Medidata 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 to improve patient experiences, accelerate clinical breakthroughs, and bring therapies to market faster. A Dassault Systèmes company (Euronext Paris: FR0014003TT8, DSY.PA), Medidata is headquartered in New York City and has been recognized as a Leader by Everest Group and IDC. Discover more at www.medidata.com and follow us @Medidata.
MEDIDATA VIDEOS
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Discover how you and your sites can benefit from Rave Companion, an easy-to-set-up and user-friendly tool that fits right into existing data entry workflows, ensuring simpler, quicker, and more accurate data entry.
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Explore this patient data surveillance (PDS) solution — which is part of Medidata Detect — and how it's providing a single workspace for CDMs to aggregate, anatomize, and review patient data from multiple sources.
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Get an inside look at this RTSM solution, a full-service and unique platform-based approach to interactive response technology.
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Discover how Medidata's Patient Insights Program is working to integrate patient perspectives throughout the software development life cycle to enhance participant experiences in clinical trials.
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Watch three short videos discussing how to achieve success in decentralized clinical trials from the patient, sponsor, and site perspectives to improve DCT outcomes.
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Medidata connects patients, sites, sponsors, and partners in a secure and scalable cloud environment. Hear from several customers as they reflect on their experience and the benefits of using Medidata’s All-In-One-Platform.
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Gain a better understanding of how Medidata’s Rave Clinical Operations product suite supports core workflows in clinical operations and helps make therapies available to the patients who need them most.
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Discuss how industries and organizations can come together with patients and patient advocate groups to foster better patient inclusion and participation in clinical trials.
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Explore how a clinical research coordinator (CRC) typically manually re-enters data from their EHR/EMR system into Rave EDC, and how Rave Companion provides automated assistance to enable the CRC to complete EDC forms.
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Discover the challenges that the evolving clinical data landscape brings to clinical data management and what next-generation clinical data management capabilities are needed to address those challenges.
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Technology and clinical trials have gone hand in hand for a very long time. With an understanding of industry needs and an eye to the future, learn about the push to greater adoption of more innovations.
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Uncover how this new app is able to increase patient engagement, allowing patients to access their portal via iOS and Android to input and share images and data for clinical trials in real time.
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In this brief roundtable session, patient advocates are interviewed to voice their views on decentralized clinical trials.
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Watch this brief video to see how the industry’s only scalable, end-to-end offering for decentralized clinical trials can connect trial experiences for patients, sites and sponsors.
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Watch this video to see how a top mid-sized CRO implemented decentralized patient services and other creative solutions to continue trials through the pandemic across therapeutic indications.
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Developments over the past two years have emphasized the pivotal role of technology in accelerating safe clinical trial development. In fact, technology tools including electronic data capture, eCOA, and centralized statistical monitoring helped Moderna to bring a COVID-19 vaccine through the full clinical trial life cycle in under a year.
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This video series explores the opportunities and challenges presented by new data capture sources, looks at how clinical data management technologies and processes are transforming, and how data managers can prepare for the future of clinical data management.
PODCASTS
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See Medidata’s unified platform of end-to-end capabilities for clinical data capture and management, including data capture covering eConsent, eCOA, RTSM, and more.
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Listen in as Medidata’s Vice President, DCTs and Patient Registries | Patient Cloud Kelly McKee talks on the podcast Pivot Points from Cramer, a brand experience and marketing agency, about treating clinical trials as continuous patient engagement rather than as a transaction to create “sustainable patients.”
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Gain insight from the Director of Clinical Data, Central Monitoring, and Oversight at Moderna Heidi McIntyre, Senior Director of RBQM R&D at Medidata Olgica Klindworth, and Senior Director of Clinical Operations Portfolio at Medidata Ken Hamill on clinical trials design and delivery.
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This episode discusses clinical trial technology adoption across patients, care teams, trial sites, and researchers and the need for industry buy-in, especially around decentralized trial technology.
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In this episode, learn how to drive diverse patient recruitment by moving from transactional, traditional strategies to innovative, people-focused approaches.
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In this episode, industry experts Kelly McKee and Alicia Staley are joined by Paul Chang, VP of Design at Medidata, to map the future of product design in clinical trials.
