Alternatives to Progeny Clinical

Compare Progeny Clinical alternatives for your business or organization using the curated list below. SourceForge ranks the best alternatives to Progeny Clinical in 2026. Compare features, ratings, user reviews, pricing, and more from Progeny Clinical competitors and alternatives in order to make an informed decision for your business.

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    ClinCapture

    ClinCapture

    ClinCapture

    At ClinCapture our mission is to build software that saves lives. Our technology lowers the cost of clinical trials by streamlining data capture processes while providing a platform that protects patient privacy. Clincapture advances the evaluation and development of drugs, biologics, and devices that demonstrate promise for the diagnosis and/or treatment of a wide range of diseases or medical conditions.
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    Komodo Health

    Komodo Health

    Komodo Health

    At Komodo Health we combine the world’s most comprehensive view of patient-encounters with innovative algorithms and decades of clinical expertise to power our Healthcare Map, the industry’s most precise view of the U.S. healthcare system. With the Healthcare Map as our foundation, we offer a suite of powerful software applications that enable you to deliver exceptional value to your customers, your colleagues, and your patients. Building your strategy using scholarly data alone is a thing of the past. Aperture was designed from the ground up to provide the most powerful view of clinical leadership and influence to drive standards of care where they matter most – whether that’s the most highly-cited author, the Twitter influencer, or the physician who sees the most patients. Open/sampled Rx & patient-level data often miss the patterns that accurately identify patients with complicated care pathways or rare diseases.
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    Volpara Health

    Volpara Health

    Volpara Health

    Facilities use Volpara Health software for early detection of breast cancer, including top US cancer screening centers. Mammography technologists rely on Volpara Health to improve mammogram quality. The most scientifically validated screening software in the breast health industry. Volpara gives you the evidence you need, right when you need it. Access to patient data for more informed breast cancer risk assessment. Each and every image we analyze improves our algorithms for early detection of breast cancer. Your aid in advocating for additional screening or genetic testing of patients. Build worklists and reports to individual preferences. Simultaneously access stats and lists from a single screen. Standardize communications for patients, referrers, and insurers. Send more compelling result letters with mammogram thumbnail images.
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    Color

    Color

    Color

    Color offers one of the most accessible, clinical-grade genetic testing services available today, analyzing genes associated with risk for common cancers and heart conditions — and how the body may process certain medications. We provide a suite of services, tools, and expertise to help you enroll new patients and activate them into care journeys relevant to them over time. We use a more complete view of patient health, incorporating an individual’s genetics, personal & family health history, and lifestyle & behavior information to surface and recommend specific care or point solutions that patients can take advantage of based on their personal risks.
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    2bPrecise

    2bPrecise

    2bPrecise

    2bPrecise delivers transformative point-of-care solutions that serve as the foundation for scalable precision medicine success. Patient not responding to first-line treatments for common conditions? Pharmacogenomics helps you identify medications that are safer and more effective. Fingertip access to test results helps eliminate “trial-and-error” prescribing practices, and accelerates patient response. Detailed genetics-focused data-gathering tools help you capture and expose risk. In-workflow Pedigree visualization allows you to identify candidates that could benefit from genetic testing, and lead you to the best course of treatment. Patient presents you with a diagnostic dilemma (e.g., symptoms such as seizures or syncope correlated with multiple conditions)? Germline tests hone in on heritable factors that can inform diagnoses. Access to meaningful and actionable results during clinical decision-making enables you to initiate preventive measures.
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    WRRisk

