ABOUT 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.
Founded by visionary CEO Dr. Michelle Longmire after discovering firsthand the difficulties of finding research patients, Medable’s platform is designed by a combination of clinicians, patients, and tech experts to ease the experience for all trial stakeholders. The result is over 150+ decentralized trials conducted across 60+ countries with over 1 million patients accessing our platform today.
A pioneer in patient-centric trials, Medable has been ranked the number one provider of decentralized clinical trials by the Everest Group, and recently collaborated with Tufts CSDD to release the first financial modeling showcasing the benefits of DCTs. Medable DCTs have now demonstrated net financial benefits of up to 5x & 14x greater than the initial upfront investment required for phase ll & phase lll studies, respectively. Additionally, our digital certification program has helped teach decentralized and patient-centric clinical trial methods to over 1,000+ of our industry peers.
Find out how Medable can partner with your organization to digitally transform your clinical protocols. Your research teams can experience benefits such as; improved patient experience, higher quality outcomes data, & savings of US$25,000,000+ for individual studies. Please visit www.Medable.com for further information.
FEATURED CONTENT
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![laboratory scientist laptop GettyImages-1302454417]( "6 Steps To Help You Choose The Right Clinical Trial Partner")
The right digital partner can unlock speed, scale, and collaboration that can transform the future of your pipeline. Learn the six steps to help you choose the right partner for your trials.
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![GettyImages-1451866321-man-lightbulb-light-ai]( "From Bottlenecks To Breakthroughs: How AI Is Transforming Translation Timelines")
Take a deeper look at AI-enabled translations and uncover how they are able to drive a remarkable 43% reduction in overall translation timelines.
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![GettyImages-2163506576-computer-ai-compliance-regulatory]( "Your Roadmap To Adopting AI agents")
A strategic roadmap can help you align people, processes, and technology for success. This strategic approach is essential for a fast and effective integration of AI agents into enterprise operations.
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![GettyImages-2036497889-lab-computer-research]( "Guidance For Using AI Agents Effectively")
By automating manual tasks and working with human counterparts, AI agents empower organizations to streamline processes and foster strategic growth
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![GettyImages-1646106148-AI-pharma-healthcare]( "AI In Clinical Trials: Key Insights From Industry Experts")
Find out what experts from the FDA are saying about AI’s ability to demonstrably impact three critical success metrics in clinical trials.
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![Removing translation]( "Removing Translation Bottlenecks With AI")
See how an AI-enabled approach eliminated the manual, time-consuming translation bottlenecks that often delay clinical trial launches.
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![GettyImages-1303406455-vial]( "Rewriting The Future Of Clinical Trials")
In an increasingly data-complex environment, eCOA is emerging as a foundational pillar for both operational agility and scientific rigor in clinical development
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![GettyImages-2154674637-AI-hand-software-ripple]( "Agentic AI And How It's Impacting Clinical Trial Research")
Since ChatGPT’s launch in 2022, artificial intelligence has transformed industries worldwide—but the next evolution, Agentic AI, promises to be even more profound.
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![fact and myth-GettyImages-1537534263]( "The Top 5 Myths About eCOA In 2025")
Projected to grow 16.1% annually through 2030, eCOA solutions are booming. Uncover the top five myths and misconceptions about eCOAs in 2025 so your clinical teams can make evidence-based decisions.
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![GettyImages-1751848523-meeting-evaluation-charts-table]( "Accelerating CRO Study Deployment At Scale")
A top-3 CRO and a top-10 pharmaceutical company partnered with Medable to help accelerate, scale, and standardize their eCOA trials. See how they accomplished it.
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![conference attendees]( "What Happened At ASCO 2025?")
ASCO 2025 underscored both the momentum in oncology innovation and the critical need to protect the infrastructure that enables it—ensuring that tomorrow’s breakthroughs remain within reach for all patients.
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![GettyImages- 1180547354 trial data]( "No More Back And Forth: Building eCOAs Right The First Time")
Clinical trial system builds have long been plagued by inefficiencies, miscommunications, and long timelines. Learn about a platform helping sponsors and CRO's overcome these challenges.
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![GettyImages-1385471311 patient tablet]( "CRO Takes Trial Build Times From Weeks To Days")
Recognizing the inefficiencies in traditional build processes, a top global CRO partnered with Medable to transform its approach to clinical trial launch.
