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661 University Avenue, Suite 460 MaRS Centre, West Tower Toronto, Ontario M5G 1M1 Canada www.ctontario.caSRERS Administration University of Ottawa Heart Institute Reminder: Institutional Research
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01
Visit the official Clinical Trials Ontario (CTO) website.
02
Create an account or log in if you already have one.
03
Select the appropriate trial types (e.g., interventional, observational).
04
Fill out the required fields including trial title, description, and objectives.
05
Provide details about the eligibility criteria for participants.
06
Include information on study locations and principal investigators.
07
Attach necessary documents such as IRB approvals and informed consent forms.
08
Review and verify all entered information for accuracy.
09
Submit the application through the portal.
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Monitor the application status and respond to any queries from CTO.

Who needs clinical trials ontario cto?

01
Researchers looking to conduct clinical trials in Ontario.
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Pharmaceutical and biotech companies seeking to test new medications.
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Healthcare institutions wanting to participate in clinical research.
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Patients who wish to enroll in clinical trials for new treatments.
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Regulatory agencies needing oversight and management of clinical trials.
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Clinical Trials Ontario (CTO) is a not-for-profit organization that facilitates the conduct of clinical trials in Ontario by providing a streamlined process, resources, and support for researchers and sponsors.
Sponsors of clinical trials conducted in Ontario are required to file with Clinical Trials Ontario.
To fill out the Clinical Trials Ontario filing, sponsors must provide detailed information about the clinical trial, including the study design, purpose, eligibility criteria, and consent process, using the provided online application platform.
The purpose of Clinical Trials Ontario is to promote the efficient conduct of clinical trials, enhance collaboration among stakeholders, and improve the quality of research in Ontario.
Required information includes trial title, objectives, methodology, study sites, investigator qualifications, participant eligibility criteria, and safety assessment protocols.
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