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DECENTRALIZED TRIALS

1:30 2020 Onsite Clinics
How State-Of-The-Art Clinical Trial Mobile Vision Clinics Work

Are you seeking a non-traditional option to complete the eye exams necessary for your ocular clinical trials? A mobile clinic may be the solution you're looking for.

25:59 Clinical Endpoints
A Framework For Selecting Reliable Clinical Endpoints From Real-World DHT Data

Dr. Andy Liu presents a case study determining which digital measure of physical activity would be a well-defined and reliable clinical endpoint in a trial including patients with diabetes.

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Comprehensive Patient Support For Clinical Trial Success

Our white-glove attention to detail and customizable, comprehensive range of services ensure that we make even the most complex challenges more manageable. Discover how we can support your needs.

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IRT And Direct-To-Patient Trials

Want to know more about the growth and expansion of IRT in the decentralized trial space? Witness how IRT is being used to support direct-to-patient delivery in this hybrid trial case study.

1:01:13 Pharma Data GettyImages-1091887430
Collect Better Oncology Trial Data, Easier

In this webinar, experts discuss how enriching oncology clinical trials with RWD generates deeper insights and improves operational efficiency to achieve better patient outcomes.

47:47 Leveraging dhts
Leveraging DHTs To Improve Data Collection And Analysis

How can wearable DHTs be leveraged to measure physical activity in patients with immunological diseases, enhancing clinical trials and advancing drug development?

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Technology Overload: Addressing Site Challenges Of Digital Trials

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.

29:36 Castor Product Spotlight New On-site ePRO
On-site ePRO Solutions For Flexible Data Collection Across Devices

Optimize flexible electronic patient-reported outcomes that allow participants to switch between site-owned devices, personal hardware, and remote completion.

22:46 Physical Activity
Digital Physical Activity Measures In Phase 3 Immunology Trials

Dr. Jie Shen, Research Fellow and Director of Digital Science at AbbVie, shares lessons learned from incorporating digital measures of physical activity into Phase 3 immunology clinical trials.

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How Optimized Trials Enhance Patient Enrollment, Retention, And More

Watch as experts from Elligo discuss the benefits, challenges, and solutions associated with optimized trials. Discover how leveraging these strategies can solve key issues in clinical research.

19:47 Enhancing Data Collection, Delivery, And Operational Efficiency
Enhancing Data Collection, Delivery, And Operational Efficiency

Remote and hybrid trial setup for cardiac monitoring can be challenging, with several but there are steps you can take to optimize cardiac monitoring workflows and data capture.

1:03:01 IQVIA ACT
Trials And Tribulations Of Electronic Patient Consent: Removing Barriers To eConsent Adoption

After a decade of dabbling with eConsent, how can sponsors and technology providers meet the demand to bring clinical trials directly to the patient at a global scale? In this webinar, you’ll learn strategies to overcome the persistent challenges in eConsent adoptio...

15:02 How Can Patient-Centric Cardiac Monitoring Enable Decentralized And Hybrid Trials
Patient-Centric Cardiac Monitoring For Decentralized And Hybrid Trials

A patient-centric approach to cardiac monitoring is helping to advance data collection and reliability during decentralized and hybrid clinical trials.

58:16 Data Analytics Strategy
Three Data Trends to Consider Now When Developing Your Decentralized Clinical Trial Strategy

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.

4:17 Medidata - Site Perspective
DCTs: The Site Perspective

Putting patients and sites on the same platform coordinates and simplifies eCOA patient data collection and provides a 360 degree view of the patient. See how through Dr. Aaliyah's story.

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Everything You Need To Know About Adopting eConsent Across Large Pharma Organizations

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.

1:44 medable oncology
Patient First Solutions For Oncology

Medable, Inc's new oncology offering is an end-to-end suite that includes an extensive eCOA library, pre-built and validated DCT applications such as Total Consent and Televisit, and protocol design consulting.

19:16 pcm trials vid 2
Clinical Trials From Home: The Role Of Research Nurses

In this presentation, speakers shed light on the advantages of home visits for clinical trials and what research nurses do to make this possible.

2:03 Cardiac Monitoring
Transforming Cardiac Monitoring With 6-Lead And 12-Lead Devices

Learn how you can monitor a large number of cardiac conditions in real-time and support clinical trials across phases and TAs.

59:47 Site Support The Cornerstone Of The Patient-Centric Digital Trial Evolution
Site Support: The Cornerstone Of The Digital Trial Evolution

Follow along as this panel of experts shares key insights from their experiences, highlighting the technologies and processes that lead to successful partnerships in patient-centric digital trials.

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Harness The Power Of eCOA In Your Next Trial

In this webinar, explore the importance of eCOAs, how they have evolved from the standard paper diaries, and what efficiencies you can realize from them.

53:35 The New Era Of Evidence Generation In Clinical Trials
The New Era Of Evidence Generation In Clinical Trials

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.

48:50 medabe webinar
Enable Next-Generation Clinical Research At Scale

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. 

1:24 Digital Data Collection
Modernizing Clinical Research With Patient-Centric Digital Data Collection

Accelerate clinical trial modernization with streamlined collection of continuous, high-precision data centered on the patient.

1:01:37 clinical_leader_presentation_92022
The Platform Shift is Here: Are you Realizing ROI Across your Portfolio of Studies?

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 trial...

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What It Really Takes To Adopt eConsent Across Large Pharma

Explore the benefits of incorporating consent management technology and discover practical strategies for developing effective change management and training programs.

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Creating The Digital Foundation For Scale In Clinical Development

Learn how CROs, pharma, and biotechs are using digital trial methods to scale efficiencies across the entirety of their clinical trial portfolio for maximum ROI.

1:33 Transformative Cardiac Solutions From AliveCor
Transformative Cardiac Solutions

While traditional ECGs require on-site visits, delaying data and increasing drop-out risk, AliveCor''s FDA-Cleared ECG devices can be used on-site as well as in decentralized and fully remote trials.

16:39 The Evolving Role Of AI And Innovation In Cardiac Monitoring
The Evolving Role Of AI And Innovation In Cardiac Monitoring

In this presentation, the panel of experts focuses on the changes AI has brought to cardiac monitoring data during clinical trials and addresses the skepticism over the use of new innovations.

3:31 Elevating the site voice
Elevating The Site Voice

A decentralized trial can be daunting for sites, but Medidata offers solutions to help site staff, sponsors, and patients move smoothly through the clinical trial process.