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Virtual Event

Oct 07, 2020 1:00 PM - Oct 09, 2020 6:30 PM

(W. Europe Standard Time)

4051 Basel, Switzerland

Future of Evidence and Smart Health Conference

Overview

Following the success of last year’s Future of Evidence and Digital Health Workshops, DIA is pleased to introduce a new two-track conference – the DIA Future of Evidence and Smart Health Conference.

In the Real World Evidence (RWE) track, we will continue discussing the quality of different types of RWE sources and how to best approach a unified framework for clinical data collection. We will explore how RWE can help optimize clinical trial design, and support decision-making for Regulators and healthcare providers (physicians and others). There will also be a particular focus on understanding how various stakeholders are leveraging RWE to advance healthcare knowledge and decision-making processes at a time when they are being increasingly delegated to AI and related technologies.

The Digital Health track will be a deep dive into the fast-evolving Digital Healthcare ecosystem and review not just novel wearables and data collection methods, but also new formats of digital intervention in Health. We will be tackling topics and concepts such as the Dynamic Dossier in the Cloud, Rapid Reviews, and Digital Therapeutics which could potentially help fulfill unmet medical needs for patients facing roadblocks in traditional therapy and intervention.

Featured topics

• Social Impact of Digital Health
• Wearables and Collection Methods
• Innovative Design Using Real-World Evidence and Novel End Points
• Real-World Evidence Collection Methods Design and Analysis
• Real-World Evidence Data Sources and Data Quality and Ethics
• The Patient Perspective on Real-World Evidence
• Digital Health – Artificial Intelligence and Machine Learning
• Blockchain
• Digital Therapeutics
• Cloud-based Systems
• Start-up Spotlights

Featured

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Exhibits

Who should attend?

  • Real World Evidence
  • Regulatory Innovation
  • Regulatory Science
  • Digital Health and Solutions
  • Patient Advocacy
  • Innovation
  • Policy
  • Epidemiology
  • Data Science
  • R&D big data
  • Data and analytics
  • Data Management, Privacy and Science
  • Artificial Intelligence and Machine Learning
  • Clinical operations and Clinical development
  • Market Access & Reimbursement
  • Bioethics

Program Committee

  • Thomas  Brookland, MSc
    Thomas Brookland, MSc EU Data and AI Policy Lead
    F. Hoffmann-La Roche Ltd, Switzerland
  • Adrian  Cassidy, PhD, MSc
    Adrian Cassidy, PhD, MSc Head Global Evidence Generation
    Novartis, Switzerland
  • Michael  Lees, MA
    Michael Lees, MA Chief Operating Officer and Head of Market Access Strategy
    PHMR Ltd, United Kingdom
  • Solène  Thieffry, MSc
    Solène Thieffry, MSc Global RWE Policy Lead
    UCB, Belgium
  • Emma  Du Four, MBA
    Emma Du Four, MBA Regulatory and R&D Policy Professional
    -, United Kingdom
  • Cécile Mathilde Ollivier, MS
    Cécile Mathilde Ollivier, MS Managing Director Europe
    Critical Path Institute, Netherlands

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