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![GettyImages-2155531148 electronic data, ePRO, eCOA]( "Why ePROs In Oncology Are Perfect For Capturing The Patient's Voice")
Recently released FDA guidance showcases why electronic patient-reported outcomes (ePROs) are ideal for capturing the “voice” of the patient. See how ePRO eases oncology trials.
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![Artificial intelligence, AI-GettyImages-1168866494]( "Key AI Trial Insights From Regulators And Consultants")
AI’s transformative impact promises more efficient, cost-effective, and successful clinical trials across the pharmaceutical landscape.
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![iStock-1074203146-computer-typing-work]( "Setting A New Client Standard In Study Closeout Timelines")
Learn how a top-10 global pharmaceutical company achieved a significantly faster time to market for a high-profile therapy.
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![Japan Globe]( "Building A Gold Standard Trial Experience In Japan")
Hear how Medable worked with a Japanese sponsor to elevate their trial experience, achieve >90% patient and site adherence, and beat their forecasted FPI date, creating new eCOA standards adopted across all the customer’s vendors.
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![GettyImages-1923661781-asian-japanese-laptop-business]( "Medable's Japanese Clinical Trial Exceeds FPI Date And eCOA Adherence")
A top-10 global pharma company aimed to address eCOA adherence and patient enrollment challenges faced by clinical trial sites in Japan. Explore an initiative to enhance the patient and site experience.
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![GettyImages-1169656849 eCOA]( "Tips For Better eCOA Experiences From Medable's Patient Caregiver Network")
Hear from patients and caregivers across various therapeutic areas as they offer tips on improving the clinical trial experience.
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![GettyImages-2095562171-data-tech-network]( "GSK And Medable Discuss The Next Phase Of DCTs")
GSK and Medable share the value of embedding DCTs into strategic goals to enhance trial accessibility, diversity, and efficiency.
CONTACT INFORMATION
Medable
525 University Ave, Suite A70
Palo Alto, CA 94301
UNITED STATES
WEBINARS
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![Medable eCOA webinar]( "Transforming Oncology Trials With Next-Gen eCOA")
With the FDA stating last fall that the “patient’s voice” is key to understanding real-world-impacts, eCOAs and ePROs are becoming quintessential tools for cancer trials.
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![top 5 myths about eCOA]( "The Top 5 Myths About eCOAs In 2025")
Join leading clinical experts as they debunk the top 5 myths about eCOA in 2025, separating fact from fiction to help clinical operations, procurement, and data management teams make smarter decisions.
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![GettyImages-1585068774 patient doctor, clinical trial, data]( "Reduce Patient And Site Burden Through Excellence In Trial Logistics")
Watch for an insightful webinar where you’ll explore the latest strategies and innovations for managing clinical trial operations with a focus on device provisioning and data workflows.
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![Oncology Cell]( "Defining And Implementing The Right Oncology Digital Strategy")
A panel of oncology experts shares how top life science companies are using a combination of DHTs, ePROs, clinical trial platforms, and more to ease oncology research and drastically reduce timelines.
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![check computer for vitals-GettyImages-1446748436]( "Maximize Control And Transparency On The Path To Study Go-Live")
Simplify the historically complicated, black-box processes around eCOA solution deployment, content storage and visualization, and global go-live.
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![The New Era Of Evidence Generation In Clinical Trials]( "The New Era Of Evidence Generation In Clinical Trials")
Learn how top pharmaceutical companies are using novel innovations to drive greater speed, scale, and access in clinical research than ever before in this webinar hosted by Musaddiq Khan, Vice President of DCT Solutions at Medable.
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![Panel Discussion]( "Harnessing The Potential Of Patient-Level Data In Clinical Trials")
Join our panel of industry leaders as they explore innovative methods and best practices for incorporating fully consented patient data in clinical trials.
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![medable tech overload thumb]( "Technology Overload: Addressing Site Challenges Of Digital Trials")
Watch as speakers explore the experiences of sites conducting digital and hybrid trials, discussing the critical benefits of a change management strategy and a unified digital trial platform.
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![amplifying evidence medable web thumb]( "Amplifying Evidence With Unified Clinical Trial Data Collection")
In this presentation, we explore the transformative potential of integrating a unified clinical trial data collection platform with intelligent automation, challenging the inadequacies of the status quo.
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![medable econsent web thumb]( "What It Really Takes To Adopt eConsent Across Large Pharma")
Explore the benefits of incorporating consent management technology and discover practical strategies for developing effective change management and training programs.
