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Get the free Clinical trial registry Authorship Cri - OAE Publishing Inc.

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Instructions to the Authors The Editorial Process Clinical trial registry Authorship Criteria Contribution Details Conflicts of Interest/ Competing Interests Submission of Manuscripts Preparation
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How to fill out clinical trial registry authorship

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How to fill out clinical trial registry authorship

01
To fill out the clinical trial registry authorship, follow these steps:
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Begin by providing the necessary identifying information, such as the title of the trial, a unique trial identification number, and the date of registration.
03
Include the names of all authors involved in the trial. Make sure to list them in the correct order according to their contributions.
04
Clearly indicate the affiliations of each author, including their institutions or organizations.
05
Specify the corresponding author, who will be responsible for communication regarding the trial.
06
Provide an email address or contact information for the corresponding author.
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Include any acknowledgments or disclosures necessary for the authorship.
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Finally, review the information entered and ensure its accuracy before submitting the registration.

Who needs clinical trial registry authorship?

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Clinical trial registry authorship is needed by individuals or research teams conducting clinical trials. It ensures transparency and accountability by identifying and acknowledging the researchers involved in the study. Additionally, it allows other researchers and the general public to evaluate the validity and credibility of the trial results.
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Clinical trial registry authorship refers to the identification of individuals or organizations responsible for the design, conduct, and overall management of a clinical trial, as recorded in a publicly accessible registry.
Researchers, sponsors, or organizations conducting clinical trials are required to file clinical trial registry authorship to comply with regulatory requirements.
To fill out clinical trial registry authorship, one should provide details about the trial's responsible parties, including names, affiliations, roles, and contact information, in accordance with the specifications of the registry being used.
The purpose of clinical trial registry authorship is to promote transparency, accountability, and integrity in clinical research by providing a clear record of who is responsible for the trial.
Information that must be reported includes the names of authors, affiliations, roles in the trial, and any relevant disclosures related to conflicts of interest.
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