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Hilton Lac-Leamy

Oct 27, 2025 7:30 AM - Oct 28, 2025 3:40 PM

3 Boulevard du Casino, Gatineau, QC J8Y 6X4, Canada

Canada Annual Meeting

The Canada Annual Meeting offers three tracks, Regulatory, Clinical, Safety and Pharmacovigilance!

Overview

Short Course: October 22 | Virtual

Meeting: October 27-28 | In-Person

The DIA Canada Annual Meeting will provide an in-depth exploration of the current pharmaceutical, medical device, and diagnostic landscapes in Canada, emphasizing Canada’s pivotal role in global healthcare product development. Offering three specialized tracks on Regulatory, Clinical, and Safety and Pharmacovigilance, the meeting will cover topics spanning from Health Canada’s latest regulatory initiatives, international collaboration, and innovative clinical practices to approaches that harness AI in drug safety and increase representation from equity-denied groups.

Attendees will have the opportunity to engage with leaders and experts from academia, regulatory bodies, and the pharmaceutical and medical device industries by gaining insights into best practices, lessons learned, and strategies to address the challenges facing stakeholders in Canada.

Participant Testimonials

Very meaningful topics, excellent speakers which allowed meaningful conversations. Size of the event also facilitates networking. - Véronique Lafrance, Senior Project Manager, Regulatory Affairs, Organon Canada

Amazing opportunity to meet PV and regulatory professionals from across Canada, learn about the challenges they face locally and in collaboration with their global affiliates. We enjoy being there every year! - Zenith PV – Exhibitor

The meeting presented a valuable learning opportunity, as we gained insights into best practices from different companies and heard the regulatory agency perspective. In addition to the professional development, DIA Canada 2024 provided an excellent networking platform to connect with peers and colleagues from across the industry and regulatory sphere. I really encourage others to join DIA's events and meetings in the future. - Vanessa Zapata, Associate Director, Regional Pharmacovigilance Officer, Merck Canada Inc.

Featured

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Continuing Education

Exhibits

Highlights & Features

Who should attend?

  • Join professionals interested in a comprehensive overview of the current biopharma pharmaceutical, medical device, and/or diagnostics landscape in Canada:

    • Pharmacovigilance and Drug Safety
    • Risk Management
    • Clinical Research, Management, and Operations
    • Regulatory Affairs and Operations
    • Medical Affairs and Scientific Communication
    • Quality Assurance
    • Life Sciences R&D
    • Project Management
    • Real-World Data and Real-World Evidence
    • Data Management

Learning objectives

  • At the conclusion of this meeting, participants should be able to:

    • Describe Health Canada’s evolving regulatory priorities and their role in advancing global collaboration and public health
    • Recognize trends in clinical research modernization, including patient engagement, trial accessibility, and innovative study approaches
    • Identify current and emerging frameworks in safety and pharmacovigilance that support compliance, data quality, and patient protection
    • Assess the impact of international and multi-stakeholder collaboration on regulatory innovation, clinical trials, and patient access
    • Discuss the role of technology and digital transformation (e.g., AI, automation, data-driven submissions) in shaping the future of regulatory affairs, safety, and clinical development
    • Explore strategies for workforce and professional development to strengthen Canada’s position in the global research and regulatory ecosystem

Short Course or Primer

To keep you at the forefront.

Oct 22, 2025

Short Course:

Tools and Methods to Evaluate the Effectiveness of Risk Minimization Measures

Program Committee

  • Melanie  Cote, MS
    Melanie Cote, MS Senior Manager, Global Regulatory Affairs
    Otsuka Pharmaceutical Development & Commercialization Inc., Canada
  • Marie-France  Goyer, MSc
    Marie-France Goyer, MSc Senior Director, Clinical Operations
    Abcellera, Canada
  • Nadia  Latif, MS
    Nadia Latif, MS Senior Manager, Pharmacovigilance
    Ipsen Biopharmaceuticals Canada Inc., Canada
  • Hocine  Abid, MD, MBA
    Hocine Abid, MD, MBA National Manager, Regulatory Operations and Enforcement Branch
    Health Canada, Canada
  • Stephanie  Anderson, MS
    Stephanie Anderson, MS Associate Director, Regulatory Affairs
    Intrinsik Corp., Canada
  • Rebecca  Barnes, MS
    Rebecca Barnes, MS Executive Director
    Network of Networks (N2), Canada
  • Katalin  Bertenyi, MSc
    Katalin Bertenyi, MSc Manager, Centre for Blood, Blood Products and Biotherapeutics
    Health Canada, Canada
  • Louise  Blythe, MSc
    Louise Blythe, MSc Head, Regulatory Affairs
    Bayer Inc. Canada, Canada
  • Anna  Bussel, MPharm
    Anna Bussel, MPharm Vice President Pharmacovigilance and Medical Information
    ClaroPV Services Inc, Canada
  • My  Dang, MBA
    My Dang, MBA Director, Regulatory Affairs
    Cencora, Canada
  • Tharany  Ganesh, MSc
    Tharany Ganesh, MSc Head, Regulatory Affairs
    AstraZeneca Canada Inc., Canada
  • Daniel  Greco, PharmD, MS, RPh
    Daniel Greco, PharmD, MS, RPh Associate Director of Patient Safety
    Bristol-Myers Squibb Company, Canada
  • Yatika  Kohli, PhD, MBA
    Yatika Kohli, PhD, MBA Chief Compliance and Strategy Officer
    NoNO Inc, Canada
  • Mei  Lam, BSN, RN
    Mei Lam, BSN, RN Associate Director Consumer Safety Regions Americas
    Haleon, Canada
  • Randy  Levitt, PhD
    Randy Levitt, PhD Director, Pharmacovigilance, Medical Information and Patient Support
    Knight Therapeutics Inc., Canada
  • Kim  McDonald-Taylor, MS, MSc
    Kim McDonald-Taylor, MS, MSc Clinical Research Consultant
    Clinical Research Association of Canada Inc., Canada
  • Amber  McLeod, PhD
    Amber McLeod, PhD Immunology, Virology, and Specialty Head, Regulatory Affairs
    Abbvie Corporation, Canada
  • Ricardo  Pasquel Cook, MD
    Ricardo Pasquel Cook, MD Safety Team Lead
    Pfizer Inc., Canada
  • Sabrina  Ramkellawan
    Sabrina Ramkellawan President and Board Director
    Clinical Research Association of Canada, Canada
  • Marcia  Sam
    Marcia Sam Senior Manager, Regulatory Affairs
    Regeneron Canada Company, Canada
  • Yulia  Vasianovich, PhD, RAC
    Yulia Vasianovich, PhD, RAC Scientific Evaluator, Marketed Health Products Directorate
    Health Canada, Canada

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