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On Demand Webinars

Events

On Demand Webinars

The clinical life science industry is constantly evolving. Having as much knowledge as possible is only going to help you grow and understand the transformation. Keeping up to date with all of the changes that occur within clinical research can be just as important as the actual study.

Medidata provides life sciences professionals with the tools, expertise, and knowledge to power smarter treatments and healthier people. We are committed to helping you answer the hopes of patients and healthcare professionals for a life-saving drug, device or treatment. You build hope. We accelerate it.

Browse through our past events to learn more about best practices to optimize your clinical research.

Next Virtual Event: Pharma & Biotech

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Watch Medidata’s Virtual Conference OnDemand where experts discuss:

  • Risk Assessment, Central Monitoring, and RTSM
  • Patient Centricity by Design: The Path to Patient-Centric Solutions
  • Enabling Clinical Trials in a Pandemic: Continue Treating Patients and Minimize Risk

NEXT Virtual Event: Medical Device & Diagnostics

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Watch Medidata’s Virtual Conference OnDemand where experts discuss:

  • eConsent – A Patient-Centered Approach Towards Improving the Informed Consent Process
  • RTSM and Medical Device Trials: Realizing the Power of a Unified Platform
  • Virtual Human Modeling: The Living Heart
  • Connecting the Next Generation of Patient Data and Devices with Deep Analytics

NEXT Virtual Event: CRO

Watch Now

Watch Medidata’s Virtual Conference OnDemand where experts discuss:

  • eConsent – A Patient-Centered Approach Towards Improving the Informed Consent Process
  • RTSM and Medical Device Trials: Realizing the Power of a Unified Platform
  • Virtual Human Modeling: The Living Heart
  • Connecting the Next Generation of Patient Data and Devices with Deep Analytics

End of Study Hacks: The New Digital Age

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Watch this webinar to learn how Sponsors and CROs are challenging the status quo by developing new models to improve end of study compliance and productivity.

COVID-19: A New Era Transforming the Clinical Trial Landscape

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Watch this webinar to learn about the changing regulatory environment with respect to clinical trials in COVID-19 world, the impact of COVID-19 on trials, trial participants, sponsors, partners, and solutions to support this challenging new era.

Clinical Trials in a Post Pandemic Era

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Watch this OnDemand webinar on the future of Clinical Trials in a Post Pandemic Era moderated by Professor Stan Kachnowski, Director of the Digital Health Strategy program at Columbia Business School.

Medidata Office Hours Series

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AS COVID-19 continues to spread, Sponsors and CROs are struggling to continue trials while maintaining patient safety and data integrity. Watch these On-Demand webinars to hear Medidata’s panel of experts discuss trial virtualization, remote consent, and rapid eCOA deployment models that will help maintain the forward momentum of your clinical trials.

Declutter the Data in your Clinical Trial: Mitigate Risk Before it Becomes an Issue

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In this webinar, you’ll hear a discussion and Q&A Chat on how to find errors, trends, and anomalies in data—through a number of statistical algorithms and tests that do not require programming—while integrating this process as part of your risk process improvement.

Clinical Trial Data Meets the Real World: Bridging the Experimental and Post-Launch Worlds

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In this webinar, you’ll hear about key considerations and best practices when combining clinical trial data with real world data to power big data analytics.

Medical Devices and Advanced Analytics: Delivering on the Promise of Connected Data

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Watch our webinar and Q&A session where we will demonstrate how Acorn AI’s Connected Patient Platform can bring insight into the vast stores of video, imaging, and electronic surgical notes created by the new generation of robotic, precision, and surgical devices.

Unleash the Power of an Integrated Imaging/EDC Platform

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In this webinar, you’ll discover what an integrated solution looks like and how it could power up your trial by reducing time and eliminating errors on data reconciliation and double data entry.

CIOs’ Perspectives: Driving Clinical Trial Innovation with a Unified Platform

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In this IT-focused webinar, you’ll hear about the need for a platform approach to clinical research, the rationale for switching from disparate systems to a unified platform, and the benefits that could be realized with a unified platform.

Synthetic Controls: Best Practices and Regulatory Perspectives

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With fewer than 10% of compounds successfully achieving Phase 1 to FDA approval status1, researchers are increasingly seeking data and methods to address key challenges.

In this 1-hour session, you will hear from former FDA leaders and industry experts.

1Source: Clinical Development Succes Rates 2006-2015, BIO Biomedtracker, Amplion

Improving Clinical Trial Quality with Best Practices for E-Clinical Technology

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The increasing challenges of clinical research are well-known; growing trial complexity, more data sources and data points, disparate systems, manual processes and more. Watch this on-demand discussion on the new strategy for managing clinical trial technology.

A Paradigm Shift to Realize Intelligent Clinical Trial Oversight

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The usual approach of adding technology and headcount to manage today’s clinical trials is not sustainable or scalable. Learn how Rave CTMS delivers expected efficiencies and more importantly, enables you to be effective.

How and Why Celgene Adopted Medidata Rave eCOA

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This incredibly informative webinar delves deeply into Celgene’s adoption of Medidata eCOA solution. If your company is looking to adopt a new eCOA solution or have issues with your current one, this webinar is a must watch.

Applying Unified E-clinical Technologies to Streamline Study Conduct

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In this webinar, Medidata will conduct an interactive demo of our intelligent platform for life sciences—exploring our broader EDC, RTSM and ePRO capabilities—and show how adopting one platform can help unify your data and workflows across study execution, allowing for rapid study startup, more streamlined execution with cleaner data, and the elimination of unnecessary reconciliation efforts.

Improving Patient Centricity with Edge Design Optimizer

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In this demo webcast, see firsthand how Rave Design Optimizer can help you improve trial execution by identifying opportunities to optimize protocol design and bolster or reinforce patient retention strategies, leading to a more patient-centric trial.

Fast Track Your Early Clinical Development Lifecycle

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Discover how early-stage solutions can give you the competitive edge you need to accelerate your clinical development lifecycle.

The New Model for eCOA: Modernizing Technology, Process and Science to Change The Game

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Join industry experts from Medidata and Syneos Health as they discuss a long-awaited new path forward to the implementation of eCOA with a solid foundation of technology, service and science.

Global Site Payments; How Clear is Your Financial View?

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Now more than ever, clinical trial sponsors and CROs share a common burden – accurate budgeting, financial planning, and timely planning. Learn how to improve financial health, fuel innovation and increase compliance with the Medidata automatic payment solution.

Utilizing a Technology-first Approach to Maximize Brand Value & Gain Competitive Advantage

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In this webinar, we highlight some of these approaches and demonstrate how data and analytics can be used to gain a competitive advantage and create differentiation.

The Promise of Real-World Data: Using Technology to Enable the Standardization, Transparency, & Replicability of RWD Research

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Watch this webinar to learn how the use of technology for deploying data and analytic standards can be utilized to meet this challenge, by facilitating the standardization, transparency, reproducibility, and replicability of RWD research.

Unified Platform Defined

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Learn the five characteristics of a unified platform and how each benefits clinical research both for a single trial and across your suite of research efforts.