacturers, integrating clinical trial management, cell manufacturing, inventory control, and supply chain logistics. It supports personalized therapy workflows with real-time autologous CGT scheduling for patient dose manufacturing and supply chain coordination. Analytics aid in production planning, delivery optimization, and cost management. The inventory system tracks temperature, shelf life, and material levels to reduce waste and prevent shortages. A production scheduler aligns manufacturing with resource availability, capacity, and demand. Clinical trial tools manage patient enrollment, cohort monitoring, and site operations. Manufacturing features include scheduling, electronic batch records and real-time process monitoring. Modules Quality Management Systems (QMS), equipment logging, and electronic lab notebooks (ELN), and Asset Management. Insight68 is GAMP and 21 CFR Part 11 compliant with full audit trails.
Insight68 provides a cloud-based, AI-driven software platform and suite of applications tailored specifically for Cell & Gene Therapy, Biotechnology, and life sciences. The platform complies with regulatory standards such as FDA 21 CFR Part 11, GAMP, and GDPR, ensuring strict traceability, Chain of Custody (COC), Chain of Identity (COI), and complete audit trails. Insight68 has a full portfolio of offering which includes Inventory, Cell & Gene Therapy Scheduling, Clinical Trials Management, Electronic Batch Records, Electronic Lab Notebook, Order Management, Regulatory Compliant Collaborative Spreadsheet, and Quality Management.