    WRRisk

    Whiterabbit.ai

    The product assigns a risk rating to a patient to drive a digital personalized screening plan for more consistent follow-up recommendations and more accurate diagnosis. This approach helps to catch cancers in the women that are at the greatest risk. WRRisk serves as a fully digital breast cancer risk assessment combining patient completed digital forms with a density assessment to provide a unified risk scorecard. WRRisk simplifies breast risk program maintenance by eliminating paper and automating many of the manual steps, from collecting forms to letter generation. The product equips patients and providers with the information they need. WRRisk Calculates 10-year and lifetime risk as well as risk-based on runner-up density.
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    Breeders Assistant
    Breeders Assistant (BA) is a specialist animal pedigree, record-keeping, and genetics analysis application for Windows 10 and Windows 11. At its simplest, it is used to produce high-quality pedigree certificates and store all breeding records in a private pedigree database held locally on your computer. BA has many advanced genetic features, including very fast inbreeding calculations. With the extended edition, it can prioritize prospective matings in a number of ways to minimize the inbreeding that would result from the mating, to maximize the influence of specific individuals within the breeding population, or to minimize the loss of genetic diversity by minimizing mean kinship. BA is supplied in several versions carefully tailored for the specific needs of breeders of pedigree cats, dogs, horses, and many other species. There is also a generic version that can be used for any animal type where a specific custom version is not provided.
    Starting Price: $125.91 one-time payment
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    Aurora

    Aurora

    Boston Advanced Analytics

    For technological efficiency, data analytics and medical necessity, Aurora is currently used by leading hospitals in the US and Europe to manage all aspects of patient IVF cycles and perform research on Cardiomyopathy patients. The science of medicine, the disease, and the decisions to be made will all change. Our software is flexible, built to allow quick and easy changes specific to your organization’s needs and standards of procedure. A 360 degree view of patient data is required for effective treatment decisions. This includes phenotype and genotype data, test and lab results, family histories, pedigrees, and text reports. All clinical data is collected, analyzed and presented in one package. Clinician can search and view in multiple ways including full display of longitudinal studies. Products are designed by software and data engineers, working closely with clinicians in each specialty.
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    FICS

    FICS

    Pi Health

    Accelerating the development of lifesaving medicines and enabling patients globally to have equal access to the highest quality of cancer care and research. Our software is revolutionizing patient access to innovative medicines & clinical trials. FICS is an innovative software that enables the collection of regulatory standard data during patient care. FICS brings together traditionally separate and non-communicating applications into a novel, end-to-end platform, paving the way for clinical trials to be done easier, faster, and with great quality.
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    Carevive

    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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    Oncora

    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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    Complion

    Complion

    Complion

    Complion’s platform is the accepted standard built specifically for clinical researchers. Our solution ensures the highest level of compliance with the greatest efficiency and the least amount of work. Allowing you to focus on what really matters — advancing and improving patient outcomes. Whether you are a Research Site, Sponsor or CRO, our eReg solution can help you address any type of clinical trial challenge, now and in the future. Reduce costs, avoid redundancy, and increase staff productivity. Easily archive, get signatures and view files from anywhere or from any device. A built-in audit trail ensures accuracy and eliminates study conduct and patient safety risks. Our clients include leading cancer centers, medical centers, hospitals, and health systems, as well as multi-specialty practices and dedicated research sites.
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    The Galen Platform

    The Galen Platform

    Ibex Medical Analytics

    Ibex Medical Analytics is the pioneer in AI-powered cancer diagnostics in pathology. We are a multidisciplinary team of entrepreneurs, data scientists, software engineers and medical experts, working together to realize our vision is transforming cancer diagnostics with AI and improving patient care. Pathologists are challenged to provide accurate and timely analysis as the number of tests increases every year. Ibex uses artificial intelligence (AI) to develop clinical-grade solutions that help detect cancer as accurately as a human pathologist. Galen Platform uses algorithms to analyze images, detect and grade cancer in biopsies and point to other findings with high clinical importance, helping pathologists reduce diagnostic error rates and enable a more efficient workflow. Ibex’s Galen™ Prostate and Galen™ Breast are the first-ever AI-based cancer detection solutions used in routine clinical practice in pathology labs, with demonstrated success in detecting missed cancer cases.
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    Omda Cytodose
    Omda’s oncology medication management solution, Omda Cytodose, uses clinically validated protocols and patient parameters to secure optimal and safer treatment for oncology patients. The system strengthens all aspects of medical care for cancer patients, with a holistic and coherent treatment flow between doctors, pharmacists, and nurses. Omda Cytodose provides support for all adult and pediatric cancers and is suitable for every type of medical cancer treatment, including chemotherapy, immunotherapy, hormone therapy, as well as supportive medication. Originally developed by clinicians at Norway’s leading cancer center, and launched in 2001, Omda Cytodose is widely used by healthcare regions across the Nordics, with millions of orders completed. It has a 15-year record of stability, reliability, and safety. Omda Cytodose is configured with clinically validated chemotherapy protocols based on national and international guidelines.
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    PedigreePoint