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In this episode, Craig Lipset, founder of Clinical Innovation Partners, sits down with Kelly McKee and Alicia Staley of Medidata to discuss the challenges of data return and how to improve patient access and clinical trial data transparency.
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Kelly Mckee of Medidata, leads a panel discussion with Jeff Kingsly DO, CEO of IACT Health, and Anne Marie Mercurio, a patient advocate to discuss the challenges and opportunities when using virtualizing technologies in clinical trials. Together they discuss lessons learned from the use of live video visits to enable clinical trial continuity along with the possibility of hybrid trials becoming the new normal for the near future.
WEBINARS
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Watch as experts from eClinical Solutions and Medidata delve into end-of-study process challenges, the transition to electronic distribution and management, the advantages of leveraging a digital platform, and more.
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Watch as presenters from Medidata dive into the most common roadblocks customers face when adopting a modern CTMS—and how to avoid them.
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As the volume and variety of clinical trial data have exploded - including electronic health records (EHR), sensors, and ePRO data - processes to manage and monitor that data have not kept pace. These processes are still grounded in a retroactive data review and reconciliation with a primary focus on eCRF data.
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This webinar aims to introduce the main regulatory themes, as well as provide a practical insight into converting regulatory theory to practical steps to enable DtP on global studies.
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Decentralized trials, once an emergent trend, are now becoming an established practice. This webinar explores the changing paradigm of study conduct to enable decentralization of clinical trials, both for patients and sites, and why it has permanently changed the paradigm for clinical execution.
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Medidata’s first webinar series for 2022 will bring industry leaders and game changers together to discuss the trends and insights in modernizing data management. This first webinar will provide best practices, practical tools and strategies that can be used today and actions to support the future "new normal". In this session, you will learn about three strategies to amp your data quality management.
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Ensuring a positive blood plasma donor experience relies on a complex network of donor, site, and manufacturing touchpoints in a heavily regulated environment. Learn how CSL Plasma created a unified solution for all plasma collection and manufacturing capabilities and how this will impact donor and site experiences.
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The need for remote access during the COVID-19 pandemic has opened the door to broad changes in how clinical trials are conducted today. Yet there is still some uncertainty around which technologies to implement, the level of on-site versus virtual (or a combination) of activities, and necessary operational changes.
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2022 will continue to blur the lines between data management and clinical operations. Hear from industry leaders from Amgen and Medidata on the process and technology needed to drive the next generation of data management.
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Learn how the rapidly evolving clinical data capture landscape influences the challenges clinical data management teams face, and the emerging technology, processes, and skillsets that can help the industry adapt.
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Watch this webinar to learn how to accelerate patient enrollment and retention by eliminating the transactional nature of clinical trials, facilitating long-term follow up and safety surveillance through post-trial engagement, and understanding key considerations, including regulatory and privacy concerns, as part of an overall decentralized trial strategy.
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Issues surrounding patient awareness of and access to clinical trials have been roadblocks to participation for many years. Finding the right patients at the right time for the right study requires a new approach focused on empowering patients long term, including both pre- and post-study engagement. Watch the available webinar to find out more.
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How do you develop COVID-19 vaccines and treatments safely in less than a year, virtually? The answer is decentralized technologies, which allows for patient participation outside of the traditional trial site and virtual clinical oversight activities, on a single platform. This session demonstrates how remote data capture linked to real time data insights helps customers get life-saving vaccines and treatments to patients in record time.
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Prior to the global pandemic, virtualization technologies were slow to adoption, with most large scale trials operating in traditional clinical settings. Now, the virtualization of clinical trials has become the industry’s new focus. In this webinar we’ll be exploring the changing paradigm of study conduct to enable virtualization of clinical trials, both for patients and sites, and why it has become the industry’s new focus.
