Canada Annual Meeting

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

Abstract Submission Deadline

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Highlights & Features

What is happening at Canada Annual Meeting

Need Approval in Order to Attend?

Download and fill out our Justification Letter to demonstrate to your supervisor why this is a must-attend event.

Event Goals and Offerings

Canada Annual Meeting Call for Abstracts

Are you a professional involved in the regulatory, clinical or safety and pharmacovigilance functional areas within a company or organization working on pharmaceuticals, drugs, medical devices, and/or diagnostics in Canada? If so, DIA wants to hear from you!

Submission Guidelines

Submit Abstract

Three Educational Tracks: Regulatory, Clinical, Safety and Pharmacovigilance

Track A: 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.

Track B: 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.

Track C: Safety and Pharmacovigilance

Our safety and 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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