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.
Addressing Operational Challenges Impeding Patient Access to Trials: Next Steps
Medidata AI provides analytics and solutions that can help you:
- Understand how data can be used to make more informed decisions around how COVID-19 impacts study enrollment, data collection and visits
- Overlay trends in COVID-19 testing and infection rates with impact on trials to identify leading indicators of recovery at a country / region / site level
- Learn how you can plan ahead and support recovery planning by tacking industry benchmarks and leading indicators
The Evolution of Trial Virtualization and its Impact on Clinical Supplies
The state of clinical supplies is changing rapidly as we see trials moving towards virtualization. The impact, logistics and strategy to account for these changes and challenges are what we explore on this webinar that face sponsors, sites, depots, CROs and particularly patients.
Financial Health for Your Oncology Research
In this session, you will learn the secret to budgeting and negotiating smart for your oncology studies. In addition, we will talk through how data collection and payment triggers can allow for a smooth payment process, especially for those conditional and/or high-ticket items within your budget.
Two Success Stories: How to Best Leverage your Strategic Consultants in IRT/RTSM
Watch this webinar to:
- Learn how to get the most out of your strategic consulting team as they provide mentoring and training
- Gain insight into best practices in executing your IRT/RTSM software from two sponsors
- Learn how a variety of vital clinical study roles are evolving in a non-traditional manner as key assets to a successful study execution
Virtual Trials vs Trial Virtualization
In this webinar we explore 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.
Watch to learn:
- Why you must define the “virtual clinical trial” around patient participation now to ensure long-term benefits to experience and outcomes
- How to streamline clinical timelines by implementing end-to-end virtualizing technologies to unify your platform approach
- The impact of virtualization technologies on sites and how to act now to ensure your ready to partner with changing future operating models
- How a combination of on-site and remote monitoring helps reduce risk, while increasing efficiency
The Emerging Role of RWE: Longitudinal Patient Insights to Bridge the Clinical and Real World
This webinar covers how longitudinal patient insights (LPI) can de-risk your clinical trials, lower the costs of follow up studies, and enhance insights.
Budget to Payments: Unify Your Clinical Trial Financial Tools to Streamline Processes
Join this webinar to engage in the following conversations:
- Clinical trial financial management elements and connecting the dots with unification
- Gaining transparency of the full investigator grant budget and payments process and eliminating roadblocks
- Obtaining the right experts for investigator grant budget and payments processes
Utilizing Patient Centric Solutions to Address Patient Burden in Rare Diseases
In this webcast, our speakers discuss why it’s so important to include the rare disease patient perspective when developing clinical trials, including:
- Unique burden patients with rare diseases face in clinical trials
- Understanding the importance data plays for the patient in trial, and why data return is critical for these patient populations
- How the design studios Infuse the patient voice in solution design
- What a patient design studio operates like
Modernizing Data Management in the D-Clinical Age
Watch this webinar to learn:
- How to bring trials to patients today by enabling the collection of digital streams from all sources
- How to discover new technology and processes needed to speed drugs to market
- How in this new age of D-Clinical, data management can transform clinical trials
Imaging AI and Machine Learning – Beyond the Hype
Watch this webinar to learn:
- How AI needs to be focusing in specific areas, as past efforts (IBM Watson) to do everything, have failed
- How to narrow down imaging problem statements that will generate better results
- How AI and Machine Learning can function as “guide rails” for radiologists
- Areas that AI and Machine Learning can increase efficiency (thus saving money) and improve quality (thus saving lives)
Clinical Trial Flexibility & Customization Needs Required by Biotechs & Next Generation Therapies
After watching this webinar, viewers will:
- Understand the unique needs of small and midsize biotech companies when conducting oncology studies
- Recognize the need for an adaptive and responsive CRO amidst the current landscape and increased demand within the growing biotechnology industry
- Understand CRO best practices for understanding and adapting to the specific needs of small and midsize biotechs
- Tailor operational and technological approaches to planning, launching and conducting studies for a growing market
Improving Access to Clinical Trials for Rare Disease Patients Through Registries
Watch this webinar and learn:
- Introducing registries as a tool for rare disease patients
- Using registries to help rare disease patients become empowered, educated, and engaged regarding clinical trial opportunities
Looking Beyond the Current Trend of Virtual Trials
Watch this webinar to learn how to leverage many virtualization technologies into a unified approach to trial virtualization and what’s next for virtual clinical trials.
