Hilton Lac-Leamy

2025 年 10 月 27 日 7:30 上午 - 2025 年 10 月 28 日 4:00 下午

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

Canada Annual Meeting

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

Abstract Submission Deadline

03

DAYS

06

HOURS

31

MINUTES

31

SECONDS

概览

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.

While we develop our 2025 agenda, please take a moment to review the 2024 final agenda.

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.

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Highlights & Features

谁应该参加?

  • Meeting Designed For:

    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

项目委员会

  • 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 Director, Clinical Operations
    Abcellera, Canada
  • Nadiya  Jirova, MSc
    Nadiya Jirova, MSc Manager, Bureau of Biologics, Radiopharmaceuticals and Self-Care Products
    Health Canada, 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 VP & Head, Regulatory Affairs
    Bayer Inc. Canada, Canada

Digital Learning Catalog

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