Clinical Trial Software and Services Partners
The conduct of a clinical trial requires numerous software and technology tools to make the trial process more efficient.
These include a clinical trials management system (CTMS), AI and machine learning, trial master files (TMF), virtual trial and remote monitoring tools, risk-based monitoring (RBM), patient diaries, electronic data capture (EDC), sensors and wearable devices, dashboards, and interactive response technology (IRT). Depending on the therapeutic area, laboratory services may also be required. Emerging eTechnologies are also being adopted in trials, including eConsent, eSource, eTMF, ePRO, and eSignatures.
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4G Clinical is driven by a single purpose: bring crucial medicines to those who need them, faster. We have revolutionized RTSM (randomization and trial supply management) and supply optimization capabilities and services from the ground up. Our best-in-class solutions, Prancer RTSM® and 4C Supply®, are driven by modern technology to bring speed and flexibility to deploy today's clinical trials and the adaptability to scale alongside your study.
ActiGraph's mission is to bring life to digital data. Built on more than twenty years of remote data capture expertise, ActiGraph is the leading provider of medical-grade wearable motion sensors for the global scientific community. ActiGraph's FDA-cleared biosensors and flexible technology ecosystem deliver high quality, continuous digital data, providing valuable insights into the real-world behaviors of clinical trial participants.
Advarra optimizes compliance and clinical trials as the premier provider of global research compliance services, including IRB, IBC, consulting, and research technology products. Clinical trial sponsors and CROs recognize Advarra as the largest integrated provider of IRB services with the greatest institutional reach among health systems, cancer centers, academic medical centers, and investigators. Forte, now part of Advarra, is the industry's leading provider of standards-based research technology.
ArisGlobal is transforming the way today's most successful Life Sciences companies bring new products to market. Our end-to-end, cloud-based drug development technology platform, LifeSphere®, automates all core functions of the drug development lifecycle. Designed with deep expertise and a long-term perspective that spans more than 30 years, LifeSphere® is a unified platform that boosts efficiency, ensures compliance, and delivers actionable insights.
Castor is a leading provider of decentralized and hybrid clinical trial solutions to democratize research. With the highest-rated eClinical platform for decentralized and hybrid clinical trials, Castor's plug-and-play platform offers rapid deployment at scale, enabling researchers to create a trial in a matter of clicks, with easy enrollment, eConsent, and real-world data capture.
Clinical ink is the global life science company that brings data, technology, and patient science together. Our deep therapeutic-area expertise, coupled with Direct Data Capture, eCOA, eConsent, telehealth, neurocognitive testing, and digital biomarkers advancements, drive the industry standard for data precision and usher in a new generation of clinical trials. By harnessing digital data, we power sponsors, CROs, researchers, and patients to recenter decentralized trials and rewrite the clinical development experience.
Cognizant's Life Sciences business unit partners with biopharmaceutical and med-tech companies to develop strategies and apply solutions to healthcare challenges across the value chain. Our services and products, including the Cognizant® Shared Investigator Platform (SIP), are digitizing interactions between sponsors and investigators across every phase, helping the industry subtract time from clinical development and add it to patient lives. With over 200,000 users across 99 countries, Cognizant SIP drives seamless collaboration among research sites and study sponsors and alleviates the administrative burden on sites.
CRIO, the leader in eSource technology, is transforming clinical research with the latest in cloud technology. CRIO's eSource system enables remote monitoring and immediate data review with a powerfully integrated eSource/EDC solution. CRIO delivers data only once - at the moment of immediacy - without re-entering into EDC, and protects data integrity with built-in compliance across 21 CFR 11, ICH-GCP, GDPR, HIPAA, and other global regulations.
Curebase is reinventing decentralized clinical trials to help the vast majority of potential patients that currently cannot access clinical research. Curebase's vision is that any patient, no matter where they are located, should be able to participate in clinical trials at home and with their own doctors. This is made possible through a unique suite of tools Curebase's has designed to engage patients in clinical trials across all settings.
Now more than ever, the clinical development path is full of make-or-break data complexities and analytical challenges. As a pioneer in evidence generation, with deep expertise in advanced analytical solutions, we are uniquely equipped to unlock the value from increasingly complex data. Life Sciences companies count on Cytel to deliver exceptional insight, minimize trial risk and accelerate the development of promising new medicines that improve human life.
Datatrak is a global clinical research and development technology platform for the life sciences industry. The Datatrak Enterprise Platform is an easy to use, cloud-based eClinical solution that empowers clinical trial users with the following products: Business Intelligence, CTMS, Trial Design, Electronic Data Capture (EDC), Medical Coding, Risk-Based Monitoring, Image Data Capture, Endpoint Adjudication, Randomization, Clinical Supply Inventory, eConsent, ePRO, and eCOA.
Datavant trials allows pharma, biotech, med device and clinical research organizations augment clinical trial insights with real world data. Datavant is a privacy compliant solution that enables researchers to de-identify, tokenize, match and connect trial data to mortality data, electronic health records, claims and more. Confirm trial eligibility, extend survival analysis, measure cost effectiveness during a study. Learn more about Datavant.
