Alternatives to ConcertAI
Compare ConcertAI alternatives for your business or organization using the curated list below. SourceForge ranks the best alternatives to ConcertAI in 2026. Compare features, ratings, user reviews, pricing, and more from ConcertAI competitors and alternatives in order to make an informed decision for your business.
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IQVIA
IQVIA
Thousands of organizations around the world trust IQVIA to speed drug development, ensure product quality and safety, improve commercial effectiveness, get the right treatments to patients, improve access to and delivery of healthcare, and ultimately drive better health outcomes. Reimagine clinical development by intelligently connecting data, technology, and analytics to optimize your trials. The result? Faster decision making and reduced risk so you can deliver life-changing therapies faster. With a foundation in data, advanced analytics, and expert insight, IQVIA brings specialized capabilities to customers across the healthcare ecosystem. Read and watch the latest from IQVIA data scientists, doctors, researchers, and other subject matter experts on the topics that matter to you. From industry trends to how we are applying our capabilities to help, you can find it here. -
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Castor EDC
Castor
Castor is a leading platform for clinical data management, offering advanced solutions for electronic data capture (EDC), patient-reported outcomes (ePRO), and eConsent. Designed to streamline clinical trials, Castor enables researchers to efficiently collect and manage data from multiple sources in a compliant, user-friendly environment. The platform also supports decentralized trials (DCTs), providing tools for remote patient recruitment, monitoring, and real-time data analysis. Castor is trusted by over 50,000 users globally, helping clinical research teams accelerate trials while ensuring high-quality data and regulatory compliance.Starting Price: $100.00/year -
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Genospace
Genospace
At Genospace, we understand that genomics is driving the development of precision medicine, yet scaling its delivery is an unsolved challenge. We’re here to help. Our platform is designed to make biomedical data meaningful and accessible to everyone, especially those on the front lines of care delivery. Arm your clinicians and researchers with the information they need to make informed decisions and join us in our mission of leveraging high-dimensional molecular data to improve individual patient outcomes and accelerate drug development and research. Large-scale population data is necessary for drug development and research. Conduct cohort-driven analyses to inform your research activities with the Genospace platform. We specialize in clinical trial research. Use the Genospace platform to match fragmented patient data to complex trial criteria and expedite patient accruals. Integrate genomic medicine into mainstream clinical care with the Genospace platform. -
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Tempus
Tempus
Tempus AI is a leading health technology company headquartered in Chicago, Illinois. Specializing in artificial intelligence and precision medicine, Tempus aims to revolutionize patient care by leveraging data and AI to develop personalized treatment plans across various medical fields, including oncology, cardiology, radiology, and depression. The company's comprehensive platform integrates genomic sequencing, clinical data, and AI-driven analytics to provide actionable insights for healthcare providers and researchers. We deliver a comprehensive view of your patients through our tissue and liquid tests, DNA and RNA sequencing, somatic and germline tests, tumor-normal matched profiling, and MRD and monitoring test options. We offer a fast, reliable platform for ordering Tempus tests, accessing patient insights, and utilizing our AI-driven technologies seamlessly. The first generative AI-enabled clinical assistant that provides access to patient insights directly at your fingertips. -
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Flatiron Horizon
Flatiron
Flatiron Health's Evidence Solutions offer a flexible approach to generating both prospective and retrospective real-world evidence, empowering life sciences companies to achieve their oncology research goals more efficiently. Central to these solutions is Flatiron Horizon, which integrates a vast repository of over 5 million de-identified patient records and 1.5 billion data points, advanced curation methods, and disease-specific machine-learning models. This platform supports various stages of the biopharma lifecycle, including discovery, clinical study design, regulatory submissions, and post-marketing commitments. Flatiron's services encompass real-world data configurations tailored to specific oncology needs, prospective evidence generation through low-interventional studies, protocol optimization, patient identification, and seamless EHR-to-EDC data transfer via Flatiron Clinical Pipe. -
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Charm Evolution
Magentus
Charm Evolution is an end-to-end oncology information management system that centralizes all chemotherapy prescribing and administration workflows to enhance safety, consistency, and accountability by replacing handwritten orders with digital prescriptions tracked through order adjustments and orphan management for accurate wastage reporting. It aggregates precise, secure patient records and treatment information from multiple sources into a single database, enabling informed, efficient decision-making at the point of care. An intelligent pathway engine automates treatment protocols, streamlines scheduling based on regimens, and supports adult and pediatric oncology and hematology with configurable treatment libraries, protocol validation, and clinical trial management. Integrated pharmacy management delivers bi‑directional compounder connectivity along with customizable worksheets and labels, while the scheduler optimizes resource allocation and reduces patient travel. -
