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International Standards for Clinical Trial Registries The registration of all interventional trials is a scientific, ethical and moral responsibility WHO Library CataloguinginPublication Data International
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International standards for clinical refer to a set of guidelines and protocols that aim to ensure the safety, quality, and consistency of clinical trials conducted around the world.
Any organization or individual involved in conducting clinical trials on an international scale is required to adhere to and file international standards for clinical.
To fill out international standards for clinical, organizations must follow the guidelines provided by the International Conference on Harmonisation (ICH) and other regulatory bodies.
The purpose of international standards for clinical is to protect the rights, safety, and well-being of clinical trial participants, ensure the credibility of trial results, and harmonize regulatory requirements across different countries.
Information that must be reported on international standards for clinical includes study protocols, informed consent forms, data collection forms, adverse event reports, and study results.
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