    PedigreePoint

    PedigreePoint

    Use PedigreePoint software to put your database on the web so others can search and display pedigrees and other reports pertaining to an entry. Typically you would use a desktop application to maintain your pedigree database then, when you're ready, publish any updates to the MySQL database used by PedPoint so users of your website can see it. A sample of the pedigree view is shown below. It shows how PedPoint can display photos and also what we call marks which are the solid blocks of color in some of the cells. These can be used to indicate that an entry has for example some genetic defect. PedigreePoint installs on a website and is written in PHP. It connects to a MySQL relational database which is usually located on the same server as the website.
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    Jeeva eClinical Cloud

    Jeeva eClinical Cloud

    Jeeva Informatics Solutions

    Jeeva's patent-pending modular solution is designed from the ground up on the most powerful cloud platform with one login from any browser-enabled mobile device for remote patient screening, education, enrollment, electronic informed consent, bi-directional communications via video calling, telemedicine, SMS, email, and evidence generation including electronic patient-reported outcomes and clinical outcomes assessments, with a modern user experience. Delays in patient recruitment & retention are keeping them up at night. Generating enough evidence of safety and efficacy of investigational new medicines is critical to get timely approval from regulatory agencies. Whether you are a patient group setting up a registry or natural history study, or a biopharma sponsor of a clinical trial, or a long-term follow-up study for gene therapy, Jeeva can save you time, and money while improving user experience for study team and trial participants.
    Starting Price: $100/mo/user
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    Medidata

    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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    The Breeder's Standard

    The Breeder's Standard

    PedFast Technologies

    ​The Breeder’s Standard® 2025 by PedFast Technologies is a comprehensive dog breeding and kennel management software designed to streamline and enhance the operations of breeders. It offers dynamic dog records with customizable fields, allowing for efficient data entry and management. The software includes a robust titles management system that accurately displays titles on pedigrees, and supports up to 65,535 photos per animal. With the PedFast™ V feature, users can rapidly enter five generations of ancestry from a single window. The Pedigree Hole Finder™ assists in identifying and filling missing ancestral information, improving both printed pedigrees and genetic calculations. Additional features encompass tracking of heats, matings, litters, and puppies, including day-by-day temperature and weight monitoring. Medical records management is facilitated through modules for vet visits, vaccinations, and medications.
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    Pedigree Assistant
    Pedigree Assistant (PA) is an app for Windows for breeders of cats, dogs, and other animals who need to print high-quality pedigree certificates. It stores the underlying breeding data so you do not need to re-enter it when adding new pedigrees. Pedigree Assistant is, in effect, like a very cut-down version of Breeders Assistant that dispenses with most features apart from producing pedigrees and storing basic animal records. It has a similar interface, though somewhat simplified to its primary purpose of producing good quality pedigrees designed to be printed. If you need other features beyond printed pedigrees you should consider Breeders Assistant. Pedigree Assistant is designed for single-user use, where the data is stored locally on your computer's hard drive, and accessed from one user account. Multi-user access of the type you seek is not available with this product. Support includes any updated releases that are released during the support period.
    Starting Price: $125.91 one-time payment
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    Qritive