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Ember
MetiStream
Unite and free your unstructured health data Interactive AI and NLP solution delivering health insights to Providers. Payers. Life Sciences. Interactive AI and NLP solution to unlock health insights from unstructured clinical notes data for: Provider. Accelerate data abstraction from and clinical validation of information contained in clinical notes. Decrease time and reduce costs required to identify care gaps, review care quality dashboards, and generate registry reports. Payer. Integrate and analyze both claims data and clinical notes to more effectively manage high risk and high cost member cohorts. Life Sciences. Rapidly match patients to clinical trials–and vice versa–using clinical trial databases and data from clinical notes. Leverage the power of real world clinical data and evidence. Ember is an end-to-end solution at the intersection of NLP and predictive analytics. Streamline. Healthcare Analytics for Unstructured Data to Improve Quality, Efficiency, and Outcomes -
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Genoox
Genoox
Through our diverse and growing community, Genoox accumulates the most relevant database and delivers actionable, real-world genomic insights that impact lives, improve clinical outcomes, and shape the business of healthcare. Our solutions are changing the face of genomics. Genoox uses the power of its community and combines public data with community data to streamline the path from DNA sample to clinical report, impacting patient care by making genomic data accessible and actionable at the point of care. Genoox enhances research and life sciences companies by providing an insight platform derived from real-world data and evidence and powered by our community with robust genomic analytics, helping researchers simplify complex genomic data and make impactful discoveries using the most advanced genetic tools and applications. Genoox helps biosystems companies such as DNA sequencing companies to bundle its state-of-the-art genomic engine with dedicated assays. -
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Sofpromed
Sofpromed
Sofpromed provides electronic data capture (EDC) systems for biotechnology, pharmaceutical, and medical device companies conducting phase I-IV clinical trials. An EDC system is a software tool used to collect, clean, and export data in clinical trials. Sofpromed’s EDC application is used in clinical trials worldwide across multiple therapeutic areas, including oncology, hematology, cardiovascular, metabolic, central nervous system (CNS), dermatology, infectious diseases, respiratory diseases, and pain, among others. Clear design, intuitive, and very easy to use. Quick data entry and navigation. Access control and data encryption. Fully web-based, no installations required. Daily data backups, seamless service. Works in multiple devices, browsers, and operating systems. Built-in monitoring, data management, and reporting tool. Meets HIPAA, GCP, and 21 CFR. Convenient billing model. monthly flat rate. -
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Cytel
Cytel
Cytel is a leading global provider of clinical trial design software, biometric services, and advanced analytics, specializing in optimizing clinical trials and assisting pharmaceutical companies in unlocking the full potential of their clinical and real-world data. Founded in 1987 by distinguished statisticians Cyrus Mehta and Nitin Patel, Cytel has been at the forefront of adaptive clinical trial technology and biostatistical science. Our software solutions, including the East Horizon platform, empower precise trial design and simulation, utilizing adaptive and Bayesian tools to optimize protocols and accelerate drug development. The East Horizon platform integrates key components of Cytel's trusted software portfolio into a unified solution with R integration, enhancing trial design capabilities. Additionally, Cytel offers the Xact software suite, a comprehensive toolkit for statistical analyses of small datasets, and sparse, and missing data. -
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AWS HealthOmics
Amazon
Securely combine the multiomic data of individuals with their medical history to deliver more personalized care. Use purpose-built data stores to support large-scale analysis and collaborative research across entire populations. Accelerate research by using scalable workflows and integrated computation tools. Protect patient privacy with HIPAA eligibility and built-in data access and logging. AWS HealthOmics helps healthcare and life science organizations and their software partners store, query, and analyze genomic, transcriptomic, and other omics data and then generate insights from that data to improve health and advance scientific discoveries. Store and analyze omics data for hundreds of thousands of patients to understand how omics variation maps to phenotypes across a population. Build reproducible and traceable clinical multiomics workflows to reduce turnaround times and increase productivity. Integrate multiomic analysis into clinical trials to test new drug candidates. -
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Amazon Comprehend Medical
Amazon
Amazon Comprehend Medical is a HIPAA-eligible natural language processing (NLP) service that uses machine learning to extract health data from medical text–no machine learning experience is required. Much of health data today is in free-form medical text like doctors’ notes, clinical trial reports, and patient health records. Manually extracting the data is a time consuming process, while automated rule-based attempts to extract the data don’t capture the full story as they fail to take context into account. As a result, the data remains unusable in large-scale analytics needed to advance the healthcare and life sciences industry and improve patient outcomes and create efficiencies. -
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Medidata
Dassault Systèmes