Encapsia is a modern, innovative and revolutionary clinical trial platform used to collect, review, analyze, and visualize all your clinical trial data. Purposefully designed to provide holistic approaches to your data, encapsia was built to function as a cohesive whole, across clinical trial functions increasing efficiencies, saving you time and money. Encapsia offers multi modal direct data capture and operates in a live, cloud-hosted, single data repository.
Florence accelerates clinical research with innovative solutions to streamline clinical trial site workflows and remote connect sponsors, CROs, and sites for access, monitoring, management, and SDR/V. The Florence platform is the industry standard with more than 7,200 research sites in 27 countries, sponsors and CROs collaborating on its network.
Greenphire is the leader in global clinical trial payment automation. Greenphire's best-in-class solutions optimize clinical trial performance by streamlining payment workflows from sponsors and CROs to sites and participants. Greenphire's ClinCard, eClinicalGPS and ConneX solutions easily handle any type of trial design and complexity, resulting in more accurate and compliant payments and travel globally for both sites and participants.
Medrio is on a mission to ease complexity in today's hybrid, decentralized, and site-based clinical trials by delivering a flexible suite of eClinical technologies and services, including EDC, eCOA, ePRO, eConsent, Direct Data Capture, and Randomization and Trial Supply Management (RTSM). Medrio is industry-recognized for delivering eClinical software with intuitive interfaces and time-saving "drag and drop" configurations as well as high-touch customer engagement, onboarding, and support services.
At Merative, we're building a more connected future in health. One where organizations can see the whole picture – and its pieces – at the highest levels of privacy and security.
We've been at the forefront of health innovation for nearly 50 years, pioneering the use of cloud, real-world data and industry-leading AI. Our name is new – but our trailblazing spirit isn't.
Informa Pharma Intelligence is the world's leading provider of drug, device, company, clinical trial and market intelligence in the competitive pharma and medtech markets. From early-stage portfolio decisions to clinical research and development and commercial planning and analysis, we offer a suite of complementary pharmaceutical business intelligence tools and solutions to support your business strategy.
inSeption distinguishes people as the most impactful variable in the outsourcing equation. Our path-breaking model attracts biopharma companies who demand a partner that shares in their drive to conduct impeccable development and will provide quality and dependable clinical solutions. We offer full outsourcing, consulting services, and functional service provider (FSP) solutions.
IQVIA Integrated Global Compliance offers a complete lifecycle approach that brings together safety, regulatory, quality, and medical information to transform how life sciences companies sustain compliance and how compliance functions perform better together.
By integrating services, technology, and analytics, we can help bring together disparate compliance functions, resulting in heightened patient safety, improved compliance performance, and proactive insights power by IQVIA Connected Intelligence.
IQVIA (NYSE:IQV) is a leading global provider of advanced analytics, technology solutions and contract research services to the life sciences industry. IQVIA applies human data science — leveraging the analytic rigor and clarity of data science to the ever-expanding scope of human science — to enable companies to reimagine and develop new approaches to clinical development and commercialization, speed innovation and accelerate improvements in healthcare outcomes.
Kayentis, a global expert in electronic data capture for patients in clinical trials, helps sponsors and CROs bring simplicity, efficiency and quality to the collection of clinical trial data from both patients and sites. Kayentis has been involved in clinical development since 2003. Over the last ten years, it has specialized in electronic Clinical Outcome Assessment (eCOA) solutions for phases II/III in a broad range of therapeutic areas.
Medable's mission is to get effective therapies to patients faster while expanding clinical research to every body, eliminating critical barriers to access such as income status, geography, & race. Medable offers a proven decentralized clinical trial platform that shortens trial timelines, creates operational efficiencies, and expands trial access to anyone worldwide using a combination of screening, eConsent, eCOA, ePRO, real-world data, connected sensors & more.
Medidata Acorn AI is a Medidata company that represents the next horizon of the industry leader's 20-year mission of powering smarter treatments and healthier people. Acorn AI is designed to make data liquid across the entire lifecycle and to answer the most important questions in R&D and commercialization for customers. Built upon the Medidata platform comprising more than 20,000 trials and 5 million patients, Acorn AI products feature one of the industry's largest structured, standardized clinical trial data repository connected with real world, translational and other datasets.
Medidata is leading the digital transformation of life sciences, creating hope for millions of patients. Medidata helps generate the evidence and insights to help pharmaceutical, biotech, medical device and diagnostic companies, and academic researchers accelerate value, minimize risk, and optimize outcomes. More than one million registered users across 1,400 customers and partners access the world's most-used platform for clinical development, commercial, and real-world data.
OCT is the leading contract research organization in Russia. Since 2005, OCT's team has conducted over 300 clinical trials in 29 therapeutic areas in Eastern Europe and the CIS region. Our team of 150+ clinical professionals provides a full range of high-quality CRO services for Phase I-IV and BE studies, with therapeutic expertise in oncology, infectious disease, and all major therapeutic indications.
