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One Farrer Hotel

Jul 15, 2025 8:30 AM - Jul 16, 2025 5:30 PM

1 Farrer Park Station Road, Singapore 217562, Singapore

DIA Singapore Annual Meeting 2025

Charting the Future: Navigating the Evolving Healthcare Landscape and Trends in Asia

Overview

Charting the Future: Navigating the Evolving Healthcare Landscape and Trends in Asia: Drug development and healthcare innovation in Asia are being rapidly reshaped by advancements in digital technologies (e.g., artificial intelligence [AI], cloud platforms), changing regulatory guidelines, and innovative clinical trial methodologies. These transformations are accelerating drug development, streamlining regulatory review processes, and enhancing patient engagement. To harness the full potential of these emerging opportunities and foster a dynamic and robust regulatory and clinical trial ecosystem, close collaborations among regulators, academia, patients, and industry are necessary. The DIA Singapore Annual Meeting 2025 invites all stakeholders to share and review the evolving healthcare landscape challenges faced and lessons learned, and to identify future trends in the clinical research and regulatory environment in Asia. Join us at DIA Singapore 2025 to navigate these transformative changes and shape the future of healthcare in Asia.

Click Here to View the Flyer

Featured topics

  • Role of AI and digital toolsin clinical trials, regulatory affairs and pharmacovigilance
  • Optimizing the implementation of regulatry pathway
  • Real-World Data (RWD) and digital innovations to enhance regulatory decision-making
  • Multi-Regional Clinical Trials and simultaneous global drug developmet
  • Decentralized Clinical Trials (DCT) and AI implementation in clinical trials

Learning objectives

Participants will enhance their understanding of key global regulatory developments from recent years, aiding in anticipating future changes and their impact in Asia, while broadening their perspectives.

This knowledge can be applied within their organizations to inform strategies for clinical development and regulatory submissions.

 

Program Committee

  • Finny  Liu, MSc, RPh
    Finny Liu, MSc, RPh APAC Regional Regulatory Policy Lead
    Roche, Singapore
  • Helene  Sou, MSc, RAC
    Helene Sou, MSc, RAC Global Regulatory Policy and Innovation
    Takeda Pharmaceutical Company Limited., Singapore
  • Sandy  Chan
    Sandy Chan Associate Director, Regulatory Policy & Intelligence Lead- Asia Pacific
    Johnson & Johnson, Singapore
  • Martin  Lim, MBA, MS
    Martin Lim, MBA, MS Co-Founder and CEO
    ONWARD Health Research, Singapore
  • Thean Soo  Lo
    Thean Soo Lo Regulatory Affairs Management Consultant
    TS Consulting, Singapore
  • Edana  Loke
    Edana Loke Director, JAPAC Regulatory Policy and Intelligence
    AbbVie Pte Ltd, Singapore, Singapore
  • Karin  Markgraf
    Karin Markgraf Head of Regulatory Affairs Asia Pacific
    Merck Healthcare, Singapore
  • Audrey  Ooi, MSc
    Audrey Ooi, MSc Head- Business Development
    Clinical Research Malaysia, Malaysia
  • Hueybee  Pey
    Hueybee Pey Senior Director, Project Leadership
    Parexel, Singapore
  • Young Joo  Park, PhD, MPH
    Young Joo Park, PhD, MPH VP, Korea, Singapore, and Southeast Asia
    DIA, Korea, Republic of
  • Jing Ping  Yeo, PhD, MBA
    Jing Ping Yeo, PhD, MBA Vice President, Clinical Operations & Head, Asia Pacific Precision for Medicine
    Precision for Medicine, Singapore
  • Jack  Wong
    Jack Wong Founder
    ARPA (Asia Regulatory Professionals Association) , Singapore
  • Kum Cheun  Wong, PharmD
    Kum Cheun Wong, PharmD Head Asia Pacific Regulatory & Development Policy
    Novartis Asia Pacific Pharmaceuticals Pte. Ltd., Singapore
  • Shun  Jin, MBA
    Shun Jin, MBA Head – BD & RA
    PharmaGend Global Medical Services Pte Ltd, Singapore

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