The Medidata Clinical Cloud is our cutting-edge platform that transforms the clinical trial experience for patients, sponsors, CROs, and research sites. As the only unified technology platform dedicated to clinical research, the Medidata clinical cloud addresses the holistic research process from start to finish. Our platform helps life science and medical device organizations cut development costs, mitigate risks, and deliver treatments and devices to market faster. No matter which products you choose for your clinical trial program, you will have access to the power of the Medidata Clinical Cloud. At Medidata, we’re leading the digital transformation of clinical research. Powered by artificial intelligence, machine learning and advanced analytics, our platform brings researchers, study managers, investigators, and patients together to accelerate research. Obtain regulatory-compliant, patient-friendly electronic informed consent for clinical trials. -
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Microsoft Cloud for Healthcare
Microsoft
Microsoft Cloud for Healthcare is a comprehensive platform designed to transform the healthcare industry through AI-powered solutions, data integration, and secure, connected experiences. The platform helps healthcare providers, payors, and life sciences organizations improve patient care, streamline operations, and enhance research capabilities. It offers tools for safeguarding sensitive data, optimizing clinical workflows, and improving patient engagement. Microsoft Cloud for Healthcare leverages actionable insights from unified clinical and operational data, enabling healthcare organizations to drive positive outcomes, increase efficiency, and reduce costs. -
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Deep Lens VIPER
Deep Lens
VIPER automates the screening process from remote patient identification (at the point of diagnosis) to qualified enrollment. Utilizing artificial intelligence, VIPER identifies and matches patients to precision trials in the narrow window of opportunity through lab-agnostic genomic data ingestion, EMR and pathology data in a way that is customized to both the patient and to the research. VIPER searches the customized matching engine to find the best available clinical trials for a patients’ specific diagnosis—at the time of diagnosis. Through workflow integration, VIPER sends real-time notifications of a patient's eligibility for available clinical trials to the entire care team in the narrow enrollment window. VIPER also provides real-time interactive dashboards with rich data mining capabilities to aggregate site and study level patient data to hit your study KPIs. -
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Dyania Health
Dyania Health
Our regulatory compliant platform empowers clinical research by algorithmically analyzing unstructured EMR data for life endangering conditions. We build technologies that expand access to the most Innovative Healthcare through Clinical Trials. We are a team focused on saving lives by providing access to healthcare therapeutic innovations that are still under investigation. We believe that every patient should be empowered and educated on their opportunities to participate in clinical trials that may offer therapies significantly saving or improving their lives. We are an advanced healthcare AI research company that have developed a computational-based platform to identify patients who match a complex set of criteria to participate in clinical trials. -
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TriNetX
TriNetX
TriNetX is a global health research network that connects healthcare organizations and life sciences companies to drive real-world research and accelerate the development of new therapies. By leveraging a self-service, HIPAA, GDPR, and LGPD-compliant platform, TriNetX enables users to access federated electronic health records, datasets, and consulting partnerships. This empowers the worldwide community to improve protocol design, streamline trial operations, refine safety signals, and enrich real-world evidence generation. The network encompasses over 275 million patients from 150 healthcare organizations across 25 countries, providing a vast and diverse dataset for research. Researchers have utilized the TriNetX network to analyze more than 26,000 protocols and present over 7,000 clinical trial opportunities to its healthcare members, significantly reducing site identification time in clinical trials by 50%. -
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Inspirata
Inspirata
Inspirata is an oncology-focused technology platform designed to optimize cancer service lines through accurate data reporting and operational efficiency. It helps healthcare organizations improve quality of care while driving revenue growth by unlocking the full value of oncology data. Inspirata uses advanced AI and automation to ensure timely, complete, and compliant cancer reporting for state and federal requirements. The platform enables real-time access to structured patient data to support research, discovery, and clinical trials. Automated casefinding and data abstraction reduce registry workload while improving accuracy. Inspirata also enhances patient navigation from diagnosis through survivorship. Overall, it empowers cancer programs to deliver better outcomes with lower operational costs. -
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MIRIO
DEEPLINK MEDICAL
Deeplink Medical has developed its offer around the MIRIO platform, which adjusts to the different use cases and needs of actors involved in medical imaging in oncology, in the clinic, and in routine. Our services rely on 3 different but complementary offers, MIRIO, a platform for the follow-up of solid tumors evaluations, and the therapeutic response of patients in oncology. The patient pathway allows a link between hospital facilities and liberal medicine. An Imaging CRO, for the follow-up of imaging data in oncological clinical trials. A scientific board supports the development of our solutions. Collaborative workflow platform structuring imaging data and radiological evaluations for patients with solid tumors allowing structuration of data in real-time (according to RECIST 1.1 and iRECIST) directly in investigation sites at the first creation of the data. Real-time evaluation of the therapeutic response of treatments according to international guidelines RECIST 1.1 and iRECIST. -
