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.
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Bioforum the Data Masters Inc.
Bioforum is a data-focused contract research organization (CRO), serving clients worldwide in optimizing the collection, standardization, and reporting of clinical research data. We strive to consistently improve and innovate data processes, enabling the most efficient data submissions for our clients across the life sciences industry worldwide. Our multidisciplinary team provides in-depth expertise and delivers high-quality solutions, including medical writing, data management, biostatistics and statistical programming.
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.
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.
Clario
For 50 years, we have led the way in delivering better clinical evidence with our clinical research data management services. In that time, our technology, expertise and know-how have helped more than 800 new drugs come to market.
Clinical ink
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
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.
eClinical Solutions
eClinical Solutions is a global provider of cloud-based enterprise software and software-driven clinical data services that accelerate digital clinical initiatives. Our intelligent clinical data cloud and data services give our clients real-time, self-service access to all their data from one centralized location; plus advanced analytics that help them make smarter, faster business decisions.
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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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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.
Medable
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
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.
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Medidata Solutions
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.
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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
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.
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.
Philips
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.
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Phlexglobal
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.
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Premier Research
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.
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 Clinical
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.
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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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Slope
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.
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ThoughtSphere
Our market-leading stacked platform creates an integrated central monitoring environment to streamline RBQM, drug safety, medical, data management, and site management tasks in a single platform. Our user-friendly solution leverages Machine Learning and Artificial Intelligence to automate processes and modernize clinical trial operations from data aggregation to the generation of validation-ready datasets.
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TransPerfect
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.
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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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YPrime
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.
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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.