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Specimen Receiving, Processing and Accessioning CLINICAL PATHOLOGY: SPECIMEN RECEIVING AREAS The Specimen Receiving Area is located at the CUTS in the Clinical Support Center on the 6th floor for
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Step 1: Start by clearly labeling the specimen container with the patient's name, date of collection, and any other required information.
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Step 2: Ensure that the submitted specimen matches the requisition form and that all necessary information is provided.
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Step 3: Review the specimen for any visible abnormalities, such as clots, hemolysis, or improper collection.
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Step 4: Document the receipt of the specimen in the laboratory information system (LIS) or any other designated tracking system.
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Step 5: Perform any required pre-analytical processing on the specimen, such as centrifugation, aliquoting, or preservation.
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Step 6: Store the specimen according to the specific storage requirements, ensuring proper temperature and conditions.
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Step 7: Communicate any issues or discrepancies with the submitting healthcare provider or ordering physician as necessary.
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Step 8: Maintain accurate records of all specimen receiving and processing activities for traceability and quality assurance purposes.

Who needs specimen receiving processing and?

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Clinical laboratories
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Medical research institutions
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Hospitals and healthcare facilities
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Pharmaceutical companies
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Forensic laboratories
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Biotechnology companies
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Diagnostic testing facilities
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Public health agencies
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Genetic testing laboratories
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Specimen receiving processing and involves the procedures for accepting and documenting incoming samples or specimens.
Laboratory staff or technicians are typically responsible for filing specimen receiving processing and.
Specimen receiving processing and is typically filled out by recording information such as specimen type, quantity, date and time received, and source.
The purpose of specimen receiving processing and is to ensure accurate and timely recording of incoming samples for further analysis.
Information such as specimen type, quantity, date and time received, and source must be reported on specimen receiving processing and.
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