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Oncora
Oncora Medical
Improving the quality of care and outcomes for cancer patients requires collaboration between physicians, scientists, cancer centers, and patients. Oncora's intuitive software platform allows all stakeholders to capture and apply real-world data for all healthcare-related decisions, for the benefit of the patient. Our products are built for healthcare professionals dedicated to improving cancer outcomes. Simplify workflow, reduce documentation burden, and optimize treatment with intelligent patient care software. Capture and visualize regulatory-grade real-world data with intuitive and dynamic software tools. Measure quality and streamline operations to improve care with advanced reporting tools. Rigorous clinical research with top cancer care professionals. Intuitive, web-based software to power your cancer center. Data and software to accelerate clinical discoveries. -
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Altis Labs Nota
Altis Labs
Altis Labs announces launch of Nota – a clinical information platform to accelerate therapeutic R&D Nota leverages. AI to predict patient outcomes from imaging data so sponsors can better prioritize their most promising therapies. Nota enables researchers to operationalize clinical trial imaging data, access predictive imaging biomarkers, and accelerate R&D at scale. Using Altis’ cloud-based software platform powered by deep learning, biopharma can incorporate comprehensive outcome predictions at the image, patient, and cohort level to improve clinical trial design and more confidently anticipate clinical endpoints. Such insights have the potential to significantly accelerate development timelines, lower drug development costs, and improve the likelihood of trial success across therapeutic areas. -
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Clinithink
Clinithink
Clinithink is a leading healthcare technology company specializing in artificial intelligence solutions that transform unstructured medical data into actionable insights. Our patented CLiX platform utilizes Clinical Natural Language Processing (CNLP) to interpret complex clinical narratives, enabling healthcare organizations to enhance patient care and operational efficiency. Clinithink offers tailored solutions across life sciences, revenue cycle management, and population health, addressing challenges such as patient cohort identification, reimbursement optimization, and disease progression tracking. Clinithink's innovative technology has garnered trust from leading pharmaceutical and healthcare organizations worldwide, positioning it at the forefront of healthcare AI and digital health advancements. CLiX is capable of understanding a vast quantity of unique and detailed clinical concepts such as; certainty, severity, laterality, and temporality. -
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Suvoda
Suvoda
Suvoda is a global clinical trial technology company specializing in complex, life-sustaining studies in therapeutic areas such as oncology, central nervous system disorders, and rare diseases. Founded in 2013, Suvoda offers an integrated platform that includes Interactive Response Technology (IRT), electronic Consent (eConsent), electronic Clinical Outcome Assessments (eCOA), and ePatient solutions, all designed to manage critical patient interactions efficiently. Their patented software architecture ensures a seamless user experience, facilitating precise randomization, drug supply management, and real-time data collection. Committed to enhancing patient comprehension and reducing site burdens, Suvoda's solutions are built to adapt to the evolving complexities of clinical trials. Headquartered near Philadelphia, with offices in Europe and Asia, Suvoda has supported over 1,500 trials across more than 85 countries. -
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NVIDIA Parabricks
NVIDIA
NVIDIA® Parabricks® is the only GPU-accelerated suite of genomic analysis applications that delivers fast and accurate analysis of genomes and exomes for sequencing centers, clinical teams, genomics researchers, and high-throughput sequencing instrument developers. NVIDIA Parabricks provides GPU-accelerated versions of tools used every day by computational biologists and bioinformaticians—enabling significantly faster runtimes, workflow scalability, and lower compute costs. From FastQ to Variant Call Format (VCF), NVIDIA Parabricks accelerates runtimes across a series of hardware configurations with NVIDIA A100 Tensor Core GPUs. Genomic researchers can experience acceleration across every step of their analysis workflows, from alignment to sorting to variant calling. When more GPUs are used, a near-linear scaling in compute time is observed compared to CPU-only systems, allowing up to 107X acceleration. -
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Owkin
Owkin
Patients from around the world suffer from complex diseases and a staggering variety of symptoms. However, they share one thing in common: Patients have a need for faster development of safer and more effective therapies. Owkin’s mission is to empower researchers in hospitals, universities, and pharmaceutical companies to: understand why drug efficacy varies from patient to patient, enhance the drug development process, and identify the best drug for the right patient to improve treatment outcomes. Owkin Loop is the foundation of Owkin’s research platform: it connects medical researchers with high-quality datasets from leading academic research centers around the world. Owkin Loop is powered by the two main components of Owkin’s Software Stack: Owkin Studio, our machine learning platform, and Owkin Connect, our federated learning framework. Owkin medical research collaborations are in Oncology, Immunology and Cardiovascular diseases. -