CONTACT INFORMATION
Medidata, a Dassault Systemes company
350 Hudson Street, 9th Floor
New York, NY 10014
UNITED STATES
Phone: 732-997-9172
Contact: Liz Lange, Lorna Protomartir
BROCHURES/DATASHEETS
- Rave TSDV - Improve CRA Efficiency And Reduce Site Burden
- Managing Risk In Clinical Trials
- Drive Efficiencies And Speed With Secure, Remote Monitoring
- The Only Platform Digitizing And Sharing All EOS Data
- Even The Most Complex Studies Reach Milestones Faster
- Unlock The Power Of Randomization And Trial Supply Management
- Cut Study Start-Up Times By Up To 50% With eCOA
- Patient-Centric, Native App Helps To Streamline TrialsPatient-Centric, Native App Helps To Streamline Trials
- Streamline And Optimize eCOA Implementation
- Capturing EHR Data In Just A Few Clicks
- One Place To Capture, Manage, Clean, And Report Clinical Research Data
- Faster, Simpler Trial Management
- Create, Collaborate, & Solve With A Global Innovators
- myMedidata - Medidata's Patient Portal
- eCOA Empowers Patients To Capture And Share Images From Any Location
- Comprehensive Data Surveillance and Risk Monitoring
- Pioneering The Next Generation Of Connected Health Solutions
- Transform Your Study On A Unified Platform
- Rave Clinical Trial Financial Management
- Powering Smarter Treatments And Healthier People
- Drive Efficiencies And Speed For Your Site With Secure, Remote Monitoring
- Medidata Professional Services Streamlines TSDV Adoption
- Rave Imaging Archive: Reliable And Compliant Access To Your Image Data After Trial Close
- Optimize Your Endpoint Adjudication On A Single Platform
- Take The Right Approach To Medical Device Clinical Trials With Rave RTSM
- Rave eTMF - Simplify Trial Oversight With Unified Document Management
- Streamline Your Medical Device And Diagnostics Trials
- Precise, Consistent, Faster Medical Coding For Clinical Trials
- Rave Grants Manager
- Patient Insights Program
- Rave RTSM: Optimize The Setup And Execution Of Repeat Visits
- Site Cloud: End Of Study (EOS)
- Rave Site Payments – The Industry’s Only Global Payment Technology Driven By EDC
- Medidata Decentralized Clinical Trials (DCT) Program
- Data-Powered Financial Management For Your Clinical Trials
- Medical Imaging In Early Phase Studies
- Rave RTSM And Edit Live Design
- Take The Right Approach To Supply Accountability
- Rave RTSM: Direct-To-Patient
- eSource: The Evolution Of Clinical Trial Data Capture
- Discover Solutions For Your Clinical Trial Challenges - Personalized Assessment
- Medidata Clinical Cloud
- Medidata eConsent – Empowering Patients Right From The Start
- Medidata RBQM – Your Path To Clinical Operations Excellence
- Re-engineer Clinical Trial Image Management
- Medidata Risk Management – Enabling Patient Safety And Data Integrity
FEATURED ARTICLES
- Accelerate Precise Medical Coding In Clinical Trials
- Finding The Right Technology For Your Clinical Development Plan
- Clinical Trials – The Ever-Changing Face Of Complexity
- TEFCA, Healthcare Data Interoperability, And Clinical Research Use Cases
- Patient Perspectives On Decentralized Clinical Trials
- Patient Perspectives On eConsent
- Blinded Randomization And Trial Supply Management Gets Support
- A Review Of The Changing Trends And Use Of eCOA In Clinical Trials
- Better Data, Better Decisions
- Advanced Analytics To Power Action Across The Trial Continuum
- DCT: Book Of Case Studies
- Data And Analytics To Power Action Across The Trial Continuum
- Patient Insights Informed Consent Engagement
- My Worst Nightmare In RSTM: Accidental Unblinding
- Revolutionizing Clinical Studies With Adaptive Trial Designs
- Busting The Top 7 Data Quality Myths In Clinical Trials
- Solving The EHR-To-EDC Challenge: A Scalable-First Approach
- Rethinking Your Imaging Strategy
- Electronic Informed Consent In Clinical Research
- Fast Data Insights Improve Productivity, Client Centricity
- Eliminating The Guesswork From Critical Decision Making
- Making Clinical Research Better For Patients With Patient Centricity By Design
- Pioneering The Next Generation Of Connected Health Solutions
- On-Demand Payment Technology Offers Accuracy, Speed, & Transparency
- Automated Trial Monitoring Workflows Make Small Teams More Efficient
- Achieving Harmonious and Optimized Site Budget Negotiations
- Detecting Variability In Adverse Event Reporting
- The Future Of Clinical Trial Oversight
- Adaptive Designs Save Time And Money: Why Aren’t They Used More Often?
- Industry Research Report: The Future Of Clinical Trials