    Qritive

    Qritive

    Making cancer diagnosis fast, accurate, and affordable. During our lifetime, 1 in 3 of us will get cancer. But cancer diagnosis is slow and expensive because doctors are not equipped with modern automated tools. Qritive provides an AI-powered solution to help doctors analyse both microscopy images and text from patient data. As a result, hospitals will be more efficient in making cancer diagnoses, allowing them to save costs. Pantheon is a CE marked vendor-agnostic digital pathology platform that enables digitization of the entire pathology lab workflow and telepathology, supports rich report generation, and provides a platform for AI analysis of pathology whole-slide images. Differentiates a wide range of benign diseases and malignancies in breast tissue.
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    Medable

    Medable

    Medable

    Medable is a software solution for researching and conducting clinical studies through a decentralized platform. The software aims to actively involve patients-contacted remotely-for obtaining the most reliable results possible. Patients can also remotely provide consent for digital examinations, and the application adapts to local languages and regulations. Right-size how your protocol is decentralized with our flexible, modular digital and DCT platform. Enable remote screening at scale, globally. Meet your studies enrollment targets faster. Develop any screening assessment. Improve consent readability with responsive layouts on web, mobile, & more. Deliver remote eConsent to patients on par with consumer digital experiences. Accommodate local regulations and languages with global flexibility. Engage patients and remove the burden of time and travel of an on-site visit. Improve patient access and engagement.
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    Liquid State Patient Engagement Platform
    Support the Patient Journey. Engage, educate and empower patients by improving your health communications. Patient Engagement Platform. Create Optimal Care Plan Establish optimal care plans for each medical pathway e.g. prostate cancer, breast cancer etc. Create Patient Engagement Pathway. Create a pathway grouping the communication rules that align with the optimal care plan. Organize Communications. Create or source communication pieces (messages, documents, videos etc.) to support various stages of the care plan. Communication Rules Create a set of communication rules detailing ‘who’ will see ‘what’ and ‘when’, delivering the communication pieces. Match Patient with Pathway. Adding a new patient to the system is a simple matter of matching their presentation with the suitable pathway. Consolidate. Bring together all patient facing communications into the one place. With the Patient Engagement Platform, you can deliver messages, documents, forms, videos, health widgets
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    Clinical Concepts

    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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    Sano

    Sano

    Sano

    Sano Genetics provides an end-to-end, 360° platform for precision-medicine and clinical-trial research that unifies patient recruitment, genetic testing, consenting, and long-term engagement to dramatically speed up and simplify study workflows. It supports custom protocol development and ethics submission documentation, digital prescreening and consent, and recruitment support through online campaigns, partner networks, and patient-advocacy groups, enabling sponsors and CROs to reach niche patient cohorts or underrepresented populations across multiple geographies. Sano offers at-home, non-invasive saliva-based DNA testing kits (as a cost-effective alternative to clinic blood draws), logistic support for sample collection and processing, reliable genetic and biomarker testing via certified labs, bioinformatics, and return of results, including genetic counselling when needed.
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    Evagene

    Evagene

    Evagene

    Clinical-grade pedigree analysis, finally in your browser. Evagene unifies pedigree drawing, clinical data modelling, Bayesian risk analysis, and AI-powered clinical interpretation in a single platform. Standard ISCN/HGNC notation. Integrated BayesMendel engine (BRCAPRO, MMRpro, PancPRO). A 180+ disease catalog with ICD-10 and OMIM codes. Blood type and trait inference from 23andMe SNP data. Zero installs.
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    OnCore

