At SNI, our clinical trials team is experienced in securing ethics approval from trusted and accredited Institutional Review Boards (IRBs) for our clients in a timely, streamlined manner that prioritizes your desired study timelines.
Ensure your trial checks all the necessary regulatory boxes before research begins
Regardless of the product type being studied, any investigator or sponsor conducting a clinical trial in Canada must obtain ethics approval prior to carrying out the study. The IRB ethics review process includes a scientific review of the research protocol, as well as a review of the submitted application form and all required supporting documents.
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.
Ready to take your product to the next stage of development?
Book a consultation with our clinical research team to discuss your study objectives, product claims of interest, and evidence generation strategy. Our experts will guide you through every step, from protocol design to data analysis, ensuring your trial meets standards for safety, efficacy, and compliance.
Contact us today to talk to a member of our team!