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Verana Health
Verana Health
Verana Health is a real‑world data platform that transforms structured and unstructured electronic health record information into de‑identified, curated, disease‑specific data modules via its clinician‑informed and AI‑enhanced VeraQ population health data engine. Aggregating data from strategic partnerships with leading medical registries (including the American Academies of Ophthalmology, Neurology, and Urological Association), it encompasses over 20,000 clinicians and roughly 90 million patient records, providing near real‑time, high‑quality datasets to power real‑world evidence generation, clinical trial site and subject identification, clinician quality reporting, and medical registry management. Accessible through cloud services such as AWS Data Exchange and Amazon Redshift, the platform offers self‑service API access, an intuitive dashboard, and customizable cohort discovery tools, while advanced AI/ML algorithms, robust data quality assessments. -
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BEKhealth
BEKhealth
BEKhealth offers an AI-powered clinical research platform centered on its BEKplatform, a unified system that extracts, interprets, and standardizes structured and unstructured electronic medical record data, including labs, diagnoses, physician notes, pathology reports, and PDFs, into a searchable, longitudinal patient graph to help life sciences and healthcare organizations rapidly identify protocol-eligible patients and optimize trial feasibility, site selection, and recruitment workflows. It employs deep learning and natural language processing to transform disorganized clinical data into actionable insights with high accuracy, generating robust queries and patient cohorts that reveal more qualified candidates than traditional manual chart review and support feasibility analyses with real-time reports and dashboards that inform decisions across research networks. -
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Mediktor
Mediktor
Mediktor is the most accurate AI medical assistant for triage and prediagnosis. We carry out clinical trials in the real world with real patients, our AI solution is clinically validated. We understand your business and we adapt our solution to create the best value proposition, aligned with your goals. We have worked for the past 10 years with Top Health Companies around the world. Our award-winning clinical trials produce relevant, compelling, clinical evidence, setting a new gold standard in the industry. Our clinical trials are carried out in the real world with real patients. Our clinical trials are led by independent researchers who design the protocols, gather data and consolidate the results. Our clinical trials are published in leading scientific journals. Our system based on artificial intelligence (AI) asks you the questions a physician would. -
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OM1
OM1
OM1 uses AI and big clinical data to dramatically improve research efficiency and clinical decision-making through high performance predictive models. OM1 Patient Finder uses proprietary, cutting-edge AI technology integrated with the OM1 Real-World Data Cloud. It incorporates different aspects of patients’ journeys from our range of data sources to identify patients at the greatest likelihood of having the target condition. We’ve built an intelligent data cloud to enable different healthcare stakeholders to cost-effectively access, analyze, and use outcomes data in a more robust, clinically meaningful, and precise way. Quickly, accurately, and more cost-effectively get to research-grade information on effectiveness, value, and safety. Quantify outcomes and demonstrate value in risk-sharing and outcomes-based payment models. -
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Exigyn
Exigyn
The best way to predict the future is to create it. Exigyn brings a financial analyst to your fingertips. Generate clinical trial scenarios, pressure-test cash runway, and still have time for dinner. Optimize trial costs by leveraging key KPIs like patient enrollment, site performance, and cost per patient. Adopt our multidimensional database for precise, detailed tracking, even down to individual vendor names. Instantly refine financial forecasts, budgets, department structures, project listings, charts of accounts, and spending, all with a single click. Streamline personnel forecasting, align headcount with clinical milestones, and optimize your organizational structure. With intuitive tools for tracking roles, salary bands, and projected hires, you can plan for the future with confidence. Our solution integrates real-time data, automating clinical accruals to save you valuable time and resources. -
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CluePoints
CluePoints
CluePoints is a cloud-based AI-driven risk-based quality management and clinical data oversight platform that leverages advanced statistics, machine learning, and deep learning to improve the integrity, accuracy, and safety of clinical trial data and processes; it provides real-time anomaly detection and centralized statistical monitoring that identifies outliers and data risks traditional methods might miss, enabling teams to manage risks proactively and accelerate issue resolution in line with FDA, EMA, and ICH guidelines. It includes specialized solutions such as Risk-Based Quality Management (RBQM) for real-time risk detection, Medical & Safety Review (MSR) for consolidated review and query workflows, Intelligent Medical Coding to automate consistent clinical coding suggestions, Intelligent Query Detection (IQD) to streamline discrepancy detection, and tools like the Site Profile & Oversight Tool (SPOT) for adaptive site monitoring. -
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Veradigm Real-World Evidence
Veradigm
