Patient & Site Solutions Partners
One of the most difficult tasks of conducting a clinical trial is the study startup process. That process includes a feasibility study to determine if there are sufficient patients to meet established inclusion and exclusion criteria, site selection, and patient recruitment.
Research has shown that as many as 85 percent of trials fail to meet enrollment timelines and 80 percent fail to finish on time. Additionally, 50 percent of sites selected to participate in studies recruit one or no patients.
Patient recruitment firms and technologies are available to help sponsor companies locate patients for studies. Technology tools such as eDiaries, text reminders, and remote monitoring tools can ease the burden on patients and increase retention rates. Additionally, there are technology tools that notify sponsor companies if and when a patient takes their trial medication. AI and machine learning solutions are also available to mine EHRs and EMRs to locate patients meeting inclusion/exclusion criteria, or to search sites to determine which ones are best suited for a trial.
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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 brings 35 years of life sciences technology innovation to deliver patient and site solutions that sponsors need. Its LifeSphere EDC, eCOA, and RTSM applications provide essential tools to engage with patients and clinical sites. LifeSphere CTMS helps sponsors manage trials from feasibility, through study startup, and closeout. With advanced automation and deep capabilities in site monitoring and payments plus unique tools for managing protocol amendments, LifeSphere CTMS increases clinical development efficiency for study teams.
Biorasi is an award-winning contract research organization accelerating drug and device clinical development for life sciences companies around the world. Since 2002, Biorasi has achieved success in bringing innovative therapies to market for our sponsors. Biorasi solves the problem of poor clinical trial performance with better patient recruitment, powerful data insights, and operational excellence. We deliver faster, higher quality clinical trials.
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.
Elligo Health Research accelerates clinical trials through healthcare with access to known patients and their HIPAA-compliant healthcare data, our IntElligo® Research Stack technology, and our eSolutions Research Accelerator PatientSelect approach. As the largest Known Patient Access Network, our ClinEdge Research Practice Management enables healthcare practices and research sites to participate in clinical trials as Research Ready.
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.
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 (NYSE:IQV) is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. IQVIA Research & Development Solutions (RDS) is the full-service clinical development partner that leverages the power of IQVIA Connected Intelligence across your entire study, from study design to site selection, enrollment and execution, so you can deliver life-changing therapies faster and without compromise.
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 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.
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 MRN we understand the complexities of today's clinical trial environment and the burden this places on patients, clients and sites.
Our services are designed to ease these burdens, from community researchers through to investigator site professional support, accelerating patient recruitment and retention.
We work to maximize the efficiency of clinical trials for drug developers, by improving the patient's experience, no matter where their community is in the world.
Novotech is the leading Asia-Pacific biotech specialist CRO with global execution capabilities. Novotech is a clinical CRO with labs, phase I facilities, and drug development consulting services. It has accumulated experience in over 3,700 clinical projects, including Phase I to Phase IV clinical trials and bioequivalence studies. Novotech is positioned to serve biopharmaceutical clients conducting clinical trials in Asia, the US and globally.
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.
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.
Pro-ficiency's mission is to eliminate protocol deviations, one study at a time, by bringing simulation to clinical trials training. The simulation approach tackles the highest risk areas of the study protocol, enabling clinical research teams to exercise critical decision-making in a risk free environment, much like a flight simulator for pilots. Allowing the study teams to practice protocol implementation and potentially make mistakes in a simulated environment, protects the patient and the study integrity.
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.
Slope provides the industry's first online eClinical Supply Chain Management (eCSCM) platform for sponsors and research sites collaborating on complex, sample-intensive, early-phase clinical trials. The Slope eCSCM platform reduces clinical trial risks, reigns in costs, improves productivity of clinical trial collaborators, and increases subject retention by moving the manual, spreadsheet-driven, and error-prone processes to a digital platform.
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.
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.
Founded by physicians committed to advancing medical science, Worldwide is out to change how the world experiences CROs – in the best possible way. From early phase and bioanalytical sciences through late phase, post-approval and real-world evidence, we provide world-class, full-service drug development services across a range of therapeutic areas, including central nervous system, cardiovascular, metabolic, general medicine, oncology and rare diseases. We never compromise on science or safety. We're never satisfied with the status quo. We're the Cure for the Common CRO.
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.