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![medable patient engagement webinar thumb]( "Enhancing The Clinical Trial Experience With Consumerization")
Clinical trial technology has transformed the ways we can engage patients. Learn from experts at Uber Health and clinical tech companies how you can supercharge the patient experience with consumerization.
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![medable clinops web thumb]( "Keeping Up With ClinOps: Why And How To Improve Delivery")
Industry experts discuss the concept of a trial platform as a service and how it can accelerate and enhance the day-to-day functions of clinical operations throughout the entire lifecycle of a study.
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![an honest assessment medable web thumb]( "An Honest Assessment Of eCOAs From A Site Perspective")
Listen to what sites have to say about the changing nature of COAs in clinical trials, including the usage of eCOA, its benefits, and ways to improve the technology.
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![medable tech overload webinar snip 2 thumb]( "Addressing Site And Sponsor Challenges In Digital Trials")
<p>While the digital transformation of clinical trials has made tremendous strides in recent years, the plethora of new technologies can overwhelm. Learn how to help sites and sponsors combat the overload of technology.</p>
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![medable web thumb]( "Keeping Patients Engaged In Clinical Trials Using Consumerization")
Today’s clinical trial participants anticipate that the convenience and flexibility they experience in their daily lives will be accommodated when entering a clinical trial. Learn how to keep participants engaged and compliant with your trial, using modern consumer experiences.
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![medable supercharge webinar thumb]( "How To Supercharge RWE Generation In Phase IV Trials")
Watch as speakers discuss their joint efforts in implementing patient-centric digital trial solutions that harness the potential of RWD, translating it into actionable Real-World Evidence insights for a sponsoring client.
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![medable create webinar thumb]( "Creating The Digital Foundation For Scale In Clinical Development")
Learn how CROs, pharma, and biotechs are using digital trial methods to scale efficiencies across the entirety of their clinical trial portfolio for maximum ROI.
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![GettyImages-1141776223 oncology]( "Enhancing Oncology Clinical Trials Through The Use Of Digital Technologies")
The most difficult clinical research just became more challenging. Learn tactics on how teams can simplify oncology research while solving new and old issues.
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![total_consent_adoption_feb_22_presentation_rev]( "Everything You Need To Know About Adopting eConsent Across Large Pharma Organizations")
Did you know that the average cost for a delayed trial is between $600,000 and $8 million per day? Discover how electronic consent management technology is helping sponsors, CROs, and sites.
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![medable patient first]( "Deploying A Unified Framework To Accelerate Recruitment And Reduce Timelines")
Learn how and why unified platforms are effective at delivering better patient access and shortening clinical trial timelines with this webinar.
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![medable digital webinar]( "The Digital Future Is Now")
Discover best practices and see real examples of how top pharmaceutical companies like GSK, Syneos, and others successfully drive the transformation of clinical development to achieve higher patient engagement and retention using digital technologies, all while emphasizing a foundational platform approach for their future trials.
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![medable webinar]( "How Technology Can Alleviate Patient Burden In Oncology Trials")
Hear from young cancer survivor Dr. Lindsay Matt, and Medable SMEs as they document what challenges patients face in clinical trials, and how to help alleviate them with modern technology.
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![clinical_leader_presentation_92022]( "The Platform Shift is Here: Are you Realizing ROI Across your Portfolio of Studies?")
Research shows that the global DCT market will reach $14B by 2026. Research also suggests that up to 90% of clinical trials are at risk of failure. Faulty trial designs, patient retention, costs and flawed data collection are drivers for the failure rate in clinical trials. The risks of study failure are reduced by taking a patient- first enterprise platform approach.
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![medable webinar 1]( "Digital Versus Digitized: Common Misconceptions About eConsent")
In this on-demand webinar attendees will learn about the common misconceptions surrounding eConsent, as well as the benefits they can realize through a digitally-enabled approach.
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![medable webinar]( "Everything You Need To Know About Hybrid/Decentralized Trials")
This webinar provides insight into an understanding of hybrid and decentralized clinical trials (DCT), the facts and fiction around decentralized trials, and why decentralized trials are not an all or nothing approach.
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![medable econsent webinar]( "Agile eConsent: Taking A Flexible Approach To Global Implementation")
Hear from industry experts on how they successfully combined agile eConsent technology with global regulatory expertise to increase enrollment rates and reduce both site and patient burden.
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![medabe webinar]( "Enable Next-Generation Clinical Research At Scale")
In this webinar, Medable SMEs take you through the end-to-end process of conducting decentralized clinical research, including benefits, common pitfalls and challenges, and more.