Veradigm Real-World Evidence (RWE) analytics platform is a cost-effective, software-as-a-service application that enables transparent and efficient analysis of real-world data. It is used by life science and clinical research organizations to explore and analyze EHR data at a granular level. The analytical platform follows OMOP standards, making it a more efficient and reliable way to generate real-world evidence. Use Veradigm RWE Analytics Platform along with data sourced from the Veradigm Network. The platform allows users to run analysis on patient populations in minutes, create reusable patient cohorts with terminology consistency across data sources, deliver repeatable retrospective studies, and conduct analysis on any dataset in the Observational Medical Outcomes Partnership (OMOP) Common Data Model (CDM), including Veradigm Network EHR Data. -
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Clinical Concepts
IVR Clinical Concepts
IVR Clinical Concepts specializes in providing virtual clinical trial technology and patient engagement solutions. Their offerings include electronic patient-reported outcomes and patient diaries, which aim to deliver better data with fewer errors, resulting in shorter timelines and lower costs. They also provide patient recruitment and outreach services, focusing on outreach, pre-screening, and real-time data collection. Their subject screening, registration, and randomization solutions are described as modular, custom, flexible, and configurable. Additionally, IVRCC offers clinical trial material management solutions designed to reduce workload while providing more control, as well as eClinical integration services to seamlessly thread data together. Their chart review services provide real-world data and clinical insights. IVRCC emphasizes custom, modular, and configurable solutions to improve the patient experience and optimize clinical trial success. -
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Carevive
Carevive
Carevive offers an EHR-integrated cancer care management platform designed to enhance patient outcomes throughout the cancer journey. The platform facilitates treatment planning by eliciting patient preferences, assessing clinical trial interests, and addressing physical and psychosocial issues to optimize decision-making. During active treatment, Carevive enables remote symptom monitoring through electronic patient-reported outcomes (ePROs), providing symptom self-management plans and guideline-driven pathways to improve quality of life and reduce hospital visits. Post-treatment, the platform supports continuous monitoring of patient-reported late effects and coordinates necessary care, including diagnostic tests for detecting new or recurrent cancers. Additionally, Carevive's applied analytics offer access to aggregated patient experience data for continuous quality improvement and support in oncology pragmatic research. -
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EDC Made Easy
AB Cube Germany GmbH
AB-Cube Germany GmbH, (formerly XClinical), is a leading European provider of eClinical technologies and the developer of the Marvin EDC platform. Marvin offers an integrated suite of clinical modules, including EDC, IWRS/RTSM, Medical Coding, ePRO, and advanced reporting tools, designed to support complex and oncology-focused clinical trials. With more than two decades of experience and a strong commitment to data quality, compliance, and innovation, AB-Cube Germany empowers sponsors, CROs, academic and research institutions worldwide to conduct efficient, high-integrity clinical studies. -
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Atropos Health
Atropos Health
Atropos Health provides on-demand evidence from real-world data to close evidence gaps in healthcare and life sciences. Proven to elevate clinical outcomes, accelerate research, and drive operational efficiency. Atropos Health rapidly transforms medical data into real-world evidence, closing evidence gaps in medicine and expediting research from months to minutes. Our core solution is a generative evidence acceleration operating system. We can securely install medical data and structure it for downstream use. Our powerful analytics tools can be used to generate evidence on demand. It can work on your data after a quick install, or immediately with our global evidence network of 160M+ patients’ records and evidence library of 10K past studies. Join top health systems and life science companies in partnering with Atropos Health to accelerate research, optimize clinical trials, inform clinical decisions, address care variation, and more. -
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Truveta
Truveta
Truveta is a health data and analytics platform dedicated to saving lives with data. By aggregating de-identified electronic health records from over 30 health systems, Truveta offers researchers access to comprehensive patient data, including clinical notes, images, and genomics. This extensive dataset encompasses more than 120 million patients, providing a representative view of patient care across the United States. Truveta Studio, the platform's integrated analytics solution, empowers researchers to analyze precise populations with powerful tools, including notebooks and dashboards, all within a secure, HIPAA-compliant environment. The platform's data is updated daily, ensuring timely insights into patient care and outcomes. Truveta's commitment to data quality is evident through its use of the Truveta Language Model, a large-language, multi-modal AI model designed to transform EHR data into clean and accurate data points for medical research. -
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Loftware Cloud Clinical Trials
Loftware
Loftware Cloud Clinical Trials is a comprehensive labeling and booklet management solution designed for the clinical trials industry. This platform helps streamline the creation, approval, and distribution of clinical trial labels, ensuring strict compliance with regulatory requirements such as FDA, EMA, and ICH. Loftware offers a centralized solution that manages labeling operations across global clinical trials, reducing errors, ensuring consistency, and improving overall efficiency. The software supports customizable templates, barcode generation, and integration with other systems to provide a seamless workflow throughout the clinical trial process. -