Optimizing Efficiency and Effectiveness with a Data-Driven Clinical Trial Management System (CTMS)
Watch this webinar and learn:
- How a data-driven approach to clinical trial management enables effective and efficient oversight of trial activities
- Strategies for taking a risk-based quality management approach to clinical trial management
- How the right CTMS can enable better workflows and tighter collaboration across clinical operations teams
Understanding the Novel Challenges in Rare Disease Clinical Development: Perspectives from Experts
Medidata recently conducted an in-depth market research study with Industry Standard Research to understand how the challenges impacting biopharma and CROs who are conducting rare disease research. Watch this on-demand webinar to learn about:
- The challenges faced by those working in the rare disease space
- Their perspectives on how well current technology meets these challenges and what improvements they would like to see in technology or analytics
- Insights into current or up-and-coming trends in rare disease clinical development
How Five COVID-19 Technology Innovations are Reducing Risk in Clinical Trials
During COVID-19, regulators and sponsors show pragmatism and flexibility in terms of mitigating challenges in the current climate. The combination of digital distribution, innovation, and flexibility enabled the clinical trial community to expedite drug development during the COVID-19 pandemic while also minimizing risks to patient and trial success. Watch this on-demand webinar to explore how new and reimagined technology innovations are addressing the impact of COVID-19.
Tackling the Challenges in Development and Clinical Adoption of Advanced Therapies
Watch this webinar to hear about the perspectives of key stakeholders on the challenges in designing Advanced Therapy Medicinal Product (ATMP) clinical trials with small patient populations, reimbursement uncertainty, and long term prospects for the commercialization of advanced therapies
[Webinar Series] The Changing Landscape of Clinical Trials
Traditional ways in which clinical trials are being conducted are being put to the test and having repercussions across the clinical trials landscape as COVID-19 continues to disrupt the world.
Watch this series of on-demand webinars where we discuss this rapidly changing situation, what you can do to manage trials more effectively and the role that technology can play to work together to vastly simplify trial management.
Next Virtual Event: Pharma & Biotech
Watch Medidata’s Virtual Conference On Demand 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
Watch Medidata’s Virtual Conference On Demand 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 Medidata’s Virtual Conference On Demand 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
[MassMedic Series] The New World: Connecting the Next Generation of Patient Data and Devices with Deep Analytics for Commercial Success
Watch this webinar to learn about a use case on the process of building the standardized, multi-faceted dataset to enable deep real-world data analysis for pre-surgical population management, surgical treatment patterns, and post-operative outcomes assessment.
[MassMedic Series] RTSM & Remote Monitoring: Realizing Quality while Mitigating Study and Site Risk for Medical Device Trials
Watch this webinar to hear Medidata experts discuss the challenges in device supply management and remote monitoring to realize quality while mitigating study and site risk during these challenging times.
[MassMedic Series] Reconsidering Trial Design Medical Device Companies to Ensure Data Capture in the Challenging COVID-19 Era
Watch this webinar to learn about considerations for adjusting data collection strategies in the middle of ongoing studies, plus trial virtualization, and how the move to decentralization will only accelerate in a post-COVID-19 world.
Virtualizing Clinical Trials: The Impact of Technology on the Patient Journey
Watch this webinar to hear about the patient’s journey and the impact of virtualizing technologies such as direct to patient trial supply management (IMP), eConsent, and other remote data capturing tools all integrated on a unified platform.
COVID-19 and Clinical Trials: Support Risk Mitigation and Recovery Plans With Data and Analytics
Watch this webinar to learn about key considerations for managing clinical trials during these turbulent times and how industry-wide trial metrics and analytics can support:
- Situation tracking by geography and therapeutic area
- Impact assessments and scenario analyses at trial and portfolio level
- Identification of leading indicators of recovery
Transforming Clinical Development and Discovery with Multi-omic Data in the Era of Precision Medicine
Watch this webinar to hear industry experts discuss key challenges, propose best practices, and share success stories illustrating how incorporating translational omics data into clinical development yielded novel insights and improved patient/study outcomes.
Maximizing the Benefits of a Unified Clinical Data Capture and Management Platform
Watch this webinar to see how leveraging multiple solutions on a unified platform streamlines processes, drives operational efficiency, eliminates reconciliation, and provides faster data insights.
Driving Quantitative Image Analysis for Early Phase Clinical Trials with Medidata and Medpace
Watch this webinar to hear experts from Medidata and Medpace discuss the role of Quantitative Imaging Biomarkers in clinical trials.
End of Study Hacks: The New Digital Age
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
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
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
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
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
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
Watch our webinar and Q&A session where we will demonstrate how Medidata 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
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
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
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
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
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
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
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
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
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
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?
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
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
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
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.