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CANADIAN CLINICAL TRIAL DATA LINKAGE SURVEY, Hay et al. ORIGINAL ARTICLELinkage of clinical trial and administrative data: a survey of cancer patient preferences A.E. Hay MB CHB, * Y.W. Lung MSC,
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To fill out the linkage of clinical trial, follow these steps:
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Begin by gathering all relevant information about the clinical trial.
03
Identify any previous linkage or related studies that have been conducted.
04
Determine the purpose of the linkage and what specific data needs to be collected.
05
Create a detailed plan outlining the methodology and data collection process.
06
Collect the necessary data from the clinical trial participants or relevant sources.
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Organize and analyze the collected data to identify any patterns or correlations.
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Interpret the findings and draw conclusions based on the data analysis.
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Prepare a report summarizing the linkage of the clinical trial and its findings.
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Review the report and make any necessary revisions or improvements.
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Present the findings to relevant stakeholders or publish the results in appropriate journals or publications.

Who needs linkage of clinical trial?

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Various individuals and organizations may need the linkage of clinical trial, including:
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- Researchers and scientists conducting the clinical trial
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- Patients and patient advocacy groups
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- Academic institutions and universities
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- Policy makers and health economists
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- Public health organizations and agencies
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Linkage of clinical trial is a form that connects the clinical trial to the corresponding regulatory approval.
The sponsor of the clinical trial is required to file the linkage of clinical trial.
The linkage of clinical trial can be filled out online through the regulatory authority's portal or submitted via mail, following the specific instructions provided.
The purpose of linkage of clinical trial is to ensure transparency and traceability between the clinical trial and its regulatory approval, allowing for monitoring and oversight.
The linkage of clinical trial typically requires information such as the unique identifier of the clinical trial, the regulatory approval number, and the product information.
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