Harnessing AI for Clinical Trial Workflow Management

Life Sciences, Clinical Trials, Drug Safety,
  • Wednesday, October 04, 2023

Join the featured speakers for an engaging webinar that delves into cutting-edge advancements in clinical trial workflow management. In this informative session, the featured speakers will explore how the power of artificial intelligence (AI) and large language models are transforming key aspects of clinical development, including redaction, clinical endpoint adjudication and central eligibility reviews. Discover how these groundbreaking technologies are streamlining processes, enhancing data security and revolutionizing the way clinical trials are conducted.

During this webinar, the expert speakers from AG Mednet, Fortrea and Cleveland Clinic will discuss the practical applications of AI and large language models, demonstrating how they can significantly improve efficiency, accuracy and compliance in critical functional areas of clinical development.

Read more...

The key highlights of the webinar include:

  • Redaction: Learn how AI-powered tools can identify and remove personally identifiable information (PII) from clinical trial documents, ensuring compliance with regulations such as the general data protection regulation (GDPR). Explore the potential for automated redaction, reducing the burden on investigator sites and contract research organizations (CROs) while maintaining data integrity
  • Data completeness and validation: Discover how AI can review site provided documents and resulting event dossiers, providing an assessment ensuring that all data necessary to adjudicate events and endpoints have been provided. This automated data quality enhancing process will make initial reviews more agile, reducing queries and delay risks
  • Process analysis and optimization: Explore how AI can help to analyze adjudication processes by looking at meta-data about how long individual steps are taking in long, multi-constituency workflows. AI can help determine where there may be bottlenecks as well as which areas could benefit from further training or workload balancing
  • Computer-aided adjudication and eligibility reviews: Discuss how future AI models different may help evaluators to focus on the right data to increase consistency and reduce the time it takes to reach consensus.  Examine whether models could reproduce for adjudicators what AI-enhanced systems have achieved in medical imaging analysis

Read Less...

Don’t miss this opportunity to stay at the forefront of clinical trial advancements. Register today for this webinar to gain valuable knowledge and insights into the future of clinical trial workflow management. Discover how AI and large language models are revolutionizing the industry, and learn how AG Mednet’s Judi platform, alongside the right CRO and academic research organization (ARO) development partners, can empower an organization to drive efficiency, compliance and success in clinical development.

Join this webinar to discover how to unlock the potential of AI in clinical trial workflow management.

Speakers

Abraham Gutman, AG Mednet

Abraham Gutman, CEO and Founder, AG Mednet

Abraham Gutman founded AG Mednet in 2005 after selling his previous company to AT&T. He is a technologist with 35 years of experience in the conception, implementation and sales of advanced software systems and platforms in fields including telecommunications and life sciences. He holds a BA in Computer Science from Cornell and an MS in Computer Science (AI) from Yale.

Message Presenter
Catherine Tyner, Fortrea

Catherine Tyner, Executive Director, Adjudication Services, Fortrea

Catherine Tyner, MA, MFA, ABD, is the Executive Director of Adjudication Services at Fortrea with over 26 years of clinical research experience. Her expertise predominantly lies in Oversight Group Management (CECs, DSMBs/DMCs), Core Laboratories, and Clinical Safety where she has made significant contributions to shaping the industry.

Throughout her career, Catherine has led the establishment and global leadership of Adjudication departments at renowned organizations such as Quintiles, Novella Clinical, and Covance (now Fortrea). With oversight of 300+ Adjudication trials across diverse therapeutic areas, she has contributed to shaping the industry’s approach to Adjudication.

Catherine was an early advocate of electronic adjudication and has provided crucial advisory insights for the development of Adjudication technology solutions. Her notable publications, conference contributions, and her seminal 2011 white paper titled “Establishment and Operation of Clinical Endpoint Committees: Best Practice for Implementation Across the Biopharmaceutical Industry” underscore her thought leadership and contributions to the body of clinical research knowledge and best practice.

