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Canada PHSA Laboratories Normal Quality Control Record Sheet 2017 free printable template

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PSA Laboratories CW Site Point of Care Title: CPC UDP 0115 Urine Dipstick Emergency Dept Form B1 Normal Quality Control Record Sheltering Dipstick Emergency Dept: Form B1 Normal Quality Control Record
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How to fill out Canada PHSA Laboratories Normal Quality Control Record

01
Begin with the title of the form at the top, ensuring it reads 'Normal Quality Control Record'.
02
Fill in the date of the quality control check.
03
Enter the name of the laboratory performing the quality control checks.
04
Document the specific tests being performed in the corresponding section.
05
Record the results of the quality control tests, making sure to include both positive and negative controls where applicable.
06
Indicate any deviations from the expected results, along with explanations as to why they occurred.
07
Include the name and signature of the technician or personnel conducting the quality control.
08
Make a note of any actions taken in response to the results, if necessary.
09
Ensure that all entries are legible and accurate before submitting the form.

Who needs Canada PHSA Laboratories Normal Quality Control Record?

01
Laboratory personnel involved in quality control processes.
02
Quality assurance teams overseeing laboratory compliance and standards.
03
Regulatory bodies that require documentation of laboratory procedures.
04
Accreditation agencies that assess laboratory practices and quality management.
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Canada PHSA Laboratories Normal Quality Control Record is a document used to track and verify the quality control processes and results within laboratories, ensuring compliance with standard operating procedures and regulatory requirements.
Laboratory personnel and quality control managers are required to file the Canada PHSA Laboratories Normal Quality Control Record to ensure that all quality control activities are documented and reviewed.
To fill out the Canada PHSA Laboratories Normal Quality Control Record, users should provide details such as the date, time of testing, parameters analyzed, control results, and any deviations or corrective actions taken.
The purpose of the Canada PHSA Laboratories Normal Quality Control Record is to maintain a documented record of quality control activities, identify trends, facilitate compliance, and support accreditation and audit processes.
The information that must be reported includes the date of testing, type of test, control data, result outcomes, reference ranges, any issues encountered, corrective actions taken, and the name of the individual completing the record.
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