OpenClinica is transforming healthcare through innovative cloud technology that simplifies running clinical trials. Proven in over 10,000 studies worldwide, the OpenClinica platform is trusted by leading biopharmaceutical companies, contract research organizations, academic institutions, and government agencies. OpenClinica is used across a wide spectrum of clinical research, including drug, device, and diagnostic trials, global health studies involving 200,000+ patients, adaptive platform trials, and clinical trials for some of the first gene therapies to be approved for market.
As a leader in Life Sciences cloud technology, Oracle Health Sciences' Clinical One and Safety One are trusted globally by professionals in both large and emerging companies engaged in clinical research and pharmacovigilance. With over 20 years' experience, Oracle Health Sciences is committed to supporting clinical development, delivering innovation to accelerate advancements, and empowering the Life Sciences industry to improve patient outcomes.
Since 2008, PCM Trials has led the way in mobile research. Our Certified Mobile Research Nurses (CMRNs) are driving the shift to patient-centric, decentralized clinical trials, giving individuals the flexibility to engage in research studies and expanding opportunities for participation.
Our CMRN certification program, coupled with protocol-specific training, ensures that patients have the best possible study experience while sponsors meet their strategic development goals in the United States and internationally.
PerkinElmer's advanced analytics and services solutions for Clinical Development help the world's leading biopharmaceutical, medical device and diagnostics manufactures discover new therapeutics faster by streamlining clinical operations, transforming risk into safety and enabling actionable decisions that can lead to better health outcomes.
Philips Pharma Solutions is an industry leader in medical imaging, cardiac safety testing and actigraphy services for clinical trials. For more than 30 years, our life science partners have relied on our scientific leadership, dedicated project teams, and advanced technology platforms to help design and optimize protocols and statistical analysis plans across a host of therapeutic areas.
Phlexglobal is the leading technology and services organization for clinical and regulatory matters with a focus on helping master a digital agenda via proven AI solutions. Phlexglobal combines software and services to offer a unique solutions portfolio with easy to achieve automation via data generation for a new level of effectiveness. The company's Trial Master File software and Regulatory Solutions are considered highly innovative in the industry.
Premier Research recognizes that when an emerging biotech is built around a single asset, focus and flexibility are critical to success. And, since many of our customers require additional infrastructure, we fill in resourcing gaps to help their product reach the patient faster. We are a mid-size CRO and offer strategies that are customized for each program, with tailored processes designed to meet highly specific needs.
Remarque Systems provides a single, easy-to-use, and effective platform to manage all of your clinical trial data. Remarque Systems brings all your data from different sources together in real time; delivers end-to-end visibility and oversight with data-driven analysis, monitoring, and risk assessment; and drives better-informed decisions with clear and conclusive analytics, reports, and visualizations.
Sikich is a leading technology and advisory consultancy that partners with biopharma, biotech and Clinical Research Organizations to streamline processes and ensure compliance, so stakeholders can do what they do best: develop new treatments for patients who need them. Offering a range of solutions and services from ERP to QMS, IT Quality & Compliance, cybersecurity, managed services, and cloud migrations, our team is dedicated to supporting life sciences companies across their growth journey.
THREAD is the industry-leading decentralized clinical trials technology and service provider, helping biopharma and CROs decentralize clinical research for sites, participants, caregivers and home health professionals. THREAD is recognized as a leader by Everest Group's DCT Product PEAK Matrix® Assessment 2021 and Frost & Sullivan's 2021 Customer Value Leadership Award. Visit THREADresearch.com to learn more.
For over 20 years, TransPerfect has helped life sciences companies conduct clinical development and commercialize products on a global scale. We bring that same level of expertise to our secure, web-based e-clinical solution, Trial Interactive. Trial Interactive enables life sciences companies to streamline the execution and commercialization of global clinical trials and collaborate on partnerships while reducing administrative burdens.
With almost a decade of experience matching and enrolling patients, Trialbee is purpose-built to reduce enrollment risk and efficiently meet global clinical trial timelines. Inspired by the shift from traditional clinical trials to hybrid and decentralized clinical trials, Trialbee has developed a data-science driven patient matching and an analytics-driven enrollment platform to provide a patient-centric journey and lower site-burden. These insights and analytics lead to tangible improvements to patient recruitment and enrollment strategies to optimize clinical trial timelines and gain operational efficiencies.
Veeva is the global leader in cloud software for the life sciences industry. Committed to innovation, product excellence, and customer success, Veeva serves more than 1,000 customers, ranging from the world's largest pharmaceutical companies to emerging biotechs. As a Public Benefit Corporation, Veeva is committed to balancing the interests of all stakeholders, including customers, employees, shareholders, and the industries it serves. For more information, visit veeva.com.
YPrime's cloud-based technology streamlines clinical trial data collection and management. YPrime's eCOA and interactive response technology (IRT) platforms introduce greater speed, precision, and data quality to clinical trials. Our consulting services help clients simplify downstream processes, while moving faster and more efficiently to their next development milestone.