    OnCore

    Advarra

    Gain visibility into all aspects of your research operations with a comprehensive, proven, and standardized clinical trial management system built through collaboration with leading academic medical centers and cancer centers. Centralize billing designation information to ensure consistency across multiple teams and systems. Improve your budgeting process, route charges correctly, and conduct more accurate auditing/monitoring of billing compliance. Gain visibility and insight into all aspects of clinical research, including comprehensive financial management, with a standardized system built in collaboration with top research institutions. Integrate OnCore with your current EMR, including turnkey interfaces with Epic and Cerner, to increase patient safety, reduce duplicate data entry, enhance billing compliance, and increase operational efficiency.
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    Noona

    Noona

    Varian

    Noona® is a patient outcomes management solution designed to engage patients in their care with real-time symptom reporting and monitoring, streamlined clinical workflows to promote evidence-based care, and access to rich data insights for better management and ongoing assessment over the course of care. Patients can report symptoms, respond to questionnaires, and communicate with their care team as often as they would like. Care teams collect highly specific, detailed information tailored to a patient’s diagnosis and treatment type for more informed decision-making. With automated prioritization, care teams can intervene with patients who have the most critical need. Over 31 available treatment modules that cover over 97 common cancer types and 244 rules-based algorithms driving assignment of symptom severity based on published guidelines. Remote deployment capabilities for fast go-live capabilities and immediate patient use.
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    Clario eCOA
    Unlock better evidence with high-quality ePRO and eClinRO. Electronic Clinical Outcome Assessments, or eCOA, measure how patients feel or function during clinical trials. By capturing clinical data electronically, you can be confident that your patient’s data is high-quality and regulatory-compliant. Put simply, eCOA avoids the quality and time issues associated with paper diaries, such as illegible answers, transcription errors and inconsistent or conflicting data. Also, the FDA recommends ePRO. Patient-reported outcomes, patients report on their health via questionnaires or assessments. Examples include quality of life or activity outcomes. The clinician reported outcomes. Health outcomes are reported by a clinician. An example may include a physical examination such as PASI. Performance outcomes are measures from specific tasks the patient is asked to perform. An example might be performing a timed task.
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    Deep Lens VIPER
    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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    Arone

    Arone

    Arone

    With over 20 years of experience in both software edition and clinical research sectors, Arone provides clinical research organizations with a complete suite of tools for patient data entry and management. Our solutions are turnkey and our team provides you with personalized support for the proper conduct of your projects and studies. Collect and manage patient data in a single tool. Arone manages the randomization of patients by randomly assigning study participants a type of treatment in order to remove bias in the study. Empower participants of clinical trials for their daily data entry. Benefit from a customized support for your projects.
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    Valar Labs

    Valar Labs

    Valar Labs

    Many decisions in cancer care are uncertain and current tools are not helping the majority of cancer patients. This is leading to unnecessary loss of life and billions of dollars of wasted cost. We are a team of multidisciplinary computer scientists and oncologists helping tackle the most pressing questions in cancer care through AI. We are building clinical grade deep learning to analyze each patient's characteristics and provide clarity to oncologists during decision making. Our AI is built with oncologists at the center and provides interpretable and actionable insights. We work with top academic medical centers and community oncologists to answer clinically important questions.
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    Clin'form

    Clin'form

    Kayentis

    Clin'form is a flexible, robust, and comprehensive electronic Clinical Outcome Assessment (eCOA) platform designed to streamline clinical trials for patients and sites, enhance data quality, and accelerate processes for research teams. It is adaptable to all protocols and populations, effective for any type of questionnaire (PRO, ObsRO, ClinRO, Diary), and caters to all age groups, from pediatric to older patients. The platform accommodates any population size, capable of managing studies ranging from a handful to over 10,000 patients across all geographic regions. Clin'form offers seamless integration with other clinical systems, ensuring a smooth workflow, and supports flexible data collection modes, including provisioned tablets or smartphones, the patient's own smartphone, web access from any browser, and interviews. Key features include an embedded tele-visit feature to plan for the unplanned, patient engagement modules to ensure high patient compliance.
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    Inspirata

    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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    Signant Health