Message Presenter
Kimberly J. Brown

Kimberly J. Brown, RN, BSN

Kimberly J. Brown has been a Registered Nurse for 40 years. She has worked in cardiology ICU and stepdowns at the Cleveland Clinic in Cleveland Ohio from 1983 to 1996. In 1996, she moved to Anchorage Alaska to help Columbia Hospitals start an Open-Heart Surgery program. She was also the Director of Critical Care there overseeing the ICU, Stepdown, ER, Cath and EP Labs. In 1998, she returned to the Cleveland Clinic and worked as an Adult and Pediatric Cardiology Clinical Trials Research Coordinator. Transitioned to C5 Research and worked as a Clinical Trials Project Manager. For the last 15 years, she has worked as the Manager of the Adjudication Group within C5 Research. During this time, she oversaw the completion of adjudication for more than 180 pharmaceutical and device trials. She co-authored multiple research abstracts, manuscripts and a book chapter during her career. She also has presented at multiple international conferences on cardiac nursing and research topics.

Message Presenter
Venugopal Menon, Vascular & Thoracic Institute

Venugopal Menon, MD, FACC, FAHA, Section Head of Clinical Cardiology, Robert and Suzanne Tomisch Department of Cardiovascular Medicine, Sydell and Arnold Miller Family Heart, Vascular & Thoracic Institute

Dr. Venu Menon is the Section Head of Clinical Cardiology in the Robert and Suzanne Tomisch Department of Cardiovascular Medicine, Sydell and Arnold Miller Family Heart, Vascular & Thoracic Institute. He is also the Director of the Cardiac Intensive Care Unit and the Cardiovascular Fellowship program and is the Mehdi Razavi Endowed Chair and Professor of Medicine at the Cleveland Clinic Lerner College of Medicine.

Dr. Menon has published more than 200 manuscripts in peer-reviewed publications with research interests in cardiac critical care and time-sensitive cardiac emergencies. Dr. Menon also has a leadership position in the Cleveland Clinic Clinical Coordinating Center for Clinical Research (C5 Research) and is involved in the conduct of clinical trials around the world, including chairmanship of the cardiovascular events committee on multiple phase III seminal clinical trials. He serves on the American Heart Association committee for scientific sessions and is the American College of Cardiology Liaison to the American Heart Association’s Emergency Cardiovascular Care committee.

Message Presenter

Who Should Attend?

This webinar will appeal to Head/Director/VPs in the following fields:

  • Clinical Operations
  • Clinical Development
  • Clinical or Drug Safety
  • Pharmacovigilance
  • Clinical Procurement/Outsourcing/Vendor Management/Alliance
  • Clinical Endpoint Adjudication
  • Clinical Endpoint Committee (CEC)
  • Data Monitoring Committee (DMC)

What You Will Learn

Learn how AI tools can be used to streamline clinical trial processes at many levels including:

  • Redaction: Learn how AI-powered tools can identify and remove personally identifiable information (PII) from clinical trial documents, ensuring compliance with regulations such as the general data protection regulation (GDPR). Explore the potential for automated redaction, reducing the burden on investigator sites and contract research organizations (CROs) while maintaining data integrity
  • Data completeness and validation: Discover how AI can review site provided documents and resulting event dossiers, providing an assessment ensuring that all data necessary to adjudicate events and endpoints have been provided. This automated data quality enhancing process will make initial reviews more agile, reducing queries and delay risks
  • Process analysis and optimization: Explore how AI can help to analyze adjudication processes by looking at meta-data about how long individual steps are taking in long, multi-constituency workflows. AI can help determine where there may be bottlenecks as well as which areas could benefit from further training or workload balancing
  • Computer-aided adjudication and eligibility reviews: Discuss how future AI models different may help evaluators to focus on the right data to increase consistency and reduce the time it takes to reach consensus.  Examine whether models could reproduce for adjudicators what AI-enhanced systems have achieved in medical imaging analysis

Xtalks Partner

AG Mednet

AG Mednet is revolutionizing the clinical trial process through Judi, the award winning clinical trial collaboration platform. Designed to empower the ecosystems that drive clinical research, the proven platform Judi streamlines workflows, facilitates communication, and accelerates the development of novel therapies for patients. The proven Judi platform is trusted by 19 of the top 20 global biopharmaceutical sponsors and 5 of the top 6 global CROs and enables clinical teams around the world to come together to seamlessly manage complex workflows in endpoint adjudication, eligibility, data safety monitoring, medical imaging, and other mission-critical areas of clinical development.

You Must Login To Register for this Free Webinar

Already have an account? LOGIN HERE. If you don’t have an account you need to create a free account.

Create Account