ASK JEAN Column: Direct access to source data and documents

17 January 2023

Question: Do investigators and institutions have to provide direct access to source data and documents related to a clinical trial monitoring, REB review, audits, and regulatory inspection?

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Regulatory Highlights: Winter 2023

17 January 2023

Consultation has re-opened for the proposed agile regulations and guidance for licensing drugs and medical devices in Canada.

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Quality Leadership Course open for applications

16 January 2023

This virtual course is designed for quality associates or equivalent persons in BC that are involved in quality initiatives, oversight, and the implementation of Quality Management System (QMS).

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