    Signant Health

    Signant Health

    Signant Health is a global evidence-generation company that helps modernize clinical trials by meeting patients where they are and reimagining the path to proof. They offer comprehensive clinical technology solutions, including electronic Clinical Outcome Assessments (eCOA), Electronic Data Capture (EDC), electronic clinician ratings, and a unified eClinical platform. Their patient engagement tools encompass a patient engagement app, eConsent, and telemedicine capabilities. Signant Health also provides clinical data and analytics services, such as COA data analytics and data aggregation and intelligence. With over 30 years of experience, they have supported thousands of trials and contributed to hundreds of drug approvals, making them a trusted partner for sponsors and CROs aiming to deliver high-quality data for trial decisions and regulatory submissions.
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    Leapcure

    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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    EvidentIQ

    EvidentIQ

    EvidentIQ

    eCOA by EvidentIQ optimizes real-time, direct-from-patient data collection by offering a simple and intuitive interface providing advanced patient assessments to enhance the patient experience and improve data quality. Customers can benefit from an end-to-end comprehensive eCOA package or create value by selecting from the various elements meeting specific requirements. Book a demo with our team of experts and see how you can improve your study ROI. eCOA by EvidentIQ brings data science services and technology together. Customers can benefit from an end-to-end comprehensive eCOA package or create value by selecting various elements meeting specific requirements. The solution can be used stand-alone as it is independent of any specific eClinical technologies such as EDC systems, but it can be integrated in any existing eClinical software landscape. It has been created to collect any patient/clinician/observer reported outcome data in a streamlined, compliant and efficient way.
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    5thPort

    5thPort

    5thPort

    5thPort is a digital patient education, engagement and eConsent platform. It can be used across individual practices, hospitals, health systems, and in clinical research. The platform utilizes high quality, prescriptive multimedia and teach-back to educate patients and their caregivers on their diagnosis, care plans, risks and benefits of recommended procedures. Once the patient is well-informed, our digital eConsent process helps to facilitate a meaningful conversation with your healthcare provider. With 5thPort, achieve the following results: 1. Save 15 to 20 minutes per consult (without spending any incremental effort) 2. Enhance the patient experience 3. Reduce patient stress on the day of their appointment 4. Empower patients to actively participate in their healthcare conversations with their provider 5. Reduce nurse burnout
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    Deep 6 AI

    Deep 6 AI

    Deep 6 AI

    Deep 6 AI disrupts the clinical trial enrollment process by transforming the way researchers identify eligible patients. Using artificial intelligence and natural language processing to mine structured and unstructured patient data, DEEP 6 AI finds more, better-matching patients for trials in minutes, not months. Deep 6 AI works with some of the most prominent health systems, pharma companies, and CROs in the world --making the DEEP 6 platform a crucial step in their clinical research workflow and greatly accelerating patients’ access to clinical trials. Deep 6 AI finds more patients for clinical trials in minutes rather than months, getting life-saving cures to people more quickly. Deep 6 AI’s software analyzes structured data, such as ICD-10 codes, and unstructured clinical data, including doctor’s notes, pathology reports, operating notes and other important medical data in free-text form that cannot be searched easily.
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    CureMetrix

    CureMetrix

    CureMetrix

    Leveraging the power of Artificial Intelligence (AI) CureMetrix is committed to advancing technology that improves disease detection and cancer survival rates across the globe. We believe that providing radiologists with the most advanced technology to support their evaluation of mammograms will support improved clinical and financial outcomes along with increased assurance for imaging centers, hospital systems and the patients they care for. Results from preliminary studies across thousands of images suggest that our algorithm can reduce false-positive rates that may lead to unnecessary follow-up procedures and undue anxiety among patients. We are developing powerful technology that could enable health care providers to hone in on even the most microscopic changes more quickly and accurately than ever before. We are designing our image analysis platform to improve the evaluation of dense breasts using mammography.
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    Unlearn

