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Department of Clinical Laboratory Genetics Genome Diagnostics & Cancer Cytogenetics Somatic Testing Toronto General Hospital Eaton Wing 11444, 200 Elizabeth Street Toronto, Ontario M5G 2C4 Head: Tracy
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01
Start by gathering the necessary information such as patient details, specimen type, and clinical history.
02
Ensure that the requisition form is properly labeled with relevant patient and laboratory identifiers.
03
Specify the tests to be performed by indicating the required panels, markers, or antibodies.
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Provide clear instructions on any special requirements or additional tests that need to be performed.
05
Complete the billing and insurance information accurately, including any necessary authorizations.
06
Obtain the appropriate signatures and date the requisition form.
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Double-check all the information to ensure accuracy and completeness.
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Submit the filled-out requisition form to the flow cytometry department as per the specified procedure.

Who needs flow cytometry requisition department?

01
Flow cytometry requisition department is needed by healthcare professionals, such as doctors, researchers, and laboratory technicians who require flow cytometry testing for diagnostic, research, or monitoring purposes.
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Institutions and organizations involved in medical or scientific studies may also utilize the flow cytometry requisition department.
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The flow cytometry requisition department is a specialized department responsible for processing and managing requests related to flow cytometry analysis, which is a technique used to measure the characteristics of cells or particles in a fluid using lasers.
Clinicians, researchers, or laboratory personnel who need flow cytometry services for their samples are required to file with the flow cytometry requisition department.
To fill out a flow cytometry requisition, one typically needs to provide patient information, clinical history, specific tests required, sample type, and any additional details relevant to the analysis.
The purpose of the flow cytometry requisition department is to ensure that samples are accurately processed and analyzed, facilitating the correct interpretation of results for clinical or research purposes.
Information that must be reported includes patient identification, sample type, specific tests requested, date of sample collection, and relevant clinical details.
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