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661 University Avenue, Suite 460 MaRS Centre, West Tower Toronto, Ontario M5G 1M1 Canada www.ctontario.caDocumented Institutional Ethics Requirements Hamilton Health Sciences Corporation Privacy Policy
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Step 1: Visit the Clinical Trials Ontario website.
02
Step 2: Create an account if you don't already have one.
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Step 3: Login to your account.
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Step 4: Fill out the required information about the clinical trial you are conducting, such as the study title, objectives, methodology, and participant criteria.
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Step 5: Provide any additional details or documents requested by the application form.
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Step 6: Review and verify all the information you have entered.
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Step 7: Submit your completed application.
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Step 8: Wait for the application to be reviewed and approved.
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Step 9: Once approved, you will receive further instructions from Clinical Trials Ontario on how to proceed.

Who needs clinical trials ontario?

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Clinical Trials Ontario is needed by researchers, healthcare professionals, and organizations that are conducting clinical trials.
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It is also necessary for individuals or groups who wish to participate in clinical trials as participants.
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Clinical Trials Ontario helps facilitate the recruitment and management of participants, as well as ensure ethical standards are met in the conduct of clinical trials.
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Clinical Trials Ontario (CTO) is an organization that aims to streamline the process of conducting clinical trials in Ontario by providing support, resources, and a framework to facilitate the efficient conduct of these trials.
Sponsors or organizations conducting clinical trials, including pharmaceutical companies, biotechnology firms, and research institutions, are required to file clinical trials in Ontario.
To fill out a clinical trial application in Ontario, sponsors must complete the designated application form, providing comprehensive details about the trial, including objectives, methodology, eligibility criteria, and any other required documentation as outlined by Clinical Trials Ontario.
The purpose of Clinical Trials Ontario is to enhance the efficiency and effectiveness of clinical trials in the province, ensure compliance with regulatory standards, promote best practices, and ultimately improve patient access to innovative treatments.
Information that must be reported includes the trial's title, objectives, design, methodology, ethical considerations, participant eligibility criteria, study duration, and any potential risks associated with the trial.
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