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Ottawa Conference and Event Centre

Nov 07, 2023 7:30 AM - Nov 08, 2023 4:10 PM

200 Coventry Road, Ottawa, ON K1K 4S3, Canada

Canada Annual Meeting

The Canada Annual Meeting offers Three Tracks, Regulatory, Clinical, Pharmacovigilance!

Highlights & Features

What is happening at Canada Annual Meeting

  • Three tracks: Regulatory, Clinical, and Pharmacovigilance,
  • Exhibit Hall with 40+ exhibiting companies
  • DIA Mobile App - receive all need to know information, build your agenda, and network with attendees

Event Goals and Offerings

  • Discuss policy updates and priorities shared directly from Health Canada
  • Stay up to date with emerging trends and technologies effecting life sciences professionals in Canada
  • Establish and foster relationships with life sciences professionals in Canada
  • Gain additional insights, education, and knowledge to analyze relevant challenges and opportunities for life sciences professionals in Canada

Why You Can't Miss it

  • Discussions on policy updates and priorities shared directly from Health Canada
  • Updates on emerging trends and tech impacting professionals like you across Canada
  • Opportunity to establish and foster relationships with like-minded global professionals

Tracks

Regulatory

The regulatory track provides opportunities for information sharing, use cases, and best practices relating to Canada’s regulatory landscape as it applies to regulatory requirements, new developments, and innovation for life sciences R&D.


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Clinical

Today, modern pharmaceutical, medical device, and diagnostic products are advancing at an unprecedented speed. Sessions in this track will focus on clinical research development and operations for industry. Those interested in this track will gain an understanding of Health Canada’s approach to the modernization of clinical trial regulations and gain further perspectives from patients and those in the life sciences R&D industry.


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Pharmacovigilance

Our pharmacovigilance track will provide a comprehensive overview of Canada’s regulatory environment in the field of clinical safety and pharmacovigilance for pharmaceutical products and medical devices.


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