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IRB & Regulatory Approvals

Ensure your trial checks all the necessary regulatory boxes before research begins

Regardless of the product type being studied, any investigator or sponsor who is looking to conduct a clinical trial in Canada must obtain ethics approval from a trusted and accredited Institutional Review Board (IRB) prior to carrying out the clinical trial.

The IRB ethics review process typically includes a scientific review of the research protocol, and completion of an application form with required supporting documents.

At SNI, our clinical trials team is experienced in securing ethics approval for our clients in a timely, streamlined manner that prioritizes your desired study timelines.

We have strong working relationships with the IRB and other Canadian regulatory bodies for each product type, making the submission process and continued ethics review simple and efficient.

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