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![human-heart-cardiac]( "Accelerate Time To Target Endpoint In Cardiometabolic Studies Using Patient-Centered Technology Solutions")
In this webinar, industry experts share their perspectives on how to address drug development challenges within cardiometabolic clinical studies and provide input on the impact of new regulatory guidance such as the DEPICT Act.
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![Data Analytics Strategy]( "Three Data Trends to Consider Now When Developing Your Decentralized Clinical Trial Strategy")
In this free webinar, learn how to update your clinical data strategy that ensures you can scale trials globally while decreasing the overall burden on sites and patients.
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![Pharma Data GettyImages-1091887430]( "Collect Better Oncology Trial Data, Easier")
In this webinar, experts discuss how enriching oncology clinical trials with RWD generates deeper insights and improves operational efficiency to achieve better patient outcomes.
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![GettyImages-1311429557-vaccine-shot]( "The New Vaccine Race: Why A Decentralized Approach Wins")
What does it take to get vaccine trials up and running quickly and efficiently? As it turns out, the best answer is DCT. Learn why in the available webinar.
FEATURED SOLUTIONS
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![Futuristic visualisation of modern innovative AI technologies-GettyImages-2170346048]( "AI Agents To Build, Integrate, And Innovate")
Built specifically for life sciences, this AI-powered platform is designed to automate and streamline the clinical trial process.
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![GettyImages-1326241306-research-computer-brain-scan]( "The Big Impact Of Medable AI")
Streamline your clinical trial study creation by automating and accelerating the eCOA build process. Generative AI models perform your repetitive configurations and significantly shorten build times.
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![Medable Feature image]( "Explore Medable Studio")
Achieve unprecedented control over the study creation and deployment process with a no-code interface.
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![medable studio thumb]( "Medable Studio")
More than just a builder, Medable Studio offers unmatched control over study creation and launch, eliminating the common roadblocks of study startup and empowering users throughout the process.
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![GettyImages-1310126023-test-tube-vaccine-lab-glove]( "How And Why We Decided To Bring 'Pathways' To Market")
Over the past year, this author has collaborated closely with a diverse team of clinicians and research experts to enhance Medable's research methodologies across various therapeutic domains.
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![GettyImages-1372091146 patient ipad]( "Improving The Patient Experience With Total Consent")
Increased outreach, heightened involvement, superior quality. Tour this comprehensive consent management solution that enhances participant access and improves the overall patient experience.
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![GettyImages-1304430076 oncology ps]( "Patient-First Solutions For Oncology")
Stay connected with your patients and their data by simplifying collection for sites and sponsors while keeping participants safe, comfortable, and engaged from any location.
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![GettyImages-1094389542 patient]( "Discover Our Mission: Making Clinical Trials Easily Accessible For Everyone")
Learn about our mission of making clinical trials easy to participate in around the world, as well as what Medable can do for you, with this overview.
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![Novel therapeutics: gene and cell therapies, nanoparticles, and combination]( "Medable Therapeutic Area Pathways")
Accelerate research and drive operational efficiencies with multi-modal, scalable digital solutions for oncology, vaccine, and cardiovascular / metabolic studies.
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![GettyImages-1311429557-vaccine-shot]( "The #1 Rated Leader In DCT Now Offers The Vaccine Pathway")
Explore an expertly crafted package of programs, products, and expertise addressing the unique challenges of vaccine research.
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![person using ipad iStock-1029343476]( "Medable eCOA")
Medable eCOA is designed to enhance your decentralized trial capabilities with all features native to the platform. Modular by design, use what you need, not what you don’t.
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![Preparing For eConsent - A Step By Step Guide For Site Personnel]( "eConsent: Optimize Access")
Learn how to optimize patient access to clinical research with a modern eConsent platform that delivers an engaging, flexible and scalable user experience.
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![GettyImages-1124543330 (1) ps]( "Research For Every Body: A Mission For Inclusive Access To Medicine")
Limited access to clinical trials has had a direct impact on the development of new medicines. Explore Medable's vision to open scientific research to the world using a platform designed for everybody, every biology, everywhere.
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![GettyImages-1370896437-doctor-patient-oncology-cancer]( "Choose An Oncology Offering Designed Around Patient Experience")
Examine this factsheet to see how Medable’s oncology offering simplifies data collection for sites and sponsors while keeping patients safe, comfortable, and engaged from any location.