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LARVOL CLIN
LARVOL
The LARVOL CLIN platform delivers comprehensive, AI-powered data intelligence and analytics tailored for oncology and drug-development professionals by aggregating more than 100,000 cancer clinical trials along with detailed results, digitized Kaplan-Meier curves and forest plots, and real-time social-media reactions from over 5,000 oncologists. Users can search by condition, intervention, or trial ID within a single streamlined interface offering expert-curated insights and visual dashboards for data-driven decision-making. The system also covers conference tracking, biomarker and diagnostics databases, and market-intelligence reports from over 25,000 sources, including regulatory communications, clinical-trial registries, and scientific congresses. Built to support pharma and biotech teams in understanding trial outcomes, trends, mechanisms of action, biomarkers, and disease pipelines, the platform integrates deep search filters, heat-maps, real-time alerts, and more. -
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SciSpace BioMed Agent
SciSpace
SciSpace BioMed is a domain-native AI “co-scientist” for biomedical research that combines a vast literature database with 150+ integrated bio-tools and 100+ academic databases and software suites to streamline complex research workflows, from genomics and single-cell analysis to drug discovery and clinical genomics. It enables researchers to ask natural-language questions, ingest datasets, interpret variants or multi-omics data, design cloning or wet-lab workflows, reason about clinical or disease biology, and generate publication-ready outputs (e.g., figures, tables, and presentations) with full transparency and citations. Users can interact with scientific papers via “chat with PDF,” highlight confusing text, math, or tables, and get clear explanations, ideal for understanding difficult methods or concepts. For literature review or exploratory research, its AI-driven semantic search accesses millions of papers and returns citation-backed summaries.Starting Price: $12 per month -
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Inovalon ONE Platform
Inovalon
The industry-leading capabilities of the Inovalon ONE® Platform empower our clients and partners to succeed by leveraging extensive industry connectivity, massive primary-source real-world datasets, sophisticated analytics, and powerful cloud-based technologies to improve the outcomes and economics of healthcare. At the core of healthcare today is the need to aggregate and analyze large amounts of disparate data, garner meaningful insight from the results, and use these insights to drive material change in patient outcomes, business performance, and healthcare economics. Our analytics and capabilities are used by more than 20,000 customers and are informed by the primary source data of more than 69.5 billion medical events across one million physicians, 611,000 clinical settings, and 350 million unique patients. -
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assisTek
assisTek
AssisTek is a leader in innovative clinical technology solutions for clinical research, offering custom clinical software solutions to streamline and enhance patient data collection. With over 25 years of excellence, they have supported more than 800 clinical research trials across 46 therapeutic areas, including over 500 multinational Phase I–IV clinical trials. Their eCOA solutions are highly scalable, customizable, and efficient, powered by a proven, cloud-based technology platform. AssisTek's product suite includes TEK eCOA Tablet, designed to support any questionnaire used in a clinical trial, TEK eDiary for capturing patient-reported outcomes at home, TEK Configurator for building clinical trial projects from start to finish, and TEK Study Portal for eClinical tracking, training, and reports in one place. Their systems and services have made them the top choice for collection and analytics among patients and clinicians. -
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PicnicHealth
PicnicHealth
PicnicHealth connects patients and researchers to deliver the most complete, fit-for-purpose real-world data. By working directly with patients who contribute their medical data to research, we can build the most complete picture of patient health across all of their providers, not just one care site or specialist. Building the right cohort of patients is easy with our existing patient communities and rapid recruitment through dozens of established direct-to-patient channels. Patients sign up and consent to participate in 10 minutes and get access to their medical records. Do you have patients in ongoing registries or trials? Send them to PicnicHealth and we’ll get them set up. Our research platform delivers customized real-world data at the patient level. Specify the data elements to extract from medical records, including doctors' notes, narrative text, and more. Our unique, patient-centric approach to real-world data empowers patients to contribute more. -
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Reliant AI
Reliant AI
Accuracy, speed, confidence. Introducing generative AI to commercial biopharma. Simplify the labor-intensive process of collecting, organizing, and inspecting vast amounts of complex data. Get straight to decision-critical insights with 100% confidence, every time. With our AI-powered data manipulation and verification platform, you'll never lose track of your workstreams again. Gather, refine, and check your data, all in one place. Search public and private databases by key drug characteristics. Segment drugs and trials by detailed patient profiles. Extract the data you need in plain English. Support your findings by linking answers back to their source. Focus your time and energy on synthesizing high-quality outputs from data rather than menially sifting through it. Our specialized LLMs enable researchers to perform asset scans 4.8x faster than by hand. We index over 38M scientific publications, conference abstracts, and clinical trials. All the data you need, when you need it. -