    Unlearn

    Unlearn

    Advancing AI to eliminate trial and error in medicine. Our digital twins enable confident and quick clinical trials. We work in neuroscience, immunology, metabolic disease, and more. TwinRCTs reach full enrollment sooner because they require fewer patients to achieve the same power as traditional trial designs. Shorten time to enrollment in late-stage studies. TwinRCTs improve the ability to observe treatment effects in early-stage studies by increasing power without adding more patients. Make confident decisions from early-stage studies and attract study participants. TwinRCTs give participants a greater chance of receiving the experimental treatment because they use smaller control groups. Position clinical trials with digital twins for regulatory success. Unlearn is engineering the future of medicine with artificial intelligence. We invent and deploy new types of generative models trained on extensive patient-level data from previous studies.
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    iKnowMed

    iKnowMed

    McKesson

    Improve the quality and efficiency of cancer treatment across all care settings. Designed in close collaboration with oncologists, iKnowMedSM is an electronic health record (EHR) that intuitively delivers the right patient information, at the right time, across nearly any device. Updated with the best in user experience and design and a one-of-a-kind mobile experience, iKnowMed EHR provides comprehensive point-of-care treatment decision support and customizable features for integration into existing workflows. Provide comprehensive clinical support for your patients, leveraging a continuously updated library of oncology treatment regimens, drug availability and clinical outcomes. Access evidence-based clinical guidelines and pathways at the point of need. Provide up-to-date treatment options integrated with information on treatment costs, insurance coverage and reimbursement data.
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    My Care Plus
    My Care PlusSM empowers patients with a personal connection to a more informed and empowered healthcare journey. Through the portal, they can gain online access to their personal health record, easily communicate with their providers, and review a recently expanded library of patient education resources. Provide patients with access to their comprehensive care plan, health information, and condition/medication education from leading cancer resources, anytime, anywhere. Answer patients’ non-urgent questions with secure messaging or broadcast messages to all of your patients. Increase patient awareness of the benefits of using your patient portal with customizable marketing materials, videos, and additional resources. Meet Meaningful Use objectives with all the features needed to help your practice meet stage 1 and stage 2 objectives. Clinical decision support, practice performance and analytics.
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    Genomenon

    Genomenon

    Genomenon

    Pharma companies need comprehensive genomic information to drive successful precision medicine programs, but decisions are often made using only a fraction of the data available, about 10%. Genomenon delivers 100% of the data. An efficient and cost-effective natural history research solution for pharma, ProdigyTM Patient Landscapes support the development of rare disease therapies by enhancing insights contained in retrospective and prospective health data. Using a powerful AI-driven approach, Genomenon delivers a comprehensive and expert assessment of every patient in the published medical literature, in a fraction of the time. Don’t miss anything, get insight into every genomic biomarker published in the medical literature. Every scientific assertion is supported by empirical evidence from the medical literature. Identify all genetic drivers and pinpoint which variants are known to be pathogenic according to ACMG clinical standards.
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    Koneksa

    Koneksa

    Koneksa

    Koneksa is a leading digital biomarker company for the pharmaceutical and biotechnology industries, specializing in developing, testing, and validating digital biomarkers to help clients understand the impact of their treatments on patients. Founded in 2013, Koneksa provides end-to-end remote clinical trial support, leveraging digital health technology, therapeutic expertise, and rapid patient-friendly remote data collection to gain better insights into patient health. Their validated, novel data algorithms are ready to deploy in treatment development programs, enabling the identification of signals earlier and faster than traditional measures. Koneksa's cloud-based SaaS platform allows multiple endpoints to be fed in real-time, giving immediate access to data and empowering confident, cost-saving decisions early in trials. The platform's ability to collect high-volume remote data with increased frequency offers ecologically valid measures and opportunities to reduce sample size.
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    Suvoda

