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Healthcare SingaporeClinical TrialsClinical trials are regulated by the Health Products Regulations Group of the Health Sciences Authority of Singapore. All clinical trials on medicinal products conducted
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Clinical trials are regulated to ensure the safety and efficacy of new treatments before they are approved for use in patients.
Any organization or individual conducting a clinical trial is required to file with the appropriate regulatory authorities.
Clinical trial sponsors must submit detailed protocols, informed consent documents, and information on the study design, endpoints, and statistical analysis plans.
The purpose of regulating clinical trials is to protect the rights and welfare of trial participants, ensure the integrity of the data, and assess the risks and benefits of new treatments.
Information on the study design, participant eligibility criteria, intervention details, data collection and analysis plans, adverse event reporting procedures, and ethical considerations must be reported on clinical trials.
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