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Instructions to the AuthorsThe Editorial Process|Clinical Trial Registry|Authorship Criteria| Contribution Details| Conflicts of Interest/ Competing Interests|Submission of Manuscripts|Preparation
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The Clinical Ink eSource Platform is a digital solution used in clinical trials to capture, manage, and analyze data electronically, enhancing the efficiency and accuracy of clinical data collection.
Typically, clinical trial sponsors, investigators, and sites involved in conducting clinical research are required to utilize and file data through the Clinical Ink eSource Platform.
To fill out the Clinical Ink eSource Platform, users need to log in to the platform, navigate to the relevant clinical trial, and enter the required data following the established protocols and guidelines provided within the system.
The purpose of the Clinical Ink eSource Platform is to streamline the clinical trial process by allowing real-time data capture, ensuring data integrity, and facilitating better compliance with regulatory requirements.
Information that must be reported includes patient demographics, clinical findings, adverse events, study outcomes, and any other trial-specific data as required by the regulatory authorities.
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