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REDCap Cloud
REDCap Cloud
REDCap Cloud is a unified data-science platform that enables organizations to collect, integrate, standardize, analyze, and share real-world and regulatory-grade clinical and research data using a single standards-based system. It supports the full lifecycle of randomized clinical trials and real-world evidence studies by offering modules for complex trial design and deployment, a clinical data hub that converges eCRF and non-eCRF sources, real-time operational and data insights via AI/ML, eSource and EHR connectivity, patient engagement (ePRO/eCOA, wearable devices) for hybrid or decentralized trials, analytics including synthetic control arms and digital twins, and global compliance with security standards, all built to reduce data-silos, eliminate vendor fragmentation, deliver bidirectional data flows and give sponsors, CROs and health-systems end-to-end visibility and control across site performance, study data quality and regulatory readiness. -
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Partek Flow
Partek
Partek bioinformatics software delivers powerful statistical and visualization tools in an easy-to-use interface. Researchers of all skill levels are empowered to explore genomic data quicker and easier than ever before. We turn data into discovery®. Pre-installed workflows and pipelines in our intuitive point-and-click interface make sophisticated NGS and array analysis attainable for any scientist. Custom and public statistical algorithms work in concert to easily and precisely distill NGS data into biological insights. Genome browser, Venn diagrams, heat maps, and other interactive visualizations reveal the biology of your next-generation sequencing and array data in brilliant color. Our Ph.D. scientists are always just a phone call away and ready to help with your NGS analysis any time you have questions. Designed specifically for the compute-intensive needs of next-generation sequencing applications with flexible installation and user management options. -
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Leapcure
Leapcure
Leapcure is a leading patient recruitment and engagement platform that connects clinical trial sponsors with eligible patients. Utilizing advanced technology and strategies, we enhance trial participation and improve patient outcomes. Our platform streamlines the recruitment process, ensuring that trials are populated with suitable candidates quickly and efficiently. Leapcure is dedicated to advancing medical research by making clinical trials more accessible and effective. We work closely with sponsors and patients to facilitate smooth and successful trial experiences, ultimately contributing to the development of new treatments and therapies. -
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Claude for Healthcare
Anthropic
Claude for Healthcare is a HIPAA-ready AI platform built on Anthropic’s advanced Claude models that helps healthcare organizations move faster without sacrificing safety, accuracy, or compliance by connecting to trusted medical, payer, and clinical data sources. It enables use cases such as prior authorization review, insurance claims appeals, clinical documentation generation, patient message triage, care coordination, and other administrative workflows by validating provider credentials, medical codes, coverage requirements, and drafting recommendations or summaries with traceable sources for verification. Claude can integrate with industry standards and databases, including CMS coverage policies, ICD-10 codes, provider registries, and PubMed, and supports secure connection to personal health records (e.g., lab results and medical histories) with user consent so patients or clinicians can get plain-language summaries and insights.Starting Price: $17 per month -
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OpenText for Life Sciences
OpenText
OpenText™ Information Management solutions help life sciences organizations leverage insights from data and content to improve decision-making processes and accelerate product development. Integrate, manage, and securely exchange data across people, systems and things. Leverage information assets from R&D to commercialization. Freedom of choice with cloud-native software that can run anywhere. OpenText for life sciences accelerates the discovery process by extracting actionable insights that drive pipeline innovation. Capture and manage research papers into electronic lab notebooks with intelligent capture. Find insights with text mining. Extract knowledge trapped in the unstructured text contained in clinical trial reports, study protocols, clinical safety and efficiency findings. Find out how to intelligently analyze, classify and extract clinical trial documents to reduce the risk of costly stops and starts. -
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Inato
Inato
We’re building a global clinical trial marketplace to create greater visibility, access, and engagement across a more diverse population of doctors and their patients. At Inato, we’re on a mission to bring clinical research to each and every patient, regardless of who they are and where they live. Marketplaces have proven transformational in broadening access to many, we believe that we can achieve this in clinical research. We shine a light on the hundreds of community sites around the world that are looking to offer more trials to their patients, while helping them realize their full research potential. We reliably match the right sites to the right trial on a global scale. Our end-to-end support model ensures sponsors can confidently partner with a broader range of sites around the world. Matching research sites to the right clinical trial protocols, unlocking site potential worldwide.