    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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    Cenduit IRT
    Today’s Interactive Response Technology (IRT) systems are increasingly complex. Flexible and configurable IRT matters - with IRT data as the source of record for recruitment, clinical trial drop-out rates, patient visits, and other crucial data. Choose a platform that’s user-friendly, mobile-ready, and comprehensive - embedded in quality, flexibility and expertise. Choose comfort with complex therapeutic expertise in today’s risk-based eClinical environment. Combining the right technology, subject matter expertise and commitment to service we empower clinical trials to deliver patient outcomes. Deep clinical and supply chain knowledge drives innovation and provides clients with control over their Randomization and Trial Supply Management (RTSM) processes. Our innovative suite of tools drives distinctive levels of quality control, site efficiency and patient compliance. Our IRT platform can meet the needs of almost any study, enabling fully validated deployment in as little as 30 days.
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    HEKMA

    HEKMA

    HEKMA

    HEKMA is an AI-powered clinical trial intelligence company focused on accelerating clinical research by improving patient recruitment, trial feasibility, and patient engagement. The company serves CROs, pharmaceutical sponsors, hospitals, and patients through an integrated platform that connects electronic health records (EHRs), AI-driven trial matching, clinical trial management, and patient engagement tools. Its mission is to reduce enrollment delays, improve access to clinical trials; particularly for underserved populations and make clinical research more efficient, transparent, and patient-centric. HEKMA combines expertise in healthcare, artificial intelligence, and clinical operations while maintaining compliance with industry standards such as HIPAA, 21 CFR Part 11, GDPR, and HL7/FHIR.
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    PedPro

    PedPro

    Tenset

    PedPro is an animal breeding and pedigree software product that prints your pedigrees and stores your breeding records. It is available for Windows computers. Initially, it operates as a 30-day trial version. After the trial period purchase a registration code for the full, unrestricted, version. PedPro remembers the details of animals previously entered and saved in the data file. If you've previously stored your pedigrees in either of these other products, transfer them easily into PedPro without having to use CSV/text import/export. Not all data is transferred, please check suitability first. Optionally include wrights inbreeding coefficient in pedigrees. Choose how many generations are used in the computation. Include photos in the pedigree, including selecting a watermark image to appear behind the pedigree. The full version of PedPro has a limit of 1,000,000 animals in a single data file. You can have as many data files as you like.
    Starting Price: $125.91 one-time payment
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    Aiforia

    Aiforia

    Aiforia

    Aiforia equips pathologists and scientists in preclinical and clinical labs with powerful deep learning and cloud-based technology to advance their image analysis tasks and workflows. From empowering researchers in the identification of novel biomarkers of disease, and supporting R&D scientists in speeding up the time-to-market of novel drugs, to helping pathologists enhance the accuracy of cancer diagnostics, Aiforia has the expertise and experience to transform healthcare all the way from discovery to diagnosis. For clinical pathology labs aiming to increase productivity and improve diagnostic accuracy, the Aiforia Clinical Suites offer a portfolio of tools for AI-supported diagnostics, intelligent visualization, QC, and automated pre- and post-screening. We are currently developing Suites for some of the world’s most prevalent cancers and have CE-IVD marking for AI models in lung and breast cancer.
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    Digimed-MD

    Digimed-MD

    Digimed Innovation

    Digimed-MD is among the first software available on the market to increase the accuracy of analyzes and diagnoses, create a proactive environment, improve monitoring of vital signs, and summarize a patient's history. Digimed-MD is specially designed to offer tools for improving patient follow-up as well as vital signs monitoring to healthcare professionals. In addition, it includes the following features. Demographic profile of the patient (demographic information, family doctor, pharmacist), clinical profile of the patient (allergies, medications, operations, illnesses), social and medical history of the patient. Therapeutic Nursing Plan, electronic form to enter clinical data manually (blood pressure, lipid profile, healthy weight, Framingham risk), electronic form to enter the clinical notes of a consultation.
    Starting Price: $197 one-time payment