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Template Version Date: November 2022PROTOCOL TEMPLATE CLINICAL TRIALSThis protocol template is intended for research projects that are considered clinical trials. A clinical trial is defined as \”
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How to fill out wch-protocol-template-secondary-use-or-retrospective- template

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How to fill out wch-protocol-template-secondary-use-or-retrospective

01
Begin by opening the WCH Protocol Template for Secondary Use or Retrospective.
02
Fill out the required sections such as study title, principal investigator, study objectives, data sources, inclusion/exclusion criteria, and data analysis plan.
03
Provide details on how the data will be collected, stored, and accessed for secondary use or retrospective purposes.
04
Include any additional information or documentation required by the institution or ethics committee.
05
Review the completed template for accuracy and completeness before submission.

Who needs wch-protocol-template-secondary-use-or-retrospective?

01
Researchers or investigators who are planning to conduct secondary use or retrospective studies using existing data sources.
02
Institutions or ethics committees that require a standardized protocol template for approving secondary use or retrospective studies.

What is WCH-Protocol-Template-Secondary-Use-or-Retrospective- ... Form?

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The wch-protocol-template-secondary-use-or-retrospective is a form used to document secondary use or retrospective studies in the context of research protocols.
Researchers and institutions conducting secondary use or retrospective studies are required to file the wch-protocol-template-secondary-use-or-retrospective form.
The form should be filled out with accurate and detailed information regarding the secondary use or retrospective study, including research objectives, study design, data sources, and ethical considerations.
The purpose of the form is to ensure transparency and compliance with ethical and legal standards in secondary use or retrospective research studies.
Information such as research objectives, study design, data sources, participant consent procedures, and data handling processes must be reported on the form.
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