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Establishing a Data Ecosystem Using Automation to Optimize Regulatory-Compliant Clinical Trials



Webinar Date/Time: Thursday, May 23, 2024 at 10am EDT | 7am PDT | 3pm BST | 4pm CEST

Gain insight from this webinar series on leveraging technology to optimize clinical trial protocols and outcomes that comply with stringent regulatory requirements.

Register Free: https://www.pharmexec.com/pe/data-ecosystem

Event Overview:

Significant advances in technology are providing new opportunities to collect and utilize real-world data to establish better clinical trial protocols that have a patient-centric focus and the ability to transform healthcare. However, it is important to understand how such applications work and their impact on safety.

This webcast series uncovers the concerns of safety professionals and other stakeholders involved in the development and implementation of clinical trial protocols in the digital era and highlights methods to best apply digital data into routine practice to best optimize trial success and adhere to strict regulatory guidance.

Key Learning Objectives

  • The value of real-world data to safety programs tied to clinical trials.
  • Learn about new innovations to use clinical, genomic, and other data to develop machine learning algorithms and deliver insights to improve patient care.
  • Challenges and solutions for setting up studies across the eClinical technology landscape
  • Strategies to leverage innovative systems and optimize trial outcomes with patient safety in mind.

Who Should Attend

  • VPs and QPPVs of safety
  • Case processing specialists
  • Safety evaluators
  • Safety IT professionals
  • Safety managers
  • Clinical researchers, data scientists, and clinical decision teams responsible for:
    • Clinical development planning, study design, and study planning
    • Clinical data management, collecting and evaluating trial metrics
    • Standards conformant study deliverables
    • Project management of studies, process optimization, and operational excellence

Full Agenda
Thursday, May 23rd:
10:00 am EDT Oracle and Cerner: A Leap Forward in Safety
Michael Fronstin, Global Head of Clinical Research and Consulting; Oracle Cerner Enviza
Bruce Palsulich, Vice President of Product Strategy; Oracle Health Sciences 

11:00 am EDT Automating Study Setup with a Digital Data Flow
Julie Smiley, Sr. Director, Life Sciences Product Strategy; Oracle, and other non-Oracle speakers.

12:00 pm EDT Building a Thriving Culture of Innovation in Pharmacovigilance
Non-Oracle speakers


Michael Fronstin
Global Head of Clinical Research and Consulting
Oracle Cerner Enviza

Bruce Palsulich
Vice President of Product Strategy
Oracle Health Sciences

Julie Smiley
Sr. Director, Life Sciences Product Strategy

Register Free: https://www.pharmexec.com/pe/data-ecosystem

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