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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Meet the team responsible for ensuring the scientific rigor and outcomes of Medable’s clinical trial platform, and uncover how they’ve been pioneering eCOA and ePRO research for decades.
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The rise of SaaS (software-as-a-service) has transformed industries, including life sciences, by enabling new possibilities. See how it’s already helping life science organizations around the world today.
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It’s no secret that more trials are going digital. Here from a panel of industry experts including Sanofi, Bayer, and the Clinical Trials Transformation Initiative (CTTI) as they discuss the evolution of digital trials and share their experiences.
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See how life science companies are using software as a service (SaaS) to bring new benefits to study startup, data collection, and more with this short blog.
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Disparate data systems present challenges, yet clinical trial platforms provide centralized integration, standardization, advanced analytics, and strong security for an efficient solution.
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What does the ICF amendment or revision process look like within a digital platform and is this harder or easier than traditional paper-based approaches?
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It’s apparent to those who have used it that the “e” in eConsent could stand for much more than 'electronic'. Duke’s new research shows why participants prefer an eConsent experience bolstered with videos, media, questions, and more.
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Learn how SaaS technology can revolutionize clinical trial launches by improving transparency, increasing control, and streamlining efficiency.
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Learn how digital data is helping the pharmaceutical industry tackle its most daunting challenge; the 12 year, $3 billion average to bring a new drug to market.
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As trials continue to digitize, learn how connected sensors, COAs, PROs, and other forms of data will come together to form the evidence of tomorrow.
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Recent research from the Tufts Center for the Study of Drug Development (CSDD) illuminated the substantial ROI of digital endpoints in clinical trials. Discover how to transform your trials today.
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Learn how a top-10 pharmaceutical client was able to "fundamentally transform the way they execute clinical trials" with the digitization and standardization of pain maps in a diabetic polyneuropathy trial.
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Discover how eCOA use drove >90% adherence across an extensive weight management master protocol clinical trial with multiple sub-studies across 70+ research sites.
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Explore how digitizing clinical trial processes, such as paperless "body map" assessments, can enhance efficiency and standardization in pharmaceutical trials.
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Discover how Medable and industry leaders are accelerating clinical research and transforming patient care in the era of digital innovation.
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Although non-verbal conversations between friends are now primarily conducted through text messages or similar apps, see why email remains the standard mode for businesses and organizations.
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Despite the rise of digital solutions in healthcare, paper consent forms are still common in today’s clinical trials. Unfortunately, these paper forms pose significant challenges in retaining the documentation of informed consent for centrally stored biospecimens.
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Discover our associates' insights on the key developments from ASCO 2024 that are set to shape the future of cancer care and patient outcomes.
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Explore how innovative strategies are cutting clinical trial times in half and accelerating the delivery of life-saving treatments.
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Oncology trials are notorious for presenting participants and sites with many challenges. With the FDA having put its support behind digital tools, learn how they make oncology trials easier for everyone.
CONTACT INFORMATION
Medable
525 University Ave, Suite A70
Palo Alto, CA 94301
UNITED STATES
WEBINARS
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Hear from a panel of oncology experts as they showcase 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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Simplify the historically complicated, black-box processes around eCOA solution deployment, content storage and visualization, and global go-live.
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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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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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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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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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Explore the benefits of incorporating consent management technology and discover practical strategies for developing effective change management and training programs.
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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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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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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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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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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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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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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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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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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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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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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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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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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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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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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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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.