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661 University Avenue, Suite 460
MaRS Center, West Tower
Toronto, Ontario
M5G 1M1 Canada
www.ctontario.caSRERS Administration
Sunny brook Health Sciences Center
Reminder: Institutional Research Administration
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Clinical Trials Ontario is a regulatory framework and process established to facilitate the conduct of clinical trials in Ontario, Canada, ensuring adherence to ethical standards and supporting patient safety.
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Researchers, sponsors, or institutions conducting clinical trials in Ontario are required to file clinical trials Ontario in.
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To fill out clinical trials Ontario in, one must complete the designated application forms provided by the provincial regulatory body, ensuring all required information and documentation is accurately submitted.
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The purpose of clinical trials Ontario in is to ensure that clinical trials are conducted safely, ethically, and in compliance with regulatory standards, while promoting transparency and accountability.
What information must be reported on clinical trials ontario in?
Information required for reporting includes trial protocol details, participant recruitment strategies, informed consent processes, safety monitoring plans, and any adverse events.
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