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. Advarra's Research Site Cloud includes the OnCore and Clinical Conductor CTMS platforms, Advarra eRegulatory Management System, and Advarra eSource system, used by hundreds of academic institutions, cancer centers, health systems, and sites. And Advarra's Longboat platform enables efficient, compliant, patient-centric workflows benefitting all research stakeholders.
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.
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 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 internationally recognized as the leading Asia Pacific-centered Biotech CRO with global execution capabilities. Novotech is a clinical CRO with labs, phase I facilities, drug development consulting services, and FDA regulatory expertise and has experience in over 5,000 clinical projects, including Phase I to Phase IV clinical trials and bioequivalence studies. Novotech is positioned to serve biotech clients conducting clinical trials in Asia Pacific, the US, and Europe.
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 believes in a holistic approach to clinical development. From regulatory consulting, to product development, to innovative study designs and patient-centric solutions, we consider your study from every angle to maximize success. Our Built for Biotech℠ model is rooted in flexibility, and we are dedicated to helping the most innovative biotech, specialty pharma and medtech companies take their best ideas from concept to commercialization.
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.
From travel and compliance to expenses and beyond, Scout Clinical has patient service needs covered for industry-leading pharmaceutical, biotechnology, medical device and CRO companies. Since 2016, Scout has offered stress-free, confidential, and personalized solutions for patient stipends, reimbursements, lodging and travel anywhere in the world. Scout Clinical is dedicated to helping patients stick with it.
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.
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.