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.

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.

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.