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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ActiGraph
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
Advarra advances the way clinical research is conducted: bringing life sciences companies, CROs, research sites, investigators, and academia together at the intersection of safety, technology, and collaboration. With trusted review solutions, innovative technologies, experienced consultants, and deep-seated connections across the industry, Advarra helps move research forward.
Anju Software
Anju is a customer-first organization providing adaptable life science solutions for clinical research, medical affairs, and data science. TrialMaster, IRMS MAX, and TA Scan, the company's flagship products, reduce complexities in the drug and device discovery and commercialization process allowing our customers to enhance the quality of their patients' lives. Anju is a portfolio company of Abry Partners serving the worldwide pharmaceutical, biotech, and contract research life sciences markets.
Capabilities
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Castor
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.
Cencora PharmaLex
Cencora PharmaLex guides pharma, biotech, and medtech clients from early strategic planning activities and non-clinical requirements through clinical development, regulatory submission processes and post-approval / maintenance post-launch activities. Our experts use technology-elevated solutions to support clients through the entire product lifecycle.
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Citeline
Citeline powers a full suite of complementary business intelligence offerings to meet the evolving needs of health care professionals to accelerate the connection of treatments to patients and patients to treatments. These patient-focused solutions and services deliver and analyze data used to drive clinical, commercial and regulatory-related decisions and create real-world opportunities for growth.
Cognizant
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.
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CRIO
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.
Crucial Data Solutions
Crucial Data Solutions (CDS) is the leading developer of validated, fully customizable eClinical software. Our unified, end-to-end platform, TrialKit, is purpose-built for clinical research teams to design, deploy, and manage studies in days—no programming required. With a cloud-based, open architecture, TrialKit gives research teams the flexibility to manage all types of studies across all phases of development.
Florence Healthcare
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.
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Greenphire
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.
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Halloran Consulting
Halloran Consulting Group is a life science consulting firm, partnering to enrich product development and business growth. We have five expertise areas: Clinical Development and Operations, Data and Technology, Regulatory Affairs and Operations, Quality & Compliance, Organizational Excellence, and Project Leadership & Program Management. As a specialized consulting firm, Halloran brings a fresh perspective to propel life science organizations towards innovation, efficiency, and breakthrough discoveries.
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inSeption Group
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.
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IQVIA Technologies
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.
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Kayentis
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.
Komodo Health
Komodo Health is a data-insights and technology company focused on reducing the burden of disease. Clinical Development teams in Life Sciences partner with Komodo to optimize every facet of drug research and development — from assessing disease incidence to advancing clinical trial diversity to incorporating evidence generation during trials.
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Medidata AI
Medidata AI provides unparalleled clinical data, advanced analytics, and industry expertise for pharmaceutical, biotech, and medical device leaders, to help reimagine what is possible, uncover the breakthrough insights, make confident decisions, and pursue continuous innovation. Our suite of solutions is backed by an integrated team of scientists, physicians, technologists, and ex-regulatory officials who bring deep expertise to answer your most important questions.
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Medidata Solutions, Inc.
Medidata, a Dassault Systèmes company, is powering smarter treatments and healthier people through digital solutions to support clinical trials. With over 20 years of groundbreaking technological innovation across more than 30,000 trials and 9 million patients, Medidata offers industry-leading expertise, analytics-powered insights, and the largest patient-level historical clinical trial data set in the world. More than 1 million registered users across 2,100+ customers trust Medidata's seamless, end-to-end platform.
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Mednet
Mednet is a leading healthcare technology company specializing in eClinical solutions designed for the global life sciences community. Pharmaceutical, medical device, biotechnology and Contract Research Organizations (CROs) around the world have trusted Mednet for over 21 years to deliver the technology innovation, experience and reliability they need for success.
Medrio
Trusted globally by sponsors, CROs, and sites, Medrio strives to improve 100 million lives through efficient and secure clinical trials. With nearly two decades of expertise, Medrio offers scalable solutions and unparalleled customer support to industry leaders in pharmaceuticals, biotech, medical devices, diagnostics, and more. Medrio's suite of solutions: CDMS/EDC, eCOA/ePRO, eConsent, and RTSM, optimizes workflows for regulatory readiness, ensuring quality data capture.
OCT Clinical
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
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.
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PCM Trials
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.
Revvity Signals Software, Inc.
Revvity Signals Software'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.
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Scout
From travel and compliance to expenses and beyond, Scout 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 is dedicated to helping patients stick with it.
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Signant Health
Signant Health is an evidence-generation company focused on leveraging software, deep therapeutic and scientific knowledge, and operational expertise to consistently capture, aggregate, and reveal quality evidence for clinical studies across all trial models. For more than 25 years, over 600 sponsors and CROs have trusted Signant solutions for remote and site-based eCOA, EDC, eConsent, RTSM, supply chain management, and data quality analytics.
Sikich
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.
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ThoughtSphere
ThoughtSphere is a market-leading clinical data & analytics technology company. Our clinical data platform works across data capture applications to provide integrated data processing capabilities to support clinical trial operations from data aggregation to the generation of validation-ready datasets. The next generation data lake and flexible end-user offerings allow organizations to socialize data, automate cross-functional review cycles, and generate reliable data faster.
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Veristat, Inc.
Veristat, a global clinical research organization (CRO), enables sponsors to solve the unique and complex challenges associated with accelerating therapies through clinical development to regulatory approval. With more than 26 years' experience in clinical trial planning and execution, Veristat is equipped to support any development program. Our team has prepared over 100 marketing applications for approval with global regulatory authorities in the last 10 years alone.
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Zelta
Zelta™ by Merative is a clinical trials solution business that includes both a clinical data management and acquisition platform and consulting, enablement, and extension services. Zelta's unified cloud-hosted platform supports all phases and complexities of research, including over 450 phase III trials.